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

Samer KaraMohamed

Showing results (1-10 of 10) with videos related to

Pageof 1
Sort By:
American Journal of Respiratory and Critical Care Medicine|January 6, 2007
Secreted modular calcium-binding protein 2 haplotypes are associated with pulmonary functionJemma B Wilk, Alan Herbert, Christina M Shoemaker, et al.
American Heart Journal|March 27, 2007
Fucosyltransferase 3 polymorphism and atherothrombotic disease in the Framingham Offspring StudyLuc Djoussé, Samer Karamohamed, Alan G Herbert, et al.
Obesity (Silver Spring, Md.)|September 22, 2006
BMI modifies associations of IL-6 genotypes with insulin resistance: the Framingham StudyAlan Herbert, Chunyu Liu, Samer Karamohamed, et al.
The American Journal of Cardiology|July 16, 2005
Influence of alcohol dehydrogenase 1C polymorphism on the alcohol-cardiovascular disease association (from the Framingham Offspring Study)Luc Djoussé, Daniel Levy, Alan G Herbert, et al.
Brain Research|February 3, 2007
Sepiapterin reductase expression is increased in Parkinson's disease brain tissueJennifer E Tobin, Jing Cui, Jemma B Wilk, et al.
Human Molecular Genetics|December 25, 2007
Recurrent 16p11.2 microdeletions in autismRavinesh A Kumar, Samer KaraMohamed, Jyotsna Sudi, et al.
Diabetes|May 27, 2003
Polymorphisms in the insulin-degrading enzyme gene are associated with type 2 diabetes in men from the NHLBI Framingham Heart StudySamer Karamohamed, Serkalem Demissie, Jeannine Volcjak, et al.
Plos One|February 27, 2009
Association and mutation analyses of 16p11.2 autism candidate genesRavinesh A Kumar, Christian R Marshall, Judith A Badner, et al.
Biological Psychiatry|April 1, 2008
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorderSusan L Christian, Camille W Brune, Jyotsna Sudi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 21, 2005
Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD studySamer Karamohamed, L I Golbe, M H Mark, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
American Journal of Respiratory and Critical Care Medicine|January 6, 2007
Secreted modular calcium-binding protein 2 haplotypes are associated with pulmonary functionJemma B Wilk, Alan Herbert, Christina M Shoemaker, et al.
American Heart Journal|March 27, 2007
Fucosyltransferase 3 polymorphism and atherothrombotic disease in the Framingham Offspring StudyLuc Djoussé, Samer Karamohamed, Alan G Herbert, et al.
Obesity (Silver Spring, Md.)|September 22, 2006
BMI modifies associations of IL-6 genotypes with insulin resistance: the Framingham StudyAlan Herbert, Chunyu Liu, Samer Karamohamed, et al.
The American Journal of Cardiology|July 16, 2005
Influence of alcohol dehydrogenase 1C polymorphism on the alcohol-cardiovascular disease association (from the Framingham Offspring Study)Luc Djoussé, Daniel Levy, Alan G Herbert, et al.
Brain Research|February 3, 2007
Sepiapterin reductase expression is increased in Parkinson's disease brain tissueJennifer E Tobin, Jing Cui, Jemma B Wilk, et al.
Human Molecular Genetics|December 25, 2007
Recurrent 16p11.2 microdeletions in autismRavinesh A Kumar, Samer KaraMohamed, Jyotsna Sudi, et al.
Diabetes|May 27, 2003
Polymorphisms in the insulin-degrading enzyme gene are associated with type 2 diabetes in men from the NHLBI Framingham Heart StudySamer Karamohamed, Serkalem Demissie, Jeannine Volcjak, et al.
Plos One|February 27, 2009
Association and mutation analyses of 16p11.2 autism candidate genesRavinesh A Kumar, Christian R Marshall, Judith A Badner, et al.
Biological Psychiatry|April 1, 2008
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorderSusan L Christian, Camille W Brune, Jyotsna Sudi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 21, 2005
Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD studySamer Karamohamed, L I Golbe, M H Mark, et al.
Pageof 1