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Bioinformatics (Oxford, England)
|
October 2, 2014
Consensus Genotyper for Exome Sequencing (CGES): improving the quality of exome variant genotypes
Vassily Trubetskoy, Alex Rodriguez, Uptal Dave, et al.
Journal of Neurodevelopmental Disorders
|
September 2, 2011
Repetitive behavior profiles: Consistency across autism spectrum disorder cohorts and divergence from Prader-Willi syndrome
Cindi G Flores, Gregory Valcante, Steve Guter, et al.
American Journal of Human Genetics
|
January 9, 2008
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism
Dan E Arking, David J Cutler, Camille W Brune, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
January 22, 2011
A genotype resource for postmortem brain samples from the Autism Tissue Program
Richard F Wintle, Anath C Lionel, Pingzhao Hu, et al.
Neuroscience Letters
|
April 28, 2005
Vitamin D receptor variants in 192 patients with schizophrenia and other psychiatric diseases
Jin Yan, Jinong Feng, Nick Craddock, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
October 2, 2004
Pharmacogenetic risk factors for osteonecrosis of the hip among children with leukemia
Mary V Relling, Wenjian Yang, Soma Das, et al.
Behavior Genetics
|
November 20, 2015
Separating Family-Level and Direct Exposure Effects of Smoking During Pregnancy on Offspring Externalizing Symptoms: Bridging the Behavior Genetic and Behavior Teratologic Divide
Ryne Estabrook, Suena H Massey, Caron A C Clark, et al.
Human Molecular Genetics
|
April 29, 2005
Global gene expression as a function of germline genetic variation
Deborah French, Mark R Wilkinson, Wenjian Yang, et al.
Archives of General Psychiatry
|
July 5, 2006
Association testing of the positional and functional candidate gene SLC1A1/EAAC1 in early-onset obsessive-compulsive disorder
Diane E Dickel, Jeremy Veenstra-VanderWeele, Nancy J Cox, et al.
Human Molecular Genetics
|
December 25, 2007
Recurrent 16p11.2 microdeletions in autism
Ravinesh A Kumar, Samer KaraMohamed, Jyotsna Sudi, et al.
Page
of 21
Search research articles
Search
Showing results (131-140 of 205) with videos related to
Sort By:
Page
of 21
Bioinformatics (Oxford, England)
|
October 2, 2014
Consensus Genotyper for Exome Sequencing (CGES): improving the quality of exome variant genotypes
Vassily Trubetskoy, Alex Rodriguez, Uptal Dave, et al.
Journal of Neurodevelopmental Disorders
|
September 2, 2011
Repetitive behavior profiles: Consistency across autism spectrum disorder cohorts and divergence from Prader-Willi syndrome
Cindi G Flores, Gregory Valcante, Steve Guter, et al.
American Journal of Human Genetics
|
January 9, 2008
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism
Dan E Arking, David J Cutler, Camille W Brune, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
January 22, 2011
A genotype resource for postmortem brain samples from the Autism Tissue Program
Richard F Wintle, Anath C Lionel, Pingzhao Hu, et al.
Neuroscience Letters
|
April 28, 2005
Vitamin D receptor variants in 192 patients with schizophrenia and other psychiatric diseases
Jin Yan, Jinong Feng, Nick Craddock, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
October 2, 2004
Pharmacogenetic risk factors for osteonecrosis of the hip among children with leukemia
Mary V Relling, Wenjian Yang, Soma Das, et al.
Behavior Genetics
|
November 20, 2015
Separating Family-Level and Direct Exposure Effects of Smoking During Pregnancy on Offspring Externalizing Symptoms: Bridging the Behavior Genetic and Behavior Teratologic Divide
Ryne Estabrook, Suena H Massey, Caron A C Clark, et al.
Human Molecular Genetics
|
April 29, 2005
Global gene expression as a function of germline genetic variation
Deborah French, Mark R Wilkinson, Wenjian Yang, et al.
Archives of General Psychiatry
|
July 5, 2006
Association testing of the positional and functional candidate gene SLC1A1/EAAC1 in early-onset obsessive-compulsive disorder
Diane E Dickel, Jeremy Veenstra-VanderWeele, Nancy J Cox, et al.
Human Molecular Genetics
|
December 25, 2007
Recurrent 16p11.2 microdeletions in autism
Ravinesh A Kumar, Samer KaraMohamed, Jyotsna Sudi, et al.
Page
of 21