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Lance P. Doucette
Lance P. Doucette
University of Alberta
Biology
Disease
Gene
Exome sequencing
Genetics
4
Papers
1
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0
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Autosomal Dominant Non-Syndromic Hearing Loss Maps to DFNA33 (13q34) and Co-Segregates with Splice Site Variants in ATP11A, A Phospholipid Flippase Gene
2021
Justin A. Pater
Cindy Penney
Darren D. O’Rielly
Anne Griffin
Mordechai Shohat
Ortal Barel
Curtis R. French
Sushma Singh
Salem Werdyani
Taylor Burt
Nelly Abdelfatah
Jim Houston
Lance P. Doucette
Jessica Squires
Nicole M. Roslin
Daniel Vincent
Pascale Marquis
Geoffrey Woodland
Susan G. Stanton
Terry-Lynn Young
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PEX6 mutations in peroxisomal biogenesis disorders: an Usher syndrome mimic
2021
Matthew D. Benson
Kimberly M. Papp
Geoffrey A. Casey
Alina Radziwon
Chris D. St. Laurent
Lance P. Doucette
Ian M. MacDonald
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Whole exome sequencing reveals putatively novel associations in retinopathies and drusen formation.
2021
European Journal of Human Genetics
Lance P. Doucette
Nicole C L Noel
Yi Zhai
Manlong Xu
Oana Caluseriu
Stephanie C. Hoang
Alina Radziwon
Ian M. MacDonald
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Whole Exome Sequencing of Unknown Retinal Disease Cases: The Alberta Perspective
2019
Investigative Ophthalmology & Visual Science
Lance P. Doucette
Stephanie C. Hoang
Alina Radziwon
Ian M. MacDonald
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