Howard Trachtman
University of Michigan(US)University of Michigan–Ann Arbor(US)Michigan United(US)Michigan Medicine(US)
Publications by Year
Research Areas
Renal Diseases and Glomerulopathies, Chronic Kidney Disease and Diabetes, Complement system in diseases, Electrolyte and hormonal disorders, Pediatric Urology and Nephrology Studies
Most-Cited Works
- → Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III(1997)863 cited
- → APOL1 Genetic Variants in Focal Segmental Glomerulosclerosis and HIV-Associated Nephropathy(2011)844 cited
- → Genetic heterogeneity of Barter's syndrome revealed by mutations in the K+ channel, ROMK(1996)820 cited
- → MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis(2008)703 cited
- → Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities(2012)626 cited
- → Soluble Urokinase Receptor and Chronic Kidney Disease(2015)411 cited
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