Publications
Below is a partial list of the publications where MAF has contributed. The publication list has mainly been compiled by MAF staff and may contain errors as well as most likely there are other published papers that we are unaware of.
2021
Krebs, G., D. Mataix-Cols, F. Rijsdijk, C. Rück, P. Lichtenstein, S. Lundström, H. Larsson, T. C. Eley and L. Fernández de la Cruz (2021). ”Concurrent and prospective associations of obsessive-compulsive symptoms with suicidality in young adults: A genetically-informative study.” J Affect Disord 281: 422-430.
2020
Esberg, A., S. Haworth, R. Kuja-Halkola, P. K. E. Magnusson and I. Johansson (2020). ”Heritability of Oral Microbiota and Immune Responses to Oral Bacteria.” Microorganisms 8(8).
Jacobson, P., M. Peltonen, P. A. Svensson, M. Taube, J. C. Andersson-Assarsson, K. Sjoholm, C. Bouchard, B. Carlsson and L. M. S. Carlsson (2020). ”9p21.3 Coronary Artery Disease Locus Identifies Patients With Treatment Benefit From Bariatric Surgery in the Nonrandomized Prospective Controlled Swedish Obese Subjects Study.” Circ Genom Precis Med 13(5): 460-465.
Johansson, V., S. Erhardt, G. Engberg, M. Kegel, M. Bhat, L. Schwieler, K. Blennow, H. Zetterberg, T. D. Cannon, L. Wetterberg, C. M. Hultman and M. Landén (2020). ”Twin study shows association between monocyte chemoattractant protein-1 and kynurenic acid in cerebrospinal fluid.” Eur Arch Psychiatry Clin Neurosci 270(7): 933-938.
Kere, M., O. Gruzieva, V. Ullemar, C. Söderhäll, D. Greco, I. Kull, A. Bergström, G. Pershagen, C. Almqvist and E. Melén (2020). ”Effects of inhaled corticosteroids on DNA methylation in peripheral blood cells in children with asthma.” Allergy 75(3): 688-691.
Kerekes, N., B. Zouini, E. Karlsson, E. Cederholm, P. Lichtenstein, H. Anckarsäter and M. Råstam (2020). ”Conduct disorder and somatic health in children: a nationwide genetically sensitive study.” BMC Psychiatry 20(1): 595.
Laan, L., J. Klar, M. Sobol, J. Hoeber, M. Shahsavani, M. Kele, A. Fatima, M. Zakaria, G. Annerén, A. Falk, J. Schuster and N. Dahl (2020). ”DNA methylation changes in Down syndrome derived neural iPSCs uncover co-dysregulation of ZNF and HOX3 families of transcription factors.” Clin Epigenetics 12(1): 9.
Laukka, E. J., Y. Köhncke, G. Papenberg, L. Fratiglioni and L. Bäckman (2020). ”Combined genetic influences on episodic memory decline in older adults without dementia.” Neuropsychology 34(6): 654-666.
Merid, S. K., A. Novoloaca, G. C. Sharp, L. K. Küpers, A. T. Kho, R. Roy, L. Gao, I. Annesi-Maesano, P. Jain, M. Plusquin, M. Kogevinas, C. Allard, F. O. Vehmeijer, N. Kazmi, L. A. Salas, F. I. Rezwan, H. Zhang, S. Sebert, D. Czamara, S. L. Rifas-Shiman, P. E. Melton, D. A. Lawlor, G. Pershagen, C. V. Breton, K. Huen, N. Baiz, L. Gagliardi, T. S. Nawrot, E. Corpeleijn, P. Perron, L. Duijts, E. A. Nohr, M. Bustamante, S. L. Ewart, W. Karmaus, S. Zhao, C. M. Page, Z. Herceg, M. R. Jarvelin, J. Lahti, A. A. Baccarelli, D. Anderson, P. Kachroo, C. L. Relton, A. Bergström, B. Eskenazi, M. H. Soomro, P. Vineis, H. Snieder, L. Bouchard, V. W. Jaddoe, T. I. A. Sørensen, M. Vrijheid, S. H. Arshad, J. W. Holloway, S. E. Håberg, P. Magnus, T. Dwyer, E. B. Binder, D. L. DeMeo, J. M. Vonk, J. Newnham, K. G. Tantisira, I. Kull, J. L. Wiemels, B. Heude, J. Sunyer, W. Nystad, M. C. Munthe-Kaas, K. Räikkönen, E. Oken, R. C. Huang, S. T. Weiss, J. M. Antó, J. Bousquet, A. Kumar, C. Söderhäll, C. Almqvist, A. Cardenas, O. Gruzieva, C. J. Xu, S. E. Reese, J. Kere, P. Brodin, O. Solomon, M. Wielscher, N. Holland, A. Ghantous, M. F. Hivert, J. F. Felix, G. H. Koppelman, S. J. London and E. Melén (2020). ”Epigenome-wide meta-analysis of blood DNA methylation in newborns and children identifies numerous loci related to gestational age.” Genome Med 12(1): 25.
Neufeld, J., A. Hagström, A. Van’t Westeinde, K. Lundin, É. Cauvet, C. Willfors, J. Isaksson, P. Lichtenstein and S. Bölte (2020). ”Global and local visual processing in autism – a co-twin-control study.” J Child Psychol Psychiatry 61(4): 470-479.
Piko, P., S. Fiatal, N. A. Werissa, B. B. Bekele, G. Racz, Z. Kosa, J. Sandor and R. Adany (2020). ”The Effect of Haplotypes in the CETP and LIPC Genes on the Triglycerides to HDL-C Ratio and Its Components in the Roma and Hungarian General Populations.” Genes (Basel) 11(1).
Soltész, B., P. Pikó, J. Sándor, Z. Kósa, R. Ádány and S. Fiatal (2020). ”The genetic risk for hypertension is lower among the Hungarian Roma population compared to the general population.” PLoS One 15(6): e0234547.
Van’t Westeinde, A., É. Cauvet, R. Toro, R. Kuja-Halkola, J. Neufeld, K. Mevel and S. Bölte (2020). ”Sex differences in brain structure: a twin study on restricted and repetitive behaviors in twin pairs with and without autism.” Mol Autism 11(1): 1.
von Walden, F., R. Fernandez-Gonzalo, J. Pingel, J. McCarthy, P. Stål and E. Pontén (2020). ”Epigenetic Marks at the Ribosomal DNA Promoter in Skeletal Muscle Are Negatively Associated With Degree of Impairment in Cerebral Palsy.” Front Pediatr 8: 236.
Vänskä, S., T. Luostarinen, I. Baussano, D. Apter, T. Eriksson, K. Natunen, P. Nieminen, J. Paavonen, V. N. Pimenoff, E. Pukkala, A. Söderlund-Strand, G. Dubin, G. Garnett, J. Dillner and M. Lehtinen (2020). ”Vaccination With Moderate Coverage Eradicates Oncogenic Human Papillomaviruses If a Gender-Neutral Strategy Is Applied.” J Infect Dis 222(6): 948-956.
2019
Dahlin, A. M., C. Wibom, U. Andersson, D. M. Hougaard, J. Bybjerg-Grauholm, I. Deltour, C. M. Hultman, A. K. Kähler, R. Karlsson, U. Hjalmars and B. Melin (2019). ”Genetic Variants in the 9p21.3 Locus Associated with Glioma Risk in Children, Adolescents, and Young Adults: A Case-Control Study.” Cancer Epidemiol Biomarkers Prev 28(7): 1252-1258.
Fiatal, S., P. Pikó, Z. Kósa, J. Sándor and R. Ádány (2019). ”Genetic profiling revealed an increased risk of venous thrombosis in the Hungarian Roma population.” Thromb Res 179: 37-44.
Gaertner, V. D., S. Michel, J. A. Curtin, V. Pulkkinen, N. Acevedo, C. Söderhäll, A. von Berg, A. Bufe, O. Laub, E. Rietschel, A. Heinzmann, B. Simma, C. Vogelberg, G. Pershagen, E. Melén, A. Simpson, A. Custovic, J. Kere and M. Kabesch (2019). ”Nocturnal asthma is affected by genetic interactions between RORA and NPSR1.” Pediatr Pulmonol 54(6): 847-857.
Gray, P., T. Luostarinen, S. Vänskä, T. Eriksson, C. Lagheden, I. Man, J. Palmroth, V. N. Pimenoff, A. Söderlund-Strand, J. Dillner and M. Lehtinen (2019). ”Occurrence of human papillomavirus (HPV) type replacement by sexual risk-taking behaviour group: Post-hoc analysis of a community randomized clinical trial up to 9 years after vaccination (IV).” Int J Cancer 145(3): 785-796.
Gruzieva, O., C. J. Xu, P. Yousefi, C. Relton, S. K. Merid, C. V. Breton, L. Gao, H. E. Volk, J. I. Feinberg, C. Ladd-Acosta, K. Bakulski, C. Auffray, N. Lemonnier, M. Plusquin, A. Ghantous, Z. Herceg, T. S. Nawrot, C. Pizzi, L. Richiardi, F. Rusconi, P. Vineis, M. Kogevinas, J. F. Felix, L. Duijts, H. T. den Dekker, V. W. V. Jaddoe, J. L. Ruiz, M. Bustamante, J. M. Antó, J. Sunyer, M. Vrijheid, K. B. Gutzkow, R. Grazuleviciene, C. Hernandez-Ferrer, I. Annesi-Maesano, J. Lepeule, J. Bousquet, A. Bergström, I. Kull, C. Söderhäll, J. Kere, U. Gehring, B. Brunekreef, A. C. Just, R. J. Wright, C. Peng, D. R. Gold, I. Kloog, D. L. DeMeo, G. Pershagen, G. H. Koppelman, S. J. London, A. A. Baccarelli and E. Melén (2019). ”Prenatal Particulate Air Pollution and DNA Methylation in Newborns: An Epigenome-Wide Meta-Analysis.” Environ Health Perspect 127(5): 57012.
Gruzieva, O., S. K. Merid, S. Chen, N. Mukherjee, A. M. Hedman, C. Almqvist, E. Andolf, Y. Jiang, J. Kere, A. Scheynius, C. Söderhäll, V. Ullemar, W. Karmaus, E. Melén, S. H. Arshad and G. Pershagen (2019). ”DNA Methylation Trajectories During Pregnancy.” Epigenet Insights 12: 2516865719867090.
Isaksson, J., A. Van’t Westeinde, É. Cauvet, R. Kuja-Halkola, K. Lundin, J. Neufeld, C. Willfors and S. Bölte (2019). ”Social Cognition in Autism and Other Neurodevelopmental Disorders: A Co-twin Control Study.” J Autism Dev Disord 49(7): 2838-2848.
Johansson, V., C. M. Hultman, I. Kizling, L. Martinsson, J. Borg, A. Hedman and T. D. Cannon (2019). ”The schizophrenia and bipolar twin study in Sweden (STAR).” Schizophr Res 204: 183-192.
Persson, E., E. Asutay, M. Heilig, A. Löfberg, N. Pedersen, D. Västfjäll and G. Tinghög (2019). ”Variation in the μ-Opioid Receptor Gene (OPRM1) Does Not Moderate Social-Rejection Sensitivity in Humans.” Psychol Sci 30(7): 1050-1062.
Reese, S. E., C. J. Xu, H. T. den Dekker, M. K. Lee, S. Sikdar, C. Ruiz-Arenas, S. K. Merid, F. I. Rezwan, C. M. Page, V. Ullemar, P. E. Melton, S. S. Oh, I. V. Yang, K. Burrows, C. Söderhäll, D. D. Jima, L. Gao, R. Arathimos, L. K. Küpers, M. Wielscher, P. Rzehak, J. Lahti, C. Laprise, A. M. Madore, J. Ward, B. D. Bennett, T. Wang, D. A. Bell, J. M. Vonk, S. E. Håberg, S. Zhao, R. Karlsson, E. Hollams, D. Hu, A. J. Richards, A. Bergström, G. C. Sharp, J. F. Felix, M. Bustamante, O. Gruzieva, R. L. Maguire, F. Gilliland, N. Baïz, E. A. Nohr, E. Corpeleijn, S. Sebert, W. Karmaus, V. Grote, E. Kajantie, M. C. Magnus, A. K. Örtqvist, C. Eng, A. H. Liu, I. Kull, V. W. V. Jaddoe, J. Sunyer, J. Kere, C. Hoyo, I. Annesi-Maesano, S. H. Arshad, B. Koletzko, B. Brunekreef, E. B. Binder, K. Räikkönen, E. Reischl, J. W. Holloway, M. R. Jarvelin, H. Snieder, N. Kazmi, C. V. Breton, S. K. Murphy, G. Pershagen, J. M. Anto, C. L. Relton, D. A. Schwartz, E. G. Burchard, R. C. Huang, W. Nystad, C. Almqvist, A. J. Henderson, E. Melén, L. Duijts, G. H. Koppelman and S. J. London (2019). ”Epigenome-wide meta-analysis of DNA methylation and childhood asthma.” J Allergy Clin Immunol 143(6): 2062-2074.
Romagnoni, A., S. Jégou, K. Van Steen, G. Wainrib and J. P. Hugot (2019). ”Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data.” Sci Rep 9(1): 10351.
Szentkereszty-Kovács, Z., S. Fiatal, A. Szegedi, D. Kovács, E. Janka, K. Herszényi, P. Holló, P. Nikamo, M. Ståhle, É. Remenyik and D. Törőcsik (2019). ”The prevalence of ADH1B and OPRM1 alleles predisposing for alcohol consumption are increased in the Hungarian psoriasis population.” Arch Dermatol Res 311(6): 435-442.
Takeda, K., I. Kou, N. Otomo, A. Grauers, Y. H. Fan, Y. Ogura, Y. Takahashi, Y. Momozawa, E. Einarsdottir, J. Kere, M. Matsumoto, Y. Qiu, Y. Q. Song, P. Gerdhem, K. Watanabe and S. Ikegawa (2019). ”A multiethnic meta-analysis defined the association of rs12946942 with severe adolescent idiopathic scoliosis.” J Hum Genet 64(5): 493-498.
Werissa, N. A., P. Piko, S. Fiatal, Z. Kosa, J. Sandor and R. Adany (2019). ”SNP-Based Genetic Risk Score Modeling Suggests No Increased Genetic Susceptibility of the Roma Population to Type 2 Diabetes Mellitus.” Genes (Basel) 10(11).
Wu, W. Y., G. Johansson, C. Wibom, T. Brännström, A. Malmström, R. Henriksson, I. Golovleva, M. L. Bondy, U. Andersson, A. M. Dahlin and B. Melin (2019). ”The Genetic Architecture of Gliomagenesis-Genetic Risk Variants Linked to Specific Molecular Subtypes.” Cancers (Basel) 11(12).
Ämmälä, A. J., A. S. Urrila, A. Lahtinen, O. Santangeli, A. Hakkarainen, K. Kantojärvi, A. E. Castaneda, N. Lundbom, M. Marttunen and T. Paunio (2019). ”Epigenetic dysregulation of genes related to synaptic long-term depression among adolescents with depressive disorder and sleep symptoms.” Sleep Med 61: 95-103.
2018
Benedek, P., M. Eriksson, K. Duvefelt, A. Freyschuss, M. Frick, P. Lundman, L. Nylund and K. Szummer (2018). ”Genetic testing for familial hypercholesterolemia among survivors of acute coronary syndrome.” J Intern Med 284(6): 674-684.
Checknita, D., T. J. Ekström, E. Comasco, K. W. Nilsson, J. Tiihonen and S. Hodgins (2018). ”Associations of monoamine oxidase A gene first exon methylation with sexual abuse and current depression in women.” J Neural Transm (Vienna) 125(7): 1053-1064.
Enander, J., V. Z. Ivanov, D. Mataix-Cols, R. Kuja-Halkola, B. Ljótsson, S. Lundström, A. Pérez-Vigil, B. Monzani, P. Lichtenstein and C. Rück (2018). ”Prevalence and heritability of body dysmorphic symptoms in adolescents and young adults: a population-based nationwide twin study.” Psychol Med 48(16): 2740-2747.
Kou, I., K. Watanabe, Y. Takahashi, Y. Momozawa, A. Khanshour, A. Grauers, H. Zhou, G. Liu, Y. H. Fan, K. Takeda, Y. Ogura, T. Zhou, Y. Iwasaki, M. Kubo, Z. Wu, M. Matsumoto, E. Einarsdottir, J. Kere, D. Huang, G. Qiu, Y. Qiu, C. A. Wise, Y. Q. Song, N. Wu, P. Su, P. Gerdhem and S. Ikegawa (2018). ”A multi-ethnic meta-analysis confirms the association of rs6570507 with adolescent idiopathic scoliosis.” Sci Rep 8(1): 11575.
Li, W., M. Middha, M. Bicak, D. D. Sjoberg, E. Vertosick, A. Dahlin, C. Häggström, G. Hallmans, A. C. Rönn, P. Stattin, O. Melander, D. Ulmert, H. Lilja and R. J. Klein (2018). ”Genome-wide Scan Identifies Role for AOX1 in Prostate Cancer Survival.” Eur Urol 74(6): 710-719.
Myers, L., A. Van’t Westeinde, R. Kuja-Halkola, K. Tammimies and S. Bölte (2018). ”2D:4D Ratio in Neurodevelopmental Disorders: A Twin Study.” J Autism Dev Disord 48(9): 3244-3252.
Ogura, Y., K. Takeda, I. Kou, A. Khanshour, A. Grauers, H. Zhou, G. Liu, Y. H. Fan, T. Zhou, Z. Wu, Y. Takahashi, M. Matsumoto, E. Einarsdottir, J. Kere, D. Huang, G. Qiu, L. Xu, Y. Qiu, C. A. Wise, Y. Q. Song, N. Wu, P. Su, P. Gerdhem, K. Watanabe and S. Ikegawa (2018). ”An international meta-analysis confirms the association of BNC2 with adolescent idiopathic scoliosis.” Sci Rep 8(1): 4730.
Payton, N. M., G. Kalpouzos, D. Rizzuto, L. Fratiglioni, M. Kivipelto, L. Bäckman and E. J. Laukka (2018). ”Combining Cognitive, Genetic, and Structural Neuroimaging Markers to Identify Individuals with Increased Dementia Risk.” J Alzheimers Dis 64(2): 533-542.
Stenberg Hammar, K., K. Niespodziana, M. van Hage, J. Kere, R. Valenta, G. Hedlin and C. Söderhäll (2018). ”Reduced CDHR3 expression in children wheezing with rhinovirus.” Pediatr Allergy Immunol 29(2): 200-206.
Xu, C. J., C. Söderhäll, M. Bustamante, N. Baïz, O. Gruzieva, U. Gehring, D. Mason, L. Chatzi, M. Basterrechea, S. Llop, M. Torrent, F. Forastiere, M. P. Fantini, K. C. L. Carlsen, T. Haahtela, A. Morin, M. Kerkhof, S. K. Merid, B. van Rijkom, S. A. Jankipersadsing, M. J. Bonder, S. Ballereau, C. J. Vermeulen, R. Aguirre-Gamboa, J. C. de Jongste, H. A. Smit, A. Kumar, G. Pershagen, S. Guerra, J. Garcia-Aymerich, D. Greco, L. Reinius, R. R. C. McEachan, R. Azad, V. Hovland, P. Mowinckel, H. Alenius, N. Fyhrquist, N. Lemonnier, J. Pellet, C. Auffray, P. van der Vlies, C. C. van Diemen, Y. Li, C. Wijmenga, M. G. Netea, M. F. Moffatt, W. Cookson, J. M. Anto, J. Bousquet, T. Laatikainen, C. Laprise, K. H. Carlsen, D. Gori, D. Porta, C. Iñiguez, J. R. Bilbao, M. Kogevinas, J. Wright, B. Brunekreef, J. Kere, M. C. Nawijn, I. Annesi-Maesano, J. Sunyer, E. Melén and G. H. Koppelman (2018). ”DNA methylation in childhood asthma: an epigenome-wide meta-analysis.” Lancet Respir Med 6(5): 379-388.
2017
Acevedo, N., S. Ezer, S. Kebede Merid, V. D. Gaertner, C. Söderhäll, M. D’Amato, M. Kabesch, E. Melén, J. Kere and V. Pulkkinen (2017). ”Neuropeptide S (NPS) variants modify the signaling and risk effects of NPS Receptor 1 (NPSR1) variants in asthma.” PLoS One 12(5): e0176568.
Bogo, R., A. Farah, K. K. Karlsson, N. L. Pedersen, M. Svartengren and Å. Skjönsberg (2017). ”Prevalence, Incidence Proportion, and Heritability for Tinnitus: A Longitudinal Twin Study.” Ear Hear 38(3): 292-300.
Bonfiglio, F., P. G. Hysi, W. Ek, V. Karhunen, N. V. Rivera, M. Männikkö, H. Nordenstedt, M. Zucchelli, F. Bresso, F. Williams, H. Tornblom, P. K. Magnusson, N. L. Pedersen, J. Ronkainen, P. T. Schmidt and M. D’Amato (2017). ”A meta-analysis of reflux genome-wide association studies in 6750 Northern Europeans from the general population.” Neurogastroenterol Motil 29(2).
