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Plos One
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July 23, 2013
Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium
Megan L Grove, Bing Yu, Barbara J Cochran, et al.
Nature Communications
|
February 19, 2016
Mutations in the nuclear bile acid receptor FXR cause progressive familial intrahepatic cholestasis
Natalia Gomez-Ospina, Carol J Potter, Rui Xiao, et al.
Cell Reports. Medicine
|
June 22, 2023
Integrating genetics and metabolomics from multi-ethnic and multi-fluid data reveals putative mechanisms for age-related macular degeneration
Xikun Han, Ines Lains, Jun Li, et al.
Genetics
|
June 22, 2023
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants
Jonah Einson, Dafni Glinos, Eric Boerwinkle, et al.
Biorxiv : the Preprint Server for Biology
|
February 13, 2023
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants
Jonah Einson, Dafni Glinos, Eric Boerwinkle, et al.
BMC Genomics
|
April 19, 2015
Assessing structural variation in a personal genome-towards a human reference diploid genome
Adam C English, William J Salerno, Oliver A Hampton, et al.
Plos One
|
October 21, 2014
The challenges of genome-wide interaction studies: lessons to learn from the analysis of HDL blood levels
Elisabeth M van Leeuwen, Françoise A S Smouter, Tony Kam-Thong, et al.
American Journal of Respiratory and Critical Care Medicine
|
May 5, 2026
Mosaic Loss of Y chromosome associates with lung function, emphysema and epigenetic aging
Woei-Yuh Saw, Kangjin Kim, Yichen Huang, et al.
Circulation
|
August 25, 2010
Independent susceptibility markers for atrial fibrillation on chromosome 4q25
Steven A Lubitz, Moritz F Sinner, Kathryn L Lunetta, et al.
Brain : a Journal of Neurology
|
March 13, 2019
Association of variants in HTRA1 and NOTCH3 with MRI-defined extremes of cerebral small vessel disease in older subjects
Aniket Mishra, Ganesh Chauhan, Marie-Helene Violleau, et al.
Page
of 118
Search research articles
Search
Showing results (761-770 of 1,171) with videos related to
Sort By:
Page
of 118
Plos One
|
July 23, 2013
Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium
Megan L Grove, Bing Yu, Barbara J Cochran, et al.
Nature Communications
|
February 19, 2016
Mutations in the nuclear bile acid receptor FXR cause progressive familial intrahepatic cholestasis
Natalia Gomez-Ospina, Carol J Potter, Rui Xiao, et al.
Cell Reports. Medicine
|
June 22, 2023
Integrating genetics and metabolomics from multi-ethnic and multi-fluid data reveals putative mechanisms for age-related macular degeneration
Xikun Han, Ines Lains, Jun Li, et al.
Genetics
|
June 22, 2023
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants
Jonah Einson, Dafni Glinos, Eric Boerwinkle, et al.
Biorxiv : the Preprint Server for Biology
|
February 13, 2023
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants
Jonah Einson, Dafni Glinos, Eric Boerwinkle, et al.
BMC Genomics
|
April 19, 2015
Assessing structural variation in a personal genome-towards a human reference diploid genome
Adam C English, William J Salerno, Oliver A Hampton, et al.
Plos One
|
October 21, 2014
The challenges of genome-wide interaction studies: lessons to learn from the analysis of HDL blood levels
Elisabeth M van Leeuwen, Françoise A S Smouter, Tony Kam-Thong, et al.
American Journal of Respiratory and Critical Care Medicine
|
May 5, 2026
Mosaic Loss of Y chromosome associates with lung function, emphysema and epigenetic aging
Woei-Yuh Saw, Kangjin Kim, Yichen Huang, et al.
Circulation
|
August 25, 2010
Independent susceptibility markers for atrial fibrillation on chromosome 4q25
Steven A Lubitz, Moritz F Sinner, Kathryn L Lunetta, et al.
Brain : a Journal of Neurology
|
March 13, 2019
Association of variants in HTRA1 and NOTCH3 with MRI-defined extremes of cerebral small vessel disease in older subjects
Aniket Mishra, Ganesh Chauhan, Marie-Helene Violleau, et al.
Page
of 118