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Edwin H Cook

Showing results (131-140 of 205) with videos related to

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Bioinformatics (Oxford, England)|October 2, 2014
Consensus Genotyper for Exome Sequencing (CGES): improving the quality of exome variant genotypesVassily 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 syndromeCindi 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 autismDan 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 ProgramRichard 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 diseasesJin 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 leukemiaMary 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 DivideRyne 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 variationDeborah 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 disorderDiane E Dickel, Jeremy Veenstra-VanderWeele, Nancy J Cox, et al.
Human Molecular Genetics|December 25, 2007
Recurrent 16p11.2 microdeletions in autismRavinesh A Kumar, Samer KaraMohamed, Jyotsna Sudi, et al.
Pageof 21

Showing results (131-140 of 205) with videos related to

Sort By:
Pageof 21
Bioinformatics (Oxford, England)|October 2, 2014
Consensus Genotyper for Exome Sequencing (CGES): improving the quality of exome variant genotypesVassily 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 syndromeCindi 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 autismDan 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 ProgramRichard 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 diseasesJin 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 leukemiaMary 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 DivideRyne 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 variationDeborah 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 disorderDiane E Dickel, Jeremy Veenstra-VanderWeele, Nancy J Cox, et al.
Human Molecular Genetics|December 25, 2007
Recurrent 16p11.2 microdeletions in autismRavinesh A Kumar, Samer KaraMohamed, Jyotsna Sudi, et al.
Pageof 21