Chiang, H. H., C. Forsell, A. K. Lindström, L. Lilius, H. Thonberg, I. Nennesmo and C. Graff (2017). ”No common founder for C9orf72 expansion mutation in Sweden.” J Hum Genet 62(2): 321-324.
Diószegi, J., S. Fiatal, R. Tóth, Á. Moravcsik-Kornyicki, Z. Kósa, J. Sándor, M. McKee and R. Ádány (2017). ”Distribution Characteristics and Combined Effect of Polymorphisms Affecting Alcohol Consumption Behaviour in the Hungarian General and Roma Populations.” Alcohol Alcohol 52(1): 104-111.
Donahue, K., N. Långström, S. Lundström, P. Lichtenstein and M. Forsman (2017). ”Familial Factors, Victimization, and Psychological Health Among Sexual Minority Adolescents in Sweden.” Am J Public Health 107(2): 322-328.
Einarsdottir, E., A. Grauers, J. Wang, H. Jiao, S. A. Escher, A. Danielsson, A. Simony, M. Andersen, S. B. Christensen, K. Åkesson, I. Kou, A. M. Khanshour, A. Ohlin, C. Wise, S. Ikegawa, J. Kere and P. Gerdhem (2017). ”CELSR2 is a candidate susceptibility gene in idiopathic scoliosis.” PLoS One 12(12): e0189591.
Gref, A., S. K. Merid, O. Gruzieva, S. Ballereau, A. Becker, T. Bellander, A. Bergström, Y. Bossé, M. Bottai, M. Chan-Yeung, E. Fuertes, D. Ierodiakonou, R. Jiang, S. Joly, M. Jones, M. S. Kobor, M. Korek, A. L. Kozyrskyj, A. Kumar, N. Lemonnier, E. MacIntyre, C. Ménard, D. Nickle, M. Obeidat, J. Pellet, M. Standl, A. Sääf, C. Söderhäll, C. M. T. Tiesler, M. van den Berge, J. M. Vonk, H. Vora, C. J. Xu, J. M. Antó, C. Auffray, M. Brauer, J. Bousquet, B. Brunekreef, W. J. Gauderman, J. Heinrich, J. Kere, G. H. Koppelman, D. Postma, C. Carlsten, G. Pershagen and E. Melén (2017). ”Genome-Wide Interaction Analysis of Air Pollution Exposure and Childhood Asthma with Functional Follow-up.” Am J Respir Crit Care Med 195(10): 1373-1383.
Henström, M., F. Hadizadeh, A. Beyder, F. Bonfiglio, T. Zheng, G. Assadi, J. Rafter, L. Bujanda, L. Agreus, A. Andreasson, A. Dlugosz, G. Lindberg, P. T. Schmidt, P. Karling, B. Ohlsson, N. J. Talley, M. Simren, S. Walter, M. Wouters, G. Farrugia and M. D’Amato (2017). ”TRPM8 polymorphisms associated with increased risk of IBS-C and IBS-M.” Gut 66(9): 1725-1727.
Huang, H., M. Fang, L. Jostins, M. Umićević Mirkov, G. Boucher, C. A. Anderson, V. Andersen, I. Cleynen, A. Cortes, F. Crins, M. D’Amato, V. Deffontaine, J. Dmitrieva, E. Docampo, M. Elansary, K. K. Farh, A. Franke, A. S. Gori, P. Goyette, J. Halfvarson, T. Haritunians, J. Knight, I. C. Lawrance, C. W. Lees, E. Louis, R. Mariman, T. Meuwissen, M. Mni, Y. Momozawa, M. Parkes, S. L. Spain, E. Théâtre, G. Trynka, J. Satsangi, S. van Sommeren, S. Vermeire, R. J. Xavier, R. K. Weersma, R. H. Duerr, C. G. Mathew, J. D. Rioux, D. P. B. McGovern, J. H. Cho, M. Georges, M. J. Daly and J. C. Barrett (2017). ”Fine-mapping inflammatory bowel disease loci to single-variant resolution.” Nature 547(7662): 173-178.
Ivanov, V. Z., A. Nordsletten, D. Mataix-Cols, E. Serlachius, P. Lichtenstein, S. Lundström, P. K. E. Magnusson, R. Kuja-Halkola and C. Rück (2017). ”Heritability of hoarding symptoms across adolescence and young adulthood: A longitudinal twin study.” PLoS One 12(6): e0179541.
Johansson, V., J. Jakobsson, R. G. Fortgang, H. Zetterberg, K. Blennow, T. D. Cannon, C. M. Hultman, L. Wetterberg and M. Landén (2017). ”Cerebrospinal fluid microglia and neurodegenerative markers in twins concordant and discordant for psychotic disorders.” Eur Arch Psychiatry Clin Neurosci 267(5): 391-402.
Johnson, A. C., R. Bogo, A. Farah, K. K. Karlsson, P. Muhr, M. Sjöström, E. B. Svensson, Å. Skjönsberg and M. Svartengren (2017). ”Influence of well-known risk factors for hearing loss in a longitudinal twin study.” Int J Audiol 56(sup1): 63-73.
Márquez, A., L. Vidal-Bralo, L. Rodríguez-Rodríguez, M. A. González-Gay, A. Balsa, I. González-Álvaro, P. Carreira, N. Ortego-Centeno, M. M. Ayala-Gutiérrez, F. J. García-Hernández, M. F. González-Escribano, J. M. Sabio, C. Tolosa, A. Suárez, A. González, L. Padyukov, J. Worthington, T. Vyse, M. E. Alarcón-Riquelme and J. Martín (2017). ”A combined large-scale meta-analysis identifies COG6 as a novel shared risk locus for rheumatoid arthritis and systemic lupus erythematosus.” Ann Rheum Dis 76(1): 286-294.
Mortera-Blanco, T., M. Dimitriou, P. S. Woll, M. Karimi, E. Elvarsdottir, S. Conte, M. Tobiasson, M. Jansson, I. Douagi, M. Moarii, L. Saft, E. Papaemmanuil, S. E. W. Jacobsen and E. Hellström-Lindberg (2017). ”SF3B1-initiating mutations in MDS-RSs target lymphomyeloid hematopoietic stem cells.” Blood 130(7): 881-890.
Muurinen, M., K. Hannula-Jouppi, L. E. Reinius, C. Söderhäll, S. K. Merid, A. Bergström, E. Melén, G. Pershagen, M. Lipsanen-Nyman, D. Greco and J. Kere (2017). ”Hypomethylation of HOXA4 promoter is common in Silver-Russell syndrome and growth restriction and associates with stature in healthy children.” Sci Rep 7(1): 15693.
Nagy, K., S. Fiatal, J. Sándor and R. Ádány (2017). ”Distinct Penetrance of Obesity-Associated Susceptibility Alleles in the Hungarian General and Roma Populations.” Obes Facts 10(5): 444-457.
Pikó, P., S. Fiatal, Z. Kósa, J. Sándor and R. Ádány (2017). ”Data to genetic risk assessment on high-density cholesterol level associated polymorphisms in Hungarian general and Roma populations.” Data Brief 14: 354-359.
Pikó, P., S. Fiatal, Z. Kósa, J. Sándor and R. Ádány (2017). ”Genetic factors exist behind the high prevalence of reduced high-density lipoprotein cholesterol levels in the Roma population.” Atherosclerosis 263: 119-126.
Täljemark, J., M. Råstam, P. Lichtenstein, H. Anckarsäter and N. Kerekes (2017). ”The coexistence of psychiatric and gastrointestinal problems in children with restrictive eating in a nationwide Swedish twin study.” J Eat Disord 5: 25.
Uhlin, E., H. Rönnholm, K. Day, M. Kele, K. Tammimies, S. Bölte and A. Falk (2017). ”Derivation of human iPS cell lines from monozygotic twins in defined and xeno free conditions.” Stem Cell Res 18: 22-25.
Weidner, J., L. Jarenbäck, K. de Jong, J. M. Vonk, M. van den Berge, C. A. Brandsma, H. M. Boezen, D. Sin, Y. Bossé, D. Nickle, J. Ankerst, L. Bjermer, D. S. Postma, A. Faiz and E. Tufvesson (2017). ”Sulfatase modifying factor 1 (SUMF1) is associated with Chronic Obstructive Pulmonary Disease.” Respir Res 18(1): 77.
Vincent, P. H., E. Benedikz, P. Uhlén, O. Hovatta and E. Sundström (2017). ”Expression of Pluripotency Markers in Nonpluripotent Human Neural Stem and Progenitor Cells.” Stem Cells Dev 26(12): 876-887.
2016
Abolhassani, H., A. Aghamohammadi and L. Hammarström (2016). ”Monogenic mutations associated with IgA deficiency.” Expert Rev Clin Immunol 12(12): 1321-1335.
Assadi, G., L. Vesterlund, F. Bonfiglio, L. Mazzurana, L. Cordeddu, D. Schepis, J. Mjösberg, S. Ruhrmann, A. Fabbri, V. Vukojevic, P. Percipalle, F. A. Salomons, J. Laurencikiene, L. Törkvist, J. Halfvarson and M. D’Amato (2016). ”Functional Analyses of the Crohn’s Disease Risk Gene LACC1.” PLoS One 11(12): e0168276.
Berglind, D., P. Müller, M. Willmer, I. Sinha, P. Tynelius, E. Näslund, K. Dahlman-Wright and F. Rasmussen (2016). ”Differential methylation in inflammation and type 2 diabetes genes in siblings born before and after maternal bariatric surgery.” Obesity (Silver Spring) 24(1): 250-261.
Borg, J., S. Cervenka, R. Kuja-Halkola, G. J. Matheson, E. G. Jönsson, P. Lichtenstein, S. Henningsson, T. Ichimiya, H. Larsson, P. Stenkrona, C. Halldin and L. Farde (2016). ”Contribution of non-genetic factors to dopamine and serotonin receptor availability in the adult human brain.” Mol Psychiatry 21(8): 1077-1084.
Ellinghaus, D., L. Jostins, S. L. Spain, A. Cortes, J. Bethune, B. Han, Y. R. Park, S. Raychaudhuri, J. G. Pouget, M. Hübenthal, T. Folseraas, Y. Wang, T. Esko, A. Metspalu, H. J. Westra, L. Franke, T. H. Pers, R. K. Weersma, V. Collij, M. D’Amato, J. Halfvarson, A. B. Jensen, W. Lieb, F. Degenhardt, A. J. Forstner, A. Hofmann, S. Schreiber, U. Mrowietz, B. D. Juran, K. N. Lazaridis, S. Brunak, A. M. Dale, R. C. Trembath, S. Weidinger, M. Weichenthal, E. Ellinghaus, J. T. Elder, J. N. Barker, O. A. Andreassen, D. P. McGovern, T. H. Karlsen, J. C. Barrett, M. Parkes, M. A. Brown and A. Franke (2016). ”Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci.” Nat Genet 48(5): 510-518.
Eriksson, J. M., S. Lundström, P. Lichtenstein, S. Bejerot and E. Eriksson (2016). ”Effect of co-twin gender on neurodevelopmental symptoms: a twin register study.” Mol Autism 7: 8.
Fiatal, S., R. Tóth, Á. Moravcsik-Kornyicki, Z. Kósa, J. Sándor, M. McKee and R. Ádány (2016). ”High Prevalence of Smoking in the Roma Population Seems to Have No Genetic Background.” Nicotine Tob Res 18(12): 2260-2267.
Fortgang, R. G., C. M. Hultman and T. D. Cannon (2016). ”Coping Styles in Twins Discordant for Schizophrenia, Bipolar Disorder, and Depression.” Clin Psychol Sci 4(2): 216-228.
Fortgang, R. G., C. M. Hultman, T. G. van Erp and T. D. Cannon (2016). ”Multidimensional assessment of impulsivity in schizophrenia, bipolar disorder, and major depressive disorder: testing for shared endophenotypes.” Psychol Med 46(7): 1497-1507.
Ghasimi, S., C. Wibom, A. M. Dahlin, T. Brännström, I. Golovleva, U. Andersson and B. Melin (2016). ”Genetic risk variants in the CDKN2A/B, RTEL1 and EGFR genes are associated with somatic biomarkers in glioma.” J Neurooncol 127(3): 483-492.
Günaydın, G., J. Nordgren, S. Sharma and L. Hammarström (2016). ”Association of elevated rotavirus-specific antibody titers with HBGA secretor status in Swedish individuals: The FUT2 gene as a putative susceptibility determinant for infection.” Virus Res 211: 64-68.
Henmyr, V., C. Lind-Halldén, D. Carlberg, C. Halldén, E. Melén, M. Wickman, A. Bergström, T. Säll and L. O. Cardell (2016). ”Characterization of genetic variation in TLR8 in relation to allergic rhinitis.” Allergy 71(3): 333-341.
Hovey, D., M. Lindstedt, A. Zettergren, L. Jonsson, A. Johansson, J. Melke, N. Kerekes, H. Anckarsäter, P. Lichtenstein, S. Lundström and L. Westberg (2016). ”Antisocial behavior and polymorphisms in the oxytocin receptor gene: findings in two independent samples.” Mol Psychiatry 21(7): 983-988.
Joubert, B. R., J. F. Felix, P. Yousefi, K. M. Bakulski, A. C. Just, C. Breton, S. E. Reese, C. A. Markunas, R. C. Richmond, C. J. Xu, L. K. Küpers, S. S. Oh, C. Hoyo, O. Gruzieva, C. Söderhäll, L. A. Salas, N. Baïz, H. Zhang, J. Lepeule, C. Ruiz, S. Ligthart, T. Wang, J. A. Taylor, L. Duijts, G. C. Sharp, S. A. Jankipersadsing, R. M. Nilsen, A. Vaez, M. D. Fallin, D. Hu, A. A. Litonjua, B. F. Fuemmeler, K. Huen, J. Kere, I. Kull, M. C. Munthe-Kaas, U. Gehring, M. Bustamante, M. J. Saurel-Coubizolles, B. M. Quraishi, J. Ren, J. Tost, J. R. Gonzalez, M. J. Peters, S. E. Håberg, Z. Xu, J. B. van Meurs, T. R. Gaunt, M. Kerkhof, E. Corpeleijn, A. P. Feinberg, C. Eng, A. A. Baccarelli, S. E. Benjamin Neelon, A. Bradman, S. K. Merid, A. Bergström, Z. Herceg, H. Hernandez-Vargas, B. Brunekreef, M. Pinart, B. Heude, S. Ewart, J. Yao, N. Lemonnier, O. H. Franco, M. C. Wu, A. Hofman, W. McArdle, P. Van der Vlies, F. Falahi, M. W. Gillman, L. F. Barcellos, A. Kumar, M. Wickman, S. Guerra, M. A. Charles, J. Holloway, C. Auffray, H. W. Tiemeier, G. D. Smith, D. Postma, M. F. Hivert, B. Eskenazi, M. Vrijheid, H. Arshad, J. M. Antó, A. Dehghan, W. Karmaus, I. Annesi-Maesano, J. Sunyer, A. Ghantous, G. Pershagen, N. Holland, S. K. Murphy, D. L. DeMeo, E. G. Burchard, C. Ladd-Acosta, H. Snieder, W. Nystad, G. H. Koppelman, C. L. Relton, V. W. Jaddoe, A. Wilcox, E. Melén and S. J. London (2016). ”DNA Methylation in Newborns and Maternal Smoking in Pregnancy: Genome-wide Consortium Meta-analysis.” Am J Hum Genet 98(4): 680-696.
Kaartokallio, T., A. I. Lokki, H. Peterson, K. Kivinen, L. Hiltunen, E. Salmela, T. Lappalainen, P. Maanselkä, S. Heino, S. Knuutila, A. Sayed, L. Poston, S. P. Brennecke, M. P. Johnson, L. Morgan, E. K. Moses, J. Kere and H. Laivuori (2016). ”Preeclampsia does not share common risk alleles in 9p21 with coronary artery disease and type 2 diabetes.” Ann Med 48(5): 330-336.
Kalpouzos, G., D. Rizzuto, L. Keller, J. Fastbom, G. Santoni, S. Angleman, C. Graff, L. Bäckman and L. Fratiglioni (2016). ”Telomerase Gene (hTERT) and Survival: Results From Two Swedish Cohorts of Older Adults.” J Gerontol A Biol Sci Med Sci 71(2): 188-195.
Kovamees, O., A. Shemyakin, M. Eriksson, B. Angelin and J. Pernow (2016). ”Arginase inhibition improves endothelial function in patients with familial hypercholesterolaemia irrespective of their cholesterol levels.” J Intern Med 279(5): 477-484.
Lester, N., D. Garcia, S. Lundström, S. Brändström, M. Råstam, N. Kerekes, T. Nilsson, C. R. Cloninger and H. Anckarsäter (2016). ”The genetic and environmental structure of the character sub-scales of the temperament and character inventory in adolescence.” Ann Gen Psychiatry 15: 10.
2015
Acevedo, N., L. E. Reinius, D. Greco, A. Gref, C. Orsmark-Pietras, H. Persson, G. Pershagen, G. Hedlin, E. Melen, A. Scheynius, J. Kere and C. Soderhall (2015). ”Risk of childhood asthma is associated with CpG-site polymorphisms, regional DNA methylation and mRNA levels at the GSDMB/ORMDL3 locus.” Hum Mol Genet 24(3): 875-890.
Bogo, R., A. Farah, A. C. Johnson, K. K. Karlsson, N. L. Pedersen, M. Svartengren and Å. Skjönsberg (2015). ”The role of genetic factors for hearing deterioration across 20 years: a twin study.” J Gerontol A Biol Sci Med Sci 70(5): 647-653.
Fuertes, E., C. Soderhall, N. Acevedo, A. Becker, M. Brauer, M. Chan-Yeung, F. N. Dijk, J. Heinrich, J. de Jongste, G. H. Koppelman, D. S. Postma, J. Kere, A. L. Kozyrskyj, G. Pershagen, A. Sandford, M. Standl, C. M. Tiesler, M. Waldenberger, M. Westman, C. Carlsten and E. Melen (2015). ”Associations between the 17q21 region and allergic rhinitis in 5 birth cohorts.” J Allergy Clin Immunol 135(2): 573-576.
Glad, C. A., L. M. Carlsson, O. Melander, P. Almgren, L. Sjöström, S. Nilsson, I. Larsson, P. A. Svensson and G. Johannsson (2015). ”The GH receptor exon 3 deleted/full-length polymorphism is associated with central adiposity in the general population.” Eur J Endocrinol 172(2): 123-128.
Grauers, A., J. Wang, E. Einarsdottir, A. Simony, A. Danielsson, K. Åkesson, A. Ohlin, K. Halldin, P. Grabowski, M. Tenne, H. Laivuori, I. Dahlman, M. Andersen, S. B. Christensen, M. K. Karlsson, H. Jiao, J. Kere and P. Gerdhem (2015). ”Candidate gene analysis and exome sequencing confirm LBX1 as a susceptibility gene for idiopathic scoliosis.” Spine J 15(10): 2239-2246.
Hafrén, L., E. Einarsdottir, E. Kentala, S. Hammarén-Malmi, M. F. Bhutta, C. J. MacArthur, B. Wilmot, M. Casselbrant, Y. P. Conley, D. E. Weeks, E. M. Mandel, O. Vaarala, A. Kallio, M. Melin, J. K. Nieminen, E. Leinonen, J. Kere and P. S. Mattila (2015). ”Predisposition to Childhood Otitis Media and Genetic Polymorphisms within the Toll-Like Receptor 4 (TLR4) Locus.” PLoS One 10(7): e0132551.
Jiao, H., P. Arner, P. Gerdhem, R. J. Strawbridge, E. Näslund, A. Thorell, A. Hamsten, J. Kere and I. Dahlman (2015). ”Exome sequencing followed by genotyping suggests SYPL2 as a susceptibility gene for morbid obesity.” Eur J Hum Genet 23(9): 1216-1222.
Karimi, M., C. Nilsson, M. Dimitriou, M. Jansson, H. Matsson, P. Unneberg, S. Lehmann, J. Kere and E. Hellström-Lindberg (2015). ”High-throughput mutational screening adds clinically important information in myelodysplastic syndromes and secondary or therapy-related acute myeloid leukemia.” Haematologica 100(6): e223-225.
Kunz, M., I. R. König, A. Schillert, J. Kruppa, A. Ziegler, H. Grallert, M. Müller-Nurasyid, W. Lieb, A. Franke, A. Ranki, J. Panelius, S. Koskenmies, T. Hasan, J. Kere, A. C. Rönn, J. C. Simon, E. Schmidt, J. Wenzel, T. Tüting, J. Landsberg, T. Zeller, S. Blankenberg, R. Gläser, N. Patsinakidis, A. Kuhn and S. M. Ibrahim (2015). ”Genome-wide association study identifies new susceptibility loci for cutaneous lupus erythematosus.” Exp Dermatol 24(7): 510-515.
Laukka, E. J., M. Lövdén, G. Kalpouzos, G. Papenberg, L. Keller, C. Graff, T. Q. Li, L. Fratiglioni and L. Bäckman (2015). ”Microstructural White Matter Properties Mediate the Association between APOE and Perceptual Speed in Very Old Persons without Dementia.” PLoS One 10(8): e0134766.
