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Human Molecular Genetics
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October 24, 2008
Disruption of the neurexin 1 gene is associated with schizophrenia
Dan Rujescu, Andres Ingason, Sven Cichon, et al.
Plos Genetics
|
February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders
Claire S Leblond, Jutta Heinrich, Richard Delorme, et al.
Nature Genetics
|
August 20, 2008
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder
Manuel A R Ferreira, Michael C O'Donovan, Yan A Meng, et al.
Nature Genetics
|
January 8, 2008
The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm
Anna Helgadottir, Gudmar Thorleifsson, Kristinn P Magnusson, et al.
Cell Reports
|
July 16, 2020
Meta-Analysis of the Alzheimer's Disease Human Brain Transcriptome and Functional Dissection in Mouse Models
Ying-Wooi Wan, Rami Al-Ouran, Carl G Mangleburg, et al.
Nature Genetics
|
February 28, 2018
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
Antonio F Pardiñas, Peter Holmans, Andrew J Pocklington, et al.
Nature
|
August 1, 2008
Large recurrent microdeletions associated with schizophrenia
Hreinn Stefansson, Dan Rujescu, Sven Cichon, et al.
Nature Genetics
|
June 5, 2019
Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
Antonio F Pardiñas, Peter Holmans, Andrew J Pocklington, et al.
Human Molecular Genetics
|
July 28, 2011
Common variants at VRK2 and TCF4 conferring risk of schizophrenia
Stacy Steinberg, Simone de Jong, , et al.
Biological Psychiatry
|
July 23, 2013
A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation
, , Elvira Bramon, et al.
Page
of 18
Search research articles
Search
Showing results (161-170 of 176) with videos related to
Sort By:
Page
of 18
Human Molecular Genetics
|
October 24, 2008
Disruption of the neurexin 1 gene is associated with schizophrenia
Dan Rujescu, Andres Ingason, Sven Cichon, et al.
Plos Genetics
|
February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders
Claire S Leblond, Jutta Heinrich, Richard Delorme, et al.
Nature Genetics
|
August 20, 2008
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder
Manuel A R Ferreira, Michael C O'Donovan, Yan A Meng, et al.
Nature Genetics
|
January 8, 2008
The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm
Anna Helgadottir, Gudmar Thorleifsson, Kristinn P Magnusson, et al.
Cell Reports
|
July 16, 2020
Meta-Analysis of the Alzheimer's Disease Human Brain Transcriptome and Functional Dissection in Mouse Models
Ying-Wooi Wan, Rami Al-Ouran, Carl G Mangleburg, et al.
Nature Genetics
|
February 28, 2018
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
Antonio F Pardiñas, Peter Holmans, Andrew J Pocklington, et al.
Nature
|
August 1, 2008
Large recurrent microdeletions associated with schizophrenia
Hreinn Stefansson, Dan Rujescu, Sven Cichon, et al.
Nature Genetics
|
June 5, 2019
Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
Antonio F Pardiñas, Peter Holmans, Andrew J Pocklington, et al.
Human Molecular Genetics
|
July 28, 2011
Common variants at VRK2 and TCF4 conferring risk of schizophrenia
Stacy Steinberg, Simone de Jong, , et al.
Biological Psychiatry
|
July 23, 2013
A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation
, , Elvira Bramon, et al.
Page
of 18