Urinary beta-2 microglobulin increases whereas TIMP-2 and IGFBP7 decline after unilateral nephrectomy in healthy kidney donors von de Rooij, Esther N. M., Hoogeveen, Ellen K., Romijn, Fred P. H. T. M., van der Kooy, Sandra W., Veighey, Kristin V., Dekker, Friedo W., van Kooten, Cees, Cobbaert, Christa M., de Fijter, Johan W.

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Voclosporin and the Antiviral Effect Against SARS-CoV-2 in Immunocompromised Kidney Patients von Arends, Eline J., Meziyerh, Soufian, Moes, Dirk Jan A.R., Kamerling, Sylvia W.A., van der Kooy, Sandra, Ogando, Natacha S., Snijder, Eric J., van Hemert, Martijn, Visser, Leo G., Feltkamp, Mariet C.W., Claas, Eric C.J., Rabelink, Ton J., van Kooten, Cees, de Vries, Aiko P.J., Teng, Y.K. Onno

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PhenoScore quantifies phenotypic variation for rare genetic diseases by combining facial analysis with other clinical features using a machine-learning framework von Dingemans, Alexander J. M., Hinne, Max, Truijen, Kim M. G., Goltstein, Lia, van Reeuwijk, Jeroen, de Leeuw, Nicole, Schuurs-Hoeijmakers, Janneke, Pfundt, Rolph, Diets, Illja J., den Hoed, Joery, de Boer, Elke, Coenen-van der Spek, Jet, Jansen, Sandra, van Bon, Bregje W., Jonis, Noraly, Ockeloen, Charlotte W., Vulto-van Silfhout, Anneke T., Kleefstra, Tjitske, Koolen, David A., Campeau, Philippe M., Palmer, Elizabeth E., Van Esch, Hilde, Lyon, Gholson J., Alkuraya, Fowzan S., Rauch, Anita, Marom, Ronit, Baralle, Diana, van der Sluijs, Pleuntje J., Santen, Gijs W. E., Kooy, R. Frank, van Gerven, Marcel A. J., Vissers, Lisenka E. L. M., de Vries, Bert B. A.

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Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP von Van Dijck, Anke, Vulto-van Silfhout, Anneke T., Cappuyns, Elisa, van der Werf, Ilse M., Mancini, Grazia M., Tzschach, Andreas, Bernier, Raphael, Gozes, Illana, Eichler, Evan E., Romano, Corrado, Lindstrand, Anna, Nordgren, Ann, Bakshi, Madhura, Wilson, Meredith, Berman, Yemina, Dickson, Rebecca, Fransen, Erik, Helsmoortel, Céline, Van den Ende, Jenneke, Van der Aa, Nathalie, van de Wijdeven, Marina J., Rosenblum, Jessica, Monteiro, Fabíola, Kok, Fernando, Quercia, Nada, Bowdin, Sarah, Dyment, David, Chitayat, David, Alkhunaizi, Ebba, Boonen, Susanne E., Keren, Boris, Jacquette, Aurelia, Faivre, Laurence, Bezieau, Stephane, Isidor, Bertrand, Rieß, Angelika, Moog, Ute, Lynch, Sally Ann, McVeigh, Terri, Elpeleg, Orly, Smeland, Marie Falkenberg, Fannemel, Madeleine, van Haeringen, Arie, Maas, Saskia M., Veenstra-Knol, H.E., Schouten, Meyke, Willemsen, Marjolein H., Marcelis, Carlo L., Ockeloen, Charlotte, van der Burgt, Ineke, Feenstra, Ilse, van der Smagt, Jasper, Jezela-Stanek, Aleksandra, Krajewska-Walasek, Malgorzata, González-Lamuño, Domingo, Anderlid, Britt-Marie, Malmgren, Helena, Nordenskjöld, Magnus, Hurst, Jane, Metcalfe, Kay, Mansour, Sahar, Lachlan, Katherine, Clayton-Smith, Jill, Hendon, Laura G., Abdulrahman, Omar A., Morrow, Eric, McMillan, Clare, Gerdts, Jennifer, Peeden, Joseph, Schrier Vergano, Samantha A., Valentino, Caitlin, Chung, Wendy K., Ozmore, Jillian R., Bedrosian-Sermone, Sandra, Treat, Kayla, Hughes, Susan Starling, Safina, Nicole, Le Pichon, Jean-Baptiste, McGuire, Marianne, Infante, Elena, Madan-Khetarpal, Suneeta, Desai, Sonal, Benke, Paul, Krokosky, Alyson, Cristian, Ingrid, Baker, Laura, Gripp, Karen, Stessman, Holly A., Eichenberger, Jacob, Jayakar, Parul, Manning, Melanie Ann, Slattery, Leah, Kvarnung, Malin, Kleefstra, Tjitske, de Vries, Bert B.A., Küry, Sébastien, Rosenfeld, Jill A., Meuwissen, Marije E., Vandeweyer, Geert, Kooy, R. Frank