Liu, J. Z., S. van Sommeren, H. Huang, S. C. Ng, R. Alberts, A. Takahashi, S. Ripke, J. C. Lee, L. Jostins, T. Shah, S. Abedian, J. H. Cheon, J. Cho, N. E. Dayani, L. Franke, Y. Fuyuno, A. Hart, R. C. Juyal, G. Juyal, W. H. Kim, A. P. Morris, H. Poustchi, W. G. Newman, V. Midha, T. R. Orchard, H. Vahedi, A. Sood, J. Y. Sung, R. Malekzadeh, H. J. Westra, K. Yamazaki, S. K. Yang, J. C. Barrett, B. Z. Alizadeh, M. Parkes, T. Bk, M. J. Daly, M. Kubo, C. A. Anderson and R. K. Weersma (2015). ”Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.” Nat Genet 47(9): 979-986.
Marenholz, I., J. Esparza-Gordillo, F. Rüschendorf, A. Bauerfeind, D. P. Strachan, B. D. Spycher, H. Baurecht, P. Margaritte-Jeannin, A. Sääf, M. Kerkhof, M. Ege, S. Baltic, M. C. Matheson, J. Li, S. Michel, W. Q. Ang, W. McArdle, A. Arnold, G. Homuth, F. Demenais, E. Bouzigon, C. Söderhäll, G. Pershagen, J. C. de Jongste, D. S. Postma, C. Braun-Fahrländer, E. Horak, L. M. Ogorodova, V. P. Puzyrev, E. Y. Bragina, T. J. Hudson, C. Morin, D. L. Duffy, G. B. Marks, C. F. Robertson, G. W. Montgomery, B. Musk, P. J. Thompson, N. G. Martin, A. James, P. Sleiman, E. Toskala, E. Rodriguez, R. Fölster-Holst, A. Franke, W. Lieb, C. Gieger, A. Heinzmann, E. Rietschel, T. Keil, S. Cichon, M. M. Nöthen, C. E. Pennell, P. D. Sly, C. O. Schmidt, A. Matanovic, V. Schneider, M. Heinig, N. Hübner, P. G. Holt, S. Lau, M. Kabesch, S. Weidinger, H. Hakonarson, M. A. R. Ferreira, C. Laprise, M. B. Freidin, J. Genuneit, G. H. Koppelman, E. Melén, M. H. Dizier, A. J. Henderson and Y. A. Lee (2015). ”Meta-analysis identifies seven susceptibility loci involved in the atopic march.” Nat Commun 6: 8804.
Matsson, H., M. Huss, H. Persson, E. Einarsdottir, E. Tiraboschi, J. Nopola-Hemmi, J. Schumacher, N. Neuhoff, A. Warnke, H. Lyytinen, G. Schulte-Korne, M. M. Nothen, P. H. Leppanen, M. Peyrard-Janvid and J. Kere (2015). ”Polymorphisms in DCDC2 and S100B associate with developmental dyslexia.” J Hum Genet.
Mezei, Z. A., Z. Bereczky, É. Katona, R. Gindele, E. Balogh, S. Fiatal, L. Balogh, I. Czuriga, R. Ádány, I. Édes and L. Muszbek (2015). ”Factor XIII B subunit polymorphisms and the risk of coronary artery disease.” Int J Mol Sci 16(1): 1143-1159.
Mousavi, F., S. Rozsa, T. Nilsson, T. Archer, H. Anckarsäter and D. Garcia (2015). ”Personality and intelligence: persistence, not self-directedness, cooperativeness or self-transcendence, is related to twins’ cognitive abilities.” PeerJ 3: e1195.
Paternoster, L., M. Standl, J. Waage, H. Baurecht, M. Hotze, D. P. Strachan, J. A. Curtin, K. Bønnelykke, C. Tian, A. Takahashi, J. Esparza-Gordillo, A. C. Alves, J. P. Thyssen, H. T. den Dekker, M. A. Ferreira, E. Altmaier, P. M. Sleiman, F. L. Xiao, J. R. Gonzalez, I. Marenholz, B. Kalb, M. P. Yanes, C. J. Xu, L. Carstensen, M. M. Groen-Blokhuis, C. Venturini, C. E. Pennell, S. J. Barton, A. M. Levin, I. Curjuric, M. Bustamante, E. Kreiner-Møller, G. A. Lockett, J. Bacelis, S. Bunyavanich, R. A. Myers, A. Matanovic, A. Kumar, J. Y. Tung, T. Hirota, M. Kubo, W. L. McArdle, A. J. Henderson, J. P. Kemp, J. Zheng, G. D. Smith, F. Rüschendorf, A. Bauerfeind, M. A. Lee-Kirsch, A. Arnold, G. Homuth, C. O. Schmidt, E. Mangold, S. Cichon, T. Keil, E. Rodríguez, A. Peters, A. Franke, W. Lieb, N. Novak, R. Fölster-Holst, M. Horikoshi, J. Pekkanen, S. Sebert, L. L. Husemoen, N. Grarup, J. C. de Jongste, F. Rivadeneira, A. Hofman, V. W. Jaddoe, S. G. Pasmans, N. J. Elbert, A. G. Uitterlinden, G. B. Marks, P. J. Thompson, M. C. Matheson, C. F. Robertson, J. S. Ried, J. Li, X. B. Zuo, X. D. Zheng, X. Y. Yin, L. D. Sun, M. A. McAleer, G. M. O’Regan, C. M. Fahy, L. E. Campbell, M. Macek, M. Kurek, D. Hu, C. Eng, D. S. Postma, B. Feenstra, F. Geller, J. J. Hottenga, C. M. Middeldorp, P. Hysi, V. Bataille, T. Spector, C. M. Tiesler, E. Thiering, B. Pahukasahasram, J. J. Yang, M. Imboden, S. Huntsman, N. Vilor-Tejedor, C. L. Relton, R. Myhre, W. Nystad, A. Custovic, S. T. Weiss, D. A. Meyers, C. Söderhäll, E. Melén, C. Ober, B. A. Raby, A. Simpson, B. Jacobsson, J. W. Holloway, H. Bisgaard, J. Sunyer, N. M. P. Hensch, L. K. Williams, K. M. Godfrey, C. A. Wang, D. I. Boomsma, M. Melbye, G. H. Koppelman, D. Jarvis, W. I. McLean, A. D. Irvine, X. J. Zhang, H. Hakonarson, C. Gieger, E. G. Burchard, N. G. Martin, L. Duijts, A. Linneberg, M. R. Jarvelin, M. M. Noethen, S. Lau, N. Hübner, Y. A. Lee, M. Tamari, D. A. Hinds, D. Glass, S. J. Brown, J. Heinrich, D. M. Evans and S. Weidinger (2015). ”Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis.” Nat Genet 47(12): 1449-1456.
Pettersson, E., A. Sjolander, C. Almqvist, H. Anckarsater, B. M. D’Onofrio, P. Lichtenstein and H. Larsson (2015). ”Birth weight as an independent predictor of ADHD symptoms: a within-twin pair analysis.” J Child Psychol Psychiatry 56(4): 453-459.
Ragnarsson, O., C. A. Glad, R. Bergthorsdottir, E. G. Almqvist, E. Ekerstad, H. Widell, B. Wangberg and G. Johannsson (2015). ”Body composition and bone mineral density in women with Cushing’s syndrome in remission and the association with common genetic variants influencing glucocorticoid sensitivity.” Eur J Endocrinol 172(1): 1-10.
Sundin, M., M. Remberger, H. Lindqvist, B. Omazic, B. Sundberg, M. Uzunel and J. Winiarski (2015). ”Hypogammaglobulinemia in children after allogeneic hematopoietic stem cell transplantation: a cytokine mediated immunoglobulin isotype class switch arrest?” Pediatr Blood Cancer 62(5): 890-896.
Söderlund-Strand, A., A. Wikström and J. Dillner (2015). ”Evaluation of human papillomavirus DNA detection in samples obtained for routine Chlamydia trachomatis screening.” J Clin Virol 64: 88-91.
Wibom, C., F. Späth, A. M. Dahlin, H. Langseth, E. Hovig, P. Rajaraman, T. B. Johannesen, U. Andersson and B. Melin (2015). ”Investigation of established genetic risk variants for glioma in prediagnostic samples from a population-based nested case-control study.” Cancer Epidemiol Biomarkers Prev 24(5): 810-816.
Xu, W. L., N. L. Pedersen, L. Keller, G. Kalpouzos, H. X. Wang, C. Graff, B. Winblad, L. Bäckman and L. Fratiglioni (2015). ”HHEX_23 AA Genotype Exacerbates Effect of Diabetes on Dementia and Alzheimer Disease: A Population-Based Longitudinal Study.” PLoS Med 12(7): e1001853.
2014
Barbosa, E. J., C. A. Glad, A. G. Nilsson, N. Bosaeus, H. F. Nystrom, P. A. Svensson, B. A. Bengtsson, S. Nilsson, I. Bosaeus, C. L. Boguszewski and G. Johannsson (2014). ”Extracellular water and blood pressure in adults with growth hormone (GH) deficiency: a genotype-phenotype association study.” PLoS One 9(8): e105754.
Becker, J., D. Czamara, T. S. Scerri, F. Ramus, V. Csepe, J. B. Talcott, J. Stein, A. Morris, K. U. Ludwig, P. Hoffmann, F. Honbolygo, D. Toth, F. Fauchereau, C. Bogliotti, S. Iannuzzi, Y. Chaix, S. Valdois, C. Billard, F. George, I. Soares-Boucaud, C. L. Gerard, S. van der Mark, E. Schulz, A. Vaessen, U. Maurer, K. Lohvansuu, H. Lyytinen, M. Zucchelli, D. Brandeis, L. Blomert, P. H. Leppanen, J. Bruder, A. P. Monaco, B. Muller-Myhsok, J. Kere, K. Landerl, M. M. Nothen, G. Schulte-Korne, S. Paracchini, M. Peyrard-Janvid and J. Schumacher (2014). ”Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.” Eur J Hum Genet 22(5): 675-680.
Dahgam, S., L. Modig, A. Torinsson Naluai, A. C. Olin and F. Nyberg (2014). ”Haplotypes of the inducible nitric oxide synthase gene are strongly associated with exhaled nitric oxide levels in adults: a population-based study.” J Med Genet 51(7): 449-454.
Darki, F., M. Peyrard-Janvid, H. Matsson, J. Kere and T. Klingberg (2014). ”DCDC2 polymorphism is associated with left temporoparietal gray and white matter structures during development.” J Neurosci 34(43): 14455-14462.
Ek, W. E., A. Reznichenko, S. Ripke, B. Niesler, M. Zucchelli, N. V. Rivera, P. T. Schmidt, N. L. Pedersen, P. Magnusson, N. J. Talley, E. G. Holliday, L. Houghton, M. Gazouli, G. Karamanolis, G. Rappold, B. Burwinkel, H. Surowy, J. Rafter, G. Assadi, L. Li, E. Papadaki, D. Gambaccini, S. Marchi, R. Colucci, C. Blandizzi, R. Barbaro, P. Karling, S. Walter, B. Ohlsson, H. Tornblom, F. Bresso, A. Andreasson, A. Dlugosz, M. Simren, L. Agreus, G. Lindberg, G. Boeckxstaens, M. Bellini, V. Stanghellini, G. Barbara, M. J. Daly, M. Camilleri, M. M. Wouters and M. D’Amato (2014). ”Exploring the genetics of irritable bowel syndrome: a GWA study in the general population and replication in multinational case-control cohorts.” Gut.
Garcia, D., A. Stråge, S. Lundström, S. Radovic, S. Brändström, M. Råstam, T. Nilsson, C. R. Cloninger, N. Kerekes and H. Anckarsäter (2014). ”Responsibility and cooperativeness are constrained, not determined.” Front Psychol 5: 308.
Glad, C. A., E. J. Barbosa, H. Filipsson Nystrom, L. M. Carlsson, S. Nilsson, A. G. Nilsson, P. A. Svensson and G. Johannsson (2014). ”SNPs within the GH-signaling pathway are associated with the early IGF1 response to GH replacement therapy in GHD adults.” Eur J Endocrinol 170(1): 101-107.
Henstrom, M., M. Zucchelli, C. Soderhall, A. Bergstrom, J. Kere, E. Melen, O. Olen and M. D’Amato (2014). ”NPSR1 polymorphisms influence recurrent abdominal pain in children: a population-based study.” Neurogastroenterol Motil 26(10): 1417-1425.
Holliday, E. G., J. Attia, S. Hancock, N. Koloski, M. McEvoy, R. Peel, M. D’Amato, L. Agreus, H. Nyhlin, A. Andreasson, A. E. Almazar, Y. A. Saito, R. J. Scott and N. J. Talley (2014). ”Genome-wide association study identifies two novel genomic regions in irritable bowel syndrome.” Am J Gastroenterol 109(5): 770-772.
Karlsson, R., M. Aly, M. Clements, L. Zheng, J. Adolfsson, J. Xu, H. Gronberg and F. Wiklund (2014). ”A population-based assessment of germline HOXB13 G84E mutation and prostate cancer risk.” Eur Urol 65(1): 169-176.
Kerekes, N., S. Lundstrom, Z. Chang, A. Tajnia, P. Jern, P. Lichtenstein, T. Nilsson and H. Anckarsater (2014). ”Oppositional defiant- and conduct disorder-like problems: neurodevelopmental predictors and genetic background in boys and girls, in a nationwide twin study.” PeerJ 2: e359.
Pantzar, A., E. J. Laukka, A. R. Atti, G. Papenberg, L. Keller, C. Graff, L. Fratiglioni and L. Backman (2014). ”Interactive effects of KIBRA and CLSTN2 polymorphisms on episodic memory in old-age unipolar depression.” Neuropsychologia 62: 137-142.
Ragnarsson, O., C. A. Glad, P. Berglund, R. Bergthorsdottir, D. N. Eder and G. Johannsson (2014). ”Common genetic variants in the glucocorticoid receptor and the 11beta-hydroxysteroid dehydrogenase type 1 genes influence long-term cognitive impairments in patients with Cushing’s syndrome in remission.” J Clin Endocrinol Metab 99(9): E1803-1807.
Soderqvist, S., H. Matsson, M. Peyrard-Janvid, J. Kere and T. Klingberg (2014). ”Polymorphisms in the dopamine receptor 2 gene region influence improvements during working memory training in children and adolescents.” J Cogn Neurosci 26(1): 54-62.
Wouters, M. M., D. Lambrechts, M. Knapp, I. Cleynen, P. Whorwell, L. Agreus, A. Dlugosz, P. T. Schmidt, J. Halfvarson, M. Simren, B. Ohlsson, P. Karling, S. Van Wanrooy, S. Mondelaers, S. Vermeire, G. Lindberg, R. Spiller, G. Dukes, M. D’Amato and G. Boeckxstaens (2014). ”Genetic variants in CDC42 and NXPH1 as susceptibility factors for constipation and diarrhoea predominant irritable bowel syndrome.” Gut 63(7): 1103-1111.
2013
Acevedo, N., A. Saaf, C. Soderhall, E. Melen, J. Mandelin, C. O. Pietras, S. Ezer, P. Karisola, J. Vendelin, G. B. Gennas, J. Yli-Kauhaluoma, H. Alenius, E. von Mutius, G. Doekes, C. Braun-Fahrlander, J. Riedler, M. van Hage, M. D’Amato, A. Scheynius, G. Pershagen, J. Kere and V. Pulkkinen (2013). ”Interaction between retinoid acid receptor-related orphan receptor alpha (RORA) and neuropeptide S receptor 1 (NPSR1) in asthma.” PLoS One 8(4): e60111.
Beaudoin, M., P. Goyette, G. Boucher, K. S. Lo, M. A. Rivas, C. Stevens, A. Alikashani, M. Ladouceur, D. Ellinghaus, L. Torkvist, G. Goel, C. Lagace, V. Annese, A. Bitton, J. Begun, S. R. Brant, F. Bresso, J. H. Cho, R. H. Duerr, J. Halfvarson, D. P. McGovern, G. Radford-Smith, S. Schreiber, P. L. Schumm, Y. Sharma, M. S. Silverberg, R. K. Weersma, M. D’Amato, S. Vermeire, A. Franke, G. Lettre, R. J. Xavier, M. J. Daly and J. D. Rioux (2013). ”Deep resequencing of GWAS loci identifies rare variants in CARD9, IL23R and RNF186 that are associated with ulcerative colitis.” PLoS Genet 9(9): e1003723.
Bloom, R. J., A. K. Kahler, A. L. Collins, G. Chen, T. D. Cannon, C. Hultman and P. F. Sullivan (2013). ”Comprehensive analysis of copy number variation in monozygotic twins discordant for bipolar disorder or schizophrenia.” Schizophr Res 146(1-3): 289-290.
Bornelov, S., A. Saaf, E. Melen, A. Bergstrom, B. Torabi Moghadam, V. Pulkkinen, N. Acevedo, C. Orsmark Pietras, M. Ege, C. Braun-Fahrlander, J. Riedler, G. Doekes, M. Kabesch, M. van Hage, J. Kere, A. Scheynius, C. Soderhall, G. Pershagen and J. Komorowski (2013). ”Rule-based models of the interplay between genetic and environmental factors in childhood allergy.” PLoS One 8(11): e80080.
Garcia, D., S. Lundstrom, S. Brandstrom, M. Rastam, C. R. Cloninger, N. Kerekes, T. Nilsson and H. Anckarsater (2013). ”Temperament and character in the Child and Adolescent Twin Study in Sweden (CATSS): comparison to the general population, and genetic structure analysis.” PLoS One 8(8): e70475.
Ivanov, V. Z., D. Mataix-Cols, E. Serlachius, P. Lichtenstein, H. Anckarsater, Z. Chang, C. H. Gumpert, S. Lundstrom, N. Langstrom and C. Ruck (2013). ”Prevalence, comorbidity and heritability of hoarding symptoms in adolescence: a population based twin study in 15-year olds.” PLoS One 8(7): e69140.
Laukka, E. J., M. Lovden, A. Herlitz, S. Karlsson, B. Ferencz, A. Pantzar, L. Keller, C. Graff, L. Fratiglioni and L. Backman (2013). ”Genetic effects on old-age cognitive functioning: a population-based study.” Psychol Aging 28(1): 262-274.
Mehlig, K., K. Leander, U. de Faire, F. Nyberg, C. Berg, A. Rosengren, L. Bjorck, H. Zetterberg, K. Blennow, G. Tognon, K. Toren, E. Strandhagen, L. Lissner and D. Thelle (2013). ”The association between plasma homocysteine and coronary heart disease is modified by the MTHFR 677C>T polymorphism.” Heart 99(23): 1761-1765.
Melin, B., A. M. Dahlin, U. Andersson, Z. Wang, R. Henriksson, G. Hallmans, M. L. Bondy, C. Johansen, M. Feychting, A. Ahlbom, C. M. Kitahara, S. S. Wang, A. M. Ruder, T. Carreón, M. A. Butler, P. D. Inskip, M. Purdue, A. W. Hsing, L. Mechanic, E. Gillanders, M. Yeager, M. Linet, S. J. Chanock, P. Hartge and P. Rajaraman (2013). ”Known glioma risk loci are associated with glioma with a family history of brain tumours — a case-control gene association study.” Int J Cancer 132(10): 2464-2468.
Rastam, M., J. Taljemark, A. Tajnia, S. Lundstrom, P. Gustafsson, P. Lichtenstein, C. Gillberg, H. Anckarsater and N. Kerekes (2013). ”Eating problems and overlap with ADHD and autism spectrum disorders in a nationwide twin study of 9- and 12-year-old children.” ScientificWorldJournal 2013: 315429.
Reinius, L. E., A. Gref, A. Saaf, N. Acevedo, M. Joerink, M. Kupczyk, M. D’Amato, A. Bergstrom, E. Melen, A. Scheynius, S. E. Dahlen, G. Pershagen, C. Soderhall and J. Kere (2013). ”DNA methylation in the Neuropeptide S Receptor 1 (NPSR1) promoter in relation to asthma and environmental factors.” PLoS One 8(1): e53877.
Weidinger, S., S. A. Willis-Owen, Y. Kamatani, H. Baurecht, N. Morar, L. Liang, P. Edser, T. Street, E. Rodriguez, G. M. O’Regan, P. Beattie, R. Folster-Holst, A. Franke, N. Novak, C. M. Fahy, M. C. Winge, M. Kabesch, T. Illig, S. Heath, C. Soderhall, E. Melen, G. Pershagen, J. Kere, M. Bradley, A. Lieden, M. Nordenskjold, J. I. Harper, W. H. McLean, S. J. Brown, W. O. Cookson, G. M. Lathrop, A. D. Irvine and M. F. Moffatt (2013). ”A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis.” Hum Mol Genet 22(23): 4841-4856.
2012
Angst, M. S., L. C. Lazzeroni, N. G. Phillips, D. R. Drover, M. Tingle, A. Ray, G. E. Swan and J. D. Clark (2012). ”Aversive and reinforcing opioid effects: a pharmacogenomic twin study.” Anesthesiology 117(1): 22-37.
