Uptake of Lipids by the Entomophilic Nematode Romanomermis culicivorax.
Ian R. Burford , Terry-Lynn Young , Roger Gordon
Journal of Nematology 14 ( 4) 492 -495
7
1982
Methods and compositions for detecting progressive hearing loss
Nelly Abdelfatah , Anne Griffin , Terry-Lynn Young
2014
Long-Term Clinical Outcome of Arrhythmogenic Right Ventricular Cardiomyopathy in Individuals With a p.S358L Mutation in TMEM43 Following Implantable Cardioverter Defibrillator Therapy.
Kathleen A. Hodgkinson , A.J. Howes , Paul Boland , Xiou Seegar Shen
Circulation-arrhythmia and Electrophysiology 9 ( 3)
21
2016
Empirical and physiological assessment of in vitro growth in the mermithid nematode Romanomermis culicivorax
Roger Gordon , Marcel Cornect , Terry-Lynn Young , Kenneth T. Kean
Canadian Journal of Zoology 68 ( 3) 511 -516
1990
Exercise and arrhythmic risk in TMEM43 p.S358L arrhythmogenic right ventricular cardiomyopathy
Frédéric L. Paulin , Kathleen A. Hodgkinson , Sarah MacLaughlan , Susan N. Stuckless
Heart Rhythm 17 ( 7) 1159 -1166
2
2020
Novel Usher syndrome pathogenic variants identified in cases with hearing and vision loss.
Justin A. Pater , Jane Green , Darren D. O’Rielly , Anne Griffin
BMC Medical Genetics 20 ( 1) 1 -9
4
2019
Canadian Bardet-Biedl syndrome family reduces the critical region of BBS3 (3p) and presents with a variable phenotype
Terry-Lynn Young , Mike O. Woods , Patrick S. Parfrey , Jane S. Green
American Journal of Medical Genetics 78 ( 5) 461 -467
50
1998
Genetic Heterogeneity of Bardet–Biedl Syndrome in a Distinct Canadian Population: Evidence for a Fifth Locus
Michael O. Woods , Terry-Lynn Young , Patrick S. Parfrey , Donna Hefferton
Genomics 55 ( 1) 2 -9
61
1999
Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease.
Kim Cryns , Theru A. Sivakumaran , Jody M.W. Van den Ouweland , Ronald J.E. Pennings
Human Mutation 22 ( 4) 275 -287
147
2003
A novel deletion in SMPX causes a rare form of X-linked progressive hearing loss in two families due to a founder effect.
Nelly Abdelfatah , Nancy Merner , Jim Houston , Tammy Benteau
Human Mutation 34 ( 1) 66 -69
17
2013
Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan
Zubair M Ahmed , Xiaoyan Cindy Li , Shontell D Powell , Saima Riazuddin
BMC Medical Genetics 5 ( 1) 24 -24
29
2004
X-Linked Hearing Loss: Two Gene Mutation Examples Provide Generalizable Implications for Clinical Care
Susan G Stanton , Anne Griffin , Tracy L Stockley , Christine Brown
American Journal of Audiology 23 ( 2) 190 -200
10
2014
Using next-generation sequencing for the diagnosis of rare disorders: a family with retinitis pigmentosa and skeletal abnormalities.
Kasmintan A Schrader , Alireza Heravi-Moussavi , Paula J Waters , Janine Senz
The Journal of Pathology 225 ( 1) 12 -18
28
2011
Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15
Lance Doucette , Nancy D Merner , Sandra Cooke , Elizabeth Ives
European Journal of Human Genetics 17 ( 5) 554 -564
24
2009
A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly
Lance Doucette , Jane Green , Bridget Fernandez , Gordon J Johnson
European Journal of Human Genetics 19 ( 3) 293 -299
27
2011
“There are days I wish it wasn’t there, and there’s days I realize I’m lucky”: A qualitative study of psychological sequelae to the implantable cardioverter defibrillator as a treatment for the prevention of sudden cardiac death in arrhythmogenic right ventricular cardiomyopathy:
Holly Etchegary , Daryl Pullman , Sean P Connors , Charlene Simmonds
JRSM Cardiovascular Disease 6 204800401769861
2017
The genetic architecture of Stargardt macular dystrophy (STGD1): a longitudinal 40-year study in a genetic isolate
Jane S. Green , Darren D. O’Rielly , Justin A. Pater , Jim Houston
European Journal of Human Genetics 28 ( 7) 925 -937
2
2020
A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effect
Justin A Pater , Tammy Benteau , Anne Griffin , Cindy Penney
Human Genetics 136 ( 1) 107 -118
10
2017
Identification of a novel in-frame deletion in KCNQ4 (DFNA2A) and evidence of multiple phenocopies of unknown origin in a family with ADSNHL
Nelly Abdelfatah , David A McComiskey , Lance Doucette , Anne Griffin
European Journal of Human Genetics 21 ( 10) 1112 -1119
12
2013
EFFECTS OF SEVERAL INSECT GROWTH REGULATORS ON EGG HATCH AND SUBSEQUENT DEVELOPMENT IN THE CABBAGE MAGGOT DELIA RADICUM (L.) (DIPTERA: ANTHOMYIIDAE)
Terry-Lynn Young , Roger Gordon , Marcel Cornect
Canadian Entomologist 119 ( 5) 481 -488
5
1987