Terry-Lynn Young

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 5

Top Venues

Human genetics

European journal of human genetics : EJHG

BMC medical genetics

Genes

Western University

Memorial University (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Western University Mar 19 2015

Canada

Adjunct Research Professor :: Comm Sci and Disorders-EC

Eastern Health May 01 2003

Canada

Medical Scientist :: Laboratory Medicine Program

Memorial University May 01 2003

Canada

Professor :: Faculty of Medicine, Discipline of Genetics

Education History

Memorial University Apr 10 1995 - Jan 02 2000

Canada

PHD :: Discipline of Genetics

Memorial University Jan 02 1984 - May 01 1989

Canada

MSC :: Biology

Memorial University Sep 05 1978 - Apr 16 1983

Canada

BSC :: Biology

Publications

Sushma Singh, Cindy Penney, Anne Griffin, Geoffrey Woodland, Salem Werdyani, Tammy A Benteau, Nelly Abdelfatah, Jessica Squires, Beverly King, Jim Houston, Matthew J Dyer, Nicole M Roslin, Daniel Vincent, Pascale Marquis, Darren D O'Rielly, Kathy Hodgkinson, Taylor Burt, Ashley Baker, Susan G Stanton, Terry-Lynn Young
Highly variable hearing loss due to POU4F3 (c.37del) is revealed by longitudinal, frequency specific analyses. European journal of human genetics : EJHG (2023)
Justin A Pater, Cindy Penney, Darren D O'Rielly, Anne Griffin, Lara Kamal, Zippora Brownstein, Barbara Vona, Chana Vinkler, Mordechai Shohat, Ortal Barel, Curtis R French, Sushma Singh, Salem Werdyani, Taylor Burt, Nelly Abdelfatah, Jim Houston, Lance P Doucette, Jessica Squires, Fabian Glaser, Nicole M Roslin, Daniel Vincent, Pascale Marquis, Geoffrey Woodland, Touati Benoukraf, Alexia Hawkey-Noble, Karen B Avraham, Susan G Stanton, Terry-Lynn Young
Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene. Human genetics 141 (3-4) (2022)
Alexia Hawkey-Noble, Justin A Pater, Roshni Kollipara, Meriel Fitzgerald, Alexandre S Maekawa, Christopher S Kovacs, Terry-Lynn Young, Curtis R French
Mutation of foxl1 Results in Reduced Cartilage Markers in a Zebrafish Model of Otosclerosis. Genes 13 (7) (2022)
Nelly Abdelfatah, Ahmed A Mostafa, Curtis R French, Lance P Doucette, Cindy Penney, Matthew B Lucas, Anne Griffin, Valerie Booth, Christopher Rowley, Jessica E Besaw, Lisbeth Tranebjærg, Nanna Dahl Rendtorff, Kathy A Hodgkinson, Leichelle A Little, Sumit Agrawal, Lorne Parnes, Tony Batten, Susan Moore, Pingzhao Hu, Justin A Pater, Jim Houston, Dante Galutira, Tammy Benteau, Courtney MacDonald, Danielle French, Darren D O'Rielly, Susan G Stanton, Terry-Lynn Young
A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) gene. Human genetics (2021)
Justin A Pater, Jane Green, Darren D O'Rielly, Anne Griffin, Jessica Squires, Taylor Burt, Sara Fernandez, Bridget Fernandez, Jim Houston, Jiayi Zhou, Nicole M Roslin, Terry-Lynn Young
Novel Usher syndrome pathogenic variants identified in cases with hearing and vision loss. BMC medical genetics 20 (1) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Terry-Lynn Young