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Omar Gustafsson

Showing results (11-20 of 23) with videos related to

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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 Genetics|February 3, 2009
Variant in the sequence of the LINGO1 gene confers risk of essential tremorHreinn Stefansson, Stacy Steinberg, Hjorvar Petursson, et al.
Biological Psychiatry|March 19, 2011
At-risk variant in TCF7L2 for type II diabetes increases risk of schizophreniaThomas Hansen, Andrés Ingason, Srdjan Djurovic, et al.
The American Journal of Psychiatry|February 18, 2011
Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illnessAndrés Ingason, George Kirov, Ina Giegling, et al.
Human Molecular Genetics|June 14, 2011
Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degenerationYi Yu, Tushar R Bhangale, Jesen Fagerness, et al.
Biological Psychiatry|May 8, 2012
Replication study and meta-analysis in European samples supports association of the 3p21.1 locus with bipolar disorderEvangelos Vassos, Stacy Steinberg, Sven Cichon, 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.
NPJ Genomic Medicine|December 22, 2017
Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlationsSigurgeir Olafsson, Pernilla Stridh, Steffan Daniël Bos, et al.
American Journal of Human Genetics|March 1, 2011
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorderSven Cichon, Thomas W Mühleisen, Franziska A Degenhardt, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
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 Genetics|February 3, 2009
Variant in the sequence of the LINGO1 gene confers risk of essential tremorHreinn Stefansson, Stacy Steinberg, Hjorvar Petursson, et al.
Biological Psychiatry|March 19, 2011
At-risk variant in TCF7L2 for type II diabetes increases risk of schizophreniaThomas Hansen, Andrés Ingason, Srdjan Djurovic, et al.
The American Journal of Psychiatry|February 18, 2011
Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illnessAndrés Ingason, George Kirov, Ina Giegling, et al.
Human Molecular Genetics|June 14, 2011
Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degenerationYi Yu, Tushar R Bhangale, Jesen Fagerness, et al.
Biological Psychiatry|May 8, 2012
Replication study and meta-analysis in European samples supports association of the 3p21.1 locus with bipolar disorderEvangelos Vassos, Stacy Steinberg, Sven Cichon, 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.
NPJ Genomic Medicine|December 22, 2017
Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlationsSigurgeir Olafsson, Pernilla Stridh, Steffan Daniël Bos, et al.
American Journal of Human Genetics|March 1, 2011
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorderSven Cichon, Thomas W Mühleisen, Franziska A Degenhardt, et al.
Pageof 3