Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

John R Gilbert

Showing results (71-80 of 98) with videos related to

Pageof 10
Sort By:
Age (Dordrecht, Netherlands)|July 10, 2012
Linkage and association of successful aging to the 6q25 region in large Amish kindredsDigna R Velez Edwards, John R Gilbert, James E Hicks, et al.
American Journal of Medical Genetics|February 13, 2002
Genomic screen and follow-up analysis for autistic disorderYujun Shao, Chantelle M Wolpert, Kimberly L Raiford, et al.
Neurology. Genetics|April 12, 2016
Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer diseaseMartin A Kohli, Holly N Cukier, Kara L Hamilton-Nelson, et al.
Neuroscience Letters|July 6, 2004
Analysis of European mitochondrial haplogroups with Alzheimer disease riskJoelle M van der Walt, Yulia A Dementieva, Eden R Martin, et al.
Plos One|March 3, 2012
MCP1 SNPs and pulmonary tuberculosis in cohorts from West Africa, the USA and Argentina: lack of association or epistasis with IL12B polymorphismsDigna R Velez Edwards, Alessandra Tacconelli, Christian Wejse, et al.
American Journal of Medical Genetics. Part A|November 15, 2006
Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15Abee L Boyles, David S Enterline, Preston H Hammock, et al.
Molecular Autism|January 14, 2014
Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disordersHolly N Cukier, Nicole D Dueker, Susan H Slifer, et al.
Human Molecular Genetics|May 1, 2012
Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathwaysAnthony J Griswold, Deqiong Ma, Holly N Cukier, et al.
JAMA Neurology|July 25, 2017
Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal TransportBrian W Kunkle, Badri N Vardarajan, Adam C Naj, et al.
Plos One|February 23, 2011
Interleukin 12B (IL12B) genetic variation and pulmonary tuberculosis: a study of cohorts from The Gambia, Guinea-Bissau, United States and ArgentinaGerard A J Morris, Digna R Velez Edwards, Philip C Hill, et al.
Pageof 10

Showing results (71-80 of 98) with videos related to

Sort By:
Pageof 10
Age (Dordrecht, Netherlands)|July 10, 2012
Linkage and association of successful aging to the 6q25 region in large Amish kindredsDigna R Velez Edwards, John R Gilbert, James E Hicks, et al.
American Journal of Medical Genetics|February 13, 2002
Genomic screen and follow-up analysis for autistic disorderYujun Shao, Chantelle M Wolpert, Kimberly L Raiford, et al.
Neurology. Genetics|April 12, 2016
Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer diseaseMartin A Kohli, Holly N Cukier, Kara L Hamilton-Nelson, et al.
Neuroscience Letters|July 6, 2004
Analysis of European mitochondrial haplogroups with Alzheimer disease riskJoelle M van der Walt, Yulia A Dementieva, Eden R Martin, et al.
Plos One|March 3, 2012
MCP1 SNPs and pulmonary tuberculosis in cohorts from West Africa, the USA and Argentina: lack of association or epistasis with IL12B polymorphismsDigna R Velez Edwards, Alessandra Tacconelli, Christian Wejse, et al.
American Journal of Medical Genetics. Part A|November 15, 2006
Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15Abee L Boyles, David S Enterline, Preston H Hammock, et al.
Molecular Autism|January 14, 2014
Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disordersHolly N Cukier, Nicole D Dueker, Susan H Slifer, et al.
Human Molecular Genetics|May 1, 2012
Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathwaysAnthony J Griswold, Deqiong Ma, Holly N Cukier, et al.
JAMA Neurology|July 25, 2017
Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal TransportBrian W Kunkle, Badri N Vardarajan, Adam C Naj, et al.
Plos One|February 23, 2011
Interleukin 12B (IL12B) genetic variation and pulmonary tuberculosis: a study of cohorts from The Gambia, Guinea-Bissau, United States and ArgentinaGerard A J Morris, Digna R Velez Edwards, Philip C Hill, et al.
Pageof 10