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American Journal of Epidemiology
|
October 6, 2017
Current Challenges and New Opportunities for Gene-Environment Interaction Studies of Complex Diseases
Kimberly McAllister, Leah E Mechanic, Christopher Amos, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 26, 2013
Association of DXA-derived bone mineral density and fat mass with African ancestry
Heather M Ochs-Balcom, Leah Preus, Jean Wactawski-Wende, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 2, 2012
Common variation in the LRRK2 gene is a risk factor for Parkinson's disease
Ignacio F Mata, Harvey Checkoway, Carolyn M Hutter, et al.
Gastroenterology
|
February 17, 2015
A model to determine colorectal cancer risk using common genetic susceptibility loci
Li Hsu, Jihyoun Jeon, Hermann Brenner, et al.
Clinical Pharmacology and Therapeutics
|
November 7, 2017
Research Directions in Genetic Predispositions to Stevens-Johnson Syndrome / Toxic Epidermal Necrolysis
Teri A Manolio, Carolyn M Hutter, Mark Avigan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 17, 2017
Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centers
Rashesh V Sanghvi, Christian J Buhay, Bradford C Powell, et al.
Nature
|
October 29, 2020
Strategic vision for improving human health at The Forefront of Genomics
Eric D Green, Chris Gunter, Leslie G Biesecker, et al.
Cell
|
April 7, 2018
Perspective on Oncogenic Processes at the End of the Beginning of Cancer Genomics
Li Ding, Matthew H Bailey, Eduard Porta-Pardo, et al.
Carcinogenesis
|
November 21, 2015
Common genetic variation and survival after colorectal cancer diagnosis: a genome-wide analysis
Amanda I Phipps, Michael N Passarelli, Andrew T Chan, et al.
American Journal of Human Genetics
|
October 28, 2008
CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290
Nicholas T Gorden, Heleen H Arts, Melissa A Parisi, et al.
Page
of 26
Search research articles
Search
Showing results (231-240 of 260) with videos related to
Sort By:
Page
of 26
American Journal of Epidemiology
|
October 6, 2017
Current Challenges and New Opportunities for Gene-Environment Interaction Studies of Complex Diseases
Kimberly McAllister, Leah E Mechanic, Christopher Amos, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 26, 2013
Association of DXA-derived bone mineral density and fat mass with African ancestry
Heather M Ochs-Balcom, Leah Preus, Jean Wactawski-Wende, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 2, 2012
Common variation in the LRRK2 gene is a risk factor for Parkinson's disease
Ignacio F Mata, Harvey Checkoway, Carolyn M Hutter, et al.
Gastroenterology
|
February 17, 2015
A model to determine colorectal cancer risk using common genetic susceptibility loci
Li Hsu, Jihyoun Jeon, Hermann Brenner, et al.
Clinical Pharmacology and Therapeutics
|
November 7, 2017
Research Directions in Genetic Predispositions to Stevens-Johnson Syndrome / Toxic Epidermal Necrolysis
Teri A Manolio, Carolyn M Hutter, Mark Avigan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 17, 2017
Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centers
Rashesh V Sanghvi, Christian J Buhay, Bradford C Powell, et al.
Nature
|
October 29, 2020
Strategic vision for improving human health at The Forefront of Genomics
Eric D Green, Chris Gunter, Leslie G Biesecker, et al.
Cell
|
April 7, 2018
Perspective on Oncogenic Processes at the End of the Beginning of Cancer Genomics
Li Ding, Matthew H Bailey, Eduard Porta-Pardo, et al.
Carcinogenesis
|
November 21, 2015
Common genetic variation and survival after colorectal cancer diagnosis: a genome-wide analysis
Amanda I Phipps, Michael N Passarelli, Andrew T Chan, et al.
American Journal of Human Genetics
|
October 28, 2008
CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290
Nicholas T Gorden, Heleen H Arts, Melissa A Parisi, et al.
Page
of 26