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drs. K.L.L. (Kirsten) Cuba

drs. K.L.L. (Kirsten) Cuba

Assistant Professor

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Research Output (80)

AGORA, a data- and biobank for birth defects and childhood cancer

van Rooij Iris A L M, van der Zanden Loes F M, Bongers Ernie M H F, Renkema Kirsten Y, Wijers Charlotte H W, Thonissen Michelle, Dokter Elisabeth M J, Marcelis Carlo L M, de Blaauw Ivo, Wijnen Marc H W A, Hoogerbrugge Peter M, Bokkerink Jos P M, Schreuder Michiel F, Koster-Kamphuis Linda, Cornelissen Elisabeth A M, Kapusta Livia, van Heijst Arno F J, Liem Kian D, de Gier Robert P E, Kuijpers-Jagtman Anne Marie, Admiraal Ronald J C, Bergé Stefaan J, van der Biezen Jan Jaap, Verdonck An, Vander Poorten Vincent, Hens Greet, Roosenboom Jasmien, Lilien Marc R, de Jong Tom P, Broens Paul, Wijnen Rene, Brooks Alice, Franke Barbara, Brunner Han G, Carels Carine E L, Knoers Nine V A M, Feitz Wout F J, Roeleveld Nel Aug 2016, In: Birth Defects Research Part A - Clinical and Molecular Teratology. 106 , p. 675–684

Maternal risk factors involved in specific congenital anomalies of the kidney and urinary tract:A case-control study

Groen In 't Woud Sander, Renkema Kirsten Y, Schreuder Michiel F, Wijers Charlotte H W, van der Zanden Loes F M, Knoers Nine V A M, Feitz Wout F J, Bongers Ernie M H F, Roeleveld Nel, van Rooij Iris A L M 4 Apr 2016, In: Birth Defects Research Part A - Clinical and Molecular Teratology. 106 , p. 596–603

De novo 14q24.2q24.3 microdeletion including IFT43 is associated with intellectual disability, skeletal anomalies, cardiac anomalies, and myopia

Stokman Marijn F, Oud Machteld M, van Binsbergen Ellen, Slaats Gisela G, Nicolaou Nayia, Renkema Kirsten Y, Nijman Isaac J , Roepman Ronald, Giles Rachel H, Arts Heleen H, Knoers Nine V A M, van Haelst Mieke M 19 Feb 2016, In: American Journal of Medical Genetics. Part A. 170 , p. 1566-1569

Prioritization and burden analysis of rare variants in 208 candidate genes suggest they do not play a major role in CAKUT

Nicolaou Nayia, Pulit Sara L, Nijman Isaac J, Monroe Glen R, Feitz Wout F J, Schreuder Michiel F, van Eerde Albertien M, de Jong Tom P V M, Giltay Jacques C, van der Zwaag Bert, Havenith Marlies R, Zwakenberg Susan, van der Zanden Loes F M, Poelmans Geert, Cornelissen Elisabeth A M, Lilien Marc R, Franke Barbara, Roeleveld Nel, van Rooij Iris A L M, Cuppen Edwin, Bongers Ernie M H F, Giles Rachel H, Knoers Nine V A M, Renkema Kirsten Y Feb 2016, In: Kidney International. 89 , p. 476-86 11 p.

Wnt5a Deficiency Leads to Anomalies in Ureteric Tree Development, Tubular Epithelial Cell Organization and Basement Membrane Integrity Pointing to a Role in Kidney Collecting Duct Patterning

Pietilä Ilkka, Prunskaite-Hyyryläinen Renata, Kaisto Susanna, Tika Elisavet, van Eerde Albertien M, Salo Antti M, Garma Leonardo, Miinalainen Ilkka, Feitz Wout F, Bongers Ernie M H F, Juffer André, Knoers Nine V A M, Renkema Kirsten Y, Myllyharju Johanna, Vainio Seppo J 2016, In: PLoS ONE [E]. 11 15 p.

Genetic, environmental, and epigenetic factors involved in CAKUT

Nicolaou Nayia, Renkema Kirsten Y, Bongers Ernie M H F, Giles Rachel H, Knoers Nine V A M Dec 2015, In: Nature Reviews. Nephrology. 11 , p. 720-731 12 p.

TARGETED PANEL SEQUENCING OF 399 RENAL GENES RECLASSIFIES PRIMARY DISEASE DIAGNOSES IN YOUNG ESRD PATIENTS

Van Eerde Albertien M., De Borst Martin H., Van der Zwaag Bert, Peters Edith J., Renkema Kirsten Y., Elferink Martin, Van Zon Patrick H. A., Lilien Marc R., Van Haaften Gijs W., Giles Rachel H., Navis Gerjan J., Knoers Nine V. A. M. Sep 2015, In: Pediatric Nephrology. 30 , p. 1548-1548 1 p.

KOUNCIL:Kidney-Oriented Understanding of Correcting Ciliopathies

Stokman M., Oud M., Van Reeuwijk J., Lilien M., Van De Kar N., Nijman I., Gilissen C., Kroes H. Y., Bongers E., Geijsen N., Kamsteeg E., Cuppen E., Roepman R., Giles R., Renkema K., Arts H., Knoers N. 13 Jul 2015, In: Cilia [E]. 4

Mutations of the SLIT2–ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract

Hwang Daw Yang, Kohl Stefan, Fan Xueping, Vivante Asaf, Chan Stefanie, Dworschak Gabriel C., Schulz Julian, van Eerde Albertien M., Hilger Alina C., Gee Heon Yung, Pennimpede Tracie, Herrmann Bernhard G., van de Hoek Glenn, Renkema Kirsten Y., Schell Christoph, Huber Tobias B., Reutter Heiko M., Soliman Neveen A., Stajic Natasa, Bogdanovic Radovan, Kehinde Elijah O., Lifton Richard P., Tasic Velibor, Lu Weining, Hildebrandt Friedhelm 31 May 2015, In: Human Genetics. 134 , p. 905-916 12 p.

Diabetes-Induced Congenital Anomalies of the Kidney and Urinary Tract (CAKUT):Nurture and Nature at Work?

Renkema Kirsten Y., Verhaar Marianne C., Knoers Nine V. A. M. May 2015, In: American Journal of Kidney Diseases. 65 , p. 644-646 3 p.

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