Whitney Wooderchak‐Donahue

Author

Also Known As

W. Wooderchak-Donahue, Whitney L Wooderchak-Donahue, Whitney L. Wooderchak-Donahue, Whitney L. Wooderchak‐Donahue, Whitney Wooderchak-Donahue, Whitney Wooderchak‐Donahue, Whitney L. Wooderchak-Donahue

Publications

1.9K

Citations

H-Index

Concepts

All Affiliations

University of Utah ARUP Laboratories (United States)ARUP Institute for Clinical and Experimental Pathology Stanford University Centro de Investigaciones Biológicas Margarita Salas

About

Whitney Wooderchak‐Donahue is an author at University of Utah specializing in medicine, pathology, and hematology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	613
2	Engineering	1	1	27
3	Natural Sciences	1	1	49
4	Biochemistry	1	1	49
5	Biomolecular Engineering	1	1	49

Whitney Wooderchak‐Donahue

Publications

1.2K

Citations

H-Index

Page 1

	Year	Citations
BMP9 Mutations Cause a Vascular-Anomaly Syndrome with Phenotypic Overlap with Hereditary Hemorrhagic Telangiectasia Whitney Wooderchak‐Donahue, Jamie McDonald, Brendan O’Fallon, The American Journal of Human Genetics Vascular-anomaly SyndromeMendelian DisorderHereditary Hemorrhagic TelangiectasiaGenetic DisorderGenetics	2013	302
<i>RASA1</i> somatic mutation and variable expressivity in capillary malformation/arteriovenous malformation (CM/AVM) syndrome Colleen Macmurdo, Whitney Wooderchak‐Donahue, Pinar Bayrak‐Toydemir, American Journal of Medical Genetics Part A	2016	103
Expanding the clinical and molecular findings in RASA1 capillary malformation-arteriovenous malformation Whitney Wooderchak‐Donahue, Peter Johnson, Jamie McDonald, European Journal of Human Genetics Vascular DiseaseMolecular FindingsVasculitisVascular MalformationVascular Surgery	2018	71
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, Genetics in Medicine Curaçao Diagnostic CriteriaHereditary Hemorrhagic TelangiectasiaGeneticsHematologyPathology	2020	68
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, American Journal of Medical Genetics Part A	2015	65
Phenotype of CM-AVM2 caused by variants in EPHB4: how much overlap with hereditary hemorrhagic telangiectasia (HHT)? Whitney Wooderchak‐Donahue, Gülsen Akay, Kevin J. Whitehead, Genetics in Medicine Much OverlapHereditary Hemorrhagic TelangiectasiaGenetic DisorderGeneticsGenetic Epidemiology	2019	57
Genetic Variants Associated with Port-Wine Stains Alice Frigerio, Karol Wright, Whitney Wooderchak‐Donahue, PLoS ONE	2015	51
Substrate-Induced Control of Product Formation by Protein Arginine Methyltransferase 1 Shanying Gui, Whitney Wooderchak‐Donahue, Tianzhu Zang, Biochemistry Molecular RegulationEpigenetic ChangeMolecular BiologySubstrate-induced ControlEnzymatic Modification	2012	49
A support vector machine for identification of single-nucleotide polymorphisms from next-generation sequencing data Brendan O’Fallon, Whitney Wooderchak‐Donahue, David K. Crockett Bioinformatics	2013	45
RASA1 analysis: Clinical and molecular findings in a series of consecutive cases Whitney Wooderchak‐Donahue, David A. Stevenson, Jamie McDonald, European Journal of Medical Genetics UrologyMolecular FindingsMedicineHistopathologyPathology	2011	39

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