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Nature Genetics
|
August 18, 2022
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
Jack M Fu, F Kyle Satterstrom, Minshi Peng, et al.
Nature Genetics
|
February 27, 2019
Identification of common genetic risk variants for autism spectrum disorder
Jakob Grove, Stephan Ripke, Thomas D Als, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 4, 2026
Altered neurodevelopmental trajectories of brain structure in Tourette syndrome and Chronic Tic Disorders
Yin Jin, Yuxin Guo, Jonathan M Koller, et al.
Nature Genetics
|
June 22, 2026
Co-expression-based models improve eQTL predictions for transcriptome-wide association studies and highlight new schizophrenia-associated genes
Fabiana Rossi, Leonardo Sportelli, Gianluca C Kikidis, et al.
Nature
|
November 4, 2014
Synaptic, transcriptional and chromatin genes disrupted in autism
Silvia De Rubeis, Xin He, Arthur P Goldberg, et al.
Nature Genetics
|
April 2, 2025
Psychiatric genetics in the diverse landscape of Latin American populations
Estela M Bruxel, Diego L Rovaris, Sintia I Belangero, et al.
American Journal of Human Genetics
|
April 29, 2014
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
Dalila Pinto, Elsa Delaby, Daniele Merico, et al.
Human Genetics
|
October 15, 2011
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
Jillian P Casey, Tiago Magalhaes, Judith M Conroy, et al.
Biological Psychiatry
|
June 8, 2021
Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders
Gabriëlla A M Blokland, Jakob Grove, Chia-Yen Chen, et al.
Human Molecular Genetics
|
July 31, 2012
Individual common variants exert weak effects on the risk for autism spectrum disorders
Richard Anney, Lambertus Klei, Dalila Pinto, et al.
Page
of 37
Search research articles
Search
Showing results (331-340 of 361) with videos related to
Sort By:
Page
of 37
Nature Genetics
|
August 18, 2022
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
Jack M Fu, F Kyle Satterstrom, Minshi Peng, et al.
Nature Genetics
|
February 27, 2019
Identification of common genetic risk variants for autism spectrum disorder
Jakob Grove, Stephan Ripke, Thomas D Als, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 4, 2026
Altered neurodevelopmental trajectories of brain structure in Tourette syndrome and Chronic Tic Disorders
Yin Jin, Yuxin Guo, Jonathan M Koller, et al.
Nature Genetics
|
June 22, 2026
Co-expression-based models improve eQTL predictions for transcriptome-wide association studies and highlight new schizophrenia-associated genes
Fabiana Rossi, Leonardo Sportelli, Gianluca C Kikidis, et al.
Nature
|
November 4, 2014
Synaptic, transcriptional and chromatin genes disrupted in autism
Silvia De Rubeis, Xin He, Arthur P Goldberg, et al.
Nature Genetics
|
April 2, 2025
Psychiatric genetics in the diverse landscape of Latin American populations
Estela M Bruxel, Diego L Rovaris, Sintia I Belangero, et al.
American Journal of Human Genetics
|
April 29, 2014
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
Dalila Pinto, Elsa Delaby, Daniele Merico, et al.
Human Genetics
|
October 15, 2011
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
Jillian P Casey, Tiago Magalhaes, Judith M Conroy, et al.
Biological Psychiatry
|
June 8, 2021
Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders
Gabriëlla A M Blokland, Jakob Grove, Chia-Yen Chen, et al.
Human Molecular Genetics
|
July 31, 2012
Individual common variants exert weak effects on the risk for autism spectrum disorders
Richard Anney, Lambertus Klei, Dalila Pinto, et al.
Page
of 37