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

Omer Weissbrod

Showing results (11-20 of 42) with videos related to

Pageof 5
Sort By:
Bioinformatics (Oxford, England)|February 9, 2017
GLINT: a user-friendly toolset for the analysis of high-throughput DNA-methylation array dataElior Rahmani, Reut Yedidim, Liat Shenhav, et al.
Scientific Reports|November 13, 2014
Further improvements to linear mixed models for genome-wide association studiesChristian Widmer, Christoph Lippert, Omer Weissbrod, et al.
Nature Communications|December 8, 2020
Improving the informativeness of Mendelian disease-derived pathogenicity scores for common diseaseSamuel S Kim, Kushal K Dey, Omer Weissbrod, et al.
Studies in Health Technology and Informatics|April 21, 2017
Fast and Efficient Feature Engineering for Multi-Cohort Analysis of EHR DataMichal Ozery-Flato, Chen Yanover, Assaf Gottlieb, et al.
Elife|October 12, 2021
Utility of polygenic embryo screening for disease depends on the selection strategyTodd Lencz, Daniel Backenroth, Einat Granot-Hershkovitz, et al.
Nature Medicine|November 3, 2023
Bacterial SNPs in the human gut microbiome associate with host BMILiron Zahavi, Amit Lavon, Lee Reicher, et al.
Genetics|October 14, 2017
RL-SKAT: An Exact and Efficient Score Test for Heritability and Set TestsRegev Schweiger, Omer Weissbrod, Elior Rahmani, et al.
Nature Communications|November 23, 2018
Detecting heritable phenotypes without a model using fast permutation testing for heritability and set-testsRegev Schweiger, Eyal Fisher, Omer Weissbrod, et al.
Nature Genetics|January 6, 2026
MultiSuSiE improves multi-ancestry fine-mapping in All of Us whole-genome sequencing dataJordan Rossen, Huwenbo Shi, Benjamin J Strober, et al.
Medrxiv : the Preprint Server for Health Sciences|May 27, 2024
MultiSuSiE improves multi-ancestry fine-mapping in All of Us whole-genome sequencing dataJordan Rossen, Huwenbo Shi, Benjamin J Strober, et al.
Pageof 5

Showing results (11-20 of 42) with videos related to

Sort By:
Pageof 5
Bioinformatics (Oxford, England)|February 9, 2017
GLINT: a user-friendly toolset for the analysis of high-throughput DNA-methylation array dataElior Rahmani, Reut Yedidim, Liat Shenhav, et al.
Scientific Reports|November 13, 2014
Further improvements to linear mixed models for genome-wide association studiesChristian Widmer, Christoph Lippert, Omer Weissbrod, et al.
Nature Communications|December 8, 2020
Improving the informativeness of Mendelian disease-derived pathogenicity scores for common diseaseSamuel S Kim, Kushal K Dey, Omer Weissbrod, et al.
Studies in Health Technology and Informatics|April 21, 2017
Fast and Efficient Feature Engineering for Multi-Cohort Analysis of EHR DataMichal Ozery-Flato, Chen Yanover, Assaf Gottlieb, et al.
Elife|October 12, 2021
Utility of polygenic embryo screening for disease depends on the selection strategyTodd Lencz, Daniel Backenroth, Einat Granot-Hershkovitz, et al.
Nature Medicine|November 3, 2023
Bacterial SNPs in the human gut microbiome associate with host BMILiron Zahavi, Amit Lavon, Lee Reicher, et al.
Genetics|October 14, 2017
RL-SKAT: An Exact and Efficient Score Test for Heritability and Set TestsRegev Schweiger, Omer Weissbrod, Elior Rahmani, et al.
Nature Communications|November 23, 2018
Detecting heritable phenotypes without a model using fast permutation testing for heritability and set-testsRegev Schweiger, Eyal Fisher, Omer Weissbrod, et al.
Nature Genetics|January 6, 2026
MultiSuSiE improves multi-ancestry fine-mapping in All of Us whole-genome sequencing dataJordan Rossen, Huwenbo Shi, Benjamin J Strober, et al.
Medrxiv : the Preprint Server for Health Sciences|May 27, 2024
MultiSuSiE improves multi-ancestry fine-mapping in All of Us whole-genome sequencing dataJordan Rossen, Huwenbo Shi, Benjamin J Strober, et al.
Pageof 5