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Gregory McInnes

Showing results (1-10 of 11) with videos related to

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Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|March 10, 2021
Drug Response Pharmacogenetics for 200,000 UK Biobank ParticipantsGregory McInnes, Russ B Altman
Clinical Pharmacology and Therapeutics|June 29, 2021
Genomewide Association Studies in PharmacogenomicsGregory McInnes, Sook Wah Yee, Yash Pershad, et al.
Clinical Pharmacology and Therapeutics|November 25, 2020
Pharmacogenetics at Scale: An Analysis of the UK BiobankGregory McInnes, Adam Lavertu, Katrin Sangkuhl, et al.
Bioinformatics (Oxford, England)|September 30, 2017
Cloud-based interactive analytics for terabytes of genomic variants dataCuiping Pan, Gregory McInnes, Nicole Deflaux, et al.
Bioinformatics (Oxford, England)|December 7, 2018
Global Biobank Engine: enabling genotype-phenotype browsing for biobank summary statisticsGregory McInnes, Yosuke Tanigawa, Chris DeBoever, et al.
Plos Computational Biology|November 2, 2020
Transfer learning enables prediction of CYP2D6 haplotype functionGregory McInnes, Rachel Dalton, Katrin Sangkuhl, et al.
International Journal of Molecular Sciences|September 9, 2022
Genetic Variation among Pharmacogenes in the Sardinian PopulationMaria Laura Idda, Magdalena Zoledziewska, Silvana Anna Maria Urru, et al.
Nature Immunology|February 13, 2023
Apolipoprotein C3 induces inflammasome activation only in its delipidated formCheng-Chieh Hsu, Baohai Shao, Jenny E Kanter, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 7, 2022
Functional genomics of OCTN2 variants informs protein-specific variant effect predictor for Carnitine Transporter DeficiencyMegan L Koleske, Gregory McInnes, Julia E H Brown, et al.
American Journal of Human Genetics|April 2, 2021
Opportunities and challenges for the computational interpretation of rare variation in clinically important genesGregory McInnes, Andrew G Sharo, Megan L Koleske, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|March 10, 2021
Drug Response Pharmacogenetics for 200,000 UK Biobank ParticipantsGregory McInnes, Russ B Altman
Clinical Pharmacology and Therapeutics|June 29, 2021
Genomewide Association Studies in PharmacogenomicsGregory McInnes, Sook Wah Yee, Yash Pershad, et al.
Clinical Pharmacology and Therapeutics|November 25, 2020
Pharmacogenetics at Scale: An Analysis of the UK BiobankGregory McInnes, Adam Lavertu, Katrin Sangkuhl, et al.
Bioinformatics (Oxford, England)|September 30, 2017
Cloud-based interactive analytics for terabytes of genomic variants dataCuiping Pan, Gregory McInnes, Nicole Deflaux, et al.
Bioinformatics (Oxford, England)|December 7, 2018
Global Biobank Engine: enabling genotype-phenotype browsing for biobank summary statisticsGregory McInnes, Yosuke Tanigawa, Chris DeBoever, et al.
Plos Computational Biology|November 2, 2020
Transfer learning enables prediction of CYP2D6 haplotype functionGregory McInnes, Rachel Dalton, Katrin Sangkuhl, et al.
International Journal of Molecular Sciences|September 9, 2022
Genetic Variation among Pharmacogenes in the Sardinian PopulationMaria Laura Idda, Magdalena Zoledziewska, Silvana Anna Maria Urru, et al.
Nature Immunology|February 13, 2023
Apolipoprotein C3 induces inflammasome activation only in its delipidated formCheng-Chieh Hsu, Baohai Shao, Jenny E Kanter, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 7, 2022
Functional genomics of OCTN2 variants informs protein-specific variant effect predictor for Carnitine Transporter DeficiencyMegan L Koleske, Gregory McInnes, Julia E H Brown, et al.
American Journal of Human Genetics|April 2, 2021
Opportunities and challenges for the computational interpretation of rare variation in clinically important genesGregory McInnes, Andrew G Sharo, Megan L Koleske, et al.
Pageof 2