Epigenome-Wide Association Study of Cognitive Functioning in Middle-Aged Monozygotic Twins by Anna Starnawska, Anna Starnawska, Anna Starnawska, Qihua Tan, Qihua Tan, Matt McGue, Matt McGue, Ole Mors, Ole Mors, Ole Mors, Anders D. Børglum, Anders D. Børglum, Anders D. Børglum, Kaare Christensen, Kaare Christensen, Kaare Christensen, Kaare Christensen, Mette Nyegaard, Mette Nyegaard, Mette Nyegaard, Lene Christiansen, Lene Christiansen

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DNA Methylation Analysis of BRD1 Promoter Regions and the Schizophrenia rs138880 Risk Allele. by Mads Dyrvig, Per Qvist, Jacek Lichota, Knud Larsen, Mette Nyegaard, Anders D Børglum, Jane H Christensen

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Exploring associations between constipation, severity of neurofibromatosis type 1 and NF1 mutational spectrum by Cecilie Ejerskov, Mette Gaustadnes, John R. Ostergaard, klaus Krogh, Kasper Thorsen, Anders D. Borglum, Annette Haagerup

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CtIP Mutations Cause Seckel and Jawad Syndromes. by Per Qvist, Pablo Huertas, Sonia Jimeno, Mette Nyegaard, Muhammad J Hassan, Stephen P Jackson, Anders D Børglum

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Discordant associations of educational attainment with ASD and ADHD implicate a polygenic form of pleiotropy by Ellen Verhoef, Jakob Grove, Chin Yang Shapland, Ditte Demontis, Stephen Burgess, Dheeraj Rai, Anders D. Børglum, Beate St Pourcain

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Maternal pregnancy-related infections and autism spectrum disorder—the genetic perspective by Ron Nudel, Wesley K. Thompson, Anders D. Børglum, David M. Hougaard, Preben B. Mortensen, Thomas Werge, Merete Nordentoft, Michael E. Benros

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Polymorphism in serotonin receptor 3B is associated with pain catastrophizing. by Emilia Horjales-Araujo, Ditte Demontis, Ellen Kielland Lund, Nanna Brix Finnerup, Anders D Børglum, Troels Staehelin Jensen, Peter Svensson, Lene Vase

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Lung function discordance in monozygotic twins and associated differences in blood DNA methylation by Anneli C. S. Bolund, Anna Starnawska, Martin R. Miller, Vivi Schlünssen, Vibeke Backer, Anders D. Børglum, Kaare Christensen, Qihua Tan, Lene Christiansen, Torben Sigsgaard

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Phenotypic and ancestry-related assortative mating in autism by Jing Zhang, J. Dylan Weissenkampen, Rachel L. Kember, iPSYCH Consortium, Jakob Grove, Anders D. Børglum, Elise B. Robinson, Edward S. Brodkin, Laura Almasy, Maja Bucan, Ronnie Sebro

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Polygenic Heterogeneity Across Obsessive-Compulsive Disorder Subgroups Defined by a Comorbid Diagnosis by Nora I. Strom, Nora I. Strom, Nora I. Strom, Nora I. Strom, Jakob Grove, Jakob Grove, Jakob Grove, Sandra M. Meier, Marie Bækvad-Hansen, Marie Bækvad-Hansen, Judith Becker Nissen, Thomas Damm Als, Thomas Damm Als, Thomas Damm Als, Matthew Halvorsen, Merete Nordentoft, Merete Nordentoft, Merete Nordentoft, Preben B. Mortensen, Preben B. Mortensen, Preben B. Mortensen, Preben B. Mortensen, David M. Hougaard, David M. Hougaard, Thomas Werge, Thomas Werge, Thomas Werge, Thomas Werge, Ole Mors, Ole Mors, Anders D. Børglum, Anders D. Børglum, Anders D. Børglum, James J. Crowley, Jonas Bybjerg-Grauholm, Jonas Bybjerg-Grauholm, Manuel Mattheisen, Manuel Mattheisen, Manuel Mattheisen

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Pharmacogenetic genotype and phenotype frequencies in a large Danish population-based case-cohort sample by Carin A. T. C. Lunenburg, Janne P. Thirstrup, Jonas Bybjerg-Grauholm, Marie Bækvad-Hansen, David M. Hougaard, Merete Nordentoft, Thomas Werge, Anders D. Børglum, Ole Mors, Preben B. Mortensen, Christiane Gasse

