Michelle P. Winn - Concepedia

Author

Michelle P. Winn

Also Known As

A. A. Abdalla, Hall, Gentzon, Kelvin Lynn, M Winn, M. P. Winn, M. Winn, Michelle P Winn, Michelle P. Winn, Michelle Winn

Publications

4.3K

Citations

H-Index

Concepts

All Affiliations

Duke Medical Center Duke University Hospital Center for Human Genetics Duke University Beaumont Hospital

About

Michelle P. Winn is an author at Duke Medical Center specializing in medicine, nephrology, and glomerulonephritis.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	17	2.7K
2	Cell Biology	6	6	1.8K
3	Cellular Physiology	3	3	455
4	Public Health	2	2	144
5	Engineering	1	1	50

Michelle P. Winn

Publications

3.5K

Citations

H-Index

Page 1

	Year	Citations
A Mutation in the <i>TRPC6</i> Cation Channel Causes Familial Focal Segmental Glomerulosclerosis Michelle P. Winn, Peter J. Conlon, Kelvin L. Lynn, Science Glomerular DiseaseRenal PathologyImmunologyPathologyGlomerulonephritis	2005	1.1K
Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomerulosclerosis Shreeram Akilesh, Hani Suleiman, Haiyang Yu, Journal of Clinical Investigation Glomerular DiseaseSpecialized Epithelial CellPathologyCytoskeletonCellular Physiology	2011	259
Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis Andrew F. Malone, Paul J. Phelan, Gentzon Hall, Kidney International GlomerulonephritisUrologyRenal PathologyPathologyScleroderma	2014	232
TRPC1 Channels Are Critical for Hypertrophic Signaling in the Heart Malini Seth, Zhu-Shan Zhang, Lan Mao, Circulation Research	2009	220
Parkin mutations and susceptibility alleles in late‐onset Parkinson's disease Sofia A. Oliveira, William K. Scott, Eden R. Martin, Annals of Neurology	2003	211
Mutations in the Gene That Encodes the F-Actin Binding Protein Anillin Cause FSGS Rasheed Gbadegesin, Gentzon Hall, Adebowale Adeyemo, Journal of the American Society of Nephrology GeneticsRenal PathologyMolecular BiologyMolecular GeneticsCytoskeleton	2014	153
HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome Rasheed Gbadegesin, Adebowale Adeyemo, Nicholas J.A. Webb, Journal of the American Society of Nephrology	2014	145
TRPC6 Enhances Angiotensin II-induced Albuminuria Jason Eckel, Peter Lavin, Elizabeth Finch, Journal of the American Society of Nephrology Cellular PhysiologyMolecular PharmacologyGlomerulonephritisRenal FunctionTrpc6 Mutations	2011	130
A Hybrid CFHR3-1 Gene Causes Familial C3 Glomerulopathy Talat H. Malik, Peter Lavin, Elena Goicoechea de Jorge, Journal of the American Society of Nephrology GeneticsRenal PathologyImmunologyInnate Immune SystemPathology	2012	129
Linkage of a Gene Causing Familial Focal Segmental Glomerulosclerosis to Chromosome 11 and Further Evidence of Genetic Heterogeneity Michelle P. Winn, Peter J. Conlon, Kelvin L. Lynn, Genomics Glomerular DiseaseGlomerulonephritisMendelian DisorderGenetic DisorderMedicine	1999	126

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