JillianKateriWarejkoMD

PubMed

• 4 citations
  Epidemiology and Risk Factors for Hemodialysis Access-Associated Infections in Children: A Prospective Cohort Study From the SCOPE Collaborative.
  Rebecca L Ruebner, Heidi Gruhler De Souza, Troy Richardson, Badreldin Bedri, Olivera Marsenic, Franca Iorember, Jillian K Warejko, Bradley A Warady, Alicia M Neu> ;American Journal of Kidney Diseases. 2022 Aug 1
• 1 citations
  An unusual cause of relapsing peritonitis in a patient on peritoneal dialysis.
  James T Nugent, Christine Crana, Jillian K Warejko> ;Seminars in Dialysis. 2022 Nov 1
• 1 citations
  The scope of treatment of pediatric IgA vasculitis nephritis and its outcome: a Pediatric Nephrology Research Consortium study.
  Mahmoud Kallash, Beth A Vogt, Ahmed Zeid, Ei Khin, Mohammed Najjar, Ahmad Aldughiem, Elizabeth Benoit, Brian Stotter, Michelle Rheault, Jillian K Warejko, Ankana Daga> ;Pediatric Nephrology. 2022 Nov 1
• 1 citations
  An initiative to improve pneumococcal immunization counseling in children with nephrotic syndrome.
  Ibrahim Sandokji, Linda S Anderson, Jillian K. Warejko, Beth L. Emerson, Jason H. Greenberg> ;Pediatric Nephrology. 2021 Nov 3
• Fanconi syndrome, nephrotic-range proteinuria, and hypoalbuminemia in a newborn-Occam's razor or Hickam's dictum? Answers.
  James T Nugent, Juliann Reardon, Christine Crana, Jason H Greenberg, Jillian K Warejko, Julie E Goodwin> ;Pediatric Nephrology. 2022 Jan 1
• Fanconi syndrome, nephrotic-range proteinuria, and hypoalbuminemia in a newborn-Occam's razor or Hickam's dictum? Questions.
  James T Nugent, Juliann Reardon, Christine Crana, Jason H Greenberg, Jillian K Warejko, Julie E Goodwin> ;Pediatric Nephrology. 2022 Jan 1
• 2 citations
  Atypical hemolytic uremic syndrome due to DGKE mutation and response to eculizumab: lessons for the clinical nephrologist.
  Danya Husain, Brian Barron, Anya Golkowski Barron, Ibrahim Sandokji, Olivera Marsenic, Jillian K. Warejko> ;Journal of Nephrology. 2021 Mar 22
• 8 citations
  Identification of novel mutations and phenotype in the steroid resistant nephrotic syndrome gene NUP93 : a case report
  Ibrahim Sandokji, Jonathan Marquez, Weizhen Ji, Cynthia A. Zerillo, Monica Konstantino, Saquib A. Lakhani, Mustafa K. Khokha, Jillian K. Warejko> ;BMC Nephrology. 2019 Jul 17
• 19 citations
  Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome.
  Daniela A. Braun, Jillian K. Warejko, Shazia Ashraf, Weizhen Tan, Ankana Daga, Ronen Schneider, Tobias Hermle, Tilman Jobst-Schwan, Eugen Widmeier, Amar J. Majmundar, ...> ;Nephrology, Dialysis, Transplantation. 2019 Mar 1
• 12 citations
  Panel sequencing distinguishes monogenic forms of nephritis from nephrosis in children
  David Schapiro, Ankana Daga, Jennifer A. Lawson, Amar J. Majmundar, Svjetlana Lovric, Weizhen Tan, Jillian K. Warejko, Inés Fessi, Jia Rao, Merlin Airik, Heon Yung Gee...> ;Nephrology, Dialysis, Transplantation. 2019 Mar 1
• 78 citations
  Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients.
  Nina Mann, Daniela A. Braun, Kassaundra Amann, Weizhen Tan, Shirlee Shril, Dervla M. Connaughton, Makiko Nakayama, Ronen Schneider, Thomas M. Kitzler, Amelie T. van de...> ;Journal of the American Society of Nephrology. 2019 Feb 1
• 47 citations
  Mutations in WDR4 as a new cause of Galloway-Mowat syndrome.
