Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Benjamin M Neale

Showing results (221-230 of 293) with videos related to

Pageof 30
Sort By:
American Journal of Human Genetics|June 5, 2018
Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic SpectrumAndrea Ganna, F Kyle Satterstrom, Seyedeh M Zekavat, et al.
Cell|August 2, 2022
A cross-disorder dosage sensitivity map of the human genomeRyan L Collins, Joseph T Glessner, Eleonora Porcu, et al.
Nature|December 6, 2023
A genomic mutational constraint map using variation in 76,156 human genomesSiwei Chen, Laurent C Francioli, Julia K Goodrich, et al.
Cell Genomics|February 13, 2023
Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomesKonrad J Karczewski, Matthew Solomonson, Katherine R Chao, et al.
Nature Genetics|January 26, 2023
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domainsDitte Demontis, G Bragi Walters, Georgios Athanasiadis, et al.
Nature|February 4, 2021
Author Correction: A structural variation reference for medical and population geneticsRyan L Collins, Harrison Brand, Konrad J Karczewski, et al.
Nature Genetics|October 3, 2018
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran ProgramDerek Klarin, Scott M Damrauer, Kelly Cho, et al.
Nature Communications|September 14, 2016
Erratum: A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitisManuel A Rivas, Daniel Graham, Patrick Sulem, et al.
Nature Genetics|March 1, 2023
Author Correction: Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domainsDitte Demontis, G Bragi Walters, Georgios Athanasiadis, et al.
Nature|May 29, 2020
A structural variation reference for medical and population geneticsRyan L Collins, Harrison Brand, Konrad J Karczewski, et al.
Pageof 30

Showing results (221-230 of 293) with videos related to

Sort By:
Pageof 30
American Journal of Human Genetics|June 5, 2018
Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic SpectrumAndrea Ganna, F Kyle Satterstrom, Seyedeh M Zekavat, et al.
Cell|August 2, 2022
A cross-disorder dosage sensitivity map of the human genomeRyan L Collins, Joseph T Glessner, Eleonora Porcu, et al.
Nature|December 6, 2023
A genomic mutational constraint map using variation in 76,156 human genomesSiwei Chen, Laurent C Francioli, Julia K Goodrich, et al.
Cell Genomics|February 13, 2023
Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomesKonrad J Karczewski, Matthew Solomonson, Katherine R Chao, et al.
Nature Genetics|January 26, 2023
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domainsDitte Demontis, G Bragi Walters, Georgios Athanasiadis, et al.
Nature|February 4, 2021
Author Correction: A structural variation reference for medical and population geneticsRyan L Collins, Harrison Brand, Konrad J Karczewski, et al.
Nature Genetics|October 3, 2018
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran ProgramDerek Klarin, Scott M Damrauer, Kelly Cho, et al.
Nature Communications|September 14, 2016
Erratum: A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitisManuel A Rivas, Daniel Graham, Patrick Sulem, et al.
Nature Genetics|March 1, 2023
Author Correction: Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domainsDitte Demontis, G Bragi Walters, Georgios Athanasiadis, et al.
Nature|May 29, 2020
A structural variation reference for medical and population geneticsRyan L Collins, Harrison Brand, Konrad J Karczewski, et al.
Pageof 30