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Rongling Li

Showing results (51-60 of 104) with videos related to

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BMC Genomic Data|August 7, 2023
The single-cell transcriptome and chromatin accessibility datasets of peripheral blood mononuclear cells in Chinese holstein cattleXiao Wang, Yahui Gao, Cong-Jun Li, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|November 29, 2008
Association of the ACTN3 genotype and physical functioning with age in older adultsMatthew J Delmonico, Joseph M Zmuda, Brent C Taylor, et al.
Journal of the American Medical Informatics Association : JAMIA|March 28, 2013
Validation of electronic medical record-based phenotyping algorithms: results and lessons learned from the eMERGE networkKatherine M Newton, Peggy L Peissig, Abel Ngo Kho, et al.
Plos One|March 6, 2014
Admixture mapping and subsequent fine-mapping suggests a biologically relevant and novel association on chromosome 11 for type 2 diabetes in African AmericansJanina M Jeff, Loren L Armstrong, Marylyn D Ritchie, et al.
Thrombosis and Haemostasis|February 17, 2017
Identification of unique venous thromboembolism-susceptibility variants in African-AmericansJohn A Heit, Sebastian M Armasu, Bryan M McCauley, et al.
Plos Genetics|November 3, 2011
Role of exonic variation in chemokine receptor genes on AIDS: CCRL2 F167Y association with pneumocystis pneumoniaPing An, Rongling Li, Ji Ming Wang, et al.
Science Translational Medicine|April 22, 2011
Electronic medical records for genetic research: results of the eMERGE consortiumAbel N Kho, Jennifer A Pacheco, Peggy L Peissig, et al.
BMC Medical Genomics|August 19, 2016
eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variantsAnurag Verma, Shefali S Verma, Sarah A Pendergrass, et al.
Human Genetics|April 30, 2022
The clinical utility of polygenic risk scores in genomic medicine practices: a systematic reviewJudit Kumuthini, Brittany Zick, Angeliki Balasopoulou, et al.
Frontiers in Genetics|January 8, 2015
Imputation and quality control steps for combining multiple genome-wide datasetsShefali S Verma, Mariza de Andrade, Gerard Tromp, et al.
Pageof 11

Showing results (51-60 of 104) with videos related to

Sort By:
Pageof 11
BMC Genomic Data|August 7, 2023
The single-cell transcriptome and chromatin accessibility datasets of peripheral blood mononuclear cells in Chinese holstein cattleXiao Wang, Yahui Gao, Cong-Jun Li, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|November 29, 2008
Association of the ACTN3 genotype and physical functioning with age in older adultsMatthew J Delmonico, Joseph M Zmuda, Brent C Taylor, et al.
Journal of the American Medical Informatics Association : JAMIA|March 28, 2013
Validation of electronic medical record-based phenotyping algorithms: results and lessons learned from the eMERGE networkKatherine M Newton, Peggy L Peissig, Abel Ngo Kho, et al.
Plos One|March 6, 2014
Admixture mapping and subsequent fine-mapping suggests a biologically relevant and novel association on chromosome 11 for type 2 diabetes in African AmericansJanina M Jeff, Loren L Armstrong, Marylyn D Ritchie, et al.
Thrombosis and Haemostasis|February 17, 2017
Identification of unique venous thromboembolism-susceptibility variants in African-AmericansJohn A Heit, Sebastian M Armasu, Bryan M McCauley, et al.
Plos Genetics|November 3, 2011
Role of exonic variation in chemokine receptor genes on AIDS: CCRL2 F167Y association with pneumocystis pneumoniaPing An, Rongling Li, Ji Ming Wang, et al.
Science Translational Medicine|April 22, 2011
Electronic medical records for genetic research: results of the eMERGE consortiumAbel N Kho, Jennifer A Pacheco, Peggy L Peissig, et al.
BMC Medical Genomics|August 19, 2016
eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variantsAnurag Verma, Shefali S Verma, Sarah A Pendergrass, et al.
Human Genetics|April 30, 2022
The clinical utility of polygenic risk scores in genomic medicine practices: a systematic reviewJudit Kumuthini, Brittany Zick, Angeliki Balasopoulou, et al.
Frontiers in Genetics|January 8, 2015
Imputation and quality control steps for combining multiple genome-wide datasetsShefali S Verma, Mariza de Andrade, Gerard Tromp, et al.
Pageof 11