Researchclopedia

Research Researchers Institutions Topics Submit About

Command Palette

Search for a command to run...

Researchclopedia

Research Researchers Institutions About

© 2026 Researchclopedia. Powered by OpenAlex under CC0 license.

Christopher N. Vlangos | Researchclopedia

Back to researchers

Christopher N. Vlangos

36

Works

5,707

Citations

24

h-index

27

i10-index

Research Topics

Genomic variations and chromosomal abnormalities Renal Diseases and Glomerulopathies Genomics and Rare Diseases

Affiliations

Virginia Commonwealth University2008–2016

University of Michigan–Ann Arbor2006–2013

Michigan United2009–2013

Michigan Medicine2007–2007

Tempus Labs (United States)2021–2023

Top Works

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics

Sarah S. Kalia,Kathy Adelman,et al.

20161,688 citations

Renal and related cancers

Genetic factors in colorectal cancer

Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible

Bernward Hinkes,Roger C. Wiggins,et al.

2006557 citations

ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

David T. Miller,Kristy Lee,et al.

2021553 citations

Nephrotic Syndrome in the First Year of Life: Two Thirds of Cases Are Caused by Mutations in 4 Genes (<i>NPHS1</i>, <i>NPHS2</i>, <i>WT1</i>, and <i>LAMB2</i>)

Bernward Hinkes,Bettina E. Mucha,et al.

2007435 citations

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness

Saskia F. Heeringa,Gil Chernin,et al.

2011394 citations

Mutations in RAI1 associated with Smith–Magenis syndrome

Rebecca E. Slager,Tiffany Lynn Newton,et al.

2003357 citations

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

David T. Miller,Kristy Lee,et al.

2021252 citations

A Novel TRPC6 Mutation That Causes Childhood FSGS

Saskia F. Heeringa,Clemens Möller,et al.

2009170 citations

A Systematic Approach to Mapping Recessive Disease Genes in Individuals from Outbred Populations

Friedhelm Hildebrandt,Saskia F. Heeringa,et al.

2009162 citations