Darren D. O’Rielly

Author

Darren D. O’Rielly

Memorial University of Newfoundland ORCID

Also Known As

Abdul Noor, D D O'Rielly, D. O'Rielly, D. O'rielly, D. O’Rielly, D.D. O'Rielly, DARREN D. O’RIELLY, Darren D O'Rielly, Darren D O‘Rielly, Darren D O’Rielly

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

Memorial University of Newfoundland University of Toronto Hospital for Sick Children SickKids Foundation St. John’s Health Sciences Centre

About

Darren D. O’Rielly is an author at Memorial University of Newfoundland specializing in medicine, genetics, and molecular diagnostics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	65
2	Arts	1	1	16
3	Natural Sciences	1	1	24
4	Cell Biology	1	1	15
5	Cellular Physiology	1	1	15

Darren D. O’Rielly

Publications

474

Citations

H-Index

Page 1

	Year	Citations
The Genetics of Psoriasis and Psoriatic Arthritis Darren D. O’Rielly, Meghna Jani, Proton Rahman, The Journal of Rheumatology	2019	60
Extending the scope of diagnostic chromosome analysis: Detection of single gene defects using high-resolution SNP microarrays Damien L. Bruno, Zornitza Stark, David J. Amor, Human Mutation	2011	49
Increased Expression of Cyclooxygenase and Nitric Oxide Isoforms, and Exaggerated Sensitivity to Prostaglandin E2, in the Rat Lumbar Spinal Cord 3 Days after L5–L6 Spinal Nerve Ligation Darren D. O’Rielly, Christopher W. Loomis Anesthesiology	2006	47
Inhibition of Spinal Prostaglandin Synthesis Early after L5/L6 Nerve Ligation Prevents the Development of Prostaglandin-dependent and Prostaglandin-independent Allodynia in the Rat Michael P. Hefferan, Darren D. O’Rielly, Christopher W. Loomis Anesthesiology	2003	45
Quantifying Differences in Heritability among Psoriatic Arthritis (PsA), Cutaneous Psoriasis (PsC) and Psoriasis vulgaris (PsV) Quan Li, Vinod Chandran, Lam C. Tsoi, Scientific Reports	2020	37
Genome-Wide Signatures of ‘Rearrangement Hotspots’ within Segmental Duplications in Humans Mohammed Uddin, Mitch Sturge, Lynette Peddle, PLoS ONE GeneticsGenomic MechanismMolecular BiologyMolecular GeneticsGenomics	2011	24
Integrated Genomics Identifies Convergence of Ankylosing Spondylitis with Global Immune Mediated Disease Pathways Mohammed Uddin, D. Codner, S M Mahmud Hasan, Scientific Reports	2015	24
Mutational Landscape of Autism Spectrum Disorder Brain Tissue Marc Woodbury‐Smith, Sylvia Lamoureux, Ghausia Begum, Genes	2022	21
Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene Justin A. Pater, Cindy Penney, Darren D. O’Rielly, Human Genetics	2022	20
Private rare deletions in SEC16A and MAMDC4 may represent novel pathogenic variants in familial axial spondyloarthritis Darren D. O’Rielly, Mohammed Uddin, D. Codner, Annals of the Rheumatic Diseases	2015	18

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