Hreinn Stefansson
Hreinn Stefansson
Head of CNS division, deCODE genetics
Verified email at decode.is - Homepage
Title
Cited by
Cited by
Year
Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes
SFA Grant, G Thorleifsson, I Reynisdottir, R Benediktsson, A Manolescu, ...
Nature genetics 38 (3), 320-323, 2006
23652006
Neuregulin 1 and susceptibility to schizophrenia
H Stefansson, H Petursson, E Sigurdsson, V Steinthorsdottir, ...
The American Journal of Human Genetics 71 (4), 877-892, 2002
18822002
Large recurrent microdeletions associated with schizophrenia
H Stefansson, D Rujescu, S Cichon, OPH Pietiläinen, A Ingason, ...
nature 455 (7210), 232, 2008
17822008
Common variants conferring risk of schizophrenia
H Stefansson, RA Ophoff, S Steinberg, OA Andreassen, S Cichon, ...
Nature 460 (7256), 744-747, 2009
16522009
Association between microdeletion and microduplication at 16p11. 2 and autism
LA Weiss, Y Shen, JM Korn, DE Arking, DT Miller, R Fossdal, ...
New England Journal of Medicine 358 (7), 667-675, 2008
16252008
Variant of TREM2 associated with the risk of Alzheimer's disease
T Jonsson, H Stefansson, S Steinberg, I Jonsdottir, PV Jonsson, ...
New England Journal of Medicine 368 (2), 107-116, 2013
16002013
Genome-wide association study identifies five new schizophrenia loci
S Ripke, AR Sanders, KS Kendler, DF Levinson, P Sklar, PA Holmans, ...
Nature genetics 43 (10), 969, 2011
15762011
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
P Hollingworth, D Harold, R Sims, A Gerrish, JC Lambert, ...
Nature genetics 43 (5), 429-435, 2011
15432011
A mutation in APP protects against Alzheimer˘s disease and age-related cognitive decline
T Jonsson, JK Atwal, S Steinberg, J Snaedal, PV Jonsson, S Bjornsson, ...
Nature 488 (7409), 96-99, 2012
14752012
A variant associated with nicotine dependence, lung cancer and peripheral arterial disease
TE Thorgeirsson, F Geller, P Sulem, T Rafnar, A Wiste, KP Magnusson, ...
Nature 452 (7187), 638-642, 2008
14712008
Biological insights from 108 schizophrenia-associated genetic loci
S Ripke, BM Neale, A Corvin, JTR Walters, KH Farh, PA Holmans, P Lee, ...
Nature 511 (7510), 421-427, 2014
14092014
Genetics of gene expression and its effect on disease
V Emilsson, G Thorleifsson, B Zhang, AS Leonardson, F Zink, J Zhu, ...
Nature 452 (7186), 423-428, 2008
13482008
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
S Ripke, C O'Dushlaine, K Chambert, JL Moran, AK Kähler, S Akterin, ...
Nature genetics 45 (10), 1150, 2013
13392013
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4
P Sklar, S Ripke, LJ Scott, OA Andreassen, S Cichon, N Craddock, ...
Nature genetics 43 (10), 977, 2011
12472011
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
MA Nalls, N Pankratz, CM Lill, CB Do, DG Hernandez, M Saad, ...
Nature genetics 46 (9), 989-993, 2014
11902014
A mega-analysis of genome-wide association studies for major depressive disorder
S Ripke, NR Wray, CM Lewis, SP Hamilton, MM Weissman, G Breen, ...
Molecular psychiatry 18 (4), 497, 2013
9622013
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
NR Wray, S Ripke, M Mattheisen, M Trzaskowski, EM Byrne, A Abdellaoui, ...
Nature genetics 50 (5), 668-681, 2018
8932018
A common inversion under selection in Europeans
H Stefansson, A Helgason, G Thorleifsson, V Steinthorsdottir, G Masson, ...
Nature genetics 37 (2), 129-137, 2005
7732005
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction
DF Gudbjartsson, US Bjornsdottir, E Halapi, A Helgadottir, P Sulem, ...
Nature genetics 41 (3), 342-347, 2009
7462009
The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm
A Helgadottir, G Thorleifsson, KP Magnusson, S Grétarsdottir, ...
Nature genetics 40 (2), 217, 2008
7432008
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