Whitney Wooderchak-Donahue
Overview
Explore the profile of Whitney Wooderchak-Donahue including associated specialties, affiliations and a list of published articles.
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19
Citations
361
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Recent Articles
1.
Whitehead K, Toydemir D, Wooderchak-Donahue W, Oakley G, McRae B, Putnam A, et al.
Int J Mol Sci
. 2024 Jul;
25(14).
PMID: 39062925
Telangiectases and arteriovenous malformations (AVMs) are the characteristic lesions of Hereditary Hemorrhagic Telangiectasia (HHT). Somatic second-hit loss-of-function variations in the HHT causative genes, and , have been described in dermal...
2.
Hodgson J, Ruiz-Llorente L, McDonald J, Quarrell O, Ugonna K, Bentham J, et al.
Mol Genet Genomic Med
. 2021 Apr;
9(12):e1685.
PMID: 33834622
Background: Disrupted endothelial BMP9/10 signaling may contribute to the pathophysiology of both hereditary hemorrhagic telangiectasia (HHT) and pulmonary arterial hypertension (PAH), yet loss of circulating BMP9 has not been confirmed...
3.
Bernard P, Wooderchak-Donahue W, Wei M, Bray S, Wood K, Parikh B, et al.
Cancers (Basel)
. 2021 Apr;
13(6).
PMID: 33799547
Patients with breast cancer often receive many drugs to manage the cancer, side effects associated with cancer treatment, and co-morbidities (i.e., polypharmacy). Drug-drug and drug-gene interactions contribute to the risk...
4.
Flores Daboub J, Grimmer J, Frigerio A, Wooderchak-Donahue W, Arnold R, Szymanski J, et al.
Cold Spring Harb Mol Case Stud
. 2020 Aug;
6(4).
PMID: 32843429
Parkes Weber syndrome is associated with autosomal dominant inheritance, caused by germline heterozygous inactivating changes in the gene, characterized by multiple micro arteriovenous fistulas and segmental overgrowth of soft tissue...
5.
McDonald J, Bayrak-Toydemir P, DeMille D, Wooderchak-Donahue W, Whitehead K
Genet Med
. 2020 Apr;
22(7):1201-1205.
PMID: 32300199
Purpose: Determine the variant detection rate for ENG, ACVRL1, and SMAD4 in individuals who meet consensus (Curaçao) criteria for the clinical diagnosis of hereditary hemorrhagic telangiectasia. Methods: Review of HHT...
6.
Ruiz-Llorente L, McDonald J, Wooderchak-Donahue W, Briggs E, Chesnutt M, Bayrak-Toydemir P, et al.
J Hum Genet
. 2019 Feb;
64(4):333-339.
PMID: 30728427
Hereditary hemorrhagic telangiectasia (HHT) is a vascular disease characterized by nose and gastrointestinal bleeding, telangiectases in skin and mucosa, and arteriovenous malformations in major internal organs. Most patients carry a...
7.
Macmurdo C, Wooderchak-Donahue W, Bayrak-Toydemir P, Le J, Wallenstein M, Milla C, et al.
Am J Med Genet A
. 2016 Mar;
170(6):1450-4.
PMID: 26969842
Germline mutations in RASA1 are associated with capillary malformation-arteriovenous malformation (CM-AVM) syndrome. CM-AVM syndrome is characterized by multi-focal capillary malformations and arteriovenous malformations. Lymphatic anomalies have been proposed as part...
8.
Arthur H, Geisthoff U, Gossage J, Hughes C, Lacombe P, Meek M, et al.
Angiogenesis
. 2015 Sep;
18(4):511-24.
PMID: 26391603
Hereditary hemorrhagic telangiectasia (HHT) is a hereditary condition that results in vascular malformations throughout the body, which have a proclivity to rupture and bleed. HHT has a worldwide incidence of...
9.
Frigerio A, Wright K, Wooderchak-Donahue W, Tan O, Margraf R, Stevenson D, et al.
PLoS One
. 2015 Jul;
10(7):e0133158.
PMID: 26192947
Background: Port-wine stains (PWS) are capillary malformations, typically located in the dermis of the head and neck, affecting 0.3% of the population. Current theories suggest that port-wine stains are caused...
10.
Wooderchak-Donahue W, VanSant-Webb C, Tvrdik T, Plant P, Lewis T, Stocks J, et al.
Am J Med Genet A
. 2015 May;
167A(8):1747-57.
PMID: 25944730
Aortopathy can be defined as aortic dilation, aneurysm, dissection, and tortuosity. Familial aortopathy may occur secondary to fibrillin-1 (FBN1) mutations in the setting of Marfan syndrome, or may occur as...