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dr. A.M. van Eerde

dr. A.M. van Eerde

Assistant Professor - medical

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Research Output (68)

NPHP1 (Nephrocystin-1) gene deletions cause adult-onset ESRD

Snoek Rozemarijn, Van Setten Jessica, Keating Brendan J., Israni Ajay K., Jacobson Pamala A., Oetting William S., Matas Arthur J., Mannon Roslyn B., Zhang Zhongyang, Zhang Weijia, Hao Ke, Murphy Barbara, Reindl-Schwaighofer Roman, Heinzl Andreas, Oberbauer Rainer, Viklicky Ondrej, Conlon Peter J., Stapleton Caragh P., Bakker Stephan J.L., Snieder Harold, Peters Edith D.J., Van Der Zwaag Bert, Knoers Nine V.A.M., De Borst Martin H., Van Eerde Albertien M. 13 apr 2018, In: Journal of the American Society of Nephrology. 29 , p. 1772-1779 8 p.

Importance of reliable variant calling and clear phenotyping when reporting on gene panel testing in renal disease

Snoek Rozemarijn, van Eerde Albertien M, Knoers Nine V A M dec 2017, In: Kidney International. 92 , p. 1325-1327 3 p.

A questionnaire survey of radiological diagnosis and management of renal dysplasia in children

Montini Giovanni, Busutti Marco, Yalcinkaya Fatos, Woolf Adrian S, Weber Stefanie, , van Eerde Albertien 24 jun 2017, In: Journal of Nephrology. 31 , p. 95-102 8 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.

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.

Pre-pregnancy advice in chronic kidney disease:do not forget genetic counseling

van Eerde Albertien M, Krediet C T Paul, Rookmaaker Maarten B, van Reekum Franka E, Knoers Nine V A M, Lely A Titia 2016, In: Kidney International. 90 , p. 905-906 2 p.

Management of a Giant Omphalocele with Non-Cross-Linked Intact Porcine-Derived Acellular Dermal Matrix (Strattice) Combined with Vacuum Therapy

Travassos Daisy Vieira, van Eerde Albertien M, Kramer William L M dec 2015, In: European journal of pediatric surgery reports. 3 , p. 61-3 3 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.

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 mei 2015, In: Human Genetics. 134 , p. 905-916 12 p.

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