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 Michelle
P. Winn, MD, is an Associate Professor in the Division
of Nephrology, Department of Medicine. Dr. Winn is
a board certified nephrologist. Her research interests include
the hereditary diseases of the human kidney. She is currently
focusing her research on familial
focal segmental glomerulosclerosis. Her other interests
include complex diseases in relation to kidney function such
as hypertensive nephropathy, end-stage renal disease and acute
renal failure.
MD, 1992, East Carolina University-School of Medicine, Greenville, NC
Residency in Internal Medicine, Duke University Medical School, Durham, NC
Fellowship in Nephrology, Duke University Medical Center, Durham, NC
Winn MP, Conlon PJ, Lynn KL, Farrington MK,
Creazzo T, Hawkins AF, Daskalakis N, Kwan SY, Ebersviller
S, Burchette JL, Pericak-Vance MA, Howell DN, Vance JM, Rosenberg
PB. A Mutation in the TRPC6 Cation Channel
Causes Familial Focal Segmental Glomerulosclerosis.
Science
2005 0: 1106215
Winn MP, Conlon PJ, Lynn KL, Howell DN, Gross
DA, Rogala AR, Smith AH, Graham FL, Bembe M, Quarles LD, Pericak-Vance
MA, Vance JM. Clinical and genetic heterogeneity
in familial focal segmental glomerulosclerosis. International
Collaborative Group for the Study of Familial Focal Segmental
Glomerulosclerosis. Kidney
International 55(4):1241-6, 1999.
Winn MP, Conlon PJ, Lynn KL, Howell DN, Slotterbeck BD, Smith
AH, Graham FL, Bembe M, Quarles LD, Pericak-Vance MA, Vance
JM. Linkage of a gene causing familial
focal segmental glomerulosclerosis to chromosome 11 and further
evidence of genetic heterogeneity. Genomics
58(2):113-20, 1999.
Conlon PJ, Lynn K, Winn MP, Quarles LD, Bembe ML, Pericak-Vance
M, Speer M, Howell DN. Spectrum of disease
in familial focal and segmental glomerulosclerosis.
Kidney
International 56(5):1863-71, 1999.
Contact:
Center for Human Genetics
DUMC Box 2903
Durham, NC 27710
Phone: 1-919-660-0038
Fax: 1-919-684-0920
E-mail: michelle.winn@duke.edu
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