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Pilot and Feasibility Studies|January 4, 2022
A physiotherapy-led transition to home intervention for older adults following emergency department discharge: protocol for a pilot feasibility randomised controlled trialMairéad Conneely, Aoife Leahy, Margaret O'Connor, et al.
BMC Medical Genetics|May 4, 2019
Novel Usher syndrome pathogenic variants identified in cases with hearing and vision lossJustin A Pater, Jane Green, Darren D O'Rielly, et al.
European Journal of Human Genetics : EJHG|February 28, 2013
Identification of a novel in-frame deletion in KCNQ4 (DFNA2A) and evidence of multiple phenocopies of unknown origin in a family with ADSNHLNelly Abdelfatah, David A McComiskey, Lance Doucette, et al.
Human Genetics|November 14, 2016
A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effectJustin A Pater, Tammy Benteau, Anne Griffin, et al.
Journal of General Internal Medicine|January 10, 2008
Programmable infusion pumps in ICUs: an analysis of corresponding adverse drug eventsTeryl K Nuckols, Anthony G Bower, Susan M Paddock, et al.
Rural and Remote Health|February 21, 2023
A physiotherapy-led transition to home intervention for older adults following Emergency Department discharge: a pilot feasibility randomised controlled trialMairéad Conneely, Aoife Leahy, Margaret O'Connor, et al.
Rand Health Quarterly|January 14, 2017
RAND/UCLA Quality-of-Care Measures for Carpal Tunnel Syndrome: Tools for Assessing Quality of Care and Appropriateness of SurgeryTeryl K Nuckols, Anne Griffin, Steven M Asch, et al.
Clinical Interventions in Aging|October 30, 2023
A Physiotherapy-Led Transition to Home Intervention for Older Adults Following Emergency Department Discharge: A Pilot Feasibility Randomised Controlled Trial (ED PLUS)Mairéad Conneely, Siobhán Leahy, Margaret O'Connor, et al.
European Journal of Human Genetics : EJHG|April 18, 2023
Highly variable hearing loss due to POU4F3 (c.37del) is revealed by longitudinal, frequency specific analysesSushma Singh, Cindy Penney, Anne Griffin, et al.
Human Genetics|March 12, 2022
Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase geneJustin A Pater, Cindy Penney, Darren D O'Rielly, et al.
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