High frequency of kidney and urinary tract anomalies in asymptomatic first-degree relatives of patients with CAKUT

Traditional and targeted exome sequencing reveals common, rare and novel functional deleterious variants in RET-signaling complex in a cohort of living US patients with urinary tract malformations

(2012) Rajshekhar Chatterjee et al.   HUMAN GENETICS

Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis

(2011) Pawaree Saisawat et al.   KIDNEY INTERNATIONAL

Novel perspectives for investigating congenital anomalies of the kidney and urinary tract (CAKUT)

(2011) K. Y. Renkema et al.   NEPHROLOGY DIALYSIS TRANSPLANTATION

Maternal Risk Factors for Congenital Urinary Anomalies: Results of a Population-based Case-control Study

(2011) Margarett Shnorhavorian et al.   UROLOGY

Organotypic specificity of key RET adaptor-docking sites in the pathogenesis of neurocristopathies and renal malformations in mice

(2010) Sanjay Jain et al.   JOURNAL OF CLINICAL INVESTIGATION

Chapter 14: Demography of the UK Paediatric Renal Replacement Therapy population in 2008

(2010) Malcolm A. Lewis et al.   NEPHRON CLINICAL PRACTICE

Genetics of congenital anomalies of the kidney and urinary tract

(2010) Renfang Song et al.   PEDIATRIC NEPHROLOGY

Clinical characteristics and outcomes of children with stage 3–5 chronic kidney disease

(2010) Tran Thi Mong Hiep et al.   PEDIATRIC NEPHROLOGY

Renal Aplasia in Humans Is Associated with RET Mutations

(2008) Michael A. Skinner et al.   AMERICAN JOURNAL OF HUMAN GENETICS

SIX2 and BMP4 Mutations Associate With Anomalous Kidney Development

(2008) S. Weber et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Chronic kidney disease in children in Turkey

(2008) Kenan Bek et al.   PEDIATRIC NEPHROLOGY