  Daniela A. Braun, Shirlee Shril, Aditi Sinha, Ronen Schneider, Weizhen Tan, Shazia Ashraf, Tobias Hermle, Tilman Jobst-Schwan, Eugen Widmeier, Amar J. Majmundar, Ankan...> ;American Journal of Medical Genetics. Part A. 2018 Aug 6
• 64 citations
  Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome
  Daniela A. Braun, Svjetlana Lovric, David Schapiro, Ronen Schneider, Jonathan Marquez, M. Asif, Muhammad Sajid Hussain, Ankana Daga, Eugen Widmeier, Jia Rao, Shazia As...> ;The Journal of Clinical Investigation. 2018 Oct 1
• 112 citations
  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, Nina Mann, Makiko Nakayama, Jing Chen, Asaf Vivante, Daw-Yang Hwang, Julian Schulz, Daniela A. Braun, Johann...> ;Journal of the American Society of Nephrology. 2018 Sep 1
• 32 citations
  GAPVD1 and ANKFY1 Mutations Implicate RAB5 Regulation in Nephrotic Syndrome
  Tobias Hermle, Ronen Schneider, David Schapiro, Daniela A. Braun, Amelie T. van der Ven, Jillian K. Warejko, Ankana Daga, Eugen Widmeier, Makiko Nakayama, Tilman Jobst...> ;Journal of the American Society of Nephrology. 2018 Aug 1
• 73 citations
  Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment.
  Shazia Ashraf, Hiroki Kudo, Jia Rao, Atsuo Kikuchi, Eugen Widmeier, Jennifer A. Lawson, Weizhen Tan, Tobias Hermle, Jillian K. Warejko, Shirlee Shril, Merlin Airik, Ti...> ;Nature Communications. 2018 May 17
• 9 citations
  Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome.
  , , , , , , , , , , , , , , , , , , , , , , , , , , > ;Hypertension. 2018 Apr 1
• 26 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, Merlin Airik, Shirlee Shril, Heon Yung Gee, Michelle A. Baum, Ghaleb Daouk, Michael A. J. Fergus...> ;Pediatric Nephrology. 2018 Feb 1
• 130 citations
  Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome
  Jillian K. Warejko, Weizhen Tan, Ankana Daga, David Schapiro, Jennifer A. Lawson, Shirlee Shril, Svjetlana Lovric, Shazia Ashraf, Jia Rao, Tobias Hermle, Tilman Jobst-...> ;Clinical Journal of the American Society of Nephrology. 2018 Jan 6
• 110 citations
  Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis
  Ankana Daga, Amar J. Majmundar, Daniela A. Braun, Heon Yung Gee, Jennifer A. Lawson, Shirlee Shril, Tilman Jobst-Schwan, Asaf Vivante, David Schapiro, Weizhen Tan, Jil...> ;Kidney International. 2018 Jan 1
• 31 citations
  Advillin acts upstream of phospholipase C ϵ1 in steroid-resistant nephrotic syndrome
  Jia Rao, Shazia Ashraf, Weizhen Tan, Amelie T. van der Ven, Heon Yung Gee, Daniela A. Braun, Krisztina Fehér, Sudeep P. George, Amin Esmaeilniakooshkghazi, Won-Il Choi...> ;The Journal of Clinical Investigation. 2017 Oct 23
• 127 citations
  Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly.
  Daniela A. Braun, Jia Rao, Géraldine Mollet, David Schapiro, Marie Claire Daugeron, Weizhen Tan, Olivier Gribouval, Olivia Boyer, Patrick Revy, Tilman Jobst-Schwan, Jo...> ;Nature Genetics. 2017 Oct 1
• 11 citations
  Single-center experience in pediatric renal transplantation using thymoglobulin induction and steroid minimization.
  Jillian K. Warejko, S. Paul Hmiel> ;Pediatric Transplantation. 2014 Dec 1
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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