Whitney Wooderchak‐Donahue

BMP9 Mutations Cause a Vascular-Anomaly Syndrome with Phenotypic Overlap with Hereditary Hemorrhagic Telangiectasia

Whitney Wooderchak‐Donahue, Jamie McDonald, Brendan O’Fallon et al. · The American Journal of Human Genetics · 2013 · 302 citations · Full text

Vascular-anomaly Syndrome, Mendelian Disorder, Hereditary Hemorrhagic Telangiectasia +11

<i>RASA1</i> somatic mutation and variable expressivity in capillary malformation/arteriovenous malformation (CM/AVM) syndrome

Colleen Macmurdo, Whitney Wooderchak‐Donahue, Pinar Bayrak‐Toydemir et al. · American Journal of Medical Genetics Part A · 2016 · 103 citations

Expanding the clinical and molecular findings in RASA1 capillary malformation-arteriovenous malformation

Whitney Wooderchak‐Donahue, Peter Johnson, Jamie McDonald et al. · European Journal of Human Genetics · 2018 · 71 citations · Full text

Vascular Disease, Molecular Findings, Vasculitis +7

Curaçao diagnostic criteria for hereditary hemorrhagic telangiectasia is highly predictive of a pathogenic variant in ENG or ACVRL1 (HHT1 and HHT2)

Jamie McDonald, Pınar Bayrak‐Toydemir, Desiree DeMille et al. · Genetics in Medicine · 2020 · 68 citations · Full text

Curaçao Diagnostic Criteria, Hereditary Hemorrhagic Telangiectasia, Genetics +5

Clinical utility of a next generation sequencing panel assay for Marfan and Marfan‐like syndromes featuring aortopathy

Whitney Wooderchak‐Donahue, Chad VanSant‐Webb, Tatiana Tvrdik et al. · American Journal of Medical Genetics Part A · 2015 · 65 citations · Full text