Niamh Ryan

8PUBLICATIONS
30CO-AUTHORS
Gene mappingGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)Neurogenetics
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Publications (8)

|May 04, 2026
Rare protein-disrupting variants in NPY5R, DLGAP1 and MAPK8IP3 segregate with OCD in two multiplex pedigrees.

|Apr 10, 2026
BICEP: an extension to indels and copy number variants for rare variant prioritisation in pedigree analysis.

Cathal Ormond, Niamh M Ryan, Aiden Corvin

|Feb 05, 2026
From Genomes to Conversations: Outreach and Engagement in Psychiatric Genetics.

Helena L Davies, Niamh M Ryan, Kylie K Reed

|Jul 30, 2024
Whole genome sequencing study of identical twins discordant for psychosis.

Cathal Ormond, Niamh M Ryan, Anna M Hedman

|Jul 19, 2023
Investigating the dark-side of the genome: a barrier to human disease variant discovery?

Niamh M Ryan, Aiden Corvin

|Jan 29, 2023
Evidence for parent-of-origin effects in autism spectrum disorder: a narrative review.

Niamh M Ryan, Elizabeth A Heron

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Frequent Collaborators

5 joint publications

Aiden Corvin

5 joint publications

Elizabeth Heron

4 joint publications

Cathal Ormond

2 joint publications

Michael Gill