Angst, M. S., N. G. Phillips, D. R. Drover, M. Tingle, A. Ray, G. E. Swan, L. C. Lazzeroni and D. J. Clark (2012). ”Pain sensitivity and opioid analgesia: a pharmacogenomic twin study.” Pain 153(7): 1397-1409.
Anthoni, H., L. E. Sucheston, B. A. Lewis, I. Tapia-Paez, X. Fan, M. Zucchelli, M. Taipale, C. M. Stein, M. E. Hokkanen, E. Castren, B. F. Pennington, S. D. Smith, R. K. Olson, J. B. Tomblin, G. Schulte-Korne, M. Nothen, J. Schumacher, B. Muller-Myhsok, P. Hoffmann, J. W. Gilger, G. W. Hynd, J. Nopola-Hemmi, P. H. Leppanen, H. Lyytinen, J. Schoumans, M. Nordenskjold, J. Spencer, D. Stanic, W. C. Boon, E. Simpson, S. Makela, J. A. Gustafsson, M. Peyrard-Janvid, S. Iyengar and J. Kere (2012). ”The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language.” Behav Genet 42(4): 509-527.
Barbosa, E. J., C. A. Glad, A. G. Nilsson, H. Filipsson Nystrom, G. Gotherstrom, P. A. Svensson, I. Vinotti, B. A. Bengtsson, S. Nilsson, C. L. Boguszewski and G. Johannsson (2012). ”Genotypes associated with lipid metabolism contribute to differences in serum lipid profile of GH-deficient adults before and after GH replacement therapy.” Eur J Endocrinol 167(3): 353-362.
Darki, F., M. Peyrard-Janvid, H. Matsson, J. Kere and T. Klingberg (2012). ”Three dyslexia susceptibility genes, DYX1C1, DCDC2, and KIAA0319, affect temporo-parietal white matter structure.” Biol Psychiatry 72(8): 671-676.
Dubois, L., K. Ohm Kyvik, M. Girard, F. Tatone-Tokuda, D. Perusse, J. Hjelmborg, A. Skytthe, F. Rasmussen, M. J. Wright, P. Lichtenstein and N. G. Martin (2012). ”Genetic and environmental contributions to weight, height, and BMI from birth to 19 years of age: an international study of over 12,000 twin pairs.” PLoS One 7(2): e30153.
Gigante, B., K. Leander, M. Vikstrom, S. Ye and U. de Faire (2012). ”Chromosome 1p13 genetic variants antagonize the risk of myocardial infarction associated with high ApoB serum levels.” BMC Cardiovasc Disord 12: 90.
Jarvinen, T. M., A. Hellquist, M. Zucchelli, S. Koskenmies, J. Panelius, T. Hasan, H. Julkunen, M. D’Amato and J. Kere (2012). ”Replication of GWAS-identified systemic lupus erythematosus susceptibility genes affirms B-cell receptor pathway signalling and strengthens the role of IRF5 in disease susceptibility in a Northern European population.” Rheumatology (Oxford) 51(1): 87-92.
Johansson, V., R. Nybom, L. Wetterberg, C. M. Hultman, T. D. Cannon, A. G. Johansson, C. J. Ekman and M. Landen (2012). ”Microscopic particles in two fractions of fresh cerebrospinal fluid in twins with schizophrenia or bipolar disorder and in healthy controls.” PLoS One 7(9): e45994.
Jostins, L., S. Ripke, R. K. Weersma, R. H. Duerr, D. P. McGovern, K. Y. Hui, J. C. Lee, L. P. Schumm, Y. Sharma, C. A. Anderson, J. Essers, M. Mitrovic, K. Ning, I. Cleynen, E. Theatre, S. L. Spain, S. Raychaudhuri, P. Goyette, Z. Wei, C. Abraham, J. P. Achkar, T. Ahmad, L. Amininejad, A. N. Ananthakrishnan, V. Andersen, J. M. Andrews, L. Baidoo, T. Balschun, P. A. Bampton, A. Bitton, G. Boucher, S. Brand, C. Büning, A. Cohain, S. Cichon, M. D’Amato, D. De Jong, K. L. Devaney, M. Dubinsky, C. Edwards, D. Ellinghaus, L. R. Ferguson, D. Franchimont, K. Fransen, R. Gearry, M. Georges, C. Gieger, J. Glas, T. Haritunians, A. Hart, C. Hawkey, M. Hedl, X. Hu, T. H. Karlsen, L. Kupcinskas, S. Kugathasan, A. Latiano, D. Laukens, I. C. Lawrance, C. W. Lees, E. Louis, G. Mahy, J. Mansfield, A. R. Morgan, C. Mowat, W. Newman, O. Palmieri, C. Y. Ponsioen, U. Potocnik, N. J. Prescott, M. Regueiro, J. I. Rotter, R. K. Russell, J. D. Sanderson, M. Sans, J. Satsangi, S. Schreiber, L. A. Simms, J. Sventoraityte, S. R. Targan, K. D. Taylor, M. Tremelling, H. W. Verspaget, M. De Vos, C. Wijmenga, D. C. Wilson, J. Winkelmann, R. J. Xavier, S. Zeissig, B. Zhang, C. K. Zhang, H. Zhao, M. S. Silverberg, V. Annese, H. Hakonarson, S. R. Brant, G. Radford-Smith, C. G. Mathew, J. D. Rioux, E. E. Schadt, M. J. Daly, A. Franke, M. Parkes, S. Vermeire, J. C. Barrett and J. H. Cho (2012). ”Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.” Nature 491(7422): 119-124.
Scerri, T. S., F. Darki, D. F. Newbury, A. J. Whitehouse, M. Peyrard-Janvid, H. Matsson, Q. W. Ang, C. E. Pennell, S. Ring, J. Stein, A. P. Morris, A. P. Monaco, J. Kere, J. B. Talcott, T. Klingberg and S. Paracchini (2012). ”The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure.” PLoS One 7(11): e50321.
Soderqvist, S., S. Bergman Nutley, M. Peyrard-Janvid, H. Matsson, K. Humphreys, J. Kere and T. Klingberg (2012). ”Dopamine, working memory, and training induced plasticity: implications for developmental research.” Dev Psychol 48(3): 836-843.
Surakka, I., J. B. Whitfield, M. Perola, P. M. Visscher, G. W. Montgomery, M. Falchi, G. Willemsen, E. J. de Geus, P. K. Magnusson, K. Christensen, T. I. Sorensen, K. H. Pietilainen, T. Rantanen, K. Silander, E. Widen, J. Muilu, I. Rahman, U. Liljedahl, A. C. Syvanen, A. Palotie, J. Kaprio, K. O. Kyvik, N. L. Pedersen, D. I. Boomsma, T. Spector, N. G. Martin, S. Ripatti and L. Peltonen (2012). ”A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol.” Twin Res Hum Genet 15(6): 691-699.
Surakka, I., J. B. Whitfield, M. Perola, P. M. Visscher, G. W. Montgomery, M. Falchi, G. Willemsen, E. J. de Geus, P. K. Magnusson, K. Christensen, T. I. Sørensen, K. H. Pietiläinen, T. Rantanen, K. Silander, E. Widén, J. Muilu, I. Rahman, U. Liljedahl, A. C. Syvänen, A. Palotie, J. Kaprio, K. O. Kyvik, N. L. Pedersen, D. I. Boomsma, T. Spector, N. G. Martin, S. Ripatti and L. Peltonen (2012). ”A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol.” Twin Res Hum Genet 15(6): 691-699.
Walum, H., P. Lichtenstein, J. M. Neiderhiser, D. Reiss, J. M. Ganiban, E. L. Spotts, N. L. Pedersen, H. Anckarsater, H. Larsson and L. Westberg (2012). ”Variation in the oxytocin receptor gene is associated with pair-bonding and social behavior.” Biol Psychiatry 71(5): 419-426.
Ziermans, T., I. Dumontheil, C. Roggeman, M. Peyrard-Janvid, H. Matsson, J. Kere and T. Klingberg (2012). ”Working memory brain activity and capacity link MAOA polymorphism to aggressive behavior during development.” Transl Psychiatry 2: e85.
2011
Alabaf, S., C. Gillberg, S. Lundström, P. Lichtenstein, N. Kerekes, M. Råstam and H. Anckarsäter (2019). ”Physical health in children with neurodevelopmental disorders.” J Autism Dev Disord 49(1): 83-95.
Aly, M., F. Wiklund, J. Xu, W. B. Isaacs, M. Eklund, M. D’Amato, J. Adolfsson and H. Gronberg (2011). ”Polygenic risk score improves prostate cancer risk prediction: results from the Stockholm-1 cohort study.” Eur Urol 60(1): 21-28.
Anedda, F., M. Zucchelli, D. Schepis, A. Hellquist, L. Corrado, S. D’Alfonso, A. Achour, G. McInerney, A. Bertorello, M. Lordal, R. Befrits, J. Bjork, F. Bresso, L. Torkvist, J. Halfvarson, J. Kere and M. D’Amato (2011). ”Multiple polymorphisms affect expression and function of the neuropeptide S receptor (NPSR1).” PLoS One 6(12): e29523.
Dumontheil, I., C. Roggeman, T. Ziermans, M. Peyrard-Janvid, H. Matsson, J. Kere and T. Klingberg (2011). ”Influence of the COMT genotype on working memory and brain activity changes during development.” Biol Psychiatry 70(3): 222-229.
Goumidi, L., K. Dahlman-Wright, I. Tapia-Paez, H. Matsson, F. Pasquier, P. Amouyel, J. Kere, J. C. Lambert and A. Meirhaeghe (2011). ”Study of estrogen receptor-alpha and receptor-beta gene polymorphisms on Alzheimer’s disease.” J Alzheimers Dis 26(3): 431-439.
Hashemi, J., C. Worrall, D. Vasilcanu, M. Fryknäs, L. Sulaiman, M. Karimi, W. H. Weng, W. O. Lui, C. Rudduck, M. Axelson, H. Jernberg-Wiklund, L. Girnita, O. Larsson and C. Larsson (2011). ”Molecular characterization of acquired tolerance of tumor cells to picropodophyllin (PPP).” PLoS One 6(3): e14757.
Jiao, H., P. Arner, J. Hoffstedt, D. Brodin, B. Dubern, S. Czernichow, F. van’t Hooft, T. Axelsson, O. Pedersen, T. Hansen, T. I. Sorensen, J. Hebebrand, J. Kere, K. Dahlman-Wright, A. Hamsten, K. Clement and I. Dahlman (2011). ”Genome wide association study identifies KCNMA1 contributing to human obesity.” BMC Med Genomics 4: 51.
Jiao, H., P. Arner, S. L. Dickson, H. Vidal, N. Mejhert, C. Henegar, M. Taube, C. Hansson, A. Hinney, P. Galan, C. Simon, A. Silveira, A. Benrick, J. O. Jansson, A. Bouloumie, D. Langin, M. Laville, C. Debard, T. Axelsson, M. Ryden, J. Kere, K. Dahlman-Wright, A. Hamsten, K. Clement and I. Dahlman (2011). ”Genetic association and gene expression analysis identify FGFR1 as a new susceptibility gene for human obesity.” J Clin Endocrinol Metab 96(6): E962-966.
Keller, L., W. Xu, H. X. Wang, B. Winblad, L. Fratiglioni and C. Graff (2011). ”The obesity related gene, FTO, interacts with APOE, and is associated with Alzheimer’s disease risk: a prospective cohort study.” J Alzheimers Dis 23(3): 461-469.
Matsson, H., K. Tammimies, M. Zucchelli, H. Anthoni, P. Onkamo, J. Nopola-Hemmi, H. Lyytinen, P. H. Leppanen, N. Neuhoff, A. Warnke, G. Schulte-Korne, J. Schumacher, M. M. Nothen, J. Kere and M. Peyrard-Janvid (2011). ”SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations.” Behav Genet 41(1): 134-140.
Narusyte, J., J. M. Neiderhiser, A. K. Andershed, B. M. D’Onofrio, D. Reiss, E. Spotts, J. Ganiban and P. Lichtenstein (2011). ”Parental criticism and externalizing behavior problems in adolescents: the role of environment and genotype-environment correlation.” J Abnorm Psychol 120(2): 365-376.
Pietras, C. O., J. Vendelin, F. Anedda, S. Bruce, M. Adner, L. Sundman, V. Pulkkinen, H. Alenius, M. D’Amato, C. Soderhall and J. Kere (2011). ”The asthma candidate gene NPSR1 mediates isoform specific downstream signalling.” BMC Pulm Med 11: 39.
Ramanujam, R., F. Piehl, R. Pirskanen, P. K. Gregersen and L. Hammarstrom (2011). ”Concomitant autoimmunity in myasthenia gravis–lack of association with IgA deficiency.” J Neuroimmunol 236(1-2): 118-122.
Rivas, M. A., M. Beaudoin, A. Gardet, C. Stevens, Y. Sharma, C. K. Zhang, G. Boucher, S. Ripke, D. Ellinghaus, N. Burtt, T. Fennell, A. Kirby, A. Latiano, P. Goyette, T. Green, J. Halfvarson, T. Haritunians, J. M. Korn, F. Kuruvilla, C. Lagace, B. Neale, K. S. Lo, P. Schumm, L. Torkvist, M. C. Dubinsky, S. R. Brant, M. S. Silverberg, R. H. Duerr, D. Altshuler, S. Gabriel, G. Lettre, A. Franke, M. D’Amato, D. P. McGovern, J. H. Cho, J. D. Rioux, R. J. Xavier and M. J. Daly (2011). ”Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease.” Nat Genet 43(11): 1066-1073.
Smedby, K. E., S. Eloranta, K. Duvefelt, M. Melbye, K. Humphreys, H. Hjalgrim and E. T. Chang (2011). ”Vitamin D receptor genotypes, ultraviolet radiation exposure, and risk of non-Hodgkin lymphoma.” Am J Epidemiol 173(1): 48-54.
Tóth, R., S. Fiatal, B. Petrovski, M. McKee and R. Adány (2011). ”Combined effect of ADH1B RS1229984, RS2066702 and ADH1C RS1693482/ RS698 alleles on alcoholism and chronic liver diseases.” Dis Markers 31(5): 267-277.
Zucchelli, M., M. Camilleri, A. N. Andreasson, F. Bresso, A. Dlugosz, J. Halfvarson, L. Torkvist, P. T. Schmidt, P. Karling, B. Ohlsson, R. H. Duerr, M. Simren, G. Lindberg, L. Agreus, P. Carlson, A. R. Zinsmeister and M. D’Amato (2011). ”Association of TNFSF15 polymorphism with irritable bowel syndrome.” Gut 60(12): 1671-1677.
2010
D’Amato, M., M. Zucchelli, M. Seddighzadeh, F. Anedda, S. Lindblad, J. Kere, L. Alfredsson, L. Klareskog and L. Padyukov (2010). ”Analysis of neuropeptide S receptor gene (NPSR1) polymorphism in rheumatoid arthritis.” PLoS One 5(2): e9315.
Fernberg, P., E. T. Chang, K. Duvefelt, H. Hjalgrim, S. Eloranta, K. M. Sorensen, A. Porwit, K. Humphreys, M. Melbye and K. Ekstrom Smedby (2010). ”Genetic variation in chromosomal translocation breakpoint and immune function genes and risk of non-Hodgkin lymphoma.” Cancer Causes Control 21(5): 759-769.
Ferreira, R. C., Q. Pan-Hammarstrom, R. R. Graham, V. Gateva, G. Fontan, A. T. Lee, W. Ortmann, E. Urcelay, M. Fernandez-Arquero, C. Nunez, G. Jorgensen, B. R. Ludviksson, S. Koskinen, K. Haimila, H. F. Clark, L. Klareskog, P. K. Gregersen, T. W. Behrens and L. Hammarstrom (2010). ”Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.” Nat Genet 42(9): 777-780.
Franke, A., D. P. McGovern, J. C. Barrett, K. Wang, G. L. Radford-Smith, T. Ahmad, C. W. Lees, T. Balschun, J. Lee, R. Roberts, C. A. Anderson, J. C. Bis, S. Bumpstead, D. Ellinghaus, E. M. Festen, M. Georges, T. Green, T. Haritunians, L. Jostins, A. Latiano, C. G. Mathew, G. W. Montgomery, N. J. Prescott, S. Raychaudhuri, J. I. Rotter, P. Schumm, Y. Sharma, L. A. Simms, K. D. Taylor, D. Whiteman, C. Wijmenga, R. N. Baldassano, M. Barclay, T. M. Bayless, S. Brand, C. Büning, A. Cohen, J. F. Colombel, M. Cottone, L. Stronati, T. Denson, M. De Vos, R. D’Inca, M. Dubinsky, C. Edwards, T. Florin, D. Franchimont, R. Gearry, J. Glas, A. Van Gossum, S. L. Guthery, J. Halfvarson, H. W. Verspaget, J. P. Hugot, A. Karban, D. Laukens, I. Lawrance, M. Lemann, A. Levine, C. Libioulle, E. Louis, C. Mowat, W. Newman, J. Panés, A. Phillips, D. D. Proctor, M. Regueiro, R. Russell, P. Rutgeerts, J. Sanderson, M. Sans, F. Seibold, A. H. Steinhart, P. C. Stokkers, L. Torkvist, G. Kullak-Ublick, D. Wilson, T. Walters, S. R. Targan, S. R. Brant, J. D. Rioux, M. D’Amato, R. K. Weersma, S. Kugathasan, A. M. Griffiths, J. C. Mansfield, S. Vermeire, R. H. Duerr, M. S. Silverberg, J. Satsangi, S. Schreiber, J. H. Cho, V. Annese, H. Hakonarson, M. J. Daly and M. Parkes (2010). ”Genome-wide meta-analysis increases to 71 the number of confirmed Crohn’s disease susceptibility loci.” Nat Genet 42(12): 1118-1125.
Glad, C. A., G. Johannsson, L. M. Carlsson and P. A. Svensson (2010). ”Rapid and high throughput genotyping of the growth hormone receptor exon 3 deleted/full-length polymorphism using a tagSNP.” Growth Horm IGF Res 20(3): 270-273.
Hasselrot, K., G. Bratt, K. Duvefelt, T. Hirbod, E. Sandstrom and K. Broliden (2010). ”HIV-1 exposed uninfected men who have sex with men have increased levels of salivary CC-chemokines associated with sexual behavior.” Aids 24(10): 1569-1575.
Keller, L., C. Murphy, H. X. Wang, L. Fratiglioni, M. Olin, M. Gafvels, I. Bjorkhem, C. Graff and S. Meaney (2010). ”A functional polymorphism in the HMGCR promoter affects transcriptional activity but not the risk for Alzheimer disease in Swedish populations.” Brain Res 1344: 185-191.
Link, J., A. R. Lorentzen, I. Kockum, K. Duvefelt, B. A. Lie, E. G. Celius, H. F. Harbo, J. Hillert and B. Brynedal (2010). ”Two HLA class I genes independently associated with multiple sclerosis.” J Neuroimmunol 226(1-2): 172-176.
Pinho, C. M., B. F. Bjork, N. Alikhani, H. G. Backman, T. Eneqvist, L. Fratiglioni, E. Glaser and C. Graff (2010). ”Genetic and biochemical studies of SNPs of the mitochondrial A beta-degrading protease, hPreP.” Neurosci Lett 469(2): 204-208.
Sillen, A., J. Brohede, L. Lilius, C. Forsell, J. Andrade, J. Odeberg, H. Ebise, B. Winblad and C. Graff (2010). ”Linkage to 20p13 including the ANGPT4 gene in families with mixed Alzheimer’s disease and vascular dementia.” J Hum Genet 55(10): 649-655.
Soderqvist, S., F. McNab, M. Peyrard-Janvid, H. Matsson, K. Humphreys, J. Kere and T. Klingberg (2010). ”The SNAP25 gene is linked to working memory capacity and maturation of the posterior cingulate cortex during childhood.” Biol Psychiatry 68(12): 1120-1125.
Toth, R., Z. Pocsai, S. Fiatal, G. Szeles, L. Kardos, B. Petrovski, M. McKee and R. Adany (2010). ”ADH1B*2 allele is protective against alcoholism but not chronic liver disease in the Hungarian population.” Addiction 105(5): 891-896.
2009
Brynedal, B., I. L. Bomfim, T. Olsson, K. Duvefelt and J. Hillert (2009). ”Differential expression, and genetic association, of CD58 in Swedish multiple sclerosis patients.” Proc Natl Acad Sci U S A 106(23): E58; author reply E59.
Dahdouh, F., H. Anthoni, I. Tapia-Paez, M. Peyrard-Janvid, G. Schulte-Korne, A. Warnke, H. Remschmidt, A. Ziegler, J. Kere, B. Muller-Myhsok, M. M. Nothen, J. Schumacher and M. Zucchelli (2009). ”Further evidence for DYX1C1 as a susceptibility factor for dyslexia.” Psychiatr Genet 19(2): 59-63.
Hellquist, A., M. Zucchelli, C. M. Lindgren, U. Saarialho-Kere, T. M. Jarvinen, S. Koskenmies, H. Julkunen, P. Onkamo, T. Skoog, J. Panelius, A. Raisanen-Sokolowski, T. Hasan, E. Widen, I. Gunnarson, E. Svenungsson, L. Padyukov, G. Assadi, L. Berglind, V. V. Makela, K. Kivinen, A. Wong, D. S. Cunningham Graham, T. J. Vyse, M. D’Amato and J. Kere (2009). ”Identification of MAMDC1 as a candidate susceptibility gene for systemic lupus erythematosus (SLE).” PLoS One 4(12): e8037.
