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Shamil R Sunyaev

Showing results (51-60 of 105) with videos related to

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Nature Communications|February 17, 2019
Quantification of frequency-dependent genetic architectures in 25 UK Biobank traits reveals action of negative selectionArmin P Schoech, Daniel M Jordan, Po-Ru Loh, et al.
The Journal of Allergy and Clinical Immunology|November 5, 2011
Genome-wide association study reveals class I MHC-restricted T cell-associated molecule gene (CRTAM) variants interact with vitamin D levels to affect asthma exacerbationsRose Du, Augusto A Litonjua, Kelan G Tantisira, et al.
American Journal of Human Genetics|February 12, 2011
Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathyDaniel M Jordan, Adam Kiezun, Samantha M Baxter, et al.
Nature Genetics|April 4, 2017
Estimating the selective effects of heterozygous protein-truncating variants from human exome dataChristopher A Cassa, Donate Weghorn, Daniel J Balick, et al.
Biorxiv : the Preprint Server for Biology|January 20, 2025
NERINE reveals rare variant associations in gene networks across multiple phenotypes and implicates an <i>SNCA-PRL-LRRK2</i> subnetwork in Parkinson's diseaseSumaiya Nazeen, Xinyuan Wang, Autumn Morrow, et al.
Nature Genetics|November 28, 2018
Reply to 'Selective effects of heterozygous protein-truncating variants'Christopher A Cassa, Donate Weghorn, Daniel J Balick, et al.
Nature|December 11, 2012
Genomic variation landscape of the human gut microbiomeSiegfried Schloissnig, Manimozhiyan Arumugam, Shinichi Sunagawa, et al.
Genome Research|June 16, 2009
Multiplex padlock targeted sequencing reveals human hypermutable CpG variationsJin Billy Li, Yuan Gao, John Aach, et al.
American Journal of Human Genetics|November 20, 2015
Leveraging Distant Relatedness to Quantify Human Mutation and Gene-Conversion RatesPier Francesco Palamara, Laurent C Francioli, Peter R Wilton, et al.
Rheumatology (Oxford, England)|October 24, 2015
An argument for early genomic sequencing in atypical cases: a WISP3 variant leads to diagnosis of progressive pseudorheumatoid arthropathy of childhoodChristopher A Cassa, Stacy E Smith, William Docken, et al.
Pageof 11

Showing results (51-60 of 105) with videos related to

Sort By:
Pageof 11
Nature Communications|February 17, 2019
Quantification of frequency-dependent genetic architectures in 25 UK Biobank traits reveals action of negative selectionArmin P Schoech, Daniel M Jordan, Po-Ru Loh, et al.
The Journal of Allergy and Clinical Immunology|November 5, 2011
Genome-wide association study reveals class I MHC-restricted T cell-associated molecule gene (CRTAM) variants interact with vitamin D levels to affect asthma exacerbationsRose Du, Augusto A Litonjua, Kelan G Tantisira, et al.
American Journal of Human Genetics|February 12, 2011
Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathyDaniel M Jordan, Adam Kiezun, Samantha M Baxter, et al.
Nature Genetics|April 4, 2017
Estimating the selective effects of heterozygous protein-truncating variants from human exome dataChristopher A Cassa, Donate Weghorn, Daniel J Balick, et al.
Biorxiv : the Preprint Server for Biology|January 20, 2025
NERINE reveals rare variant associations in gene networks across multiple phenotypes and implicates an <i>SNCA-PRL-LRRK2</i> subnetwork in Parkinson's diseaseSumaiya Nazeen, Xinyuan Wang, Autumn Morrow, et al.
Nature Genetics|November 28, 2018
Reply to 'Selective effects of heterozygous protein-truncating variants'Christopher A Cassa, Donate Weghorn, Daniel J Balick, et al.
Nature|December 11, 2012
Genomic variation landscape of the human gut microbiomeSiegfried Schloissnig, Manimozhiyan Arumugam, Shinichi Sunagawa, et al.
Genome Research|June 16, 2009
Multiplex padlock targeted sequencing reveals human hypermutable CpG variationsJin Billy Li, Yuan Gao, John Aach, et al.
American Journal of Human Genetics|November 20, 2015
Leveraging Distant Relatedness to Quantify Human Mutation and Gene-Conversion RatesPier Francesco Palamara, Laurent C Francioli, Peter R Wilton, et al.
Rheumatology (Oxford, England)|October 24, 2015
An argument for early genomic sequencing in atypical cases: a WISP3 variant leads to diagnosis of progressive pseudorheumatoid arthropathy of childhoodChristopher A Cassa, Stacy E Smith, William Docken, et al.
Pageof 11