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Chelsea Lowther, PhD

About Me
Education & Certifications
Awards
Locations
Publications

About Me

Language

English

Position

ASSISTANT PROFESSOR | Genetics and Genomic Sciences

Research Topics

Computational Biology, Genomics, Human Genetics and Genetic Disorders, Personalized Medicine, Translational Research

Multi-Disciplinary Training Areas

Artificial Intelligence and Emerging Technologies in Medicine [AIET], Genetics and Genomic Sciences [GGS]

About Me

Language

English

Position

ASSISTANT PROFESSOR | Genetics and Genomic Sciences

Research Topics

Computational Biology, Genomics, Human Genetics and Genetic Disorders, Personalized Medicine, Translational Research

Multi-Disciplinary Training Areas

Artificial Intelligence and Emerging Technologies in Medicine [AIET], Genetics and Genomic Sciences [GGS]

Education

BSc, University of Prince Edward Island

PhD, University of Toronto

Postdoc, Massachusetts General Hospital/Harvard Medical School/Broad Institute

Awards

2022

K99/R00 Transition to Independence Award

NICHD

2021

Fund for Medical Discovery Fundamental Research Fellowship Award

Massachusetts General Hospital Executive Committee on Research

2020

Charles J. Epstein Trainee Award for Excellence in Human Genetics Research – Finalist

American Society of Human Genetics

2020

Charles J. Epstein Trainee Award for Excellence in Human Genetics Research – Winner

American Society of Human Genetics

2018

Postdoctoral Fellowship

Canadian Institutes of Health Research

2015

Frederick Banting and Charles Best Canada Graduate Scholarship

Canadian Institutes of Health Research

2015

McLaughlin Centre Training Award

University of Toronto

2012

Convocation Award

Psychological Association of Prince Edward Island

2011

Robert Haines Memorial Science Award of Merit

University of Prince Edward Island

Locations

3 East 101st Street, 3 E 101st St, New York, NY, 10029

332-243-7190

Publications

Publications:24

Selected Publications

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes. Samuel F. Berkovic, Benjamin M. Neale, Gábor Zsurka, Milena Zizovic, Fritz Zimprich, Federico Zara, Felix Zahnert, Sara Zagaglia, Emrah Yücesan, Robert Yolken, Uluc Yis, Zuhal Yapıcı, Kazuhiro Yamakawa, David Wu, Randi von Wrede, Isaac Wong, Stefan Wolking, Markus Wolff, Steven M. Wolf, Samuel Wiebe, Peter Widdess-Walsh, Sarah Weckhuysen, Yvonne G. Weber, Nick Watts, Ryan G. Wagner, Sarah von Spiczak, Sophie von Brauchitsch, Markéta Vlčková, Annalisa Vetro, Maria Stella Vari, Andreas van Baalen, Luc Valton, Priya Vaidiswaran, Algirdas Utkus, Sibel Uğur-İşeri, Dilsad Turkdogan, Birute Tumiene, Meng Han Tsai, Pınar Topaloglu, Marian Todaro, Paolo Tinuper, Nicholas John Timpson, Oskari Timonen, George A. Tanteles, Randip S. Taneja, Michael E. Talkowski, Hillary R. Raynes, Lara Marcuse, Chelsea Lowther, Madeline C. Fields. Nature Neuroscience
Genetic diagnostic outcomes from a 10-year research programme in autism in Aotearoa New Zealand. Suzanne M. Musgrave, Juliet Taylor, Whitney Whitford, Alexandra Garton, Jessie Poquérusse, Victoria Hawkins, Waiora Port, Kriebashne S. Moodley, Ruth Monk, Sarah D. Knowles, Caroline Walker, Christopher Samson, Lydia Velzian, Brendan Swan, Donald R. Love, Rosamund Hill, Colette Muir, Michael E. Talkowski, Chelsea Lowther, Russell G. Snell, Klaus Lehnert, Jessie C. Jacobsen. Journal of the Royal Society of New Zealand
Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies. Chelsea Lowther, Elise Valkanas, Jessica L. Giordano, Harold Z. Wang, Benjamin B. Currall, Kathryn O'Keefe, Emma Pierce-Hoffman, Nehir E. Kurtas, Christopher W. Whelan, Stephanie P. Hao, Ben Weisburd, Vahid Jalili, Jack Fu, Isaac Wong, Ryan L. Collins, Xuefang Zhao, Christina A. Austin-Tse, Emily Evangelista, Gabrielle Lemire, Vimla S. Aggarwal, Diane Lucente, Laura D. Gauthier, Charlotte Tolonen, Nareh Sahakian, Christine Stevens, Joon Yong An, Shan Dong, Mary E. Norton, Tippi C. MacKenzie, Bernie Devlin, Kelly Gilmore, Bradford C. Powell, Alicia Brandt, Francesco Vetrini, Michelle DiVito, Stephan J. Sanders, Daniel G. MacArthur, Jennelle C. Hodge, Anne O'Donnell-Luria, Heidi L. Rehm, Neeta L. Vora, Brynn Levy, Harrison Brand, Ronald J. Wapner, Michael E. Talkowski. American Journal of Human Genetics

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