Saisawat, Pawaree

Top Publications

Top Publications Authored or Co-Authored by "Saisawat, Pawaree"

• ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling

  Journal of Clinical Investigation, Volume 123, No. 8, Year 2013, Citations 208
• Exome sequencing reveals cubilin mutation as a single-gene cause of proteinuria

  Journal of the American Society of Nephrology, Volume 22, No. 10, Year 2011, Citations 95
• Mild recessive mutations in six fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract

  Journal of the American Society of Nephrology, Volume 25, No. 9, Year 2014, Citations 94
• Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS)

  Nephrology Dialysis Transplantation, Volume 25, No. 9, Year 2010, Citations 83
• Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis

  Kidney International, Volume 81, No. 2, Year 2012, Citations 80