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

Cathal Ormond

Showing results (1-10 of 9) with videos related to

Pageof 1
Sort By:
Briefings in Bioinformatics|April 6, 2021
Converting single nucleotide variants between genome builds: from cautionary tale to solutionCathal Ormond, Niamh M Ryan, Aiden Corvin, et al.
Biorxiv : the Preprint Server for Biology|April 10, 2026
BICEP: an extension to indels and copy number variants for rare variant prioritisation in pedigree analysisCathal Ormond, Niamh M Ryan, Aiden Corvin, et al.
Scientific Reports|July 30, 2024
Investigating copy number variants in schizophrenia pedigrees using a new consensus pipeline called PECANCathal Ormond, Niamh M Ryan, William Byerley, et al.
Briefings in Bioinformatics|December 10, 2024
BICEP: Bayesian inference for rare genomic variant causality evaluation in pedigreesCathal Ormond, Niamh M Ryan, Mathieu Cap, et al.
Biological Psychiatry Global Open Science|October 26, 2023
Ultrarare Missense Variants Implicated in Utah Pedigrees Multiply Affected With SchizophreniaCathal Ormond, Niamh M Ryan, Elizabeth A Heron, et al.
NPJ Genomic Medicine|September 28, 2024
Polygenic scores stratify neurodevelopmental copy number variant carrier cognitive outcomes in the UK BiobankThomas J Dinneen, Fiana Ní Ghrálaigh, Cathal Ormond, et al.
Molecular Psychiatry|October 12, 2022
Identity-by-descent analysis of a large Tourette's syndrome pedigree from Costa Rica implicates genes involved in neuronal development and signal transductionNiamh Ryan, Cathal Ormond, Yi-Chieh Chang, et al.
Medrxiv : the Preprint Server for Health Sciences|May 4, 2026
Rare protein-disrupting variants in <i>NPY5R, DLGAP1</i> and <i>MAPK8IP3</i> segregate with OCD in two multiplex pedigreesCathal Ormond, Mathieu Cap, Yi-Chieh Chang, et al.
Translational Psychiatry|July 30, 2024
Whole genome sequencing study of identical twins discordant for psychosisCathal Ormond, Niamh M Ryan, Anna M Hedman, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Briefings in Bioinformatics|April 6, 2021
Converting single nucleotide variants between genome builds: from cautionary tale to solutionCathal Ormond, Niamh M Ryan, Aiden Corvin, et al.
Biorxiv : the Preprint Server for Biology|April 10, 2026
BICEP: an extension to indels and copy number variants for rare variant prioritisation in pedigree analysisCathal Ormond, Niamh M Ryan, Aiden Corvin, et al.
Scientific Reports|July 30, 2024
Investigating copy number variants in schizophrenia pedigrees using a new consensus pipeline called PECANCathal Ormond, Niamh M Ryan, William Byerley, et al.
Briefings in Bioinformatics|December 10, 2024
BICEP: Bayesian inference for rare genomic variant causality evaluation in pedigreesCathal Ormond, Niamh M Ryan, Mathieu Cap, et al.
Biological Psychiatry Global Open Science|October 26, 2023
Ultrarare Missense Variants Implicated in Utah Pedigrees Multiply Affected With SchizophreniaCathal Ormond, Niamh M Ryan, Elizabeth A Heron, et al.
NPJ Genomic Medicine|September 28, 2024
Polygenic scores stratify neurodevelopmental copy number variant carrier cognitive outcomes in the UK BiobankThomas J Dinneen, Fiana Ní Ghrálaigh, Cathal Ormond, et al.
Molecular Psychiatry|October 12, 2022
Identity-by-descent analysis of a large Tourette's syndrome pedigree from Costa Rica implicates genes involved in neuronal development and signal transductionNiamh Ryan, Cathal Ormond, Yi-Chieh Chang, et al.
Medrxiv : the Preprint Server for Health Sciences|May 4, 2026
Rare protein-disrupting variants in <i>NPY5R, DLGAP1</i> and <i>MAPK8IP3</i> segregate with OCD in two multiplex pedigreesCathal Ormond, Mathieu Cap, Yi-Chieh Chang, et al.
Translational Psychiatry|July 30, 2024
Whole genome sequencing study of identical twins discordant for psychosisCathal Ormond, Niamh M Ryan, Anna M Hedman, et al.
Pageof 1