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dr. K.Y. (Kirsten) Renkema

dr. K.Y. (Kirsten) Renkema

Assistant Professor

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Research Output (80)

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

Schlingmann Karl P, Jouret François, Shen Kuang, Nigam Anukrati, Arjona Francisco J, Dafinger Claudia, Houillier Pascal, Jones Deborah P, Kleinerüschkamp Felix, Oh Jun, Godefroid Nathalie, Eltan Mehmet, Güran Tülay, Burtey Stéphane, Parotte Marie-Christine, König Jens, Braun Alina, Bos Caro, Ibars Serra Maria, Rehmann Holger, Zwartkruis Fried J T, Renkema Kirsten Y, Klingel Karin, Schulze-Bahr Eric, Schermer Bernhard, Bergmann Carsten, Altmüller Janine, Thiele Holger, Beck Bodo B, Dahan Karin, Sabatini David, Liebau Max C, Vargas-Poussou Rosa, Knoers Nine V A M, Konrad Martin, de Baaij Jeroen H F Nov 2021, In: Journal of the American Society of Nephrology. 32 , p. 2885-2899 15 p.

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

van der Zanden Loes F M, van Rooij Iris A L M, Quaedackers Josine S L T, Nijman Rien J M, Steffens Martijn, de Wall Liesbeth L L, Bongers Ernie M H F, Schaefer Franz, Kirchner Marietta, Behnisch Rouven, Bayazit Aysun K, Caliskan Salim, Obrycki Lukasz, Montini Giovanni, Duzova Ali, Wuttke Matthias, Jennings Rachel, Hanley Neil A, Milmoe Natalie J, Winyard Paul J D, Renkema Kirsten Y, Schreuder Michiel F, Roeleveld Nel, Feitz Wout F J Jun 2021, In: European Urology Open Science. 28 , p. 26-35 10 p.

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

Knoers Nine V.A.M., Renkema Kirsten Y. 1 Aug 2019, In: Kidney International. 96 , p. 267-269 3 p.

Impact of next generation sequencing on our understanding of CAKUT

Nigam Anukrati, Knoers Nine V.A.M., Renkema Kirsten Y. 1 Jul 2019, In: Seminars in Cell and Developmental Biology. 91 , p. 104-110 7 p.

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

Stokman Marijn F., van der Zwaag Bert, van de Kar Nicole C.A.J., van Haelst Mieke M., van Eerde Albertien M., van der Heijden Joost W., Kroes Hester Y., Ippel Elly, Schulp Annelien J.A., van Gassen Koen L., van Rooij Iris A.L.M., Giles Rachel H., Beales Philip L., Roepman Ronald, Arts Heleen H., Bongers Ernie M.H.F., Renkema Kirsten Y., Knoers Nine V.A.M., van Reeuwijk Jeroen, Lilien Marc R. 1 Oct 2018, In: Pediatric Nephrology. 33 , p. 1701-1712 12 p.

Changes in the urinary extracellular vesicle proteome are associated with nephronophthisis-related ciliopathies

Stokman Marijn F., Bijnsdorp Irene V., Schelfhorst Tim, Pham Thang V., Piersma Sander R., Knol Jaco C., Giles Rachel H., Bongers Ernie M.H.F., Knoers Nine V.A.M., Lilien Marc R., Jiménez Connie R., Renkema Kirsten Y. 30 Jul 2018, In: Journal of Proteomics. 192 , p. 27-36 10 p.

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

Renkema Kirsten Y, Giles Rachel H, Lilien Marc R, Beales Philip L, Roepman Ronald, Oud Machteld M, Arts Heleen H, Knoers Nine V A M 2018, In: Frontiers in Pediatrics. 6 7 p.

PDE3A gene screening improves diagnostics for patients with Bilginturan syndrome (hypertension and brachydactyly syndrome)

Renkema Kirsten Y., Westermann Jonne M., Nievelstein Rutger A.J., Lo-A-Njoe Shirley M., van der Zwaag Bert, Manshande Meindert E., van Haelst Mieke M. 2018, In: Hypertension Research. 41 , p. 981-988

Genetics of kidney disease in 2016:Ingenious tactics to unravel complex kidney disease genetics

Renkema Kirsten Y, Knoers Nine V A M 19 Jan 2017, In: Nature Reviews. Nephrology. 13 , p. 67-68 2 p.

The expanding phenotypic spectra of kidney diseases:Insights from genetic studies

Stokman Marijn F., Renkema Kirsten Y., Giles Rachel H., Schaefer Franz, Knoers Nine V.A.M., Van Eerde Albertien M. 1 Aug 2016, In: Nature Reviews. Nephrology. 12 , p. 472-483 12 p.

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