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Mark J Daly

Showing results (81-90 of 530) with videos related to

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American Journal of Human Genetics|May 31, 2003
IBD5 is a general risk factor for inflammatory bowel disease: replication of association with Crohn disease and identification of a novel association with ulcerative colitisCosmas Giallourakis, Monika Stoll, Katie Miller, et al.
Genome Research|October 31, 2008
Whole population, genome-wide mapping of hidden relatednessAlexander Gusev, Jennifer K Lowe, Markus Stoffel, et al.
Nature Reviews. Genetics|November 29, 2025
Dissecting pleiotropy to gain mechanistic insights into human diseaseYon Ho Jee, Yixuan He, Wenhan Lu, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 8, 2014
Autism spectrum disorder severity reflects the average contribution of de novo and familial influencesElise B Robinson, Kaitlin E Samocha, Jack A Kosmicki, et al.
Epilepsia|October 21, 2018
Guideline-based and bioinformatic reassessment of lesion-associated gene and variant pathogenicity in focal human epilepsiesLisa-Marie Niestroj, Juanjiangmeng Du, Michael Nothnagel, et al.
Science (New York, N.Y.)|December 16, 2006
Histocompatible embryonic stem cells by parthenogenesisKitai Kim, Paul Lerou, Akiko Yabuuchi, et al.
European Journal of Human Genetics : EJHG|October 22, 2009
Genetic profile for five common variants associated with age-related macular degeneration in densely affected families: a novel analytic approachLucia Sobrin, Julian B Maller, Benjamin M Neale, et al.
Medrxiv : the Preprint Server for Health Sciences|December 16, 2024
Cystic fibrosis risk variants confer protection against inflammatory bowel diseaseMingrui Yu, Qian Zhang, Kai Yuan, et al.
Medrxiv : the Preprint Server for Health Sciences|December 11, 2023
Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure eventsHenrike O Heyne, Fanny-Dhelia Pajuste, Julian Wanner, et al.
Molecular Autism|March 22, 2013
Lack of association of rare functional variants in TSC1/TSC2 genes with autism spectrum disorderSamira Bahl, Colby Chiang, Roberta L Beauchamp, et al.
Pageof 53

Showing results (81-90 of 530) with videos related to

Sort By:
Pageof 53
American Journal of Human Genetics|May 31, 2003
IBD5 is a general risk factor for inflammatory bowel disease: replication of association with Crohn disease and identification of a novel association with ulcerative colitisCosmas Giallourakis, Monika Stoll, Katie Miller, et al.
Genome Research|October 31, 2008
Whole population, genome-wide mapping of hidden relatednessAlexander Gusev, Jennifer K Lowe, Markus Stoffel, et al.
Nature Reviews. Genetics|November 29, 2025
Dissecting pleiotropy to gain mechanistic insights into human diseaseYon Ho Jee, Yixuan He, Wenhan Lu, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 8, 2014
Autism spectrum disorder severity reflects the average contribution of de novo and familial influencesElise B Robinson, Kaitlin E Samocha, Jack A Kosmicki, et al.
Epilepsia|October 21, 2018
Guideline-based and bioinformatic reassessment of lesion-associated gene and variant pathogenicity in focal human epilepsiesLisa-Marie Niestroj, Juanjiangmeng Du, Michael Nothnagel, et al.
Science (New York, N.Y.)|December 16, 2006
Histocompatible embryonic stem cells by parthenogenesisKitai Kim, Paul Lerou, Akiko Yabuuchi, et al.
European Journal of Human Genetics : EJHG|October 22, 2009
Genetic profile for five common variants associated with age-related macular degeneration in densely affected families: a novel analytic approachLucia Sobrin, Julian B Maller, Benjamin M Neale, et al.
Medrxiv : the Preprint Server for Health Sciences|December 16, 2024
Cystic fibrosis risk variants confer protection against inflammatory bowel diseaseMingrui Yu, Qian Zhang, Kai Yuan, et al.
Medrxiv : the Preprint Server for Health Sciences|December 11, 2023
Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure eventsHenrike O Heyne, Fanny-Dhelia Pajuste, Julian Wanner, et al.
Molecular Autism|March 22, 2013
Lack of association of rare functional variants in TSC1/TSC2 genes with autism spectrum disorderSamira Bahl, Colby Chiang, Roberta L Beauchamp, et al.
Pageof 53