Katelyn E. Burgess

Copy-Number Disorders Are a Common Cause of Congenital Kidney Malformations

Simone Sanna‐Cherchi, Krzysztof Kiryluk, Katelyn E. Burgess et al. · The American Journal of Human Genetics · 2012 · 233 citations · Full text

Medicine, Genetics, Molecular Genetics +16

Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome

Simone Sanna‐Cherchi, Katelyn E. Burgess, Shannon N. Nees et al. · Kidney International · 2011 · 80 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

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 E. Burgess et al. · Pediatric Nephrology · 2013 · 20 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14