Hellquist, A., T. M. Jarvinen, S. Koskenmies, M. Zucchelli, C. Orsmark-Pietras, L. Berglind, J. Panelius, T. Hasan, H. Julkunen, M. D’Amato, U. Saarialho-Kere and J. Kere (2009). ”Evidence for genetic association and interaction between the TYK2 and IRF5 genes in systemic lupus erythematosus.” J Rheumatol 36(8): 1631-1638.
Zucchelli, M., L. Torkvist, F. Bresso, J. Halfvarson, A. Hellquist, F. Anedda, G. Assadi, G. B. Lindgren, M. Svanfeldt, M. Janson, C. L. Noble, S. Pettersson, M. Lappalainen, P. Paavola-Sakki, L. Halme, M. Farkkila, U. Turunen, J. Satsangi, K. Kontula, R. Lofberg, J. Kere and M. D’Amato (2009). ”PepT1 oligopeptide transporter (SLC15A1) gene polymorphism in inflammatory bowel disease.” Inflamm Bowel Dis 15(10): 1562-1569.
2008
Hannelius, U., E. Salmela, T. Lappalainen, G. Guillot, C. M. Lindgren, U. von Dobeln, P. Lahermo and J. Kere (2008). ”Population substructure in Finland and Sweden revealed by the use of spatial coordinates and a small number of unlinked autosomal SNPs.” BMC Genet 9: 54.
Pegelow, M., M. Peyrard-Janvid, M. Zucchelli, I. Fransson, O. Larson, J. Kere, C. Larsson and A. Karsten (2008). ”Familial non-syndromic cleft lip and palate–analysis of the IRF6 gene and clinical phenotypes.” Eur J Orthod 30(2): 169-175.
2007
Anthoni, H., M. Zucchelli, H. Matsson, B. Muller-Myhsok, I. Fransson, J. Schumacher, S. Massinen, P. Onkamo, A. Warnke, H. Griesemann, P. Hoffmann, J. Nopola-Hemmi, H. Lyytinen, G. Schulte-Korne, J. Kere, M. M. Nothen and M. Peyrard-Janvid (2007). ”A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.” Hum Mol Genet 16(6): 667-677.
Brynedal, B., K. Duvefelt, G. Jonasdottir, I. M. Roos, E. Akesson, J. Palmgren and J. Hillert (2007). ”HLA-A confers an HLA-DRB1 independent influence on the risk of multiple sclerosis.” PLoS One 2(7): e664.
Cavaco, I., S. Asimus, M. Peyrard-Janvid, P. E. Ferreira, M. I. Veiga, T. N. Hai, V. Ribeiro, M. Ashton and J. P. Gil (2007). ”The Vietnamese Khin population harbors particular N-acetyltransferase 2 allele frequencies.” Clin Chem 53(11): 1977-1979.
Fischer, H., M. Esbjornsson, R. L. Sabina, A. Stromberg, M. Peyrard-Janvid and B. Norman (2007). ”AMP deaminase deficiency is associated with lower sprint cycling performance in healthy subjects.” J Appl Physiol (1985) 103(1): 315-322.
Hannelius, U., L. Gherman, V. V. Makela, A. Lindstedt, M. Zucchelli, C. Lagerberg, G. Tybring, J. Kere and C. M. Lindgren (2007). ”Large-scale zygosity testing using single nucleotide polymorphisms.” Twin Res Hum Genet 10(4): 604-625.
Lundmark, F., K. Duvefelt and J. Hillert (2007). ”Genetic association analysis of the interleukin 7 gene (IL7) in multiple sclerosis.” J Neuroimmunol 192(1-2): 171-173.
2006
Hodgson, U., V. Pulkkinen, M. Dixon, M. Peyrard-Janvid, M. Rehn, P. Lahermo, V. Ollikainen, K. Salmenkivi, V. Kinnula, J. Kere, P. Tukiainen and T. Laitinen (2006). ”ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosis.” Am J Hum Genet 79(1): 149-154.
Schumacher, J., H. Anthoni, F. Dahdouh, I. R. Konig, A. M. Hillmer, N. Kluck, M. Manthey, E. Plume, A. Warnke, H. Remschmidt, J. Hulsmann, S. Cichon, C. M. Lindgren, P. Propping, M. Zucchelli, A. Ziegler, M. Peyrard-Janvid, G. Schulte-Korne, M. M. Nothen and J. Kere (2006). ”Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.” Am J Hum Genet 78(1): 52-62.
2005
Koillinen, H., P. Lahermo, J. Rautio, J. Hukki, M. Peyrard-Janvid and J. Kere (2005). ”A genome-wide scan of non-syndromic cleft palate only (CPO) in Finnish multiplex families.” J Med Genet 42(2): 177-184.
Peyrard-Janvid, M., M. Pegelow, H. Koillinen, C. Larsson, I. Fransson, J. Rautio, J. Hukki, O. Larson, A. L. Karsten and J. Kere (2005). ”Novel and de novo mutations of the IRF6 gene detected in patients with Van der Woude or popliteal pterygium syndrome.” Eur J Hum Genet 13(12): 1261-1267.
Ylisaukko-Oja, T., M. Peyrard-Janvid, C. M. Lindgren, K. Rehnstrom, R. Vanhala, L. Peltonen, I. Jarvela and J. Kere (2005). ”Family-based association study of DYX1C1 variants in autism.” Eur J Hum Genet 13(1): 127-130.
Zhang, Z., K. Duvefelt, F. Svensson, T. Masterman, G. Jonasdottir, H. Salter, T. Emahazion, D. Hellgren, G. Falk, T. Olsson, J. Hillert and M. Anvret (2005). ”Two genes encoding immune-regulatory molecules (LAG3 and IL7R) confer susceptibility to multiple sclerosis.” Genes Immun 6(2): 145-152.
2004
Peyrard-Janvid, M., H. Anthoni, P. Onkamo, P. Lahermo, M. Zucchelli, N. Kaminen, K. Hannula-Jouppi, J. Nopola-Hemmi, A. Voutilainen, H. Lyytinen and J. Kere (2004). ”Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene.” Hum Genet 114(5): 510-516.
Vänskä, S., T. Luostarinen, I. Baussano, D. Apter, T. Eriksson, K. Natunen, P. Nieminen, J. Paavonen, V. N. Pimenoff, E. Pukkala, A. Söderlund-Strand, G. Dubin, G. Garnett, J. Dillner and M. Lehtinen (2020). ”Vaccination With Moderate Coverage Eradicates Oncogenic Human Papillomaviruses If a Gender-Neutral Strategy Is Applied.” J Infect Dis 222(6): 948-956.
Esberg, A., S. Haworth, R. Kuja-Halkola, P. K. E. Magnusson and I. Johansson (2020). ”Heritability of Oral Microbiota and Immune Responses to Oral Bacteria.” Microorganisms 8(8).
Jacobson, P., M. Peltonen, P. A. Svensson, M. Taube, J. C. Andersson-Assarsson, K. Sjoholm, C. Bouchard, B. Carlsson and L. M. S. Carlsson (2020). ”9p21.3 Coronary Artery Disease Locus Identifies Patients With Treatment Benefit From Bariatric Surgery in the Nonrandomized Prospective Controlled Swedish Obese Subjects Study.” Circ Genom Precis Med 13(5): 460-465.
Johansson, V., S. Erhardt, G. Engberg, M. Kegel, M. Bhat, L. Schwieler, K. Blennow, H. Zetterberg, T. D. Cannon, L. Wetterberg, C. M. Hultman and M. Landén (2020). ”Twin study shows association between monocyte chemoattractant protein-1 and kynurenic acid in cerebrospinal fluid.” Eur Arch Psychiatry Clin Neurosci 270(7): 933-938.
Kere, M., O. Gruzieva, V. Ullemar, C. Söderhäll, D. Greco, I. Kull, A. Bergström, G. Pershagen, C. Almqvist and E. Melén (2020). ”Effects of inhaled corticosteroids on DNA methylation in peripheral blood cells in children with asthma.” Allergy 75(3): 688-691.
Kerekes, N., B. Zouini, E. Karlsson, E. Cederholm, P. Lichtenstein, H. Anckarsäter and M. Råstam (2020). ”Conduct disorder and somatic health in children: a nationwide genetically sensitive study.” BMC Psychiatry 20(1): 595.
Laan, L., J. Klar, M. Sobol, J. Hoeber, M. Shahsavani, M. Kele, A. Fatima, M. Zakaria, G. Annerén, A. Falk, J. Schuster and N. Dahl (2020). ”DNA methylation changes in Down syndrome derived neural iPSCs uncover co-dysregulation of ZNF and HOX3 families of transcription factors.” Clin Epigenetics 12(1): 9.
Laukka, E. J., Y. Köhncke, G. Papenberg, L. Fratiglioni and L. Bäckman (2020). ”Combined genetic influences on episodic memory decline in older adults without dementia.” Neuropsychology 34(6): 654-666.
Merid, S. K., A. Novoloaca, G. C. Sharp, L. K. Küpers, A. T. Kho, R. Roy, L. Gao, I. Annesi-Maesano, P. Jain, M. Plusquin, M. Kogevinas, C. Allard, F. O. Vehmeijer, N. Kazmi, L. A. Salas, F. I. Rezwan, H. Zhang, S. Sebert, D. Czamara, S. L. Rifas-Shiman, P. E. Melton, D. A. Lawlor, G. Pershagen, C. V. Breton, K. Huen, N. Baiz, L. Gagliardi, T. S. Nawrot, E. Corpeleijn, P. Perron, L. Duijts, E. A. Nohr, M. Bustamante, S. L. Ewart, W. Karmaus, S. Zhao, C. M. Page, Z. Herceg, M. R. Jarvelin, J. Lahti, A. A. Baccarelli, D. Anderson, P. Kachroo, C. L. Relton, A. Bergström, B. Eskenazi, M. H. Soomro, P. Vineis, H. Snieder, L. Bouchard, V. W. Jaddoe, T. I. A. Sørensen, M. Vrijheid, S. H. Arshad, J. W. Holloway, S. E. Håberg, P. Magnus, T. Dwyer, E. B. Binder, D. L. DeMeo, J. M. Vonk, J. Newnham, K. G. Tantisira, I. Kull, J. L. Wiemels, B. Heude, J. Sunyer, W. Nystad, M. C. Munthe-Kaas, K. Räikkönen, E. Oken, R. C. Huang, S. T. Weiss, J. M. Antó, J. Bousquet, A. Kumar, C. Söderhäll, C. Almqvist, A. Cardenas, O. Gruzieva, C. J. Xu, S. E. Reese, J. Kere, P. Brodin, O. Solomon, M. Wielscher, N. Holland, A. Ghantous, M. F. Hivert, J. F. Felix, G. H. Koppelman, S. J. London and E. Melén (2020). ”Epigenome-wide meta-analysis of blood DNA methylation in newborns and children identifies numerous loci related to gestational age.” Genome Med 12(1): 25.
Neufeld, J., A. Hagström, A. Van’t Westeinde, K. Lundin, É. Cauvet, C. Willfors, J. Isaksson, P. Lichtenstein and S. Bölte (2020). ”Global and local visual processing in autism – a co-twin-control study.” J Child Psychol Psychiatry 61(4): 470-479.
Piko, P., S. Fiatal, N. A. Werissa, B. B. Bekele, G. Racz, Z. Kosa, J. Sandor and R. Adany (2020). ”The Effect of Haplotypes in the CETP and LIPC Genes on the Triglycerides to HDL-C Ratio and Its Components in the Roma and Hungarian General Populations.” Genes (Basel) 11(1).
Soltész, B., P. Pikó, J. Sándor, Z. Kósa, R. Ádány and S. Fiatal (2020). ”The genetic risk for hypertension is lower among the Hungarian Roma population compared to the general population.” PLoS One 15(6): e0234547.
Van’t Westeinde, A., É. Cauvet, R. Toro, R. Kuja-Halkola, J. Neufeld, K. Mevel and S. Bölte (2020). ”Sex differences in brain structure: a twin study on restricted and repetitive behaviors in twin pairs with and without autism.” Mol Autism 11(1): 1.
von Walden, F., R. Fernandez-Gonzalo, J. Pingel, J. McCarthy, P. Stål and E. Pontén (2020). ”Epigenetic Marks at the Ribosomal DNA Promoter in Skeletal Muscle Are Negatively Associated With Degree of Impairment in Cerebral Palsy.” Front Pediatr 8: 236.
Vänskä, S., T. Luostarinen, I. Baussano, D. Apter, T. Eriksson, K. Natunen, P. Nieminen, J. Paavonen, V. N. Pimenoff, E. Pukkala, A. Söderlund-Strand, G. Dubin, G. Garnett, J. Dillner and M. Lehtinen (2020). ”Vaccination With Moderate Coverage Eradicates Oncogenic Human Papillomaviruses If a Gender-Neutral Strategy Is Applied.” J Infect Dis 222(6): 948-956.
Dahlin, A. M., C. Wibom, U. Andersson, D. M. Hougaard, J. Bybjerg-Grauholm, I. Deltour, C. M. Hultman, A. K. Kähler, R. Karlsson, U. Hjalmars and B. Melin (2019). ”Genetic Variants in the 9p21.3 Locus Associated with Glioma Risk in Children, Adolescents, and Young Adults: A Case-Control Study.” Cancer Epidemiol Biomarkers Prev 28(7): 1252-1258.
Fiatal, S., P. Pikó, Z. Kósa, J. Sándor and R. Ádány (2019). ”Genetic profiling revealed an increased risk of venous thrombosis in the Hungarian Roma population.” Thromb Res 179: 37-44.
Gaertner, V. D., S. Michel, J. A. Curtin, V. Pulkkinen, N. Acevedo, C. Söderhäll, A. von Berg, A. Bufe, O. Laub, E. Rietschel, A. Heinzmann, B. Simma, C. Vogelberg, G. Pershagen, E. Melén, A. Simpson, A. Custovic, J. Kere and M. Kabesch (2019). ”Nocturnal asthma is affected by genetic interactions between RORA and NPSR1.” Pediatr Pulmonol 54(6): 847-857.
Gray, P., T. Luostarinen, S. Vänskä, T. Eriksson, C. Lagheden, I. Man, J. Palmroth, V. N. Pimenoff, A. Söderlund-Strand, J. Dillner and M. Lehtinen (2019). ”Occurrence of human papillomavirus (HPV) type replacement by sexual risk-taking behaviour group: Post-hoc analysis of a community randomized clinical trial up to 9 years after vaccination (IV).” Int J Cancer 145(3): 785-796.
Gruzieva, O., S. K. Merid, S. Chen, N. Mukherjee, A. M. Hedman, C. Almqvist, E. Andolf, Y. Jiang, J. Kere, A. Scheynius, C. Söderhäll, V. Ullemar, W. Karmaus, E. Melén, S. H. Arshad and G. Pershagen (2019). ”DNA Methylation Trajectories During Pregnancy.” Epigenet Insights 12: 2516865719867090.
Gruzieva, O., C. J. Xu, P. Yousefi, C. Relton, S. K. Merid, C. V. Breton, L. Gao, H. E. Volk, J. I. Feinberg, C. Ladd-Acosta, K. Bakulski, C. Auffray, N. Lemonnier, M. Plusquin, A. Ghantous, Z. Herceg, T. S. Nawrot, C. Pizzi, L. Richiardi, F. Rusconi, P. Vineis, M. Kogevinas, J. F. Felix, L. Duijts, H. T. den Dekker, V. W. V. Jaddoe, J. L. Ruiz, M. Bustamante, J. M. Antó, J. Sunyer, M. Vrijheid, K. B. Gutzkow, R. Grazuleviciene, C. Hernandez-Ferrer, I. Annesi-Maesano, J. Lepeule, J. Bousquet, A. Bergström, I. Kull, C. Söderhäll, J. Kere, U. Gehring, B. Brunekreef, A. C. Just, R. J. Wright, C. Peng, D. R. Gold, I. Kloog, D. L. DeMeo, G. Pershagen, G. H. Koppelman, S. J. London, A. A. Baccarelli and E. Melén (2019). ”Prenatal Particulate Air Pollution and DNA Methylation in Newborns: An Epigenome-Wide Meta-Analysis.” Environ Health Perspect 127(5): 57012.
Isaksson, J., A. Van’t Westeinde, É. Cauvet, R. Kuja-Halkola, K. Lundin, J. Neufeld, C. Willfors and S. Bölte (2019). ”Social Cognition in Autism and Other Neurodevelopmental Disorders: A Co-twin Control Study.” J Autism Dev Disord 49(7): 2838-2848.
Johansson, V., C. M. Hultman, I. Kizling, L. Martinsson, J. Borg, A. Hedman and T. D. Cannon (2019). ”The schizophrenia and bipolar twin study in Sweden (STAR).” Schizophr Res 204: 183-192.
Persson, E., E. Asutay, M. Heilig, A. Löfberg, N. Pedersen, D. Västfjäll and G. Tinghög (2019). ”Variation in the μ-Opioid Receptor Gene (OPRM1) Does Not Moderate Social-Rejection Sensitivity in Humans.” Psychol Sci 30(7): 1050-1062.
Reese, S. E., C. J. Xu, H. T. den Dekker, M. K. Lee, S. Sikdar, C. Ruiz-Arenas, S. K. Merid, F. I. Rezwan, C. M. Page, V. Ullemar, P. E. Melton, S. S. Oh, I. V. Yang, K. Burrows, C. Söderhäll, D. D. Jima, L. Gao, R. Arathimos, L. K. Küpers, M. Wielscher, P. Rzehak, J. Lahti, C. Laprise, A. M. Madore, J. Ward, B. D. Bennett, T. Wang, D. A. Bell, J. M. Vonk, S. E. Håberg, S. Zhao, R. Karlsson, E. Hollams, D. Hu, A. J. Richards, A. Bergström, G. C. Sharp, J. F. Felix, M. Bustamante, O. Gruzieva, R. L. Maguire, F. Gilliland, N. Baïz, E. A. Nohr, E. Corpeleijn, S. Sebert, W. Karmaus, V. Grote, E. Kajantie, M. C. Magnus, A. K. Örtqvist, C. Eng, A. H. Liu, I. Kull, V. W. V. Jaddoe, J. Sunyer, J. Kere, C. Hoyo, I. Annesi-Maesano, S. H. Arshad, B. Koletzko, B. Brunekreef, E. B. Binder, K. Räikkönen, E. Reischl, J. W. Holloway, M. R. Jarvelin, H. Snieder, N. Kazmi, C. V. Breton, S. K. Murphy, G. Pershagen, J. M. Anto, C. L. Relton, D. A. Schwartz, E. G. Burchard, R. C. Huang, W. Nystad, C. Almqvist, A. J. Henderson, E. Melén, L. Duijts, G. H. Koppelman and S. J. London (2019). ”Epigenome-wide meta-analysis of DNA methylation and childhood asthma.” J Allergy Clin Immunol 143(6): 2062-2074.
Romagnoni, A., S. Jégou, K. Van Steen, G. Wainrib and J. P. Hugot (2019). ”Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data.” Sci Rep 9(1): 10351.
Szentkereszty-Kovács, Z., S. Fiatal, A. Szegedi, D. Kovács, E. Janka, K. Herszényi, P. Holló, P. Nikamo, M. Ståhle, É. Remenyik and D. Törőcsik (2019). ”The prevalence of ADH1B and OPRM1 alleles predisposing for alcohol consumption are increased in the Hungarian psoriasis population.” Arch Dermatol Res 311(6): 435-442.
Takeda, K., I. Kou, N. Otomo, A. Grauers, Y. H. Fan, Y. Ogura, Y. Takahashi, Y. Momozawa, E. Einarsdottir, J. Kere, M. Matsumoto, Y. Qiu, Y. Q. Song, P. Gerdhem, K. Watanabe and S. Ikegawa (2019). ”A multiethnic meta-analysis defined the association of rs12946942 with severe adolescent idiopathic scoliosis.” J Hum Genet 64(5): 493-498.
Werissa, N. A., P. Piko, S. Fiatal, Z. Kosa, J. Sandor and R. Adany (2019). ”SNP-Based Genetic Risk Score Modeling Suggests No Increased Genetic Susceptibility of the Roma Population to Type 2 Diabetes Mellitus.” Genes (Basel) 10(11).
Wu, W. Y., G. Johansson, C. Wibom, T. Brännström, A. Malmström, R. Henriksson, I. Golovleva, M. L. Bondy, U. Andersson, A. M. Dahlin and B. Melin (2019). ”The Genetic Architecture of Gliomagenesis-Genetic Risk Variants Linked to Specific Molecular Subtypes.” Cancers (Basel) 11(12).
Ämmälä, A. J., A. S. Urrila, A. Lahtinen, O. Santangeli, A. Hakkarainen, K. Kantojärvi, A. E. Castaneda, N. Lundbom, M. Marttunen and T. Paunio (2019). ”Epigenetic dysregulation of genes related to synaptic long-term depression among adolescents with depressive disorder and sleep symptoms.” Sleep Med 61: 95-103.
