Structural investigations of the active‐site mutant Asn156Ala of outer membrane phospholipase A: Function of the Asn–His interaction in the catalytic triad von Snijder, H.J., Van Eerde, J.H., Kingma, R.L., Kalk, K.H., Dekker, N., Egmond, M.R., Dijkstra, B.W.

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Structure and Regulation of Outer Membrane Phospholipase A von Snijder, H. J., van Eerde, J. H., Kingma, R. L., Ubarretxena, I., Kalk, K. H., Verheij, H. M., Egmond, M. R., Dekker, N., Dijkstra, B. W.

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Gain of glycosylation in integrin α3 causes lung disease and nephrotic syndrome von Nicolaou, Nayia, Margadant, Coert, Kevelam, Sietske H, Lilien, Marc R, Oosterveld, Michiel J S, Kreft, Maaike, van Eerde, Albertien M, Pfundt, Rolph, Terhal, Paulien A, van der Zwaag, Bert, Nikkels, Peter G J, Sachs, Norman, Goldschmeding, Roel, Knoers, Nine V A M, Renkema, Kirsten Y, Sonnenberg, Arnoud

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Hypomagnesaemia with varying degrees of extrarenal symptoms as a consequence of heterozygous CNNM2 variants von Bosman, Willem, Franken, Gijs A. C., de las Heras, Javier, Madariaga, Leire, Barakat, Tahsin Stefan, Oostenbrink, Rianne, van Slegtenhorst, Marjon, Perdomo-Ramírez, Ana, Claverie-Martín, Félix, van Eerde, Albertien M., Vargas-Poussou, Rosa, Dubourg, Laurence Derain, González-Recio, Irene, Martínez-Cruz, Luis Alfonso, de Baaij, Jeroen H. F., Hoenderop, Joost G. J.

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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... von 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

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

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Genetics-first approach improves diagnostics of ESKD patients <50 years old von Snoek, Rozemarijn, van Jaarsveld, Richard H, Nguyen, Tri Q, Peters, Edith D J, Elferink, Martin G, Ernst, Robert F, Rookmaaker, Maarten B, Lilien, Marc R, Spierings, Eric, Goldschmeding, Roel, Knoers, Nine V A M, van der Zwaag, Bert, van Zuilen, Arjan D, van Eerde, Albertien M

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Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNA von Viering, Daan, Schlingmann, Karl P, Hureaux, Marguerite, Nijenhuis, Tom, Mallett, Andrew, Chan, Melanie M Y, van Beek, André, van Eerde, Albertien M, Coulibaly, Jean-Marie, Vallet, Marion, Decramer, Stéphane, Pelletier, Solenne, Klaus, Günter, Kömhoff, Martin, Beetz, Rolf, Patel, Chirag, Shenoy, Mohan, Steenbergen, Eric J, Anderson, Glenn, Bongers, Ernie M H F, Bergmann, Carsten, Panneman, Daan, Rodenburg, Richard J, Kleta, Robert, Houillier, Pascal, Konrad, Martin, Vargas-Poussou, Rosa, Knoers, Nine V A M, Bockenhauer, Detlef, de Baaij, Jeroen H F

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Atrial fibrillation: trends in prevalence and antithrombotic prescriptions in the community von Joosten, L. P. T., de Boer, A. R., van Eerde, E. J. B., van Doorn, S., Hoes, A. W., Bots, M. L., Rutten, F. H., Geersing, G. J.

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Sexual dimorphism in selenium deficiency is associated with metabolic syndrome and prevalence of heart disease von Weening, Eerde H, Al-Mubarak, Ali A, Dokter, Martin M, Dickstein, Kenneth, Lang, Chim C, Ng, Leong L, Metra, Marco, van Veldhuisen, Dirk J, Touw, Daan J, de Boer, Rudolf A, Gansevoort, Ron T, Voors, Adriaan A, Bakker, Stephan J L, van der Meer, Peter, Bomer, Nils

