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

Matthieu Moisse

Showing results (51-60 of 66) with videos related to

Pageof 7
Sort By:
Frontiers in Cellular Neuroscience|January 2, 2023
Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence dataAhmad Al Khleifat, Alfredo Iacoangeli, Ashley R Jones, et al.
NPJ Genomic Medicine|January 29, 2022
Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosisAhmad Al Khleifat, Alfredo Iacoangeli, Joke J F A van Vugt, et al.
Genetic Epidemiology|November 20, 2013
Identification of new genetic susceptibility loci for breast cancer through consideration of gene-environment interactionsAnja Schoeps, Anja Rudolph, Petra Seibold, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 7, 2016
Genetic modifiers of CHEK2*1100delC-associated breast cancer riskTaru A Muranen, Dario Greco, Carl Blomqvist, et al.
Science Translational Medicine|February 23, 2022
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALSPaul J Hop, Ramona A J Zwamborn, Eilis Hannon, et al.
Human Genetics|December 10, 2014
Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer riskLuis G Carvajal-Carmona, Tracy A O'Mara, Jodie N Painter, et al.
Human Molecular Genetics|November 8, 2014
Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer riskJodie N Painter, Tracy A O'Mara, Jyotsna Batra, et al.
Nature Communications|April 25, 2019
Meta-analysis of epigenome-wide association studies in neonates reveals widespread differential DNA methylation associated with birthweightLeanne K Küpers, Claire Monnereau, Gemma C Sharp, et al.
Plos One|November 13, 2014
MicroRNA related polymorphisms and breast cancer riskSofia Khan, Dario Greco, Kyriaki Michailidou, et al.
Human Molecular Genetics|June 15, 2014
Genetic variation in mitotic regulatory pathway genes is associated with breast tumor gradeKristen S Purrington, Seth Slettedahl, Manjeet K Bolla, et al.
Pageof 7

Showing results (51-60 of 66) with videos related to

Sort By:
Pageof 7
Frontiers in Cellular Neuroscience|January 2, 2023
Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence dataAhmad Al Khleifat, Alfredo Iacoangeli, Ashley R Jones, et al.
NPJ Genomic Medicine|January 29, 2022
Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosisAhmad Al Khleifat, Alfredo Iacoangeli, Joke J F A van Vugt, et al.
Genetic Epidemiology|November 20, 2013
Identification of new genetic susceptibility loci for breast cancer through consideration of gene-environment interactionsAnja Schoeps, Anja Rudolph, Petra Seibold, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 7, 2016
Genetic modifiers of CHEK2*1100delC-associated breast cancer riskTaru A Muranen, Dario Greco, Carl Blomqvist, et al.
Science Translational Medicine|February 23, 2022
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALSPaul J Hop, Ramona A J Zwamborn, Eilis Hannon, et al.
Human Genetics|December 10, 2014
Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer riskLuis G Carvajal-Carmona, Tracy A O'Mara, Jodie N Painter, et al.
Human Molecular Genetics|November 8, 2014
Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer riskJodie N Painter, Tracy A O'Mara, Jyotsna Batra, et al.
Nature Communications|April 25, 2019
Meta-analysis of epigenome-wide association studies in neonates reveals widespread differential DNA methylation associated with birthweightLeanne K Küpers, Claire Monnereau, Gemma C Sharp, et al.
Plos One|November 13, 2014
MicroRNA related polymorphisms and breast cancer riskSofia Khan, Dario Greco, Kyriaki Michailidou, et al.
Human Molecular Genetics|June 15, 2014
Genetic variation in mitotic regulatory pathway genes is associated with breast tumor gradeKristen S Purrington, Seth Slettedahl, Manjeet K Bolla, et al.
Pageof 7