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Whitney L Wooderchak-Donahue (Whitney Wooderchak-Donahue)

Publication Activity (10 Years)

Years Active: 2018-2021
Publications (10 Years): 3

Top Topics

Transforming Growth Factor

Epithelial Mesenchymal Transition

Patient Reported Outcomes

Top Venues

Science signaling

Molecular genetics & genomic medicine

Journal of medical genetics

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

Publications

Joshua Mark Hodgson, Lidia Ruiz-Llorente, Jamie McDonald, Oliver W J Quarrell, Kelechi Ugonna, James Bentham, Rebecca Mason, Jennifer M Martin, Alejandro Sifrim, Katie Bergstrom, Pinar Bayrak-Toydemir, Whitney L Wooderchak-Donahue, Nicholas W Morrell, Robin Condliffe, Carmelo Bernabéu, Paul D Upton
Homozygous GDF2 nonsense mutations result in a loss of circulating BMP9 and BMP10 and are associated with either PAH or an "HHT-like" syndrome in children. Molecular genetics & genomic medicine (2021)
Whitney L Wooderchak-Donahue, Jamie McDonald, Andrew Farrell, Gulsen Akay, Matt Velinder, Peter Johnson, Chad VanSant-Webb, Rebecca Margraf, Eric Briggs, Kevin J Whitehead, Jennifer Thomson, Angela E Lin, Reed E Pyeritz, Gabor Marth, Pinar Bayrak-Toydemir
Genome sequencing reveals a deep intronic splicing ACVRL1 mutation hotspot in Hereditary Haemorrhagic Telangiectasia. Journal of medical genetics 55 (12) (2018)
Xuan Jiang, Whitney L Wooderchak-Donahue, Jamie McDonald, Prajakta Ghatpande, Mai Baalbaki, Melissa Sandoval, Daniel Hart, Hilary Clay, Shaun R Coughlin, Giorgio Lagna, Pinar Bayrak-Toydemir, Akiko Hata
Inactivating mutations in Drosha mediate vascular abnormalities similar to hereditary hemorrhagic telangiectasia. Science signaling 11 (513) (2018)