Cathal Ormond
Dublin, L, Ireland
Last Updated: 09/26/2026
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Found 9 publications
Rare protein-disrupting variants in NPY5R, DLGAP1 and MAPK8IP3 segregate with OCD in two multiplex pedigrees.
Journal: medRxiv : the preprint server for health sciences
Published: May 04, 2026
BICEP: an extension to indels and copy number variants for rare variant prioritisation in pedigree analysis.
Journal: bioRxiv : the preprint server for biology
Published: April 10, 2026
BICEP: Bayesian inference for rare genomic variant causality evaluation in pedigrees.
Journal: Briefings in bioinformatics
Published: June 18, 2024
Polygenic scores stratify neurodevelopmental copy number variant carrier cognitive outcomes in the UK Biobank.
Journal: NPJ genomic medicine
Published: January 03, 2024
Investigating copy number variants in schizophrenia pedigrees using a new consensus pipeline called PECAN.
Journal: Scientific reports
Published: December 19, 2023
Whole genome sequencing study of identical twins discordant for psychosis.
Journal: Translational psychiatry
Published: November 23, 2023
Ultrarare Missense Variants Implicated in Utah Pedigrees Multiply Affected With Schizophrenia.
Journal: Biological psychiatry global open science
Published: October 24, 2022
Identity-by-descent analysis of a large Tourette's syndrome pedigree from Costa Rica implicates genes involved in neuronal development and signal transduction.
Journal: Molecular psychiatry
Published: September 23, 2021
Converting single nucleotide variants between genome builds: from cautionary tale to solution.
Journal: Briefings in bioinformatics
Published: November 02, 2020
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Last Updated: 09/26/2026