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Showing results (1101-1110 of 1,201) with videos related to

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Nature Genetics|April 23, 2013
Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitisJimmy Z Liu, Johannes Roksund Hov, Trine Folseraas, et al.
Ebiomedicine|January 8, 2021
Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortiumBridget M Lin, Kelsey E Grinde, Jennifer A Brody, et al.
American Journal of Respiratory and Critical Care Medicine|July 28, 2012
Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstructionJemma B Wilk, Nick R G Shrine, Laura R Loehr, et al.
The New England Journal of Medicine|June 19, 2014
Loss-of-function mutations in APOC3, triglycerides, and coronary disease, Jacy Crosby, Gina M Peloso, et al.
Nature Communications|March 10, 2015
Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levelsElisabeth M van Leeuwen, Lennart C Karssen, Joris Deelen, et al.
Genome Research|February 1, 2015
Actionable exomic incidental findings in 6503 participants: challenges of variant classificationLaura M Amendola, Michael O Dorschner, Peggy D Robertson, et al.
Nature Genetics|February 7, 2017
Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosisBrian D Hobbs, Kim de Jong, Maxime Lamontagne, et al.
Plos Genetics|December 24, 2019
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populationsMadeline H Kowalski, Huijun Qian, Ziyi Hou, et al.
Nature|July 22, 2011
The landscape of recombination in African AmericansAnjali G Hinch, Arti Tandon, Nick Patterson, et al.
American Journal of Human Genetics|April 22, 2021
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed programYao Hu, Adrienne M Stilp, Caitlin P McHugh, et al.
Pageof 121

Showing results (1101-1110 of 1,201) with videos related to

Sort By:
Pageof 121
Nature Genetics|April 23, 2013
Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitisJimmy Z Liu, Johannes Roksund Hov, Trine Folseraas, et al.
Ebiomedicine|January 8, 2021
Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortiumBridget M Lin, Kelsey E Grinde, Jennifer A Brody, et al.
American Journal of Respiratory and Critical Care Medicine|July 28, 2012
Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstructionJemma B Wilk, Nick R G Shrine, Laura R Loehr, et al.
The New England Journal of Medicine|June 19, 2014
Loss-of-function mutations in APOC3, triglycerides, and coronary disease, Jacy Crosby, Gina M Peloso, et al.
Nature Communications|March 10, 2015
Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levelsElisabeth M van Leeuwen, Lennart C Karssen, Joris Deelen, et al.
Genome Research|February 1, 2015
Actionable exomic incidental findings in 6503 participants: challenges of variant classificationLaura M Amendola, Michael O Dorschner, Peggy D Robertson, et al.
Nature Genetics|February 7, 2017
Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosisBrian D Hobbs, Kim de Jong, Maxime Lamontagne, et al.
Plos Genetics|December 24, 2019
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populationsMadeline H Kowalski, Huijun Qian, Ziyi Hou, et al.
Nature|July 22, 2011
The landscape of recombination in African AmericansAnjali G Hinch, Arti Tandon, Nick Patterson, et al.
American Journal of Human Genetics|April 22, 2021
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed programYao Hu, Adrienne M Stilp, Caitlin P McHugh, et al.
Pageof 121