Prabha Senguttuvan

Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract

Amelie T. van der Ven, Dervla M. Connaughton, Hadas Ityel et al. · Journal of the American Society of Nephrology · 2018 · 202 citations

Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary Tract

Asaf Vivante, Daw‐Yang Hwang, Stefan Kohl et al. · Journal of the American Society of Nephrology · 2016 · 96 citations · Full text

Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations

Dervla M. Connaughton, Rufeng Dai, Danielle Owen et al. · The American Journal of Human Genetics · 2020 · 49 citations · Full text

Medicine, Genetics, Developmental Biology +1

Infections encountered in childhood nephrotics in a pediatric renal unit

Prabha Senguttuvan, K Ravanan, N Prabhu et al. · Indian Journal of Nephrology · 2004 · 37 citations

Glomerulonephritis, Medicine, Kidney Failure +7

COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans

Thomas M. Kitzler, Ronen Schneider, Stefan Kohl et al. · Human Genetics · 2019 · 24 citations · Full text

Genetic Disorder, Medicine, Genetics +9