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Talin Haritunians

Showing results (81-90 of 123) with videos related to

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Circulation. Cardiovascular Genetics|April 20, 2010
Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortiumAlanna C Morrison, Janine F Felix, L Adrienne Cupples, et al.
Nature Genetics|October 11, 2011
Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel diseaseManuel A Rivas, Mélissa Beaudoin, Agnes Gardet, et al.
Gastroenterology|August 6, 2016
A Pleiotropic Missense Variant in SLC39A8 Is Associated With Crohn's Disease and Human Gut Microbiome CompositionDalin Li, Jean-Paul Achkar, Talin Haritunians, et al.
Nature Genetics|May 12, 2009
Multiple loci associated with indices of renal function and chronic kidney diseaseAnna Köttgen, Nicole L Glazer, Abbas Dehghan, et al.
Circulation. Cardiovascular Genetics|October 2, 2010
Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factorsQiong Yang, Anna Köttgen, Abbas Dehghan, et al.
Circulation. Cardiovascular Genetics|May 7, 2010
Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortiumNicholas L Smith, Janine F Felix, Alanna C Morrison, et al.
American Journal of Human Genetics|August 27, 2021
Stratification of risk of progression to colectomy in ulcerative colitis via measured and predicted gene expressionAngela Mo, Sini Nagpal, Kyle Gettler, et al.
Diabetes|March 10, 2011
A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortiumAldi T Kraja, Dhananjay Vaidya, James S Pankow, et al.
Nature|June 29, 2017
Fine-mapping inflammatory bowel disease loci to single-variant resolutionHailiang Huang, Ming Fang, Luke Jostins, et al.
Gut|April 20, 2023
Genetic coding variant in complement factor B (CFB) is associated with increased risk for perianal Crohn's disease and leads to impaired CFB cleavage and phagocytosisMarzieh Akhlaghpour, Talin Haritunians, Shyam K More, et al.
Pageof 13

Showing results (81-90 of 123) with videos related to

Sort By:
Pageof 13
Circulation. Cardiovascular Genetics|April 20, 2010
Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortiumAlanna C Morrison, Janine F Felix, L Adrienne Cupples, et al.
Nature Genetics|October 11, 2011
Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel diseaseManuel A Rivas, Mélissa Beaudoin, Agnes Gardet, et al.
Gastroenterology|August 6, 2016
A Pleiotropic Missense Variant in SLC39A8 Is Associated With Crohn's Disease and Human Gut Microbiome CompositionDalin Li, Jean-Paul Achkar, Talin Haritunians, et al.
Nature Genetics|May 12, 2009
Multiple loci associated with indices of renal function and chronic kidney diseaseAnna Köttgen, Nicole L Glazer, Abbas Dehghan, et al.
Circulation. Cardiovascular Genetics|October 2, 2010
Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factorsQiong Yang, Anna Köttgen, Abbas Dehghan, et al.
Circulation. Cardiovascular Genetics|May 7, 2010
Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortiumNicholas L Smith, Janine F Felix, Alanna C Morrison, et al.
American Journal of Human Genetics|August 27, 2021
Stratification of risk of progression to colectomy in ulcerative colitis via measured and predicted gene expressionAngela Mo, Sini Nagpal, Kyle Gettler, et al.
Diabetes|March 10, 2011
A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortiumAldi T Kraja, Dhananjay Vaidya, James S Pankow, et al.
Nature|June 29, 2017
Fine-mapping inflammatory bowel disease loci to single-variant resolutionHailiang Huang, Ming Fang, Luke Jostins, et al.
Gut|April 20, 2023
Genetic coding variant in complement factor B (CFB) is associated with increased risk for perianal Crohn's disease and leads to impaired CFB cleavage and phagocytosisMarzieh Akhlaghpour, Talin Haritunians, Shyam K More, et al.
Pageof 13