T
Thorgeir E. Thorgeirsson
Researcher at deCODE genetics
Publications - 121
Citations - 22357
Thorgeir E. Thorgeirsson is an academic researcher from deCODE genetics. The author has contributed to research in topics: Genome-wide association study & Population. The author has an hindex of 49, co-authored 106 publications receiving 18623 citations. Previous affiliations of Thorgeir E. Thorgeirsson include Lawrence Berkeley National Laboratory & University of California, Santa Cruz.
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Journal ArticleDOI
Generalized anxiety disorder in the anxiety/depression spectrum
H. Oskarsso,Thorgeir E. Thorgeirsson,Frank Geller,H. Kolbeinsson,J.G. Stefansson,E. Lindal,A. Ingibergsdottir,Jeffrey R. Gulcher,Kari Stefansson +8 more
TL;DR: Logistic regression confirms the strong link between GAD and dysthymia and gives these disorders the possible role of a genetic bridge between anxiety and depressive disorders.
Journal ArticleDOI
Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses
Thomas Damm Als,Mitja I. Kurki,Jakob Grove,Georgios Voloudakis,Karen Therrien,Elisa Tasanko,Trine Tollerup Nielsen,J. Naamanka,Kumar Veerapen,Daniel Levy,Jaroslav Bendl,Jonas Bybjerg-Grauholm,Biao Zeng,Ditte Demontis,Anders Rosengren,Georgios Athanasiadis,Marie Bækved-Hansen,Per Qvist,G. Bragi Walters,Thorgeir E. Thorgeirsson,Hreinn Stefansson,Katherine L. Musliner,Veera M. Rajagopal,Leila Farajzadeh,Janne Pia Thirstrup,Bjarni J. Vilhjálmsson,John J. McGrath,Manuel Mattheisen,Sandra Meier,Esben Agerbo,Kari Stefansson,Merete Nordentoft,Thomas Werge,David M. Hougaard,Preben Bo Mortensen,Murray B. Stein,Joel Gelernter,Iiris Hovatta,Panos Roussos,Mark J. Daly,Ole Mors,Aarno Palotie,Anders D. Børglum +42 more
Patent
Susceptibility variants for peripheral arterial disease and abdominal aortic aneurysm
TL;DR: In this paper, the authors disclosed certain genetic variants as susceptibility variants for peripheral arterial disease (PAD) and abdominal aortic aneurysm (AAA) and related to risk management using such variants.
Journal ArticleDOI
Correction : Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank (Molecular Psychiatry, (2020), 10.1038/s41380-019-0546-6)
Jri Coleman,Kirstin L. Purves,Kas Davis,Christopher Rayner,Shing Wan Choi,Christopher Hübel,Helena Gaspar,Carol Kan,Van der Auwera S,Mark Adams,Donald M. Lyall,KW Choi,Naomi R. Wray,Stephan Ripke,Stephan Ripke,Manuel Mattheisen,Manuel Mattheisen,Maciej Trzaskowski,Maciej Trzaskowski,EM Byrne,A Abdellaoui,E Agerbo,TM Air,Tfm Andlauer,S-A Bacanu,M Baekvad-Hansen,Atf Beekman,TB Bigdeli,EB Binder,J Bryois,Henriette N. Buttenschøn,Jonas Bybjerg-Grauholm,Na Cai,Enrique Castelao,Jane H. Christensen,Clarke T,Lucía Colodro-Conde,Baptiste Couvy-Duchesne,N. Craddock,Gregory E. Crawford,Gary Davies,Ian J. Deary,Franziska Degenhardt,Eske M. Derks,Nese Direk,Conor V. Dolan,Erin C. Dunn,Erin C. Dunn,Thalia C. Eley,Escott-Price,Ffh Kiadeh,Hilary K. Finucane,Jerome C. Foo,Andreas J. Forstner,Josef Frank,M. Gill,Fernando S. Goes,Scott D. Gordon,Jakob Grove,Lisa Hall,Christine Søholm Hansen,Torben Hansen,Stefan Herms,Ian B. Hickie,Peter Hoffmann,G. Homuth,Carsten Horn,J-J Hottenga,David M. Hougaard,David