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J Karczewski

Showing results (131-140 of 144) with videos related to

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Plos Genetics|May 26, 2018
Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish populationManuel A Rivas, Brandon E Avila, Jukka Koskela, et al.
Medrxiv : the Preprint Server for Health Sciences|May 25, 2026
Systematic common and rare variant association testing in 392,030 whole genomes in <i>All of Us</i>Wenhan Lu, Robert J Carroll, Matthew Solomonson, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2026
The Biobank Rare Variant consortium powers the discovery of rare genetic associations through global collaborationDuncan S Palmer, Barney Hill, Sam Hodgson, et al.
Medrxiv : the Preprint Server for Health Sciences|April 3, 2026
Integrating 730,947 exome sequences with clinical literature improves gene discoveryJeremy Guez, Julia K Goodrich, Mikhail A Moldovan, et al.
Genetics|July 16, 2013
A new system for comparative functional genomics of Saccharomyces yeastsAmy A Caudy, Yuanfang Guan, Yue Jia, et al.
Science Translational Medicine|January 22, 2016
Quantifying prion disease penetrance using large population control cohortsEric Vallabh Minikel, Sonia M Vallabh, Monkol Lek, et al.
Nature|May 29, 2020
The mutational constraint spectrum quantified from variation in 141,456 humansKonrad J Karczewski, Laurent C Francioli, Grace Tiao, et al.
Genome Medicine|October 2, 2015
Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studiesYun R Li, Jessica van Setten, Shefali S Verma, et al.
European Heart Journal|January 30, 2014
Mendelian randomization of blood lipids for coronary heart diseaseMichael V Holmes, Folkert W Asselbergs, Tom M Palmer, et al.
Nature|August 19, 2016
Analysis of protein-coding genetic variation in 60,706 humansMonkol Lek, Konrad J Karczewski, Eric V Minikel, et al.
Pageof 15

Showing results (131-140 of 144) with videos related to

Sort By:
Pageof 15
Plos Genetics|May 26, 2018
Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish populationManuel A Rivas, Brandon E Avila, Jukka Koskela, et al.
Medrxiv : the Preprint Server for Health Sciences|May 25, 2026
Systematic common and rare variant association testing in 392,030 whole genomes in <i>All of Us</i>Wenhan Lu, Robert J Carroll, Matthew Solomonson, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2026
The Biobank Rare Variant consortium powers the discovery of rare genetic associations through global collaborationDuncan S Palmer, Barney Hill, Sam Hodgson, et al.
Medrxiv : the Preprint Server for Health Sciences|April 3, 2026
Integrating 730,947 exome sequences with clinical literature improves gene discoveryJeremy Guez, Julia K Goodrich, Mikhail A Moldovan, et al.
Genetics|July 16, 2013
A new system for comparative functional genomics of Saccharomyces yeastsAmy A Caudy, Yuanfang Guan, Yue Jia, et al.
Science Translational Medicine|January 22, 2016
Quantifying prion disease penetrance using large population control cohortsEric Vallabh Minikel, Sonia M Vallabh, Monkol Lek, et al.
Nature|May 29, 2020
The mutational constraint spectrum quantified from variation in 141,456 humansKonrad J Karczewski, Laurent C Francioli, Grace Tiao, et al.
Genome Medicine|October 2, 2015
Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studiesYun R Li, Jessica van Setten, Shefali S Verma, et al.
European Heart Journal|January 30, 2014
Mendelian randomization of blood lipids for coronary heart diseaseMichael V Holmes, Folkert W Asselbergs, Tom M Palmer, et al.
Nature|August 19, 2016
Analysis of protein-coding genetic variation in 60,706 humansMonkol Lek, Konrad J Karczewski, Eric V Minikel, et al.
Pageof 15