Taila Hartley

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 7

Top Topics

Autism Spectrum Disorder

Intellectual Disability

Dna Methylation

Genome Wide Analysis

Top Venues

Neurology. Genetics

American journal of medical genetics. Part A

American journal of medical genetics. Part C, Seminars in medical genetics

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

Publications

Ian C Smith, Chantal A Pileggi, Ying Wang, Kristin Kernohan, Taila Hartley, Hugh J Mcmillan, Marcos Loreto Sampaio, Gerd Melkus, John M Woulfe, Gaganvir Parmar, Pierre Raymond Bourque, Thanh B Nguyen, Jocelyn Christine Zwicker, C Elizabeth Pringle, Olga Jarinova, Hanns Lochmüller, David A Dyment, Bernard Brais, Kym M Boycott, null null, Siegfried Hekimi, Mary-Ellen Harper, Jodi Warman-Chardon
Novel Homozygous Variant in COQ7 in Siblings With Hereditary Motor Neuropathy. Neurology. Genetics 9 (1) (2023)
Leanne de Kock, Alexanne Cuillerier, Meredith Gillespie, Madeline Couse, Taila Hartley, Wendy Mears, Francois P Bernier, Albert E Chudley, Patrick Frosk, Sarah M Nikkel, A Micheil Innes, Julie Lauzon, Maryann Thomas, Andrea Guerin, Christine M Armour, Rosanna Weksberg, James N Scott, Debra Watkins, Shirley Harvey, Cheryl Cytrynbaum, null null, Kristin D Kernohan, Kym M Boycott
Molecular characterization of 13 patients with PIK3CA-related overgrowth spectrum using a targeted deep sequencing approach. American journal of medical genetics. Part A (2023)
Jodi Warman-Chardon, Taila Hartley, Aren Elizabeth Marshall, Arran McBride, Madeline Couse, William Macdonald, Mellissa R W Mann, Pierre Raymond Bourque, Thanh B Nguyen, Hanns Lochmüller, John M Woulfe, Marcos Loreto Sampaio, Gerd Melkus, Bernard Brais, David A Dyment, Kym M Boycott, Kristin Kernohan
Biallelic SOX8 Variants Associated With Novel Syndrome With Myopathy, Skeletal Deformities, Intellectual Disability, and Ovarian Dysfunction. Neurology. Genetics 9 (5) (2023)
Jodi Warman-Chardon, Taila Hartley, Aren Elizabeth Marshall, Arran McBride, Madeline Couse, William Macdonald, Mellissa R W Mann, Pierre Raymond Bourque, Thanh B Nguyen, Hanns Lochmüller, John M Woulfe, Marcos Loreto Sampaio, Gerd Melkus, Bernard Brais, David A Dyment, Kym M Boycott, Kristin Kernohan
Biallelic SOX8 Variants Associated With Novel Syndrome With Myopathy, Skeletal Deformities, Intellectual Disability, and Ovarian Dysfunction. Neurology. Genetics 9 (5) (2023)
Hannah G Driver, Taila Hartley, E Magda Price, Andrei L Turinsky, Orion J Buske, Matthew Osmond, Arun K Ramani, Emily Kirby, Kristin D Kernohan, Madeline Couse, Hillary Elrick, Kevin Lu, Pouria Mashouri, Aarthi Mohan, Delvin So, Conor Klamann, Hannah G B H Le, Andrea Herscovich, Christian R Marshall, Andrew Statia, Care Rare Canada Consortium, Bartha Maria Knoppers, Michael Brudno, Kym M Boycott
Genomics4RD: An integrated platform to share Canadian deep-phenotype and multiomic data for international rare disease gene discovery. Human mutation 43 (6) (2022)
Taila Hartley, Élisabeth Soubry, Meryl Acker, Matthew Osmond, Madeline Couse, Meredith K Gillespie, Yoko Ito, Aren E Marshall, Gabrielle Lemire, Lijia Huang, Caitlin Chisholm, Alison J Eaton, E Magda Price, James E Dowling, Arun K Ramani, Roberto Mendoza-Londono, Gregory Costain, Michelle M Axford, Anna Szuto, Vanda McNiven, Nadirah Damseh, Rebekah Jobling, Leanne de Kock, Bahareh A Mojarad, Ted Young, Zhuo Shao, Robin Z Hayeems, Ian D Graham, Mark A Tarnopolsky, Lauren Brady, Christine M Armour, Michael Geraghty, Julie Richer, Sarah Sawyer, Matthew Lines, Saadet Mercimek-Mahmutoglu, Melissa T Carter, Gail Graham, Peter Kannu, Joanna Lazier, Chumei Li, Ritu B Aul, Tugce B Balci, Nomazulu Dlamini, Lauren Badalato, Andrea Guerin, Jagdeep Walia, David Chitayat, Ronald Cohn, Hanna Faghfoury, Cynthia Forster-Gibson, Hernan Gonorazky, Eyal Grunebaum, Michal Inbar-Feigenberg, Natalya Karp, Chantal Morel, Alison Rusnak, Neal Sondheimer, Jodi Warman-Chardon, Priya T Bhola, Danielle K Bourque, Inara Chacon Fonseca, Lauren Chad, Pranesh Chakraborty, Karen Chong, Asif Doja, Elaine Suk-Ying Goh, Maha Saleh, null null, Beth K Potter, Christian R Marshall, David A Dyment, Kristin Kernohan, Kym M Boycott
Bridging clinical care and research in Ontario, Canada: Maximizing diagnoses from reanalysis of clinical exome sequencing data. Clinical genetics (2022)
Taila Hartley, Tuğçe B Balcı, Samantha K Rojas, Alison J Eaton, Care Rare Canada, David A Dyment, Kym M Boycott
The unsolved rare genetic disease atlas? An analysis of the unexplained phenotypic descriptions in OMIM®. American journal of medical genetics. Part C, Seminars in medical genetics 178 (4) (2019)