Concepedia
Statistics
Publications
14
Citations
1.7K
H-Index
13
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 molecular genetics, genetics, and medicine.
Publications per year
2009–2023
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 · 400 citations · Full text
Medicine, Genetics, Molecular Genetics +17
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 · 262 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 · 237 citations · Full text
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 · 128 citations · Full text
Life Sciences, Genetics, Molecular Genetics +7
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 · 122 citations · Full text
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