Whitney Wooderchak-Donahue
3PUBLICATIONS
20CO-AUTHORS
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Publications (3)
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|Apr 09, 2021
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.Joshua Hodgson, Lidia Ruiz-Llorente, Jamie McDonald
|Sep 24, 2018
Genome sequencing reveals a deep intronic splicing ACVRL1 mutation hotspot in Hereditary Haemorrhagic Telangiectasia.Whitney L Wooderchak-Donahue, Jamie McDonald, Andrew Farrell
|Jan 18, 2018
Inactivating mutations in Drosha mediate vascular abnormalities similar to hereditary hemorrhagic telangiectasia.Xuan Jiang, Whitney L Wooderchak-Donahue, Jamie McDonald
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Frequent Collaborators
2 joint publications
Jamie McDonald
1 joint publications
Xuan Jiang
1 joint publications
Mai Baalbaki
1 joint publications
Melissa Sandoval
1 joint publications
Daniel Hart
1 joint publications
Shaun Coughlin
1 joint publications
Giorgio Lagna
1 joint publications
Pinar Bayrak-Toydemir
1 joint publications
Akiko Hata
1 joint publications
Joshua Hodgson
