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

Stephane E Castel

Showing results (11-20 of 32) with videos related to

Pageof 4
Sort By:
Plos Genetics|December 14, 2019
Leveraging allelic imbalance to refine fine-mapping for eQTL studiesJennifer Zou, Farhad Hormozdiari, Brandon Jew, et al.
Cell|November 24, 2014
Dicer promotes transcription termination at sites of replication stress to maintain genome stabilityStephane E Castel, Jie Ren, Sonali Bhattacharjee, et al.
Nature Genetics|August 22, 2018
Modified penetrance of coding variants by cis-regulatory variation contributes to disease riskStephane E Castel, Alejandra Cervera, Pejman Mohammadi, et al.
Elife|June 16, 2026
Faroese whole genomes provide insight into ancestry and recent selectionIman Hamid, Ólavur Mortensen, Alba Refoyo-Martínez, et al.
Nature|October 18, 2011
RNAi promotes heterochromatic silencing through replication-coupled release of RNA Pol IIMikel Zaratiegui, Stephane E Castel, Danielle V Irvine, et al.
Cell|September 20, 2024
Nothing about us without us: Sharing results with communities that provide genomic dataSarah LeBaron von Baeyer, Rebecca M Crocker, Rindra Rakotoarivony, et al.
Science (New York, N.Y.)|October 12, 2019
Genetic regulatory variation in populations informs transcriptome analysis in rare diseasePejman Mohammadi, Stephane E Castel, Beryl B Cummings, et al.
Annals of Human Genetics|February 3, 2026
Mitonuclear Discordance and Gout, Type 2 Diabetes and Chronic Kidney Disease in Aotearoa New Zealand Indigenous Māori and Pacific PeopleRachel R Dickerson, Riku Takei, Murray Cadzow, et al.
Nature Communications|August 18, 2017
Genetic regulatory effects modified by immune activation contribute to autoimmune disease associationsSarah Kim-Hellmuth, Matthias Bechheim, Benno Pütz, et al.
BMC Genomics|November 1, 2021
Mid-pass whole genome sequencing enables biomedical genetic studies of diverse populationsAnne-Katrin Emde, Amanda Phipps-Green, Murray Cadzow, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Plos Genetics|December 14, 2019
Leveraging allelic imbalance to refine fine-mapping for eQTL studiesJennifer Zou, Farhad Hormozdiari, Brandon Jew, et al.
Cell|November 24, 2014
Dicer promotes transcription termination at sites of replication stress to maintain genome stabilityStephane E Castel, Jie Ren, Sonali Bhattacharjee, et al.
Nature Genetics|August 22, 2018
Modified penetrance of coding variants by cis-regulatory variation contributes to disease riskStephane E Castel, Alejandra Cervera, Pejman Mohammadi, et al.
Elife|June 16, 2026
Faroese whole genomes provide insight into ancestry and recent selectionIman Hamid, Ólavur Mortensen, Alba Refoyo-Martínez, et al.
Nature|October 18, 2011
RNAi promotes heterochromatic silencing through replication-coupled release of RNA Pol IIMikel Zaratiegui, Stephane E Castel, Danielle V Irvine, et al.
Cell|September 20, 2024
Nothing about us without us: Sharing results with communities that provide genomic dataSarah LeBaron von Baeyer, Rebecca M Crocker, Rindra Rakotoarivony, et al.
Science (New York, N.Y.)|October 12, 2019
Genetic regulatory variation in populations informs transcriptome analysis in rare diseasePejman Mohammadi, Stephane E Castel, Beryl B Cummings, et al.
Annals of Human Genetics|February 3, 2026
Mitonuclear Discordance and Gout, Type 2 Diabetes and Chronic Kidney Disease in Aotearoa New Zealand Indigenous Māori and Pacific PeopleRachel R Dickerson, Riku Takei, Murray Cadzow, et al.
Nature Communications|August 18, 2017
Genetic regulatory effects modified by immune activation contribute to autoimmune disease associationsSarah Kim-Hellmuth, Matthias Bechheim, Benno Pütz, et al.
BMC Genomics|November 1, 2021
Mid-pass whole genome sequencing enables biomedical genetic studies of diverse populationsAnne-Katrin Emde, Amanda Phipps-Green, Murray Cadzow, et al.
Pageof 4