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Molecular Psychiatry
|
September 23, 2015
Genome-wide autozygosity is associated with lower general cognitive ability
D P Howrigan, M A Simonson, G Davies, et al.
Nature Communications
|
September 14, 2016
Erratum: A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis
Manuel A Rivas, Daniel Graham, Patrick Sulem, et al.
Nature Genetics
|
March 1, 2023
Author Correction: Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains
Ditte Demontis, G Bragi Walters, Georgios Athanasiadis, et al.
Nature
|
May 29, 2020
A structural variation reference for medical and population genetics
Ryan L Collins, Harrison Brand, Konrad J Karczewski, et al.
Nature Genetics
|
April 28, 2018
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder
Donna M Werling, Harrison Brand, Joon-Yong An, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
August 25, 2010
Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder
Benjamin M Neale, Sarah E Medland, Stephan Ripke, et al.
Plos Genetics
|
December 6, 2019
Correction: Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
Felix Day, Tugce Karaderi, Michelle R Jones, et al.
Plos Genetics
|
December 20, 2018
Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
Felix Day, Tugce Karaderi, Michelle R Jones, et al.
Nature Genetics
|
September 17, 2008
Common variants at CD40 and other loci confer risk of rheumatoid arthritis
Soumya Raychaudhuri, Elaine F Remmers, Annette T Lee, et al.
Nature Genetics
|
April 12, 2022
Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia
Duncan S Palmer, Daniel P Howrigan, Sinéad B Chapman, et al.
Page
of 56
Search research articles
Search
Showing results (481-490 of 552) with videos related to
Sort By:
Page
of 56
Molecular Psychiatry
|
September 23, 2015
Genome-wide autozygosity is associated with lower general cognitive ability
D P Howrigan, M A Simonson, G Davies, et al.
Nature Communications
|
September 14, 2016
Erratum: A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis
Manuel A Rivas, Daniel Graham, Patrick Sulem, et al.
Nature Genetics
|
March 1, 2023
Author Correction: Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains
Ditte Demontis, G Bragi Walters, Georgios Athanasiadis, et al.
Nature
|
May 29, 2020
A structural variation reference for medical and population genetics
Ryan L Collins, Harrison Brand, Konrad J Karczewski, et al.
Nature Genetics
|
April 28, 2018
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder
Donna M Werling, Harrison Brand, Joon-Yong An, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
August 25, 2010
Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder
Benjamin M Neale, Sarah E Medland, Stephan Ripke, et al.
Plos Genetics
|
December 6, 2019
Correction: Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
Felix Day, Tugce Karaderi, Michelle R Jones, et al.
Plos Genetics
|
December 20, 2018
Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
Felix Day, Tugce Karaderi, Michelle R Jones, et al.
Nature Genetics
|
September 17, 2008
Common variants at CD40 and other loci confer risk of rheumatoid arthritis
Soumya Raychaudhuri, Elaine F Remmers, Annette T Lee, et al.
Nature Genetics
|
April 12, 2022
Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia
Duncan S Palmer, Daniel P Howrigan, Sinéad B Chapman, et al.
Page
of 56