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John R Gilbert

Showing results (61-70 of 98) with videos related to

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Plos One|May 12, 2011
Comparison of three targeted enrichment strategies on the SOLiD sequencing platformDale J Hedges, Toumy Guettouche, Shan Yang, et al.
Molecular Autism|November 5, 2011
An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in malesRen-Hua Chung, Deqiong Ma, Kai Wang, et al.
Human Genetics|May 11, 2005
SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defectsKristen L Deak, Abee L Boyles, Heather C Etchevers, et al.
Neurobiology of Aging|February 7, 2012
Vitamin D receptor and Alzheimer's disease: a genetic and functional studyLiyong Wang, Kenju Hara, Jessica M Van Baaren, et al.
Plos One|October 22, 2011
Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism riskDaria Salyakina, Holly N Cukier, Joycelyn M Lee, et al.
Molecular Autism|July 18, 2015
Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variantsAnthony J Griswold, Nicole D Dueker, Derek Van Booven, et al.
Autism Research : Official Journal of the International Society for Autism Research|October 12, 2012
The expanding role of MBD genes in autism: identification of a MECP2 duplication and novel alterations in MBD5, MBD6, and SETDB1Holly N Cukier, Joycelyn M Lee, Deqiong Ma, et al.
Human Molecular Genetics|April 18, 2015
Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesisRobert A Kozol, Holly N Cukier, Bing Zou, et al.
Plos Genetics|October 2, 2010
Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalitiesAdam C Naj, Gary W Beecham, Eden R Martin, et al.
Annals of Human Genetics|August 14, 2012
Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease geneAnna C Cummings, Lan Jiang, Digna R Velez Edwards, et al.
Pageof 10

Showing results (61-70 of 98) with videos related to

Sort By:
Pageof 10
Plos One|May 12, 2011
Comparison of three targeted enrichment strategies on the SOLiD sequencing platformDale J Hedges, Toumy Guettouche, Shan Yang, et al.
Molecular Autism|November 5, 2011
An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in malesRen-Hua Chung, Deqiong Ma, Kai Wang, et al.
Human Genetics|May 11, 2005
SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defectsKristen L Deak, Abee L Boyles, Heather C Etchevers, et al.
Neurobiology of Aging|February 7, 2012
Vitamin D receptor and Alzheimer's disease: a genetic and functional studyLiyong Wang, Kenju Hara, Jessica M Van Baaren, et al.
Plos One|October 22, 2011
Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism riskDaria Salyakina, Holly N Cukier, Joycelyn M Lee, et al.
Molecular Autism|July 18, 2015
Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variantsAnthony J Griswold, Nicole D Dueker, Derek Van Booven, et al.
Autism Research : Official Journal of the International Society for Autism Research|October 12, 2012
The expanding role of MBD genes in autism: identification of a MECP2 duplication and novel alterations in MBD5, MBD6, and SETDB1Holly N Cukier, Joycelyn M Lee, Deqiong Ma, et al.
Human Molecular Genetics|April 18, 2015
Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesisRobert A Kozol, Holly N Cukier, Bing Zou, et al.
Plos Genetics|October 2, 2010
Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalitiesAdam C Naj, Gary W Beecham, Eden R Martin, et al.
Annals of Human Genetics|August 14, 2012
Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease geneAnna C Cummings, Lan Jiang, Digna R Velez Edwards, et al.
Pageof 10