Sarah R. McWhinney

Medicine · Health Sciences

12h-index3.5kcitations15works0.02yr avg
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Research Topics

Adrenal and Paraganglionic Tumors(5), Cancer, Hypoxia, and Metabolism(4), Neuroblastoma Research and Treatments(4), Neurofibromatosis and Schwannoma Cases(3), Gastrointestinal Tumor Research and Treatment(3)

Publications15 total

Using germline genotype in cancer pharmacogenetic studies
UNC Libraries·2020Open Access
Platinum neurotoxicity pharmacogenetics
UNC Libraries·2020· 21 citedOpen Access
Using Germline Genotype in Cancer Pharmacogenetic Studies
Pharmacogenomics·2009· 37 citedOpen Access
Platinum neurotoxicity pharmacogenetics
Molecular Cancer Therapeutics·2009· 552 citedOpen Access
Familial Gastrointestinal Stromal Tumors and Germ-Line Mutations
New England Journal of Medicine·2007· 221 citedOpen Access
Clinical and molecular genetics of patients with the Carney–Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD
European Journal of Human Genetics·2007· 482 citedOpen Access
Genetics of Carney Triad: Recurrent Losses at Chromosome 1 but Lack of Germline Mutations in Genes Associated with Paragangliomas and Gastrointestinal Stromal Tumors
The Journal of Clinical Endocrinology & Metabolism·2007· 150 citedOpen Access
Germline<i>NF1</i>Mutational Spectra and Loss-of-Heterozygosity Analyses in Patients with Pheochromocytoma and Neurofibromatosis Type 1
The Journal of Clinical Endocrinology & Metabolism·2007· 134 cited
Functioning Paraganglioma and Gastrointestinal Stromal Tumor of the Jejunum in Three Women
The American Journal of Surgical Pathology·2006· 35 cited
Role of tumor supressor genes in neuroendocrine neoplasias and cardiovascular disease
OhioLink ETD Center (Ohio Library and Information Network)·2005Open Access
Large Germline Deletions of Mitochondrial Complex II Subunits SDHB and SDHD in Hereditary Paraganglioma
The Journal of Clinical Endocrinology & Metabolism·2004· 90 citedOpen Access
Early-Onset Renal Cell Carcinoma as a Novel Extraparaganglial Component of SDHB-Associated Heritable Paraganglioma
The American Journal of Human Genetics·2004· 387 citedOpen Access
Intronic Single Nucleotide Polymorphisms in the<i>RET</i>Protooncogene Are Associated with a Subset of Apparently Sporadic Pheochromocytoma and May Modulate Age of Onset
The Journal of Clinical Endocrinology & Metabolism·2003· 26 citedOpen Access
Mutazioni germinali nel feocromocitoma non sindromico
L Endocrinologo·2003
Germ-Line Mutations in Nonsyndromic Pheochromocytoma
New England Journal of Medicine·2002· 1.4k citedOpen Access

Frequent Co-authors

Charis Eng(9), Andrzej Januszewicz(5), Mariola Pęczkowska(5), Hartmut P.H. Neumann(4), Constantine A. Stratakis(4), Birke Bausch(3), Oliver Gimm(3), Howard L. McLeod(3), Barbara Pasini(3), Thalia Bei(3), Sotirios Stergiopoulos(3), Joachim Klisch(2), Carsten Altehoefer(2), Klaus Zerres(2), Wendy M. Smith(2), R. Munk(2), Tanja Manz(2), S. Glaesker(2), Thomas W. Apel(2), M. Treier(2)