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Showing results (41-50 of 59) with videos related to

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The New England Journal of Medicine|October 15, 2010
Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemiaKiran Musunuru, James P Pirruccello, Ron Do, et al.
Nature Biotechnology|August 14, 2019
Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genomeAaron M Wenger, Paul Peluso, William J Rowell, et al.
Nature Genetics|August 4, 2014
A framework for the interpretation of de novo mutation in human diseaseKaitlin E Samocha, Elise B Robinson, Stephan J Sanders, et al.
Nature|January 28, 2014
A polygenic burden of rare disruptive mutations in schizophreniaShaun M Purcell, Jennifer L Moran, Menachem Fromer, et al.
Genome Biology|September 16, 2011
The functional spectrum of low-frequency coding variationGabor T Marth, Fuli Yu, Amit R Indap, et al.
Plos Genetics|April 18, 2013
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controlsLi Liu, Aniko Sabo, Benjamin M Neale, et al.
Nature|January 6, 2022
RNA profiles reveal signatures of future health and disease in pregnancyMorten Rasmussen, Mitsu Reddy, Rory Nolan, et al.
Nature Communications|April 8, 2025
Molecular subtyping of hypertensive disorders of pregnancyMichal A Elovitz, Elaine P S Gee, Nathaniel Delaney-Busch, et al.
Neuron|January 29, 2013
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disordersElaine T Lim, Soumya Raychaudhuri, Stephan J Sanders, et al.
Science (New York, N.Y.)|February 21, 2012
A systematic survey of loss-of-function variants in human protein-coding genesDaniel G MacArthur, Suganthi Balasubramanian, Adam Frankish, et al.
Pageof 6

Showing results (41-50 of 59) with videos related to

Sort By:
Pageof 6
The New England Journal of Medicine|October 15, 2010
Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemiaKiran Musunuru, James P Pirruccello, Ron Do, et al.
Nature Biotechnology|August 14, 2019
Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genomeAaron M Wenger, Paul Peluso, William J Rowell, et al.
Nature Genetics|August 4, 2014
A framework for the interpretation of de novo mutation in human diseaseKaitlin E Samocha, Elise B Robinson, Stephan J Sanders, et al.
Nature|January 28, 2014
A polygenic burden of rare disruptive mutations in schizophreniaShaun M Purcell, Jennifer L Moran, Menachem Fromer, et al.
Genome Biology|September 16, 2011
The functional spectrum of low-frequency coding variationGabor T Marth, Fuli Yu, Amit R Indap, et al.
Plos Genetics|April 18, 2013
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controlsLi Liu, Aniko Sabo, Benjamin M Neale, et al.
Nature|January 6, 2022
RNA profiles reveal signatures of future health and disease in pregnancyMorten Rasmussen, Mitsu Reddy, Rory Nolan, et al.
Nature Communications|April 8, 2025
Molecular subtyping of hypertensive disorders of pregnancyMichal A Elovitz, Elaine P S Gee, Nathaniel Delaney-Busch, et al.
Neuron|January 29, 2013
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disordersElaine T Lim, Soumya Raychaudhuri, Stephan J Sanders, et al.
Science (New York, N.Y.)|February 21, 2012
A systematic survey of loss-of-function variants in human protein-coding genesDaniel G MacArthur, Suganthi Balasubramanian, Adam Frankish, et al.
Pageof 6