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Translating polygenic risk scores for clinical use by estimating the confidence bounds of risk prediction by Jiangming Sun, Yunpeng Wang, Lasse Folkersen, Yan Borné, Inge Amlien, Alfonso Buil, Marju Orho-Melander, Anders D. Børglum, David M. Hougaard, Regeneron Genetics Center, Olle Melander, Gunnar Engström, Thomas Werge, Kasper Lage

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Accuracy of haplotype estimation and whole genome imputation affects complex trait analyses in complex biobanks by Vivek Appadurai, Jonas Bybjerg-Grauholm, Morten Dybdahl Krebs, Anders Rosengren, Alfonso Buil, Andrés Ingason, Ole Mors, Anders D. Børglum, David M. Hougaard, Merete Nordentoft, Preben B. Mortensen, Olivier Delaneau, Thomas Werge, Andrew J. Schork

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Common schizophrenia risk variants are enriched in open chromatin regions of human glutamatergic neurons by Mads E. Hauberg, Jordi Creus-Muncunill, Jaroslav Bendl, Alexey Kozlenkov, Biao Zeng, Chuhyon Corwin, Sarah Chowdhury, Harald Kranz, Yasmin L. Hurd, Michael Wegner, Anders D. Børglum, Stella Dracheva, Michelle E. Ehrlich, John F. Fullard, Panos Roussos

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Associations between patterns in comorbid diagnostic trajectories of individuals with schizophrenia and etiological factors by Morten Dybdahl Krebs, Gonçalo Espregueira Themudo, Michael Eriksen Benros, Ole Mors, Anders D. Børglum, David Hougaard, Preben Bo Mortensen, Merete Nordentoft, Michael J. Gandal, Chun Chieh Fan, Daniel H. Geschwind, Andrew J. Schork, Thomas Werge, Wesley K. Thompson

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Postpartum and non-postpartum depression: a population-based matched case-control study comparing polygenic risk scores for severe mental disorders by Trine Munk-Olsen, Arianna Di Florio, Kathrine B. Madsen, Clara Albiñana, Merete L. Mægbæk, Veerle Bergink, Vibe G. Frøkjær, Esben Agerbo, Bjarni J. Vilhjálmsson, Thomas Werge, Merete Nordentoft, David M. Hougaard, Anders D. Børglum, Ole Mors, Preben Bo Mortensen, Xiaoqin Liu

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Cuba: exploring the history of admixture and the genetic basis of pigmentation using autosomal and uniparental markers. by Beatriz Marcheco-Teruel, Esteban J Parra, Evelyn Fuentes-Smith, Antonio Salas, Henriette N Buttenschøn, Ditte Demontis, María Torres-Español, Lilia C Marín-Padrón, Enrique J Gómez-Cabezas, Vanesa Alvarez-Iglesias, Ana Mosquera-Miguel, Antonio Martínez-Fuentes, Angel Carracedo, Anders D Børglum, Ole Mors

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ADuLT: An efficient and robust time-to-event GWAS by Emil M. Pedersen, Esben Agerbo, Oleguer Plana-Ripoll, Jette Steinbach, Morten D. Krebs, David M. Hougaard, Thomas Werge, Merete Nordentoft, Anders D. Børglum, Katherine L. Musliner, Andrea Ganna, Andrew J. Schork, Preben B. Mortensen, John J. McGrath, Florian Privé, Bjarni J. Vilhjálmsson

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Multi-PGS enhances polygenic prediction by combining 937 polygenic scores by Clara Albiñana, Zhihong Zhu, Andrew J. Schork, Andrés Ingason, Hugues Aschard, Isabell Brikell, Cynthia M. Bulik, Liselotte V. Petersen, Esben Agerbo, Jakob Grove, Merete Nordentoft, David M. Hougaard, Thomas Werge, Anders D. Børglum, Preben Bo Mortensen, John J. McGrath, Benjamin M. Neale, Florian Privé, Bjarni J. Vilhjálmsson

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A Novel Locus Harbouring a Functional CD164 Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing Impairment. by Mette Nyegaard, Nanna D Rendtorff, Morten S Nielsen, Thomas J Corydon, Ditte Demontis, Anna Starnawska, Anne Hedemand, Annalisa Buniello, Francesco Niola, Michael T Overgaard, Suzanne M Leal, Wasim Ahmad, Friedrik P Wikman, Kirsten B Petersen, Dorthe G Crüger, Jaap Oostrik, Hannie Kremer, Niels Tommerup, Morten Frödin, Karen P Steel, Lisbeth Tranebjærg, Anders D Børglum

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