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Matthias Wolf

Associate Professor · University of Michigan

Credentials: · · · · ·

History

University of Michigan
Present

Pediatric Nephrology
University of Texas Southwestern Medical Center
2009–2012
Pediatrics
1999–2002
Doctor of Medicine
1995–1999

Research

Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination
Nature Genetics · 2003 · 499 citations
The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome
Nature Genetics · 2007 · 385 citations
Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis
Nature Genetics · 2003 · 271 citations

FH
Friedhelm Hildebrandt
27 papers
John O'Toole
6 papers · 1 as a fellow
Eric Wise
4 papers
AM
Ahmad Mashmoushi
3 papers · 3 as a fellow
Anthony Bleyer
3 papers
Denise Marciano
3 papers
Abha Choudhary
2 papers
Chou-Long Huang
2 papers
Christie Thomas
2 papers
HT
Howard Trachtman
2 papers
Aakash Goyal
1 paper
AS
Abby Sunq
1 paper

Grants

Assay Development and Optimization for a High Throughput Screen to Detect Compounds Increasing Secretion of C150S Mutant Uromodulin
National Institute of Diabetes and Digestive and Kidney Diseases · R01
Contact PI · $1.8M · University of Michigan at Ann Arbor
2020–2026
Renal Regulation of the Magnesium Channel TRPM6 by Uromodulin
National Institute of Diabetes and Digestive and Kidney Diseases · R03
Contact PI · $162K · Ut Southwestern Medical Center
2017–2020
The Role of Uromodulin in the Regulation of the Renal Calcium Channel TRPV5
National Institute of Diabetes and Digestive and Kidney Diseases · K08
Contact PI · $581.3K · Ut Southwestern Medical Center
2012–2017