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

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Coffin-Siris Syndrome and the BAF Complex: Genotype-Phenotype Study in 63 Patients von Santen, Gijs W.E., Aten, Emmelien, Vulto-van Silfhout, Anneke T., Pottinger, Caroline, van Bon, Bregje W.M., van Minderhout, Ivonne J.H.M., Snowdowne, Ronelle, van der Lans, Christian A.C., Boogaard, Merel, Linssen, Margot M.L., Vijfhuizen, Linda, van der Wielen, Michiel J.R., Vollebregt, M.J. (Ellen), Breuning, Martijn H., Kriek, Marjolein, van Haeringen, Arie, den Dunnen, Johan T., Hoischen, Alexander, Clayton-Smith, Jill, de Vries, Bert B.A., Hennekam, Raoul C.M., van Belzen, Martine J., Almureikhi, Mariam, Baban, Anwar, Barbosa, Mafalda, Ben-Omran, Tawfeg, Berry, Katherine, Bigoni, Stefania, Boute, Odile, Brueton, Louise, van der Burgt, Ineke, Canham, Natalie, Chandler, Kate E., Chrzanowska, Krystyna, Collins, Amanda L., de Toni, Teresa, Dean, John, den Hollander, Nicolette S., Flore, Leigh Anne, Fryer, Alan, Gardham, Alice, Graham Jr, John M., Harrison, Victoria, Horn, Denise, Jongmans, Marjolijn C., Josifova, Dragana, Kant, Sarina G., Kapoor, Seema, Kingston, Helen, Kini, Usha, Kleefstra, Tjitske, Krajewska-Walasek, Małgorzata, Kramer, Nancy, Maas, Saskia M., Maciel, Patricia, Mancini, Grazia M.S., Maystadt, Isabelle, McKee, Shane, Milunsky, Jeff M., Nampoothiri, Sheela, Newbury-Ecob, Ruth, Nikkel, Sarah M., Parker, Michael J., Pérez-Jurado, Luis A., Robertson, Stephen P., Rooryck, Caroline, Shears, Debbie, Silengo, Margherita, Singh, Ankur, Smigiel, Robert, Soares, Gabriela, Splitt, Miranda, Stewart, Helen, Sweeney, Elizabeth, Tassabehji, May, Tuysuz, Beyhan, van Eerde, Albertien M., Vincent-Delorme, Catherine, Wilson, Louise C., Yesil, Gozde

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Novel MUC1 variant identified by massively parallel sequencing explains interstitial kidney disease in a large Dutch family von de Haan, Amber, van Eerde, Albertien M., Eijgelsheim, Mark, Rump, Patrick, van der Zwaag, Bert, Hennekam, Eric, Živná, Martina, Kmoch, Stanislav, Bleyer, Anthony J., Kidd, Kendrah, Vogt, Liffert, Knoers, Nine V.A.M., de Borst, Martin H.

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Translational strategies to uncover the etiology of congenital anomalies of the kidney and urinary tract von Vendrig, Lisanne M., ten Hoor, Mayke A. C., König, Benthe H., Lekkerkerker, Iris, Renkema, Kirsten Y., Schreuder, Michiel F., van der Zanden, Loes F. M., van Eerde, Albertien M., Groen in ’t Woud, Sander, Mulder, Jaap, Westland, Rik

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Trace element equilibrium in acute heart failure and the effect of empagliflozin von Weening, Eerde H., Al‐Mubarak, Ali A., Damman, Kevin, Voors, Adriaan A., Veldhuisen, Dirk J., Heerspink, Hiddo J.L., Schomburg, Lutz, Meer, Peter, Bomer, Nils

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NPHP1 (Nephrocystin-1) Gene Deletions Cause Adult-Onset ESRD von 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

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An Unusual Member of the Papain Superfamily: Mapping the Catalytic Cleft of the Marasmius oreades agglutinin (MOA) with a Caspase Inhibitor von Cordara, Gabriele, van Eerde, André, Grahn, Elin M, Winter, Harry C, Goldstein, Irwin J, Krengel, Ute

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Genes in the ureteric budding pathway: association study on vesico-ureteral reflux patients von van Eerde, Albertien M, Duran, Karen, van Riel, Els, de Kovel, Carolien G F, Koeleman, Bobby P C, Knoers, Nine V A M, Renkema, Kirsten Y, van der Horst, Henricus J R, Bökenkamp, Arend, van Hagen, Johanna M, van den Berg, Leonard H, Wolffenbuttel, Katja P, van den Hoek, Joop, Feitz, Wouter F, de Jong, Tom P V M, Giltay, Jacques C, Wijmenga, Cisca

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Genetic testing in a national cohort of adults with chronic kidney disease of unknown origin von de Haan, Amber, Eijgelsheim, Mark, Vogt, Liffert, Hoorn, Ewout J, Rotmans, Joris I, Fortrie, Gijs, Marsman, Roos F J, Rothuizen, Tonia C, Spijker, H Siebe, Claus, Laura R, Konings, Constantijn J A M, Waanders, Femke, Doornebal, Joan, Kramer, Andrea B, Adema, Aaltje Y, van der Zwaag, Bert, van Eerde, Albertien M, Knoers, Nine V A M, de Borst, Martin H

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A teacher’s learning process in dual design research: learning to scaffold language in a multilingual mathematics classroom von Smit, J., van Eerde, H. A. A.

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