Benedek, P., M. Eriksson, K. Duvefelt, A. Freyschuss, M. Frick, P. Lundman, L. Nylund and K. Szummer (2018). ”Genetic testing for familial hypercholesterolemia among survivors of acute coronary syndrome.” J Intern Med 284(6): 674-684.
Checknita, D., T. J. Ekström, E. Comasco, K. W. Nilsson, J. Tiihonen and S. Hodgins (2018). ”Associations of monoamine oxidase A gene first exon methylation with sexual abuse and current depression in women.” J Neural Transm (Vienna) 125(7): 1053-1064.
Enander, J., V. Z. Ivanov, D. Mataix-Cols, R. Kuja-Halkola, B. Ljótsson, S. Lundström, A. Pérez-Vigil, B. Monzani, P. Lichtenstein and C. Rück (2018). ”Prevalence and heritability of body dysmorphic symptoms in adolescents and young adults: a population-based nationwide twin study.” Psychol Med 48(16): 2740-2747.
Kou, I., K. Watanabe, Y. Takahashi, Y. Momozawa, A. Khanshour, A. Grauers, H. Zhou, G. Liu, Y. H. Fan, K. Takeda, Y. Ogura, T. Zhou, Y. Iwasaki, M. Kubo, Z. Wu, M. Matsumoto, E. Einarsdottir, J. Kere, D. Huang, G. Qiu, Y. Qiu, C. A. Wise, Y. Q. Song, N. Wu, P. Su, P. Gerdhem and S. Ikegawa (2018). ”A multi-ethnic meta-analysis confirms the association of rs6570507 with adolescent idiopathic scoliosis.” Sci Rep 8(1): 11575.
Li, W., M. Middha, M. Bicak, D. D. Sjoberg, E. Vertosick, A. Dahlin, C. Häggström, G. Hallmans, A. C. Rönn, P. Stattin, O. Melander, D. Ulmert, H. Lilja and R. J. Klein (2018). ”Genome-wide Scan Identifies Role for AOX1 in Prostate Cancer Survival.” Eur Urol 74(6): 710-719.
Myers, L., A. Van’t Westeinde, R. Kuja-Halkola, K. Tammimies and S. Bölte (2018). ”2D:4D Ratio in Neurodevelopmental Disorders: A Twin Study.” J Autism Dev Disord 48(9): 3244-3252.
Ogura, Y., K. Takeda, I. Kou, A. Khanshour, A. Grauers, H. Zhou, G. Liu, Y. H. Fan, T. Zhou, Z. Wu, Y. Takahashi, M. Matsumoto, E. Einarsdottir, J. Kere, D. Huang, G. Qiu, L. Xu, Y. Qiu, C. A. Wise, Y. Q. Song, N. Wu, P. Su, P. Gerdhem, K. Watanabe and S. Ikegawa (2018). ”An international meta-analysis confirms the association of BNC2 with adolescent idiopathic scoliosis.” Sci Rep 8(1): 4730.
Payton, N. M., G. Kalpouzos, D. Rizzuto, L. Fratiglioni, M. Kivipelto, L. Bäckman and E. J. Laukka (2018). ”Combining Cognitive, Genetic, and Structural Neuroimaging Markers to Identify Individuals with Increased Dementia Risk.” J Alzheimers Dis 64(2): 533-542.
Stenberg Hammar, K., K. Niespodziana, M. van Hage, J. Kere, R. Valenta, G. Hedlin and C. Söderhäll (2018). ”Reduced CDHR3 expression in children wheezing with rhinovirus.” Pediatr Allergy Immunol 29(2): 200-206.
Xu, C. J., C. Söderhäll, M. Bustamante, N. Baïz, O. Gruzieva, U. Gehring, D. Mason, L. Chatzi, M. Basterrechea, S. Llop, M. Torrent, F. Forastiere, M. P. Fantini, K. C. L. Carlsen, T. Haahtela, A. Morin, M. Kerkhof, S. K. Merid, B. van Rijkom, S. A. Jankipersadsing, M. J. Bonder, S. Ballereau, C. J. Vermeulen, R. Aguirre-Gamboa, J. C. de Jongste, H. A. Smit, A. Kumar, G. Pershagen, S. Guerra, J. Garcia-Aymerich, D. Greco, L. Reinius, R. R. C. McEachan, R. Azad, V. Hovland, P. Mowinckel, H. Alenius, N. Fyhrquist, N. Lemonnier, J. Pellet, C. Auffray, P. van der Vlies, C. C. van Diemen, Y. Li, C. Wijmenga, M. G. Netea, M. F. Moffatt, W. Cookson, J. M. Anto, J. Bousquet, T. Laatikainen, C. Laprise, K. H. Carlsen, D. Gori, D. Porta, C. Iñiguez, J. R. Bilbao, M. Kogevinas, J. Wright, B. Brunekreef, J. Kere, M. C. Nawijn, I. Annesi-Maesano, J. Sunyer, E. Melén and G. H. Koppelman (2018). ”DNA methylation in childhood asthma: an epigenome-wide meta-analysis.” Lancet Respir Med 6(5): 379-388.
Acevedo, N., S. Ezer, S. Kebede Merid, V. D. Gaertner, C. Söderhäll, M. D’Amato, M. Kabesch, E. Melén, J. Kere and V. Pulkkinen (2017). ”Neuropeptide S (NPS) variants modify the signaling and risk effects of NPS Receptor 1 (NPSR1) variants in asthma.” PLoS One 12(5): e0176568.
Bogo, R., A. Farah, K. K. Karlsson, N. L. Pedersen, M. Svartengren and Å. Skjönsberg (2017). ”Prevalence, Incidence Proportion, and Heritability for Tinnitus: A Longitudinal Twin Study.” Ear Hear 38(3): 292-300.
Bonfiglio, F., P. G. Hysi, W. Ek, V. Karhunen, N. V. Rivera, M. Männikkö, H. Nordenstedt, M. Zucchelli, F. Bresso, F. Williams, H. Tornblom, P. K. Magnusson, N. L. Pedersen, J. Ronkainen, P. T. Schmidt and M. D’Amato (2017). ”A meta-analysis of reflux genome-wide association studies in 6750 Northern Europeans from the general population.” Neurogastroenterol Motil 29(2).
Chiang, H. H., C. Forsell, A. K. Lindström, L. Lilius, H. Thonberg, I. Nennesmo and C. Graff (2017). ”No common founder for C9orf72 expansion mutation in Sweden.” J Hum Genet 62(2): 321-324.
Diószegi, J., S. Fiatal, R. Tóth, Á. Moravcsik-Kornyicki, Z. Kósa, J. Sándor, M. McKee and R. Ádány (2017). ”Distribution Characteristics and Combined Effect of Polymorphisms Affecting Alcohol Consumption Behaviour in the Hungarian General and Roma Populations.” Alcohol Alcohol 52(1): 104-111.
Donahue, K., N. Långström, S. Lundström, P. Lichtenstein and M. Forsman (2017). ”Familial Factors, Victimization, and Psychological Health Among Sexual Minority Adolescents in Sweden.” Am J Public Health 107(2): 322-328.
Einarsdottir, E., A. Grauers, J. Wang, H. Jiao, S. A. Escher, A. Danielsson, A. Simony, M. Andersen, S. B. Christensen, K. Åkesson, I. Kou, A. M. Khanshour, A. Ohlin, C. Wise, S. Ikegawa, J. Kere and P. Gerdhem (2017). ”CELSR2 is a candidate susceptibility gene in idiopathic scoliosis.” PLoS One 12(12): e0189591.
Gref, A., S. K. Merid, O. Gruzieva, S. Ballereau, A. Becker, T. Bellander, A. Bergström, Y. Bossé, M. Bottai, M. Chan-Yeung, E. Fuertes, D. Ierodiakonou, R. Jiang, S. Joly, M. Jones, M. S. Kobor, M. Korek, A. L. Kozyrskyj, A. Kumar, N. Lemonnier, E. MacIntyre, C. Ménard, D. Nickle, M. Obeidat, J. Pellet, M. Standl, A. Sääf, C. Söderhäll, C. M. T. Tiesler, M. van den Berge, J. M. Vonk, H. Vora, C. J. Xu, J. M. Antó, C. Auffray, M. Brauer, J. Bousquet, B. Brunekreef, W. J. Gauderman, J. Heinrich, J. Kere, G. H. Koppelman, D. Postma, C. Carlsten, G. Pershagen and E. Melén (2017). ”Genome-Wide Interaction Analysis of Air Pollution Exposure and Childhood Asthma with Functional Follow-up.” Am J Respir Crit Care Med 195(10): 1373-1383.
Henström, M., F. Hadizadeh, A. Beyder, F. Bonfiglio, T. Zheng, G. Assadi, J. Rafter, L. Bujanda, L. Agreus, A. Andreasson, A. Dlugosz, G. Lindberg, P. T. Schmidt, P. Karling, B. Ohlsson, N. J. Talley, M. Simren, S. Walter, M. Wouters, G. Farrugia and M. D’Amato (2017). ”TRPM8 polymorphisms associated with increased risk of IBS-C and IBS-M.” Gut 66(9): 1725-1727.
Huang, H., M. Fang, L. Jostins, M. Umićević Mirkov, G. Boucher, C. A. Anderson, V. Andersen, I. Cleynen, A. Cortes, F. Crins, M. D’Amato, V. Deffontaine, J. Dmitrieva, E. Docampo, M. Elansary, K. K. Farh, A. Franke, A. S. Gori, P. Goyette, J. Halfvarson, T. Haritunians, J. Knight, I. C. Lawrance, C. W. Lees, E. Louis, R. Mariman, T. Meuwissen, M. Mni, Y. Momozawa, M. Parkes, S. L. Spain, E. Théâtre, G. Trynka, J. Satsangi, S. van Sommeren, S. Vermeire, R. J. Xavier, R. K. Weersma, R. H. Duerr, C. G. Mathew, J. D. Rioux, D. P. B. McGovern, J. H. Cho, M. Georges, M. J. Daly and J. C. Barrett (2017). ”Fine-mapping inflammatory bowel disease loci to single-variant resolution.” Nature 547(7662): 173-178.
Ivanov, V. Z., A. Nordsletten, D. Mataix-Cols, E. Serlachius, P. Lichtenstein, S. Lundström, P. K. E. Magnusson, R. Kuja-Halkola and C. Rück (2017). ”Heritability of hoarding symptoms across adolescence and young adulthood: A longitudinal twin study.” PLoS One 12(6): e0179541.
Johansson, V., J. Jakobsson, R. G. Fortgang, H. Zetterberg, K. Blennow, T. D. Cannon, C. M. Hultman, L. Wetterberg and M. Landén (2017). ”Cerebrospinal fluid microglia and neurodegenerative markers in twins concordant and discordant for psychotic disorders.” Eur Arch Psychiatry Clin Neurosci 267(5): 391-402.
Johnson, A. C., R. Bogo, A. Farah, K. K. Karlsson, P. Muhr, M. Sjöström, E. B. Svensson, Å. Skjönsberg and M. Svartengren (2017). ”Influence of well-known risk factors for hearing loss in a longitudinal twin study.” Int J Audiol 56(sup1): 63-73.
Márquez, A., L. Vidal-Bralo, L. Rodríguez-Rodríguez, M. A. González-Gay, A. Balsa, I. González-Álvaro, P. Carreira, N. Ortego-Centeno, M. M. Ayala-Gutiérrez, F. J. García-Hernández, M. F. González-Escribano, J. M. Sabio, C. Tolosa, A. Suárez, A. González, L. Padyukov, J. Worthington, T. Vyse, M. E. Alarcón-Riquelme and J. Martín (2017). ”A combined large-scale meta-analysis identifies COG6 as a novel shared risk locus for rheumatoid arthritis and systemic lupus erythematosus.” Ann Rheum Dis 76(1): 286-294.
Mortera-Blanco, T., M. Dimitriou, P. S. Woll, M. Karimi, E. Elvarsdottir, S. Conte, M. Tobiasson, M. Jansson, I. Douagi, M. Moarii, L. Saft, E. Papaemmanuil, S. E. W. Jacobsen and E. Hellström-Lindberg (2017). ”SF3B1-initiating mutations in MDS-RSs target lymphomyeloid hematopoietic stem cells.” Blood 130(7): 881-890.
Muurinen, M., K. Hannula-Jouppi, L. E. Reinius, C. Söderhäll, S. K. Merid, A. Bergström, E. Melén, G. Pershagen, M. Lipsanen-Nyman, D. Greco and J. Kere (2017). ”Hypomethylation of HOXA4 promoter is common in Silver-Russell syndrome and growth restriction and associates with stature in healthy children.” Sci Rep 7(1): 15693.
Nagy, K., S. Fiatal, J. Sándor and R. Ádány (2017). ”Distinct Penetrance of Obesity-Associated Susceptibility Alleles in the Hungarian General and Roma Populations.” Obes Facts 10(5): 444-457.
Pikó, P., S. Fiatal, Z. Kósa, J. Sándor and R. Ádány (2017). ”Data to genetic risk assessment on high-density cholesterol level associated polymorphisms in Hungarian general and Roma populations.” Data Brief 14: 354-359.
Pikó, P., S. Fiatal, Z. Kósa, J. Sándor and R. Ádány (2017). ”Genetic factors exist behind the high prevalence of reduced high-density lipoprotein cholesterol levels in the Roma population.” Atherosclerosis 263: 119-126.
Täljemark, J., M. Råstam, P. Lichtenstein, H. Anckarsäter and N. Kerekes (2017). ”The coexistence of psychiatric and gastrointestinal problems in children with restrictive eating in a nationwide Swedish twin study.” J Eat Disord 5: 25.
Uhlin, E., H. Rönnholm, K. Day, M. Kele, K. Tammimies, S. Bölte and A. Falk (2017). ”Derivation of human iPS cell lines from monozygotic twins in defined and xeno free conditions.” Stem Cell Res 18: 22-25.
Weidner, J., L. Jarenbäck, K. de Jong, J. M. Vonk, M. van den Berge, C. A. Brandsma, H. M. Boezen, D. Sin, Y. Bossé, D. Nickle, J. Ankerst, L. Bjermer, D. S. Postma, A. Faiz and E. Tufvesson (2017). ”Sulfatase modifying factor 1 (SUMF1) is associated with Chronic Obstructive Pulmonary Disease.” Respir Res 18(1): 77.
Vincent, P. H., E. Benedikz, P. Uhlén, O. Hovatta and E. Sundström (2017). ”Expression of Pluripotency Markers in Nonpluripotent Human Neural Stem and Progenitor Cells.” Stem Cells Dev 26(12): 876-887.
Abolhassani, H., A. Aghamohammadi and L. Hammarström (2016). ”Monogenic mutations associated with IgA deficiency.” Expert Rev Clin Immunol 12(12): 1321-1335.
Assadi, G., L. Vesterlund, F. Bonfiglio, L. Mazzurana, L. Cordeddu, D. Schepis, J. Mjösberg, S. Ruhrmann, A. Fabbri, V. Vukojevic, P. Percipalle, F. A. Salomons, J. Laurencikiene, L. Törkvist, J. Halfvarson and M. D’Amato (2016). ”Functional Analyses of the Crohn’s Disease Risk Gene LACC1.” PLoS One 11(12): e0168276.
Berglind, D., P. Müller, M. Willmer, I. Sinha, P. Tynelius, E. Näslund, K. Dahlman-Wright and F. Rasmussen (2016). ”Differential methylation in inflammation and type 2 diabetes genes in siblings born before and after maternal bariatric surgery.” Obesity (Silver Spring) 24(1): 250-261.
Borg, J., S. Cervenka, R. Kuja-Halkola, G. J. Matheson, E. G. Jönsson, P. Lichtenstein, S. Henningsson, T. Ichimiya, H. Larsson, P. Stenkrona, C. Halldin and L. Farde (2016). ”Contribution of non-genetic factors to dopamine and serotonin receptor availability in the adult human brain.” Mol Psychiatry 21(8): 1077-1084.
Ellinghaus, D., L. Jostins, S. L. Spain, A. Cortes, J. Bethune, B. Han, Y. R. Park, S. Raychaudhuri, J. G. Pouget, M. Hübenthal, T. Folseraas, Y. Wang, T. Esko, A. Metspalu, H. J. Westra, L. Franke, T. H. Pers, R. K. Weersma, V. Collij, M. D’Amato, J. Halfvarson, A. B. Jensen, W. Lieb, F. Degenhardt, A. J. Forstner, A. Hofmann, S. Schreiber, U. Mrowietz, B. D. Juran, K. N. Lazaridis, S. Brunak, A. M. Dale, R. C. Trembath, S. Weidinger, M. Weichenthal, E. Ellinghaus, J. T. Elder, J. N. Barker, O. A. Andreassen, D. P. McGovern, T. H. Karlsen, J. C. Barrett, M. Parkes, M. A. Brown and A. Franke (2016). ”Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci.” Nat Genet 48(5): 510-518.
Eriksson, J. M., S. Lundström, P. Lichtenstein, S. Bejerot and E. Eriksson (2016). ”Effect of co-twin gender on neurodevelopmental symptoms: a twin register study.” Mol Autism 7: 8.
Fiatal, S., R. Tóth, Á. Moravcsik-Kornyicki, Z. Kósa, J. Sándor, M. McKee and R. Ádány (2016). ”High Prevalence of Smoking in the Roma Population Seems to Have No Genetic Background.” Nicotine Tob Res 18(12): 2260-2267.
Fortgang, R. G., C. M. Hultman and T. D. Cannon (2016). ”Coping Styles in Twins Discordant for Schizophrenia, Bipolar Disorder, and Depression.” Clin Psychol Sci 4(2): 216-228.
Fortgang, R. G., C. M. Hultman, T. G. van Erp and T. D. Cannon (2016). ”Multidimensional assessment of impulsivity in schizophrenia, bipolar disorder, and major depressive disorder: testing for shared endophenotypes.” Psychol Med 46(7): 1497-1507.
Ghasimi, S., C. Wibom, A. M. Dahlin, T. Brännström, I. Golovleva, U. Andersson and B. Melin (2016). ”Genetic risk variants in the CDKN2A/B, RTEL1 and EGFR genes are associated with somatic biomarkers in glioma.” J Neurooncol 127(3): 483-492.
Günaydın, G., J. Nordgren, S. Sharma and L. Hammarström (2016). ”Association of elevated rotavirus-specific antibody titers with HBGA secretor status in Swedish individuals: The FUT2 gene as a putative susceptibility determinant for infection.” Virus Res 211: 64-68.
Henmyr, V., C. Lind-Halldén, D. Carlberg, C. Halldén, E. Melén, M. Wickman, A. Bergström, T. Säll and L. O. Cardell (2016). ”Characterization of genetic variation in TLR8 in relation to allergic rhinitis.” Allergy 71(3): 333-341.
Hovey, D., M. Lindstedt, A. Zettergren, L. Jonsson, A. Johansson, J. Melke, N. Kerekes, H. Anckarsäter, P. Lichtenstein, S. Lundström and L. Westberg (2016). ”Antisocial behavior and polymorphisms in the oxytocin receptor gene: findings in two independent samples.” Mol Psychiatry 21(7): 983-988.
Joubert, B. R., J. F. Felix, P. Yousefi, K. M. Bakulski, A. C. Just, C. Breton, S. E. Reese, C. A. Markunas, R. C. Richmond, C. J. Xu, L. K. Küpers, S. S. Oh, C. Hoyo, O. Gruzieva, C. Söderhäll, L. A. Salas, N. Baïz, H. Zhang, J. Lepeule, C. Ruiz, S. Ligthart, T. Wang, J. A. Taylor, L. Duijts, G. C. Sharp, S. A. Jankipersadsing, R. M. Nilsen, A. Vaez, M. D. Fallin, D. Hu, A. A. Litonjua, B. F. Fuemmeler, K. Huen, J. Kere, I. Kull, M. C. Munthe-Kaas, U. Gehring, M. Bustamante, M. J. Saurel-Coubizolles, B. M. Quraishi, J. Ren, J. Tost, J. R. Gonzalez, M. J. Peters, S. E. Håberg, Z. Xu, J. B. van Meurs, T. R. Gaunt, M. Kerkhof, E. Corpeleijn, A. P. Feinberg, C. Eng, A. A. Baccarelli, S. E. Benjamin Neelon, A. Bradman, S. K. Merid, A. Bergström, Z. Herceg, H. Hernandez-Vargas, B. Brunekreef, M. Pinart, B. Heude, S. Ewart, J. Yao, N. Lemonnier, O. H. Franco, M. C. Wu, A. Hofman, W. McArdle, P. Van der Vlies, F. Falahi, M. W. Gillman, L. F. Barcellos, A. Kumar, M. Wickman, S. Guerra, M. A. Charles, J. Holloway, C. Auffray, H. W. Tiemeier, G. D. Smith, D. Postma, M. F. Hivert, B. Eskenazi, M. Vrijheid, H. Arshad, J. M. Antó, A. Dehghan, W. Karmaus, I. Annesi-Maesano, J. Sunyer, A. Ghantous, G. Pershagen, N. Holland, S. K. Murphy, D. L. DeMeo, E. G. Burchard, C. Ladd-Acosta, H. Snieder, W. Nystad, G. H. Koppelman, C. L. Relton, V. W. Jaddoe, A. Wilcox, E. Melén and S. J. London (2016). ”DNA Methylation in Newborns and Maternal Smoking in Pregnancy: Genome-wide Consortium Meta-analysis.” Am J Hum Genet 98(4): 680-696.
