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, Ali G. Gharavi, Anna Latos-Bielenska> ;Pediatric Nephrology. 2014 Feb 1
• 162 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, Dexter Hadley, Shannon N. Nees, Miguel Verbitsky, Brittany J. Pe...> ;American Journal of Human Genetics. 2012 Dec 7
• 57 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, Monica Dagnino, Monica Bodria, Alba Carrea, Maddalena Allegretta, ...> ;Kidney International. 2011 Aug 2

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