JillianKateriWarejkoMD

PubMed

• 137 citations
  Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly.
  Daniela A. Braun, Jia Rao, Géraldine Mollet, David Schapiro, Marie Claire Daugeron
  Nature Genetics. 2017-10-01
• 141 citations
  Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome
  Jillian K. Warejko, Weizhen Tan, Ankana Daga, David Schapiro, Jennifer A. Lawson
  Clinical Journal of the American Society of Nephrology. 2018-01-06
• 30 citations
  Analysis of 24 genes reveals a monogenic cause in 11.1% of cases with steroid-resistant nephrotic syndrome at a single center.
  Weizhen Tan, Svjetlana Lovric, Shazia Ashraf, Jia Rao, David Schapiro
  Pediatric Nephrology. 2018-02-01

Journal Articles

• Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract  
  Deborah R Stein, Friedhelm Hildebrandt, Richard P Lifton, Amar J Majmundar, Nina Mann, Jillian K Warejko, Michelle A Baum, Asaf Vivante, Nancy M Rodig, Jing Chen, Mich..., Journal of the American Society of Nephrology
• Mutations in WDR4 as a New Cause of Galloway–Mowat Syndrome  
  Amar J Majmundar, Jillian K Warejko, Jing Chen, Friedhelm Hildebrandt, Ankana Daga, American Journal of Medical Genetics Part A
• GAPVD1 and ANKFY1 Mutations Implicate RAB5 Regulation in Nephrotic Syndrome  
  Jillian K Warejko, Friedhelm Hildebrandt, Amar J Majmundar, Heidi L Rehm, Richard P Lifton, Laura S Finn, Ankana Daga, Journal of the American Society of Nephrology