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Benjamin M Neale

Showing results (241-250 of 293) 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.
Nature Genetics|March 16, 2010
Genome-wide association identifies multiple ulcerative colitis susceptibility lociDermot P B McGovern, Agnès Gardet, Leif Törkvist, et al.
Neuron|June 23, 2017
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette SyndromeAlden Y Huang, Dongmei Yu, Lea K Davis, et al.
Medrxiv : the Preprint Server for Health Sciences|June 26, 2025
The Landscape of Shared and Divergent Genetic Influences across 14 Psychiatric DisordersAndrew D Grotzinger, Josefin Werme, Wouter J Peyrot, et al.
Nature|April 13, 2012
Patterns and rates of exonic de novo mutations in autism spectrum disordersBenjamin M Neale, Yan Kou, Li Liu, et al.
Medrxiv : the Preprint Server for Health Sciences|November 6, 2024
Phenotype harmonization and analysis for The Populations Underrepresented in Mental illness Association Studies (the PUMAS Project)Ana M Ramirez-Diaz, Ana M Diaz-Zuluaga, Rocky E Stroud, 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.
Nature|February 4, 2021
Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humansKonrad J Karczewski, Laurent C Francioli, Grace Tiao, et al.
Pageof 30

Showing results (241-250 of 293) with videos related to

Sort By:
Pageof 30
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.
Nature Genetics|March 16, 2010
Genome-wide association identifies multiple ulcerative colitis susceptibility lociDermot P B McGovern, Agnès Gardet, Leif Törkvist, et al.
Neuron|June 23, 2017
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette SyndromeAlden Y Huang, Dongmei Yu, Lea K Davis, et al.
Medrxiv : the Preprint Server for Health Sciences|June 26, 2025
The Landscape of Shared and Divergent Genetic Influences across 14 Psychiatric DisordersAndrew D Grotzinger, Josefin Werme, Wouter J Peyrot, et al.
Nature|April 13, 2012
Patterns and rates of exonic de novo mutations in autism spectrum disordersBenjamin M Neale, Yan Kou, Li Liu, et al.
Medrxiv : the Preprint Server for Health Sciences|November 6, 2024
Phenotype harmonization and analysis for The Populations Underrepresented in Mental illness Association Studies (the PUMAS Project)Ana M Ramirez-Diaz, Ana M Diaz-Zuluaga, Rocky E Stroud, 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.
Nature|February 4, 2021
Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humansKonrad J Karczewski, Laurent C Francioli, Grace Tiao, et al.
Pageof 30