Kitzler, Thomas M.

Top Publications

Top Publications Authored or Co-Authored by "Kitzler, Thomas M."

• 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
• Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome

  Journal of Clinical Investigation, Volume 128, No. 10, Year 2018, Citations 73
• Mutations in PRDM15 are a novel cause of galloway-mowat syndrome

  Journal of the American Society of Nephrology, Volume 32, No. 3, Year 2021, Citations 43
• Recessive NOS1AP variants impair actin remodeling and cause glomerulopathy in humans and mice

  Science Advances, Volume 7, No. 1, Article eabe1386, Year 2021, Citations 39