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D Ritchie

Showing results (991-1000 of 1,033) with videos related to

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The Pharmacogenomics Journal|July 15, 2015
A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced coughJ D Mosley, C M Shaffer, S L Van Driest, et al.
JAMA Network Open|January 16, 2019
Exome Sequencing-Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank ParticipantsKandamurugu Manickam, Adam H Buchanan, Marci L B Schwartz, et al.
Clinical Pharmacology and Therapeutics|February 10, 2016
Genetic variation among 82 pharmacogenes: The PGRNseq data from the eMERGE networkW S Bush, D R Crosslin, A Owusu-Obeng, et al.
Biodata Mining|August 4, 2017
Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individualsEmily R Holzinger, Shefali S Verma, Carrie B Moore, et al.
Medrxiv : the Preprint Server for Health Sciences|July 20, 2021
Genetic regulation of <i>OAS1</i> nonsense-mediated decay underlies association with risk of severe COVID-19A Rouf Banday, Megan L Stanifer, Oscar Florez-Vargas, et al.
Nature Genetics|August 5, 2024
Genetic risk factors for COVID-19 and influenza are largely distinctJack A Kosmicki, Anthony Marcketta, Deepika Sharma, et al.
Science (New York, N.Y.)|December 24, 2016
Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR studyFrederick E Dewey, Michael F Murray, John D Overton, et al.
Clinical Pharmacology and Therapeutics|June 25, 2014
Design and anticipated outcomes of the eMERGE-PGx project: a multicenter pilot for preemptive pharmacogenomics in electronic health record systemsL J Rasmussen-Torvik, S C Stallings, A S Gordon, et al.
Medrxiv : the Preprint Server for Health Sciences|February 23, 2021
Genome-wide analysis in 756,646 individuals provides first genetic evidence that <i>ACE2</i> expression influences COVID-19 risk and yields genetic risk scores predictive of severe diseaseJ E Horowitz, J A Kosmicki, A Damask, et al.
Cell|January 19, 2024
A multi-cohort genome-wide association study in African ancestry individuals reveals risk loci for primary open-angle glaucomaShefali S Verma, Harini V Gudiseva, Venkata R M Chavali, et al.
Pageof 104

Showing results (991-1000 of 1,033) with videos related to

Sort By:
Pageof 104
The Pharmacogenomics Journal|July 15, 2015
A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced coughJ D Mosley, C M Shaffer, S L Van Driest, et al.
JAMA Network Open|January 16, 2019
Exome Sequencing-Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank ParticipantsKandamurugu Manickam, Adam H Buchanan, Marci L B Schwartz, et al.
Clinical Pharmacology and Therapeutics|February 10, 2016
Genetic variation among 82 pharmacogenes: The PGRNseq data from the eMERGE networkW S Bush, D R Crosslin, A Owusu-Obeng, et al.
Biodata Mining|August 4, 2017
Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individualsEmily R Holzinger, Shefali S Verma, Carrie B Moore, et al.
Medrxiv : the Preprint Server for Health Sciences|July 20, 2021
Genetic regulation of <i>OAS1</i> nonsense-mediated decay underlies association with risk of severe COVID-19A Rouf Banday, Megan L Stanifer, Oscar Florez-Vargas, et al.
Nature Genetics|August 5, 2024
Genetic risk factors for COVID-19 and influenza are largely distinctJack A Kosmicki, Anthony Marcketta, Deepika Sharma, et al.
Science (New York, N.Y.)|December 24, 2016
Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR studyFrederick E Dewey, Michael F Murray, John D Overton, et al.
Clinical Pharmacology and Therapeutics|June 25, 2014
Design and anticipated outcomes of the eMERGE-PGx project: a multicenter pilot for preemptive pharmacogenomics in electronic health record systemsL J Rasmussen-Torvik, S C Stallings, A S Gordon, et al.
Medrxiv : the Preprint Server for Health Sciences|February 23, 2021
Genome-wide analysis in 756,646 individuals provides first genetic evidence that <i>ACE2</i> expression influences COVID-19 risk and yields genetic risk scores predictive of severe diseaseJ E Horowitz, J A Kosmicki, A Damask, et al.
Cell|January 19, 2024
A multi-cohort genome-wide association study in African ancestry individuals reveals risk loci for primary open-angle glaucomaShefali S Verma, Harini V Gudiseva, Venkata R M Chavali, et al.
Pageof 104