Alison J Eaton
5PUBLICATIONS
30CO-AUTHORS
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Publications (5)
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|Nov 11, 2022
Prenatal Genetic Testing in the Era of Next Generation Sequencing: A One-Center Canadian Experience.Asra Almubarak, Dan Zhang, Mackenzie Kosak
|Mar 30, 2021
Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner syndrome.Sarah E Sheppard, Ian M Campbell, Margaret H Harr
|Mar 13, 2020
When to think outside the autozygome: Best practices for exome sequencing in "consanguineous" families.Alison Eaton, Taila Hartley, Kristin Kernohan
|Dec 24, 2018
The unsolved rare genetic disease atlas? An analysis of the unexplained phenotypic descriptions in OMIM®.Taila Hartley, Tuğçe B Balcı, Samantha K Rojas
|Sep 24, 2018
Is PNPT1-related hearing loss ever non-syndromic? Whole exome sequencing of adult siblings expands the natural history of PNPT1-related disorders.Alison Eaton, Francois P Bernier, Caitlin Goedhart
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Frequent Collaborators
2 joint publications
Kym M Boycott
1 joint publications
Ryan E Lamont
1 joint publications
A Micheil Innes
1 joint publications
Taila Hartley
1 joint publications
Tuğçe B Balcı
1 joint publications
David A Dyment
1 joint publications
Sarah E Sheppard
1 joint publications
Ian M Campbell
1 joint publications
Nina Gold
1 joint publications
Margaret Au
