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

Hilary C Martin

Showing results (31-40 of 68) with videos related to

Pageof 7
Sort By:
American Journal of Human Genetics|May 2, 2026
Meta-analysis across six global biobanks identifies recessive coding associations with complex traits and diseasesFrederik H Lassen, Georgios Kalantzis, Andrea Eoli, et al.
Nature|September 28, 2018
Common genetic variants contribute to risk of rare severe neurodevelopmental disordersMari E K Niemi, Hilary C Martin, Daniel L Rice, et al.
Nature Communications|January 28, 2021
The contribution of X-linked coding variation to severe developmental disordersHilary C Martin, Eugene J Gardner, Kaitlin E Samocha, et al.
Plos Medicine|July 9, 2026
Genetic and sociodemographic factors associated with trajectories of physical and mental health multimorbidity in a South Asian cohort in the UK: A multistate modelling analysisDaniel Stow, Ruby S M Tsang, Ioanna K Katzourou, et al.
Nature Communications|August 6, 2015
Multicohort analysis of the maternal age effect on recombinationHilary C Martin, Ryan Christ, Julie G Hussin, et al.
Nature|November 20, 2024
Examining the role of common variants in rare neurodevelopmental conditionsQin Qin Huang, Emilie M Wigdor, Daniel S Malawsky, et al.
Genome Biology|January 3, 2012
MicroRNAs and their isomiRs function cooperatively to target common biological pathwaysNicole Cloonan, Shivangi Wani, Qinying Xu, et al.
Nature|October 1, 2025
Polygenic and developmental profiles of autism differ by age at diagnosisXinhe Zhang, Jakob Grove, Yuanjun Gu, et al.
Human Molecular Genetics|August 1, 2019
Defective tubulin detyrosination causes structural brain abnormalities with cognitive deficiency in humans and miceAlistair T Pagnamenta, Pierre Heemeryck, Hilary C Martin, et al.
Medrxiv : the Preprint Server for Health Sciences|December 8, 2025
Improving type 2 diabetes polygenic risk scores by incorporating rare, low-frequency, and population-specific variantsKatie Taylor, Alicia Huerta-Chagoya, Xiaoyu Wang, et al.
Pageof 7

Showing results (31-40 of 68) with videos related to

Sort By:
Pageof 7
American Journal of Human Genetics|May 2, 2026
Meta-analysis across six global biobanks identifies recessive coding associations with complex traits and diseasesFrederik H Lassen, Georgios Kalantzis, Andrea Eoli, et al.
Nature|September 28, 2018
Common genetic variants contribute to risk of rare severe neurodevelopmental disordersMari E K Niemi, Hilary C Martin, Daniel L Rice, et al.
Nature Communications|January 28, 2021
The contribution of X-linked coding variation to severe developmental disordersHilary C Martin, Eugene J Gardner, Kaitlin E Samocha, et al.
Plos Medicine|July 9, 2026
Genetic and sociodemographic factors associated with trajectories of physical and mental health multimorbidity in a South Asian cohort in the UK: A multistate modelling analysisDaniel Stow, Ruby S M Tsang, Ioanna K Katzourou, et al.
Nature Communications|August 6, 2015
Multicohort analysis of the maternal age effect on recombinationHilary C Martin, Ryan Christ, Julie G Hussin, et al.
Nature|November 20, 2024
Examining the role of common variants in rare neurodevelopmental conditionsQin Qin Huang, Emilie M Wigdor, Daniel S Malawsky, et al.
Genome Biology|January 3, 2012
MicroRNAs and their isomiRs function cooperatively to target common biological pathwaysNicole Cloonan, Shivangi Wani, Qinying Xu, et al.
Nature|October 1, 2025
Polygenic and developmental profiles of autism differ by age at diagnosisXinhe Zhang, Jakob Grove, Yuanjun Gu, et al.
Human Molecular Genetics|August 1, 2019
Defective tubulin detyrosination causes structural brain abnormalities with cognitive deficiency in humans and miceAlistair T Pagnamenta, Pierre Heemeryck, Hilary C Martin, et al.
Medrxiv : the Preprint Server for Health Sciences|December 8, 2025
Improving type 2 diabetes polygenic risk scores by incorporating rare, low-frequency, and population-specific variantsKatie Taylor, Alicia Huerta-Chagoya, Xiaoyu Wang, et al.
Pageof 7