Senguttuvan, Prabha

Top Publications

Top Publications Authored or Co-Authored by "Senguttuvan, Prabha"

• A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome

  Journal of the American Society of Nephrology, Volume 26, No. 6, Year 2015, Citations 489
• Whole-exome sequencing identifies causative mutations in families with congenital anomalies of the kidney and urinary tract

  Journal of the American Society of Nephrology, Volume 29, No. 9, Year 2018, Citations 129
• Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations

  American Journal of Human Genetics, Volume 107, No. 4, Year 2020, Citations 99
• Exome sequencing discerns syndromes in patients from consanguineous families with congenital anomalies of the kidneys and urinary tract

  Journal of the American Society of Nephrology, Volume 28, No. 1, Year 2017, Citations 75
• Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract

  European Urology Open Science, Volume 44, Year 2022, Citations 36