Concepedia

Pawaree Saisawat

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Publications

13

Citations

1.7K

H-Index

12

Active since

2009

Affiliations

University of Michigan(Current)

Howard Hughes Medical Institute

Boston Children's Hospital

Harvard University

Children's Clinical University Hospital

Pawaree Saisawat is an author at University of Michigan specializing in medicine, genetics, and molecular genetics.

ORCID

Top concepts

Publications per year

2009–2022

13

Publications

13

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness

Saskia F. Heeringa, Gil Chernin, Moumita Chaki et al. · Journal of Clinical Investigation · 2011 · 394 citations · Full text

Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract

Daw‐Yang Hwang, Gabriel C. Dworschak, Stefan Kohl et al. · Kidney International · 2014 · 256 citations · Full text

ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling

Heon Yung Gee, Pawaree Saisawat, Shazia Ashraf et al. · Journal of Clinical Investigation · 2013 · 226 citations · Full text

, , +15

Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association

Pawaree Saisawat, Stefan Kohl, Alina C. Hilger et al. · Kidney International · 2013 · 127 citations · Full text

, , +9

Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations

Gil Chernin, Virginia Vega-Warner, Dominik S. Schoeb et al. · Clinical Journal of the American Society of Nephrology · 2010 · 109 citations · Full text

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