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Niamh M Ryan

Showing results (1-10 of 17) with videos related to

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Biological Research|July 19, 2023
Investigating the dark-side of the genome: a barrier to human disease variant discovery?Niamh M Ryan, Aiden Corvin
Journal of Applied Genetics|January 29, 2023
Evidence for parent-of-origin effects in autism spectrum disorder: a narrative reviewNiamh M Ryan, Elizabeth A Heron
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.
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.
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.
Genome Medicine|November 18, 2014
SuRFing the genomics wave: an R package for prioritising SNPs by functionalityNiamh M Ryan, Stewart W Morris, David J Porteous, et al.
Scientific Reports|December 18, 2020
Methyl-CpG-binding protein 2 mediates overlapping mechanisms across brain disordersSnow Bach, Niamh M Ryan, Paolo Guasoni, et al.
Cancer Research|March 11, 2010
BRD7, a subunit of SWI/SNF complexes, binds directly to BRCA1 and regulates BRCA1-dependent transcriptionMary T Harte, Garrett J O'Brien, Niamh M Ryan, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Biological Research|July 19, 2023
Investigating the dark-side of the genome: a barrier to human disease variant discovery?Niamh M Ryan, Aiden Corvin
Journal of Applied Genetics|January 29, 2023
Evidence for parent-of-origin effects in autism spectrum disorder: a narrative reviewNiamh M Ryan, Elizabeth A Heron
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.
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.
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.
Genome Medicine|November 18, 2014
SuRFing the genomics wave: an R package for prioritising SNPs by functionalityNiamh M Ryan, Stewart W Morris, David J Porteous, et al.
Scientific Reports|December 18, 2020
Methyl-CpG-binding protein 2 mediates overlapping mechanisms across brain disordersSnow Bach, Niamh M Ryan, Paolo Guasoni, et al.
Cancer Research|March 11, 2010
BRD7, a subunit of SWI/SNF complexes, binds directly to BRCA1 and regulates BRCA1-dependent transcriptionMary T Harte, Garrett J O'Brien, Niamh M Ryan, et al.
Pageof 2