Terry-Lynn Young

7PUBLICATIONS
12CO-AUTHORS
NeurogeneticsCultural theoryHaematological tumoursGene mappingVision science
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Publications (7)

|Jun 12, 2026
Heterozygous Nonsense Mutation in the Nuclear Transport Factor KPNA7, a Maternal Factor Active in Embryonic Tissues, Causes Autosomal Dominant Otosclerosis.

|Sep 29, 2025
Embodying hearing loss: confronting the issue and adjusting to a new norm.

April Pike, Joanne Smith-Young, Terry-Lynn Young

|Apr 18, 2023
Highly variable hearing loss due to POU4F3 (c.37del) is revealed by longitudinal, frequency specific analyses.

Sushma Singh, Cindy Penney, Anne Griffin

|Jul 27, 2022
Mutation of foxl1 Results in Reduced Cartilage Markers in a Zebrafish Model of Otosclerosis.

Alexia Hawkey-Noble, Justin A Pater, Roshni Kollipara

|Mar 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 gene.

Justin A Pater, Cindy Penney, Darren D O'Rielly

|Oct 11, 2021
A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) gene.

Nelly Abdelfatah, Ahmed A Mostafa, Curtis R French

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Frequent Collaborators

1 joint publications

Roshni Kollipara

1 joint publications

Christopher S Kovacs

1 joint publications

Nicole M Roslin

1 joint publications

Kathy Hodgkinson