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Jonathan Marchini

Showing results (51-60 of 102) with videos related to

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European Journal of Human Genetics : EJHG|January 27, 2011
The effect of genome-wide association scan quality control on imputation outcome for common variantsLorraine Southam, Kalliope Panoutsopoulou, N William Rayner, et al.
Nature Genetics|September 25, 2024
Yield of genetic association signals from genomes, exomes and imputation in the UK BiobankSheila M Gaynor, Tyler Joseph, Xiaodong Bai, et al.
Nature Communications|August 6, 2015
Multicohort analysis of the maternal age effect on recombinationHilary C Martin, Ryan Christ, Julie G Hussin, et al.
Genome Research|March 13, 2013
The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomesStephen B Montgomery, David L Goode, Erika Kvikstad, et al.
Nature Communications|March 14, 2026
Humans with function-disrupting variants in the myostatin gene (MSTN) have increased skeletal muscle mass and strength, and less adiposityJoseph L Herman, Peter Dornbos, Karl Landheer, et al.
Communications Biology|June 6, 2022
Population-scale analysis of common and rare genetic variation associated with hearing loss in adultsKavita Praveen, Lee Dobbyn, Lauren Gurski, et al.
Plos Genetics|April 19, 2014
A general approach for haplotype phasing across the full spectrum of relatednessJared O'Connell, Deepti Gurdasani, Olivier Delaneau, et al.
Nature Communications|February 24, 2026
Rare coding variants in CHRNB3 associate with reduced daily cigarette smoking across ancestriesVeera M Rajagopal, Andrey Ziyatdinov, Tyler Joseph, et al.
Nature|April 8, 2026
Population-scale repeat expansions elucidate disease risk and brain atrophyVijay Kumar Pounraja, Jae Hoon Sul, Joseph Herman, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2026
Rare protein-coding variation and the genetic architecture of height in >1.4 million individualsJack A Kosmicki, Liron Ganel, Kyoko Watanabe, et al.
Pageof 11

Showing results (51-60 of 102) with videos related to

Sort By:
Pageof 11
European Journal of Human Genetics : EJHG|January 27, 2011
The effect of genome-wide association scan quality control on imputation outcome for common variantsLorraine Southam, Kalliope Panoutsopoulou, N William Rayner, et al.
Nature Genetics|September 25, 2024
Yield of genetic association signals from genomes, exomes and imputation in the UK BiobankSheila M Gaynor, Tyler Joseph, Xiaodong Bai, et al.
Nature Communications|August 6, 2015
Multicohort analysis of the maternal age effect on recombinationHilary C Martin, Ryan Christ, Julie G Hussin, et al.
Genome Research|March 13, 2013
The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomesStephen B Montgomery, David L Goode, Erika Kvikstad, et al.
Nature Communications|March 14, 2026
Humans with function-disrupting variants in the myostatin gene (MSTN) have increased skeletal muscle mass and strength, and less adiposityJoseph L Herman, Peter Dornbos, Karl Landheer, et al.
Communications Biology|June 6, 2022
Population-scale analysis of common and rare genetic variation associated with hearing loss in adultsKavita Praveen, Lee Dobbyn, Lauren Gurski, et al.
Plos Genetics|April 19, 2014
A general approach for haplotype phasing across the full spectrum of relatednessJared O'Connell, Deepti Gurdasani, Olivier Delaneau, et al.
Nature Communications|February 24, 2026
Rare coding variants in CHRNB3 associate with reduced daily cigarette smoking across ancestriesVeera M Rajagopal, Andrey Ziyatdinov, Tyler Joseph, et al.
Nature|April 8, 2026
Population-scale repeat expansions elucidate disease risk and brain atrophyVijay Kumar Pounraja, Jae Hoon Sul, Joseph Herman, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2026
Rare protein-coding variation and the genetic architecture of height in >1.4 million individualsJack A Kosmicki, Liron Ganel, Kyoko Watanabe, et al.
Pageof 11