Kaartokallio, T., A. I. Lokki, H. Peterson, K. Kivinen, L. Hiltunen, E. Salmela, T. Lappalainen, P. Maanselkä, S. Heino, S. Knuutila, A. Sayed, L. Poston, S. P. Brennecke, M. P. Johnson, L. Morgan, E. K. Moses, J. Kere and H. Laivuori (2016). ”Preeclampsia does not share common risk alleles in 9p21 with coronary artery disease and type 2 diabetes.” Ann Med 48(5): 330-336.
Kalpouzos, G., D. Rizzuto, L. Keller, J. Fastbom, G. Santoni, S. Angleman, C. Graff, L. Bäckman and L. Fratiglioni (2016). ”Telomerase Gene (hTERT) and Survival: Results From Two Swedish Cohorts of Older Adults.” J Gerontol A Biol Sci Med Sci 71(2): 188-195.
Kovamees, O., A. Shemyakin, M. Eriksson, B. Angelin and J. Pernow (2016). ”Arginase inhibition improves endothelial function in patients with familial hypercholesterolaemia irrespective of their cholesterol levels.” J Intern Med 279(5): 477-484.
Lester, N., D. Garcia, S. Lundström, S. Brändström, M. Råstam, N. Kerekes, T. Nilsson, C. R. Cloninger and H. Anckarsäter (2016). ”The genetic and environmental structure of the character sub-scales of the temperament and character inventory in adolescence.” Ann Gen Psychiatry 15: 10.
Acevedo N, Reinius LE, Greco D, Gref A, Orsmark-Pietras C, Persson H, et al. (2015). Risk of childhood asthma is associated with CpG-site polymorphisms, regional DNA methylation and mRNA levels at the GSDMB/ORMDL3 locus. Human molecular genetics 24(3): 875-890.
Fuertes E, Soderhall C, Acevedo N, Becker A, Brauer M, Chan-Yeung M, et al. (2015). Associations between the 17q21 region and allergic rhinitis in 5 birth cohorts. The Journal of allergy and clinical immunology 135(2): 573-576.
Grauers A, Wang J, Einarsdottir E, Simony A, Danielsson A, Akesson K, et al. (2015). Candidate gene analysis and exome sequencing confirm LBX1 as a susceptibility gene for Idiopathic Scoliosis. The spine journal : official journal of the North American Spine Society.
Matsson H, Huss M, Persson H, Einarsdottir E, Tiraboschi E, Nopola-Hemmi J, et al. (2015). Polymorphisms in DCDC2 and S100B associate with developmental dyslexia. Journal of human genetics.
Pettersson E, Sjolander A, Almqvist C, Anckarsater H, D’Onofrio BM, Lichtenstein P, et al. (2015). Birth weight as an independent predictor of ADHD symptoms: a within-twin pair analysis. Journal of child psychology and psychiatry, and allied disciplines 56(4): 453-459.
Ragnarsson O, Glad CA, Bergthorsdottir R, Almqvist EG, Ekerstad E, Widell H, et al. (2015). Body composition and bone mineral density in women with Cushing’s syndrome in remission and the association with common genetic variants influencing glucocorticoid sensitivity. European journal of endocrinology / European Federation of Endocrine Societies 172(1): 1-10.
Soderlund-Strand A, Wikstrom A, Dillner J (2015). Evaluation of human papillomavirus DNA detection in samples obtained for routine Chlamydia trachomatis screening. Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology 64: 88-91.
Gunaydin G, Nordgren J, Sharma S, Hammarstrom L (2016). Association of elevated rotavirus-specific antibody titers with HBGA secretor status in Swedish individuals: The FUT2 gene as a putative susceptibility determinant for infection. Virus Res 211: 64-68.
Berglind D, Muller P, Willmer M, Sinha I, Tynelius P, Naslund E, et al. (2016). Differential methylation in inflammation and type 2 diabetes genes in siblings born before and after maternal bariatric surgery. Obesity (Silver Spring) 24(1): 250-261.
Xu WL, Pedersen NL, Keller L, Kalpouzos G, Wang HX, Graff C, et al. (2015). HHEX_23 AA Genotype Exacerbates Effect of Diabetes on Dementia and Alzheimer Disease: A Population-Based Longitudinal Study. PLoS Med 12(7): e1001853.
Mousavi F, Rozsa S, Nilsson T, Archer T, Anckarsater H, Garcia D (2015). Personality and intelligence: persistence, not self-directedness, cooperativeness or self-transcendence, is related to twins’ cognitive abilities. PeerJ 3: e1195.
Marenholz I, Esparza-Gordillo J, Ruschendorf F, Bauerfeind A, Strachan DP, Spycher BD, et al. (2015). Meta-analysis identifies seven susceptibility loci involved in the atopic march. 6: 8804.
Laukka EJ, Lovden M, Kalpouzos G, Papenberg G, Keller L, Graff C, et al. (2015). Microstructural White Matter Properties Mediate the Association between APOE and Perceptual Speed in Very Old Persons without Dementia. PLoS One 10(8): e0134766.
Kunz M, Konig IR, Schillert A, Kruppa J, Ziegler A, Grallert H, et al. (2015). Genome-wide association study identifies new susceptibility loci for cutaneous lupus erythematosus. Exp Dermatol 24(7): 510-515.
Karimi M, Nilsson C, Dimitriou M, Jansson M, Matsson H, Unneberg P, et al. (2015). High-throughput mutational screening adds clinically important information in myelodysplastic syndromes and secondary or therapy-related acute myeloid leukemia. Haematologica 100(6): e223-225.
Jiao H, Arner P, Gerdhem P, Strawbridge RJ, Naslund E, Thorell A, et al. (2015). Exome sequencing followed by genotyping suggests SYPL2 as a susceptibility gene for morbid obesity. Eur J Hum Genet 23(9): 1216-1222.
Henmyr V, Lind-Hallden C, Carlberg D, Hallden C, Melen E, Wickman M, et al. (2015). Characterization of genetic variation in TLR8 in relation to allergic rhinitis. Allergy.
Hafren L, Einarsdottir E, Kentala E, Hammaren-Malmi S, Bhutta MF, MacArthur CJ, et al. (2015). Predisposition to Childhood Otitis Media and Genetic Polymorphisms within the Toll-Like Receptor 4 (TLR4) Locus. PLoS One 10(7): e0132551.
Glad CA, Carlsson LM, Melander O, Almgren P, Sjostrom L, Nilsson S, et al. (2015). The GH receptor exon 3 deleted/full-length polymorphism is associated with central adiposity in the general population. Eur J Endocrinol 172(2): 123-128.
Ek WE, Reznichenko A, Ripke S, Niesler B, Zucchelli M, Rivera NV, et al. (2015). Exploring the genetics of irritable bowel syndrome: a GWA study in the general population and replication in multinational case-control cohorts. Gut 64(11): 1774-1782.
Bogo R, Farah A, Johnson AC, Karlsson KK, Pedersen NL, Svartengren M, et al. (2015). The role of genetic factors for hearing deterioration across 20 years: a twin study. J Gerontol A Biol Sci Med Sci 70(5): 647-653.
(2015). Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis. Nat Genet 47(12): 1449-1456.
Barbosa EJ, Glad CA, Nilsson AG, Bosaeus N, Nystrom HF, Svensson PA, et al. (2014). Extracellular water and blood pressure in adults with growth hormone (GH) deficiency: a genotype-phenotype association study. PloS one 9(8): e105754.
Becker J, Czamara D, Scerri TS, Ramus F, Csepe V, Talcott JB, et al. (2014). Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort. Eur J Hum Genet 22(5): 675-680.
Dahgam S, Modig L, Torinsson Naluai A, Olin AC, Nyberg F (2014). Haplotypes of the inducible nitric oxide synthase gene are strongly associated with exhaled nitric oxide levels in adults: a population-based study. Journal of medical genetics 51(7): 449-454.
Darki F, Peyrard-Janvid M, Matsson H, Kere J, Klingberg T (2014). DCDC2 polymorphism is associated with left temporoparietal gray and white matter structures during development. The Journal of neuroscience : the official journal of the Society for Neuroscience 34(43): 14455-14462.
Ek WE, Reznichenko A, Ripke S, Niesler B, Zucchelli M, Rivera NV, et al. (2014). Exploring the genetics of irritable bowel syndrome: a GWA study in the general population and replication in multinational case-control cohorts. Gut.
Ferencz B, Laukka EJ, Welmer AK, Kalpouzos G, Angleman S, Keller L, et al. (2014). The benefits of staying active in old age: physical activity counteracts the negative influence of PICALM, BIN1, and CLU risk alleles on episodic memory functioning. Psychology and aging 29(2): 440-449.
Garcia D, Strage A, Lundstrom S, Radovic S, Brandstrom S, Rastam M, et al. (2014). Responsibility and cooperativeness are constrained, not determined. Frontiers in psychology 5: 308.
Glad CA, Barbosa EJ, Filipsson Nystrom H, Carlsson LM, Nilsson S, Nilsson AG, et al. (2014). SNPs within the GH-signaling pathway are associated with the early IGF1 response to GH replacement therapy in GHD adults. European journal of endocrinology / European Federation of Endocrine Societies 170(1): 101-107.
Henstrom M, Zucchelli M, Soderhall C, Bergstrom A, Kere J, Melen E, et al. (2014). NPSR1 polymorphisms influence recurrent abdominal pain in children: a population-based study. Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society 26(10): 1417-1425.
Holliday EG, Attia J, Hancock S, Koloski N, McEvoy M, Peel R, et al. (2014). Genome-wide association study identifies two novel genomic regions in irritable bowel syndrome. The American journal of gastroenterology 109(5): 770-772.
Jiao H, Arner P, Gerdhem P, Strawbridge RJ, Naslund E, Thorell A, et al. (2014). Exome sequencing followed by genotyping suggests SYPL2 as a susceptibility gene for morbid obesity. Eur J Hum Genet.
Karlsson R, Aly M, Clements M, Zheng L, Adolfsson J, Xu J, et al. (2014). A population-based assessment of germline HOXB13 G84E mutation and prostate cancer risk. European urology 65(1): 169-176.
Kerekes N, Lundstrom S, Chang Z, Tajnia A, Jern P, Lichtenstein P, et al. (2014). Oppositional defiant- and conduct disorder-like problems: neurodevelopmental predictors and genetic background in boys and girls, in a nationwide twin study. PeerJ 2: e359.
Pantzar A, Laukka EJ, Atti AR, Papenberg G, Keller L, Graff C, et al. (2014). Interactive effects of KIBRA and CLSTN2 polymorphisms on episodic memory in old-age unipolar depression. Neuropsychologia 62: 137-142.
Ragnarsson O, Glad CA, Berglund P, Bergthorsdottir R, Eder DN, Johannsson G (2014). Common genetic variants in the glucocorticoid receptor and the 11beta-hydroxysteroid dehydrogenase type 1 genes influence long-term cognitive impairments in patients with Cushing’s syndrome in remission. The Journal of clinical endocrinology and metabolism 99(9): E1803-1807.
Soderlund-Strand A, Uhnoo I, Dillner J (2014). Change in population prevalences of human papillomavirus after initiation of vaccination: the high-throughput HPV monitoring study. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 23(12): 2757-2764.
Soderqvist S, Matsson H, Peyrard-Janvid M, Kere J, Klingberg T (2014). Polymorphisms in the dopamine receptor 2 gene region influence improvements during working memory training in children and adolescents. Journal of cognitive neuroscience 26(1): 54-62.
Wouters MM, Lambrechts D, Knapp M, Cleynen I, Whorwell P, Agreus L, et al. (2014). Genetic variants in CDC42 and NXPH1 as susceptibility factors for constipation and diarrhoea predominant irritable bowel syndrome. Gut 63(7): 1103-1111.
Acevedo N, Saaf A, Soderhall C, Melen E, Mandelin J, Pietras CO, et al. (2013). Interaction between retinoid acid receptor-related orphan receptor alpha (RORA) and neuropeptide S receptor 1 (NPSR1) in asthma. PloS one 8(4): e60111.
Beaudoin M, Goyette P, Boucher G, Lo KS, Rivas MA, Stevens C, et al. (2013). Deep resequencing of GWAS loci identifies rare variants in CARD9, IL23R and RNF186 that are associated with ulcerative colitis. PLoS genetics 9(9): e1003723.
Bloom RJ, Kahler AK, Collins AL, Chen G, Cannon TD, Hultman C, et al. (2013). Comprehensive analysis of copy number variation in monozygotic twins discordant for bipolar disorder or schizophrenia. Schizophrenia research 146(1-3): 289-290.
Bornelov S, Saaf A, Melen E, Bergstrom A, Torabi Moghadam B, Pulkkinen V, et al. (2013). Rule-based models of the interplay between genetic and environmental factors in childhood allergy. PloS one 8(11): e80080.
Garcia D, Lundstrom S, Brandstrom S, Rastam M, Cloninger CR, Kerekes N, et al. (2013). Temperament and character in the Child and Adolescent Twin Study in Sweden (CATSS): comparison to the general population, and genetic structure analysis. PloS one 8(8): e70475.
Ivanov VZ, Mataix-Cols D, Serlachius E, Lichtenstein P, Anckarsater H, Chang Z, et al. (2013). Prevalence, comorbidity and heritability of hoarding symptoms in adolescence: a population based twin study in 15-year olds. PloS one 8(7): e69140.
Laukka EJ, Lovden M, Herlitz A, Karlsson S, Ferencz B, Pantzar A, et al. (2013). Genetic effects on old-age cognitive functioning: a population-based study. Psychology and aging 28(1): 262-274.
Mehlig K, Leander K, de Faire U, Nyberg F, Berg C, Rosengren A, et al. (2013). The association between plasma homocysteine and coronary heart disease is modified by the MTHFR 677C>T polymorphism. Heart (British Cardiac Society) 99(23): 1761-1765.
Rastam M, Taljemark J, Tajnia A, Lundstrom S, Gustafsson P, Lichtenstein P, et al. (2013). Eating problems and overlap with ADHD and autism spectrum disorders in a nationwide twin study of 9- and 12-year-old children. TheScientificWorldJournal 2013: 315429.
Reinius LE, Gref A, Saaf A, Acevedo N, Joerink M, Kupczyk M, et al. (2013). DNA methylation in the Neuropeptide S Receptor 1 (NPSR1) promoter in relation to asthma and environmental factors. PloS one 8(1): e53877.
Weidinger S, Willis-Owen SA, Kamatani Y, Baurecht H, Morar N, Liang L, et al. (2013). A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis. Human molecular genetics 22(23): 4841-4856.
Angst MS, Lazzeroni LC, Phillips NG, Drover DR, Tingle M, Ray A, et al. (2012). Aversive and reinforcing opioid effects: a pharmacogenomic twin study. Anesthesiology 117(1): 22-37.
Angst MS, Phillips NG, Drover DR, Tingle M, Ray A, Swan GE, et al. (2012). Pain sensitivity and opioid analgesia: a pharmacogenomic twin study. Pain 153(7): 1397-1409.
Anthoni H, Sucheston LE, Lewis BA, Tapia-Paez I, Fan X, Zucchelli M, et al. (2012). The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language. Behavior genetics 42(4): 509-527.
Barbosa EJ, Glad CA, Nilsson AG, Filipsson Nystrom H, Gotherstrom G, Svensson PA, et al. (2012). Genotypes associated with lipid metabolism contribute to differences in serum lipid profile of GH-deficient adults before and after GH replacement therapy. European journal of endocrinology / European Federation of Endocrine Societies 167(3): 353-362.
Darki F, Peyrard-Janvid M, Matsson H, Kere J, Klingberg T (2012). Three dyslexia susceptibility genes, DYX1C1, DCDC2, and KIAA0319, affect temporo-parietal white matter structure. Biological psychiatry 72(8): 671-676.
Dubois L, Ohm Kyvik K, Girard M, Tatone-Tokuda F, Perusse D, Hjelmborg J, et al. (2012). Genetic and environmental contributions to weight, height, and BMI from birth to 19 years of age: an international study of over 12,000 twin pairs. PloS one 7(2): e30153.
Gigante B, Leander K, Vikstrom M, Ye S, de Faire U (2012). Chromosome 1p13 genetic variants antagonize the risk of myocardial infarction associated with high ApoB serum levels. BMC cardiovascular disorders 12: 90.
Jarvinen TM, Hellquist A, Zucchelli M, Koskenmies S, Panelius J, Hasan T, et al. (2012). Replication of GWAS-identified systemic lupus erythematosus susceptibility genes affirms B-cell receptor pathway signalling and strengthens the role of IRF5 in disease susceptibility in a Northern European population. Rheumatology (Oxford, England) 51(1): 87-92.
Johansson V, Nybom R, Wetterberg L, Hultman CM, Cannon TD, Johansson AG, et al. (2012). Microscopic particles in two fractions of fresh cerebrospinal fluid in twins with schizophrenia or bipolar disorder and in healthy controls. PloS one 7(9): e45994.
Ruau D, Dudley JT, Chen R, Phillips NG, Swan GE, Lazzeroni LC, et al. (2012). Integrative approach to pain genetics identifies pain sensitivity loci across diseases. PLoS computational biology 8(6): e1002538.
Scerri TS, Darki F, Newbury DF, Whitehouse AJ, Peyrard-Janvid M, Matsson H, et al. (2012). The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure. PloS one 7(11): e50321.
Soderqvist S, Bergman Nutley S, Peyrard-Janvid M, Matsson H, Humphreys K, Kere J, et al. (2012). Dopamine, working memory, and training induced plasticity: implications for developmental research. Developmental psychology 48(3): 836-843.
Surakka I, Whitfield JB, Perola M, Visscher PM, Montgomery GW, Falchi M, et al. (2012). A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol. Twin research and human genetics : the official journal of the International Society for Twin Studies 15(6): 691-699.
Walum H, Lichtenstein P, Neiderhiser JM, Reiss D, Ganiban JM, Spotts EL, et al. (2012). Variation in the oxytocin receptor gene is associated with pair-bonding and social behavior. Biological psychiatry 71(5): 419-426.
Ziermans T, Dumontheil I, Roggeman C, Peyrard-Janvid M, Matsson H, Kere J, et al. (2012). Working memory brain activity and capacity link MAOA polymorphism to aggressive behavior during development. Translational psychiatry 2: e85.
Aly M, Wiklund F, Xu J, Isaacs WB, Eklund M, D’Amato M, et al. (2011). Polygenic risk score improves prostate cancer risk prediction: results from the Stockholm-1 cohort study. European urology 60(1): 21-28.
Anedda F, Zucchelli M, Schepis D, Hellquist A, Corrado L, D’Alfonso S, et al. (2011). Multiple polymorphisms affect expression and function of the neuropeptide S receptor (NPSR1). PloS one 6(12): e29523.
Cosgrove VE, Rhee SH, Gelhorn HL, Boeldt D, Corley RC, Ehringer MA, et al. (2011). Structure and etiology of co-occurring internalizing and externalizing disorders in adolescents. Journal of abnormal child psychology 39(1): 109-123.
Dumontheil I, Roggeman C, Ziermans T, Peyrard-Janvid M, Matsson H, Kere J, et al. (2011). Influence of the COMT genotype on working memory and brain activity changes during development. Biological psychiatry 70(3): 222-229.
Goumidi L, Dahlman-Wright K, Tapia-Paez I, Matsson H, Pasquier F, Amouyel P, et al. (2011). Study of estrogen receptor-alpha and receptor-beta gene polymorphisms on Alzheimer’s disease. Journal of Alzheimer’s disease : JAD 26(3): 431-439.
Jiao H, Arner P, Dickson SL, Vidal H, Mejhert N, Henegar C, et al. (2011). Genetic association and gene expression analysis identify FGFR1 as a new susceptibility gene for human obesity. The Journal of clinical endocrinology and metabolism 96(6): E962-966.
Jiao H, Arner P, Hoffstedt J, Brodin D, Dubern B, Czernichow S, et al. (2011). Genome wide association study identifies KCNMA1 contributing to human obesity. BMC medical genomics 4: 51.
Keller L, Xu W, Wang HX, Winblad B, Fratiglioni L, Graff C (2011). The obesity related gene, FTO, interacts with APOE, and is associated with Alzheimer’s disease risk: a prospective cohort study. Journal of Alzheimer’s disease : JAD 23(3): 461-469.
Matsson H, Tammimies K, Zucchelli M, Anthoni H, Onkamo P, Nopola-Hemmi J, et al. (2011). SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations. Behavior genetics 41(1): 134-140.
Narusyte J, Neiderhiser JM, Andershed AK, D’Onofrio BM, Reiss D, Spotts E, et al. (2011). Parental criticism and externalizing behavior problems in adolescents: the role of environment and genotype-environment correlation. Journal of abnormal psychology 120(2): 365-376.
