Gudmundur Bragi Walters - deCODE Genet, IS-101 Reykjavik, Iceland

基本信息

Career Trajectory

Bio

G. Bragi Walters started work at deCODE genetics in 1997 and has been involved in numerous projects. In 2011 he joined the CNS department where his main focus has been on the genetics of neurodevelopmental disorders and manages the Autism Spectrum Disorder- and Attention Deficit/Hyperactivity projects.

Research Interests

Papers共 98 篇Author StatisticsCo-AuthorSimilar Experts

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Predicting ADHD in Alcohol Dependence Using Polygenic Risk Scores for ADHD

Kejal H. S. Patel,G. Bragi Walters,Hreinn Stefansson,Kari Stefansson,Franziska Degenhardt,Markus Nothen,Tracey Van Der Veen,Ditte Demontis,Anders Borglum,Mark Kristiansen,Nicholas J. Bass,Andrew McQuillin

AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS（2024）

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Developmental Language Disorder – Heritability and Genetic Correlations with Other Disorders Affecting Language

Ron Nudel, Rikke Vang Chrsitensen, Nelli Kalnak, Mischa Lundberg,Michael Schwinn, Erik Sørensen,Christina Mikkelsen,Janna Nissen, Lea Arregui Nordahl Christoffersen,Bertram Dalskov Kjerulff, Thomas Folkmann Hansen, Kristoffer Sølvsten Burgdorf,Ole Birger Vesterager Pedersen, Christian Erikstrup, Rósa S. Gísladóttir,G. Bragi Walters,Hreinn Stefánsson,Sisse Rye Ostrowski,Thomas Werge

Psychiatry Researchpp.116212, (2024)

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Multi-polygenic Scores in a Naturalistic Psychiatric Cohort: from Disorder-Specific to Transdiagnostic Perspectives

Yingjie Shi,Emma Sprooten,Peter Mulders, Janna Vrijsen,Janita Bralten, Ditte Demontis, Anders D. Borglum,G. Bragi Walters, Kari Stefansson,Philip van Eijndhoven,Indira Tendolkar,Barbara Franke,Nina Roth Mota

AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICSno. 1 (2024)

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Loss-of-function Variants in ITSN1 Confer High Risk of Parkinson’s Disease

Astros Th. Skuladottir,Vinicius Tragante,Gardar Sveinbjornsson,Hannes Helgason, Arni Sturluson,Anna Bjornsdottir,Palmi Jonsson, Vala Palmadottir,Olafur A. Sveinsson,Brynjar O. Jensson,Sigurjon A. Gudjonsson,Erna V. Ivarsdottir, Rosa S. Gisladottir, Arni F. Gunnarsson,G. Bragi Walters,Gudrun A. Jonsdottir,Thorgeir E. Thorgeirsson,Gyda Bjornsdottir,Hilma Holm,Daniel F. Gudbjartsson,Patrick Sulem,Hreinn Stefansson,Kari Stefansson

NPJ PARKINSONS DISEASEno. 1 (2024)

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Disentangling the shared genetics of ADHD, cannabis use disorder and cannabis use and prediction of cannabis use disorder in ADHD

Trine Tollerup Nielsen,Jinjie Duan,Daniel F. Levey,G. Bragi Walters,Emma C. Johnson,Thorgeir Thorgeirsson,VA Million Veteran Program,Thomas Werge,Preben Bo Mortensen,Hreinn Stefansson,Kari Stefansson,David M. Hougaard,Arpana Agrawal,Joel Gelernter,Jakob Grove,Anders D. Børglum,Ditte Demontis

medrxiv（2024）

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Homozygosity for R47H in TREM2 and the Risk of Alzheimer's Disease

Hreinn Stefansson,G Bragi Walters,Gardar Sveinbjornsson,Vinicius Tragante,Gudmundur Einarsson,Hannes Helgason,Asgeir Sigurðsson,Doruk Beyter,Audunn S Snaebjarnarson,Erna V Ivarsdottir,Gudmar Thorleifsson,Bjarni V Halldorsson,Gudmundur Norddahl,Unnur Styrkarsdottir,Arni Sturluson,Hilma Holm,Agnar Helgason, Kristjan Moore,Hannes P Eggertsson, Asmundur H Oddsson,Gudrun A Jonsdottir, Arni F Gunnarsson,Gyda Bjornsdottir,Rosa S Gisladottir,Thorgeir E Thorgeirsson,Astros Skuladottir,Daniel F Gudbjartsson,Patrick Sulem,Palmi Jonsson,Steinunn Thordardottir,Jon Snaedal,Helga Eyjolfsdottir,Byron Creese,Clive Ballard,Anne Corbett,Miguel Vasconcelos Da Silva,Dag Aarsland,Ole A Andreassen, DemGen Study Group,Geir Selbæk,Srdjan Djurovic,Eystein Stordal, Thormod Fladby,Jan Haavik,Jannicke Igland,Lasse M Giil,Sture Eriksson,Göran Hallmans,Hugo Lövheim,Karin Lopatko Lindman,Miles Trupp,Lars Forsgren,Thomas Werge,Karina Banasik,Søren Brunak,Henrik Ullum,Ruth Frikke-Schmidt,Sisse R Ostrowski,DBDS Genomic Consortium,Maria Didriksen,Erik Sørensen,Anja H Simonsen, Jørgen E Nielsen,Gunhild Waldemar,Ole B Pedersen,Christian Erikstrup,Kirk U Knowlton,Lincoln D Nadauld,Kari Stefansson, DemGen Study Group and DBDS Genomic Consortium

The New England journal of medicineno. 23 (2024): 2217-2219

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Exploring the Genetic Risk of Childhood Daytime Urinary Incontinence: A Genome-Wide Association Study

Anders Breinbjerg,Cecilie Siggaard Jørgensen,G Bragi Walters,Jakob Grove, Thomas D Als,Konstantinos Kamperis,Lilja Stéfansdóttir, Janne P Thirstrup, Britt Borg,Clara Albiñana,Bjarni J Vilhjálmsson,Viðar Ö Eðvarðsson,Hreinn Stefánsson, Preben B Mortensen,Esben Agerbo,Thomas Werge,Anders Børglum,Ditte Demontis,Kári Stefánsson,Søren Rittig,Jane Hvarregaard Christensen

The Journal of urologypp.101097JU0000000000004187-101097JU0000000000004187, (2024)

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Homozygosity for a Stop-Gain Variant in CCDC201 Causes Primary Ovarian Insufficiency

NATURE GENETICS (2024)

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INSIGHTS FROM >80 LOCI ASSOCIATED WITH ATTENTION-DEFICIT/HYPERACTIVITY DISORDER

Raymond Walters,Ditte Demontis,Georgios Athanasiadis,G. Bragi Walters,Tetyana Zayats,Daniel Howrigan, Stephen V. Faraone,Kari Stefansson,Thomas Werge,Anders Borglum,Benjamin Neale,Barbara Franke

European neuropsychopharmacology (2023): S21-S21

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