Kirsten Y. Renkema

Utrecht, UT, Netherlands

Last Updated: 09/26/2026

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Found 30 publications

Increased mTOR signaling secondary to a human ILK missense variant inhibits nephrogenesis with decreased metabolism.

Increased mTOR signaling secondary to a human ILK missense variant inhibits nephrogenesis with decreased metabolism.

Journal: Mechanisms of ageing and development

Published: June 24, 2025

Translational strategies to uncover the etiology of congenital anomalies of the kidney and urinary tract.

Translational strategies to uncover the etiology of congenital anomalies of the kidney and urinary tract.

Journal: Pediatric nephrology (Berlin, Germany)

Published: May 31, 2024

A Genome-Wide Association Study into the Aetiology of Congenital Solitary Functioning Kidney.

A Genome-Wide Association Study into the Aetiology of Congenital Solitary Functioning Kidney.

Journal: Biomedicines

Published: October 05, 2022

Uncovering risk factors for kidney injury in children with a solitary functioning kidney.

Uncovering risk factors for kidney injury in children with a solitary functioning kidney.

Journal: Kidney international

Published: June 02, 2022

CDH12 as a Candidate Gene for Kidney Injury in Posterior Urethral Valve Cases: A Genome-wide Association Study Among Patients with Obstructive Uropathies.

CDH12 as a Candidate Gene for Kidney Injury in Posterior Urethral Valve Cases: A Genome-wide Association Study Among Patients with Obstructive Uropathies.

Journal: European urology open science

Published: April 08, 2021

mTOR-Activating Mutations in RRAGD Are Causative for Kidney Tubulopathy and Cardiomyopathy.

mTOR-Activating Mutations in RRAGD Are Causative for Kidney Tubulopathy and Cardiomyopathy.

Journal: Journal of the American Society of Nephrology : JASN

Published: March 12, 2021

Maternal risk associated with the VACTERL association: A case-control study.

Maternal risk associated with the VACTERL association: A case-control study.

Journal: Birth defects research

Published: May 25, 2020

Clinical Integration of Genome Diagnostics for Congenital Anomalies of the Kidney and Urinary Tract.

Clinical Integration of Genome Diagnostics for Congenital Anomalies of the Kidney and Urinary Tract.

Journal: Clinical journal of the American Society of Nephrology : CJASN

Published: April 22, 2020

The genomic landscape of CAKUT; you gain some, you lose some.

The genomic landscape of CAKUT; you gain some, you lose some.

Journal: Kidney international

Published: February 11, 2019

The KOUNCIL Consortium: From Genetic Defects to Therapeutic Development for Nephronophthisis.

The KOUNCIL Consortium: From Genetic Defects to Therapeutic Development for Nephronophthisis.

Journal: Frontiers in pediatrics

Published: February 09, 2018

Impact of next generation sequencing on our understanding of CAKUT.

Impact of next generation sequencing on our understanding of CAKUT.

Journal: Seminars in cell & developmental biology

Published: December 25, 2017

Clinical and genetic analyses of a Dutch cohort of 40 patients with a nephronophthisis-related ciliopathy.

Clinical and genetic analyses of a Dutch cohort of 40 patients with a nephronophthisis-related ciliopathy.

Journal: Pediatric nephrology (Berlin, Germany)

Published: December 09, 2017

Showing 1-12 of 30

Last Updated: 09/26/2026