Pietras CO, Vendelin J, Anedda F, Bruce S, Adner M, Sundman L, et al. (2011). The asthma candidate gene NPSR1 mediates isoform specific downstream signalling. BMC pulmonary medicine 11: 39.
Ramanujam R, Piehl F, Pirskanen R, Gregersen PK, Hammarstrom L (2011). Concomitant autoimmunity in myasthenia gravis–lack of association with IgA deficiency. Journal of neuroimmunology 236(1-2): 118-122.
Rivas MA, Beaudoin M, Gardet A, Stevens C, Sharma Y, Zhang CK, et al. (2011). Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease. Nature genetics 43(11): 1066-1073.
Smedby KE, Eloranta S, Duvefelt K, Melbye M, Humphreys K, Hjalgrim H, et al. (2011). Vitamin D receptor genotypes, ultraviolet radiation exposure, and risk of non-Hodgkin lymphoma. American journal of epidemiology 173(1): 48-54.
Vesterlund L, Jiao H, Unneberg P, Hovatta O, Kere J (2011). The zebrafish transcriptome during early development. BMC developmental biology 11: 30.
Zucchelli M, Camilleri M, Andreasson AN, Bresso F, Dlugosz A, Halfvarson J, et al. (2011). Association of TNFSF15 polymorphism with irritable bowel syndrome. Gut 60(12): 1671-1677.
D’Amato M, Zucchelli M, Seddighzadeh M, Anedda F, Lindblad S, Kere J, et al. (2010). Analysis of neuropeptide S receptor gene (NPSR1) polymorphism in rheumatoid arthritis. PloS one 5(2): e9315.
Fernberg P, Chang ET, Duvefelt K, Hjalgrim H, Eloranta S, Sorensen KM, et al. (2010). Genetic variation in chromosomal translocation breakpoint and immune function genes and risk of non-Hodgkin lymphoma. Cancer causes & control : CCC 21(5): 759-769.
Ferreira RC, Pan-Hammarstrom Q, Graham RR, Gateva V, Fontan G, Lee AT, et al. (2010). Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. Nature genetics 42(9): 777-780.
Glad CA, Johannsson G, Carlsson LM, Svensson PA (2010). Rapid and high throughput genotyping of the growth hormone receptor exon 3 deleted/full-length polymorphism using a tagSNP. Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society 20(3): 270-273.
Hasselrot K, Bratt G, Duvefelt K, Hirbod T, Sandstrom E, Broliden K (2010). HIV-1 exposed uninfected men who have sex with men have increased levels of salivary CC-chemokines associated with sexual behavior. AIDS (London, England) 24(10): 1569-1575.
Hellquist A, Sandling JK, Zucchelli M, Koskenmies S, Julkunen H, D’Amato M, et al. (2010). Variation in STAT4 is associated with systemic lupus erythematosus in a Finnish family cohort. Annals of the rheumatic diseases 69(5): 883-886.
Jarvinen TM, Hellquist A, Koskenmies S, Einarsdottir E, Koskinen LL, Jeskanen L, et al. (2010). Tyrosine kinase 2 and interferon regulatory factor 5 polymorphisms are associated with discoid and subacute cutaneous lupus erythematosus. Experimental dermatology 19(2): 123-131.
Keller L, Murphy C, Wang HX, Fratiglioni L, Olin M, Gafvels M, et al. (2010). A functional polymorphism in the HMGCR promoter affects transcriptional activity but not the risk for Alzheimer disease in Swedish populations. Brain research 1344: 185-191.
Link J, Lorentzen AR, Kockum I, Duvefelt K, Lie BA, Celius EG, et al. (2010). Two HLA class I genes independently associated with multiple sclerosis. Journal of neuroimmunology 226(1-2): 172-176.
Pinho CM, Bjork BF, Alikhani N, Backman HG, Eneqvist T, Fratiglioni L, et al. (2010). Genetic and biochemical studies of SNPs of the mitochondrial A beta-degrading protease, hPreP. Neuroscience letters 469(2): 204-208.
Sillen A, Brohede J, Lilius L, Forsell C, Andrade J, Odeberg J, et al. (2010). Linkage to 20p13 including the ANGPT4 gene in families with mixed Alzheimer’s disease and vascular dementia. Journal of human genetics 55(10): 649-655.
Soderqvist S, McNab F, Peyrard-Janvid M, Matsson H, Humphreys K, Kere J, et al. (2010). The SNAP25 gene is linked to working memory capacity and maturation of the posterior cingulate cortex during childhood. Biological psychiatry 68(12): 1120-1125.
Torkvist L, Halfvarson J, Ong RT, Lordal M, Sjoqvist U, Bresso F, et al. (2010). Analysis of 39 Crohn’s disease risk loci in Swedish inflammatory bowel disease patients. Inflammatory bowel diseases 16(6): 907-909.
Bruce S, Nyberg F, Melen E, James A, Pulkkinen V, Orsmark-Pietras C, et al. (2009). The protective effect of farm animal exposure on childhood allergy is modified by NPSR1 polymorphisms. Journal of medical genetics 46(3): 159-167.
Brynedal B, Bomfim IL, Olsson T, Duvefelt K, Hillert J (2009). Differential expression, and genetic association, of CD58 in Swedish multiple sclerosis patients. Proceedings of the National Academy of Sciences of the United States of America 106(23): E58; author reply E59.
Dahdouh F, Anthoni H, Tapia-Paez I, Peyrard-Janvid M, Schulte-Korne G, Warnke A, et al. (2009). Further evidence for DYX1C1 as a susceptibility factor for dyslexia. Psychiatric genetics 19(2): 59-63.
Dahlman I, Nilsson M, Gu HF, Lecoeur C, Efendic S, Ostenson CG, et al. (2009). Functional and genetic analysis in type 2 diabetes of liver X receptor alleles–a cohort study. BMC medical genetics 10: 27.
Einarsdottir E, Koskinen LL, Dukes E, Kainu K, Suomela S, Lappalainen M, et al. (2009). IL23R in the Swedish, Finnish, Hungarian and Italian populations: association with IBD and psoriasis, and linkage to celiac disease. BMC medical genetics 10: 8.
Ekelund E, Bradley M, Weidinger S, Jovanovic DL, Johansson C, Lindgren CM, et al. (2009). Lack of association between neuropeptide S receptor 1 gene (NPSR1) and eczema in five European populations. Acta dermato-venereologica 89(2): 115-121.
Hellquist A, Jarvinen TM, Koskenmies S, Zucchelli M, Orsmark-Pietras C, Berglind L, et al. (2009). Evidence for genetic association and interaction between the TYK2 and IRF5 genes in systemic lupus erythematosus. The Journal of rheumatology 36(8): 1631-1638.
Hellquist A, Zucchelli M, Lindgren CM, Saarialho-Kere U, Jarvinen TM, Koskenmies S, et al. (2009). Identification of MAMDC1 as a candidate susceptibility gene for systemic lupus erythematosus (SLE). PloS one 4(12): e8037.
Kainu K, Kivinen K, Zucchelli M, Suomela S, Kere J, Inerot A, et al. (2009). Association of psoriasis to PGLYRP and SPRR genes at PSORS4 locus on 1q shows heterogeneity between Finnish, Swedish and Irish families. Experimental dermatology 18(2): 109-115.
Koskinen LL, Einarsdottir E, Dukes E, Heap GA, Dubois P, Korponay-Szabo IR, et al. (2009). Association study of the IL18RAP locus in three European populations with coeliac disease. Human molecular genetics 18(6): 1148-1155.
Lindstrom S, Adami HO, Balter K, Xu J, Zheng SL, Sun J, et al. (2009). Genetic variation in the upstream region of ERG and prostate cancer. Cancer causes & control : CCC 20(7): 1173-1180.
Massinen S, Tammimies K, Tapia-Paez I, Matsson H, Hokkanen ME, Soderberg O, et al. (2009). Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia. Human molecular genetics 18(15): 2802-2812.
Peterson H, Laivuori H, Kerkela E, Jiao H, Hiltunen L, Heino S, et al. (2009). ROCK2 allelic variants are not associated with pre-eclampsia susceptibility in the Finnish population. Molecular human reproduction 15(7): 443-449.
Zucchelli M, Torkvist L, Bresso F, Halfvarson J, Hellquist A, Anedda F, et al. (2009). PepT1 oligopeptide transporter (SLC15A1) gene polymorphism in inflammatory bowel disease. Inflammatory bowel diseases 15(10): 1562-1569.
Zucchelli M, Torkvist L, Bresso F, Halfvarson J, Soderhall C, Lee YA, et al. (2009). No association between the eczema genes COL29A1 and IL31 and inflammatory bowel disease. Inflammatory bowel diseases 15(7): 961-962.
Dahlman I, Vaxillaire M, Nilsson M, Lecoeur C, Gu HF, Cavalcanti-Proenca C, et al. (2008). Estrogen receptor alpha gene variants associate with type 2 diabetes and fasting plasma glucose. Pharmacogenetics and genomics 18(11): 967-975.
Hannelius U, Salmela E, Lappalainen T, Guillot G, Lindgren CM, von Dobeln U, et al. (2008). Population substructure in Finland and Sweden revealed by the use of spatial coordinates and a small number of unlinked autosomal SNPs. BMC genetics 9: 54.
Jiao H, Kaaman M, Dungner E, Kere J, Arner P, Dahlman I (2008). Association analysis of positional obesity candidate genes based on integrated data from transcriptomics and linkage analysis. International journal of obesity (2005) 32(5): 816-825.
Koskinen LL, Korponay-Szabo IR, Viiri K, Juuti-Uusitalo K, Kaukinen K, Lindfors K, et al. (2008). Myosin IXB gene region and gluten intolerance: linkage to coeliac disease and a putative dermatitis herpetiformis association. Journal of medical genetics 45(4): 222-227.
Ludwig KU, Roeske D, Schumacher J, Schulte-Korne G, Konig IR, Warnke A, et al. (2008). Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample. Journal of neural transmission (Vienna, Austria : 1996) 115(11): 1587-1589.
Melen E, Nyberg F, Lindgren CM, Berglind N, Zucchelli M, Nordling E, et al. (2008). Interactions between glutathione S-transferase P1, tumor necrosis factor, and traffic-related air pollution for development of childhood allergic disease. Environmental health perspectives 116(8): 1077-1084.
Mottagui-Tabar S, Hoffstedt J, Brookes AJ, Jiao H, Arner P, Dahlman I (2008). Association of ADRB1 and UCP3 gene polymorphisms with insulin sensitivity but not obesity. Hormone research 69(1): 31-36.
Nordling E, Berglind N, Melen E, Emenius G, Hallberg J, Nyberg F, et al. (2008). Traffic-related air pollution and childhood respiratory symptoms, function and allergies. Epidemiology (Cambridge, Mass.) 19(3): 401-408.
Orsmark-Pietras C, Melen E, Vendelin J, Bruce S, Laitinen A, Laitinen LA, et al. (2008). Biological and genetic interaction between tenascin C and neuropeptide S receptor 1 in allergic diseases. Human molecular genetics 17(11): 1673-1682.
Pegelow M, Peyrard-Janvid M, Zucchelli M, Fransson I, Larson O, Kere J, et al. (2008). Familial non-syndromic cleft lip and palate–analysis of the IRF6 gene and clinical phenotypes. European journal of orthodontics 30(2): 169-175.
Roos IM, Kockum I, Hillert J (2008). The interleukin 23 receptor gene in multiple sclerosis: a case-control study. Journal of neuroimmunology 194(1-2): 173-180.
Anthoni H, Zucchelli M, Matsson H, Muller-Myhsok B, Fransson I, Schumacher J, et al. (2007). A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia. Human molecular genetics 16(6): 667-677.
Brynedal B, Duvefelt K, Jonasdottir G, Roos IM, Akesson E, Palmgren J, et al. (2007). HLA-A confers an HLA-DRB1 independent influence on the risk of multiple sclerosis. PloS one 2(7): e664.
Cavaco I, Asimus S, Peyrard-Janvid M, Ferreira PE, Veiga MI, Hai TN, et al. (2007). The Vietnamese Khin population harbors particular N-acetyltransferase 2 allele frequencies. Clinical chemistry 53(11): 1977-1979.
Dahlman I, Dicker A, Jiao H, Kere J, Blomqvist L, van Harmelen V, et al. (2007). A common haplotype in the G-protein-coupled receptor gene GPR74 is associated with leanness and increased lipolysis. American journal of human genetics 80(6): 1115-1124.
D’Amato M, Bruce S, Bresso F, Zucchelli M, Ezer S, Pulkkinen V, et al. (2007). Neuropeptide s receptor 1 gene polymorphism is associated with susceptibility to inflammatory bowel disease. Gastroenterology 133(3): 808-817.
Fischer H, Esbjornsson M, Sabina RL, Stromberg A, Peyrard-Janvid M, Norman B (2007). AMP deaminase deficiency is associated with lower sprint cycling performance in healthy subjects. J Appl Physiol (1985) 103(1): 315-322.
Hannelius U, Gherman L, Makela VV, Lindstedt A, Zucchelli M, Lagerberg C, et al. (2007). Large-scale zygosity testing using single nucleotide polymorphisms. Twin research and human genetics : the official journal of the International Society for Twin Studies 10(4): 604-625.
Hellquist A, Zucchelli M, Kivinen K, Saarialho-Kere U, Koskenmies S, Widen E, et al. (2007). The human GIMAP5 gene has a common polyadenylation polymorphism increasing risk to systemic lupus erythematosus. Journal of medical genetics 44(5): 314-321.
Hiltunen L, Rautanen A, Rasi V, Kaaja R, Kere J, Krusius T, et al. (2007). An unfavorable combination of Factor V Leiden with age, weight, and blood group causes high risk of pregnancy-associated venous thrombosis: a population-based nested case-control study. Thrombosis research 119(4): 423-432.
Kivinen K, Peterson H, Hiltunen L, Laivuori H, Heino S, Tiala I, et al. (2007). Evaluation of STOX1 as a preeclampsia candidate gene in a population-wide sample. Eur J Hum Genet 15(4): 494-497.
Lundmark F, Duvefelt K, Hillert J (2007). Genetic association analysis of the interleukin 7 gene (IL7) in multiple sclerosis. Journal of neuroimmunology 192(1-2): 171-173.
Lundmark F, Duvefelt K, Iacobaeus E, Kockum I, Wallstrom E, Khademi M, et al. (2007). Variation in interleukin 7 receptor alpha chain (IL7R) influences risk of multiple sclerosis. Nature genetics 39(9): 1108-1113.
Malerba G, Lindgren CM, Xumerle L, Kiviluoma P, Trabetti E, Laitinen T, et al. (2007). Chromosome 7p linkage and GPR154 gene association in Italian families with allergic asthma. Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 37(1): 83-89.
Nilsson M, Dahlman I, Jiao H, Gustafsson JA, Arner P, Dahlman-Wright K (2007). Impact of estrogen receptor gene polymorphisms and mRNA levels on obesity and lipolysis–a cohort study. BMC medical genetics 8: 73.
O’Doherty C, Roos IM, Antiguedad A, Aransay AM, Hillert J, Vandenbroeck K (2007). ITGA4 polymorphisms and susceptibility to multiple sclerosis. Journal of neuroimmunology 189(1-2): 151-157.
Ollikainen M, Hannelius U, Lindgren CM, Abdel-Rahman WM, Kere J, Peltomaki P (2007). Mechanisms of inactivation of MLH1 in hereditary nonpolyposis colorectal carcinoma: a novel approach. Oncogene 26(31): 4541-4549.
Otonkoski T, Jiao H, Kaminen-Ahola N, Tapia-Paez I, Ullah MS, Parton LE, et al. (2007). Physical exercise-induced hypoglycemia caused by failed silencing of monocarboxylate transporter 1 in pancreatic beta cells. American journal of human genetics 81(3): 467-474.
De Jager PL, Graham R, Farwell L, Sawcer S, Richardson A, Behrens TW, et al. (2006). The role of inflammatory bowel disease susceptibility loci in multiple sclerosis and systemic lupus erythematosus. Genes and immunity 7(4): 327-334.
Ekelund E, Saaf A, Tengvall-Linder M, Melen E, Link J, Barker J, et al. (2006). Elevated expression and genetic association links the SOCS3 gene to atopic dermatitis. American journal of human genetics 78(6): 1060-1065.
Hodgson U, Pulkkinen V, Dixon M, Peyrard-Janvid M, Rehn M, Lahermo P, et al. (2006). ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosis. American journal of human genetics 79(1): 149-154.
Lundmark F, Harbo HF, Celius EG, Saarela J, Datta P, Oturai A, et al. (2006). Association analysis of the LAG3 and CD4 genes in multiple sclerosis in two independent populations. Journal of neuroimmunology 180(1-2): 193-198.
Melen E, Umerkajeff S, Nyberg F, Zucchelli M, Lindstedt A, Gullsten H, et al. (2006). Interaction between variants in the interleukin-4 receptor alpha and interleukin-9 receptor genes in childhood wheezing: evidence from a birth cohort study. Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 36(11): 1391-1398.
Schumacher J, Anthoni H, Dahdouh F, Konig IR, Hillmer AM, Kluck N, et al. (2006). Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia. American journal of human genetics 78(1): 52-62.
Dahlman I, Kaaman M, Jiao H, Kere J, Laakso M, Arner P (2005). The CIDEA gene V115F polymorphism is associated with obesity in Swedish subjects. Diabetes 54(10): 3032-3034.
Hannelius U, Lindgren CM, Melen E, Malmberg A, von Dobeln U, Kere J (2005). Phenylketonuria screening registry as a resource for population genetic studies. Journal of medical genetics 42(10): e60.
Holmkvist J, Almgren P, Parikh H, Zucchelli M, Kere J, Groop L, et al. (2005). Haplotype construction of the FRDA gene and evaluation of its role in type II diabetes. Eur J Hum Genet 13(7): 849-855.
Jiao H, Dahlman I, Eriksson P, Kere J, Arner P (2005). A common beta2-adrenoceptor gene haplotype protects against obesity in Swedish women. Obesity research 13(10): 1645-1650.
Koillinen H, Lahermo P, Rautio J, Hukki J, Peyrard-Janvid M, Kere J (2005). A genome-wide scan of non-syndromic cleft palate only (CPO) in Finnish multiplex families. Journal of medical genetics 42(2): 177-184.
Melen E, Bruce S, Doekes G, Kabesch M, Laitinen T, Lauener R, et al. (2005). Haplotypes of G protein-coupled receptor 154 are associated with childhood allergy and asthma. American journal of respiratory and critical care medicine 171(10): 1089-1095.
Peyrard-Janvid M, Pegelow M, Koillinen H, Larsson C, Fransson I, Rautio J, et al. (2005). Novel and de novo mutations of the IRF6 gene detected in patients with Van der Woude or popliteal pterygium syndrome. Eur J Hum Genet 13(12): 1261-1267.
Rautanen A, Zucchelli M, Makela S, Kere J (2005). Gene mapping with pooled samples on three genotyping platforms. Molecular and cellular probes 19(6): 408-416.
Sankelo M, Flanagan JA, Machado R, Harrison R, Rudarakanchana N, Morrell N, et al. (2005). BMPR2 mutations have short lifetime expectancy in primary pulmonary hypertension. Human mutation 26(2): 119-124.
Swanberg M, Lidman O, Padyukov L, Eriksson P, Akesson E, Jagodic M, et al. (2005). MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction. Nature genetics 37(5): 486-494.
Wu H, Cantor RM, Graham DS, Lingren CM, Farwell L, Jager PL, et al. (2005). Association analysis of the R620W polymorphism of protein tyrosine phosphatase PTPN22 in systemic lupus erythematosus families: increased T allele frequency in systemic lupus erythematosus patients with autoimmune thyroid disease. Arthritis and rheumatism 52(8): 2396-2402.
Ylisaukko-Oja T, Peyrard-Janvid M, Lindgren CM, Rehnstrom K, Vanhala R, Peltonen L, et al. (2005). Family-based association study of DYX1C1 variants in autism. Eur J Hum Genet 13(1): 127-130.
Zhang Z, Duvefelt K, Svensson F, Masterman T, Jonasdottir G, Salter H, et al. (2005). Two genes encoding immune-regulatory molecules (LAG3 and IL7R) confer susceptibility to multiple sclerosis. Genes and immunity 6(2): 145-152.
Dahlman I, Eriksson P, Kaaman M, Jiao H, Lindgren CM, Kere J, et al. (2004). alpha2-Heremans-Schmid glycoprotein gene polymorphisms are associated with adipocyte insulin action. Diabetologia 47(11): 1974-1979.
Melen E, Gullsten H, Zucchelli M, Lindstedt A, Nyberg F, Wickman M, et al. (2004). Sex specific protective effects of interleukin-9 receptor haplotypes on childhood wheezing and sensitisation. Journal of medical genetics 41(12): e123.
Peyrard-Janvid M, Anthoni H, Onkamo P, Lahermo P, Zucchelli M, Kaminen N, et al. (2004). Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene. Human genetics 114(5): 510-516
Asumalahti K, Ameen M, Suomela S, Hagforsen E, Michaelsson G, Evans J, et al. (2003). Genetic analysis of PSORS1 distinguishes guttate psoriasis and palmoplantar pustulosis. The Journal of investigative dermatology 120(4): 627-632.