Showing results (11-20 of 27) with videos related to
Sort By:
Pageof 3
The New England Journal of Medicine|July 20, 2007
A genetic risk factor for periodic limb movements in sleepHreinn Stefansson, David B Rye, Andrew Hicks, et al.Nature Communications|August 29, 2018
MAP1B mutations cause intellectual disability and extensive white matter deficitG Bragi Walters, Omar Gustafsson, Gardar Sveinbjornsson, et al.Translational Psychiatry|October 19, 2019
Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorderOlafur O Gudmundsson, G Bragi Walters, Andres Ingason, et al.Nature Neuroscience|June 9, 2015
Polygenic risk scores for schizophrenia and bipolar disorder predict creativityRobert A Power, Stacy Steinberg, Gyda Bjornsdottir, et al.Biological Psychiatry|October 8, 2015
Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European CohortBirgitte Bertelsen, Hreinn Stefánsson, Lars Riff Jensen, et al.Nature Genetics|March 26, 2015
Loss-of-function variants in ABCA7 confer risk of Alzheimer's diseaseStacy Steinberg, Hreinn Stefansson, Thorlakur Jonsson, et al.American Journal of Human Genetics|July 30, 2002
Neuregulin 1 and susceptibility to schizophreniaHreinn Stefansson, Engilbert Sigurdsson, Valgerdur Steinthorsdottir, et al.Nature Communications|September 9, 2018
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traitsThorunn Rafnar, Bjarni Gunnarsson, Olafur A Stefansson, et al.Nature Genetics|April 9, 2008
Many sequence variants affecting diversity of adult human heightDaniel F Gudbjartsson, G Bragi Walters, Gudmar Thorleifsson, et al.Human Molecular Genetics|October 24, 2008
Disruption of the neurexin 1 gene is associated with schizophreniaDan Rujescu, Andres Ingason, Sven Cichon, et al.Pageof 3