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John R Gilbert

Showing results (51-60 of 98) with videos related to

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Science (New York, N.Y.)|March 12, 2005
Complement factor H variant increases the risk of age-related macular degenerationJonathan L Haines, Michael A Hauser, Silke Schmidt, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 12, 2011
Microduplications in an autism multiplex family narrow the region of susceptibility for developmental disorders on 15q24 and implicate 7p21Holly N Cukier, Daria Salyakina, Sarah F Blankstein, et al.
Human Genetics|July 14, 2011
Mitochondrial haplogroup X is associated with successful aging in the AmishMonique D Courtenay, John R Gilbert, Lan Jiang, et al.
Neuroscience Letters|July 24, 2003
The Q7R Saitohin gene polymorphism is not associated with Alzheimer diseaseSofia A Oliveira, Eden R Martin, William K Scott, et al.
Environmental Health Perspectives|October 13, 2006
Neural tube defects and folate pathway genes: family-based association tests of gene-gene and gene-environment interactionsAbee L Boyles, Ashley V Billups, Kristen L Deak, et al.
Annals of Human Genetics|July 13, 2013
C9ORF72 intermediate repeat copies are a significant risk factor for Parkinson diseaseKaren Nuytemans, Güney Bademci, Martin M Kohli, et al.
Psychiatric Genetics|July 11, 2007
Investigation of potential gene-gene interactions between APOE and RELN contributing to autism riskAllison E Ashley-Koch, James Jaworski, De Qiong Ma, et al.
Molecular Autism|January 21, 2011
A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autismJohn P Hussman, Ren-Hua Chung, Anthony J Griswold, et al.
The American Journal of Psychiatry|May 2, 2006
Lack of association between autism and SLC25A12Raquel Rabionet, Jacob L McCauley, James M Jaworski, et al.
Annals of Human Genetics|November 8, 2012
Evaluating mitochondrial DNA variation in autism spectrum disordersAthena Hadjixenofontos, Michael A Schmidt, Patrice L Whitehead, et al.
Pageof 10

Showing results (51-60 of 98) with videos related to

Sort By:
Pageof 10
Science (New York, N.Y.)|March 12, 2005
Complement factor H variant increases the risk of age-related macular degenerationJonathan L Haines, Michael A Hauser, Silke Schmidt, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 12, 2011
Microduplications in an autism multiplex family narrow the region of susceptibility for developmental disorders on 15q24 and implicate 7p21Holly N Cukier, Daria Salyakina, Sarah F Blankstein, et al.
Human Genetics|July 14, 2011
Mitochondrial haplogroup X is associated with successful aging in the AmishMonique D Courtenay, John R Gilbert, Lan Jiang, et al.
Neuroscience Letters|July 24, 2003
The Q7R Saitohin gene polymorphism is not associated with Alzheimer diseaseSofia A Oliveira, Eden R Martin, William K Scott, et al.
Environmental Health Perspectives|October 13, 2006
Neural tube defects and folate pathway genes: family-based association tests of gene-gene and gene-environment interactionsAbee L Boyles, Ashley V Billups, Kristen L Deak, et al.
Annals of Human Genetics|July 13, 2013
C9ORF72 intermediate repeat copies are a significant risk factor for Parkinson diseaseKaren Nuytemans, Güney Bademci, Martin M Kohli, et al.
Psychiatric Genetics|July 11, 2007
Investigation of potential gene-gene interactions between APOE and RELN contributing to autism riskAllison E Ashley-Koch, James Jaworski, De Qiong Ma, et al.
Molecular Autism|January 21, 2011
A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autismJohn P Hussman, Ren-Hua Chung, Anthony J Griswold, et al.
The American Journal of Psychiatry|May 2, 2006
Lack of association between autism and SLC25A12Raquel Rabionet, Jacob L McCauley, James M Jaworski, et al.
Annals of Human Genetics|November 8, 2012
Evaluating mitochondrial DNA variation in autism spectrum disordersAthena Hadjixenofontos, Michael A Schmidt, Patrice L Whitehead, et al.
Pageof 10