KatelynElizabethBurgessMD

PubMed

• 16 citations
  The emerging role of genomics in the diagnosis and workup of congenital urinary tract defects: a novel deletion syndrome on chromosome 3q13.31-22.1
  Anna Materna-Kiryluk, Krzysztof Kiryluk, Katelyn Elizabeth Burgess, Arkadiusz Bieleninik, Simone Sanna-Cherchi
  Pediatric Nephrology. 2014-02-01
• 165 citations
  Copy-Number Disorders Are a Common Cause of Congenital Kidney Malformations
  Simone Sanna-Cherchi, Krzysztof Kiryluk, Katelyn Elizabeth Burgess, Monica Bodria, Matthew G. Sampson
  American Journal of Human Genetics. 2012-12-07
• 55 citations
  Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome
  Simone Sanna-Cherchi, Katelyn Elizabeth Burgess, Shannon N. Nees, Gianluca Caridi, Patricia L. Weng
  Kidney International. 2011-08-02

Journal Articles

• Mutations in DSTYK and dominant urinary tract malformations  
  Sanna-Cherchi S, Sampogna RV, Papeta N, Burgess KE, Nees SN, Perry BJ, Choi M, Bodria M, Liu Y, Weng PL, Lozanovski VJ, Verbitsky M, Lugani F, Sterken R, Paragas N, Ca..., New England Journal of Medicine, 8/15/2013
• Copy-number disorders are a common cause of congenital kidney malformations.  
  Sanna-Cherchi S, Kiryluk K, Burgess KE, Bodria M, Sampson MG, Hadley D, Nees SN, Verbitsky M, Perry BJ, Sterken R, Lozanovski VJ, Materna-Kiryluk A, Barlassina C, Kini..., Am J Hum Genet, 11/15/2012