Taila Hartley

6PUBLICATIONS
56CO-AUTHORS
Developmental genetics (incl. sex determination)Photonics, optoelectronics and optical communicationsEnvironmentally sustainable engineeringGene expression (incl. microarray and other genome-wide approaches)Genomics
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Publications (6)

|Jan 18, 2024
Biallelic SOX8 Variants Associated With Novel Syndrome With Myopathy, Skeletal Deformities, Intellectual Disability, and Ovarian Dysfunction.

Jodi Warman-Chardon, Taila Hartley, Aren Elizabeth Marshall

|Nov 10, 2023
Molecular characterization of 13 patients with PIK3CA-related overgrowth spectrum using a targeted deep sequencing approach.

Leanne de Kock, Alexanne Cuillerier, Meredith Gillespie

|Apr 20, 2023
Novel Homozygous Variant in COQ7 in Siblings With Hereditary Motor Neuropathy.

Ian C Smith, Chantal A Pileggi, Ying Wang

|Nov 10, 2022
Bridging clinical care and research in Ontario, Canada: Maximizing diagnoses from reanalysis of clinical exome sequencing data.

Taila Hartley, Élisabeth Soubry, Meryl Acker

|Feb 19, 2022
Genomics4RD: An integrated platform to share Canadian deep-phenotype and multiomic data for international rare disease gene discovery.

Hannah G Driver, Taila Hartley, E Magda Price

|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

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Frequent Collaborators

6 joint publications

Kym M Boycott

4 joint publications

David A Dyment

2 joint publications

Pierre R Bourque

2 joint publications

Gerd Melkus