M. Howard,Marcus Ising,Rick Jansen,I. Jones,Lisa Jones,Eric Jorgenson,James A. Knowles,Isaac S. Kohane,Julia Kraft,Warren W. Kretzschmar,Z. Kutalik,Yun Li,Penelope A. Lind,Donald J. MacIntyre,Dean F. MacKinnon,Robert Maier,W. Maier,Jonathan Marchini,Hamdi Mbarek,Patrick J. McGrath,P. McGuffin,S. E. Medland,Divya Mehta,Christel M. Middeldorp,Evelin Mihailov,Y. Milaneschi,Lili Milani,Francis M. Mondimore,Grant W. Montgomery,Sara Mostafavi,Niamh Mullins,Matthias Nauck,Bernard Ng,Michel G. Nivard,Nyholt,Paul F. O'Reilly,Hogni Oskarsson,M J Owen,Jodie N. Painter,Carsten Bøcker Pedersen,Marianne Giørtz Pedersen,Roseann E. Peterson,Erik Pettersson,Wouter J. Peyrot,Giorgio Pistis,Danielle Posthuma,Jorge A. Quiroz,Per Qvist,John P. Rice,Brien P. Riley,Margarita Rivera,Saira Saeed Mirza,Robert A. Schoevers,Eva C. Schulte,Ling Shen,Jing Shi,Stanley I. Shyn,Engilbert Sigurdsson,Gcb Sinnamon,J.H. Smit,David J. Smith,Hreinn Stefansson,Stacy Steinberg,Fabian Streit,Jana Strohmaier,Katherine E. Tansey,Henning Teismann,Alexander Teumer,Wesley K. Thompson,P. A. Thomson,Thorgeir E. Thorgeirsson,Matthew Traylor,Jens Treutlein,Trubetskoy,A.G. Uitterlinden,Daniel Umbricht,van, Hemert, Am,Alexander Viktorin,Peter M. Visscher,Yunpeng Wang,Bradley T. Webb,Shantel Weinsheimer,Jürgen Wellmann,Gonneke Willemsen,Stephanie H. Witt,Yang Wu,Hualin S. Xi,Jian Yang,Futao Zhang,Arolt,Bernard T. Baune,Kenneth I. Berger,D.I. Boomsma,Sven Cichon,Udo Dannlowski,de, Geus, Ejc,DePaulo,Enrico Domenici,Katharina Domschke,Tõnu Esko,Hans-Jörgen Grabe,Steven P. Hamilton,Caroline Hayward,A. C. Heath,Kenneth S. Kendler,Stefan Kloiber,Glyn Lewis,Qingqin S. Li,Susanne Lucae,Paf Madden,Patrick K.E. Magnusson,N. G. Martin,Andrew M. McIntosh,Andres Metspalu,Ole Mors,P. B. Mortensen,Bertram Müller-Myhsok,Merete Nordentoft,M. M. Nöthen,M O'Donovan,Sara A. Paciga,Nancy L. Pedersen,Bwjh Penninx,Roy H. Perlis,David J. Porteous,James B. Potash,Martin Preisig,M. Rietschel,Catherine Schaefer,Thomas G. Schulze,Jordan W. Smoller,K. Stefansson,Henning Tiemeier,Rudolf Uher,Henry Völzke,Myrna M. Weissman,Thomas Werge,Cathryn M. Lewis,Daphna Levinson,Gerome Breen,Anders D. Børglum,P.F. Sullivan,Evangelos Vassos,Andrea Danese,Andrea Danese,Barbara Maughan,Matthew Hotopf +215 more
TL;DR: An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Posted ContentDOI
A genome-wide meta-analysis identifies 53 sequence variants associating with carpal tunnel syndrome
Astros Skuladottir,Gyda Bjornsdottir,Egil Ferkingstad,Gudmundur V. Einarsson,Lilja Stefansdottir,Muhammad Nawaz,Thorunn A. Olafsdottir,Saedis Saevarsdottir,Graham R. Walters,Sigurdur Magnusson,Asmundur Oddson,Anna Bjornsdottir,Olafur Sveinsson,Arnor Vikingsson,Thomas Hansen,Rikke Kart Jacobsen,Christian Erikstrup,Michael Schwinn,Søren Brunak,Karina Banasik,Sisse R. Ostrowski,Anders Troelsen,Cecilie Henkel,Ole Birger Pedersen,Ingileif Jonsdottir,Daniel F. Gudbjartsson,Patrick Sulem,Thorgeir E. Thorgeirsson,Hreinn Stefansson,Kari Stefansson +29 more
TL;DR: It is suggested that the components of the extracellular matrix play a key role in the pathogenesis of CTS and the genetic component to the risk is higher in recurrent/persistent cases than nonrecurrent/nonresistant cases.