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Bortezomib before and after autologous stem cell transplantation overcomes the negative prognostic impact of renal impairment in newly diagnosed multiple myeloma: a subgroup analys... von Scheid, Christof, Sonneveld, Pieter, Schmidt-Wolf, Ingo G H, van der Holt, Bronno, el Jarari, Laila, Bertsch, Uta, Salwender, Hans, Zweegman, Sonja, Blau, Igor Wolfgang, Vellenga, Edo, Weisel, Katja, Pfreundschuh, Michael, Jie, Kon-Siong, Neben, Kai, van de Velde, Helgi, Duehrsen, Ulrich, Schaafsma, M Ron, Lindemann, Walter, Kersten, Marie José, Peter, Norma, Hänel, Mathias, Croockewit, Sandra, Martin, Hans, Wittebol, Shulamiet, Bos, Gerard Mj, van Marwijk-Kooy, Marinus, Wijermans, Pierre, Goldschmidt, Hartmut, Lokhorst, Henk M

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Prevalence of comorbidities in individuals with neurodevelopmental disorders from the aggregated phenomics data of 51,227 pediatric individuals von Dingemans, Alexander J. M., Jansen, Sandra, van Reeuwijk, Jeroen, de Leeuw, Nicole, Pfundt, Rolph, Schuurs-Hoeijmakers, Janneke, van Bon, Bregje W., Marcelis, Carlo, Ockeloen, Charlotte W., Willemsen, Marjolein, van der Sluijs, Pleuntje J., Santen, Gijs W. E., Kooy, R. Frank, Vulto-van Silfhout, Anneke T., Kleefstra, Tjitske, Koolen, David A., Vissers, Lisenka E. L. M., de Vries, Bert B. A.

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Overrepresentation of genetic variation in the AnkyrinG interactome is related to a range of neurodevelopmental disorders von van der Werf, Ilse M., Jansen, Sandra, de Vries, Petra F., Gerstmans, Amber, van de Vorst, Maartje, Van Dijck, Anke, de Vries, Bert B. A., Gilissen, Christian, Hoischen, Alexander, Vissers, Lisenka E. L. M., Kooy, R. Frank, Vandeweyer, Geert

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Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability von van der Werf, Ilse M., Van Dijck, Anke, Reyniers, Edwin, Helsmoortel, Céline, Kumar, Ajay Anand, Kalscheuer, Vera M., de Brouwer, Arjan PM, Kleefstra, Tjitske, van Bokhoven, Hans, Mortier, Geert, Janssens, Sandra, Vandeweyer, Geert, Kooy, R. Frank

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PhenoScore quantifies phenotypic variation for rare genetic diseases by combining facial analysis with other clinical features using a machine-learning framework von Dingemans, Alexander J.M, Hinne, Max, Truijen, Kim M.G, Goltstein, Lia, van Reeuwijk, Jeroen, de Leeuw, Nicole, Schuurs-Hoeijmakers, Janneke, Pfundt, Rolph, Diets, Illja J, den Hoed, Joery, de Boer, Elke, van der Spek, Jet, Jansen, Sandra, van Bon, Bregje W, Jonis, Noraly, Ockeloen, Charlotte W, Vulto-van Silfhout, Anneke T, Kleefstra, Tjitske, Koolen, David A, Campeau, Philippe M, Palmer, Elizabeth E, Van Esch, Hilde, Lyon, Gholson J, Alkuraya, Fowzan S, Rauch, Anita, Marom, Ronit, Baralle, Diana, van der Sluijs, Pleuntje J, Santen, Gijs W.E, Kooy, R. Frank, van Gerven, Marcel A.J, Vissers, Lisenka E.L.M, de Vries, Bert B.A

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PhenoScore quantifies phenotypic variation for rare genetic diseases by combining facial analysis with other clinical features using a machine-learning framework von Dingemans, Alexander J M, Hinne, Max, Truijen, Kim M G, Goltstein, Lia, van Reeuwijk, Jeroen, de Leeuw, Nicole, Schuurs-Hoeijmakers, Janneke, Pfundt, Rolph, Diets, Illja J, den Hoed, Joery, de Boer, Elke, Coenen-van der Spek, Jet, Jansen, Sandra, van Bon, Bregje W, Jonis, Noraly, Ockeloen, Charlotte W, Vulto-van Silfhout, Anneke T, Kleefstra, Tjitske, Koolen, David A, Campeau, Philippe M, Palmer, Elizabeth E, Van Esch, Hilde, Lyon, Gholson J, Alkuraya, Fowzan S, Rauch, Anita, Marom, Ronit, Baralle, Diana, van der Sluijs, Pleuntje J, Santen, Gijs W E, Kooy, R Frank

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Cohort profile: the ‘Biomarkers of heterogeneity in type 1 diabetes’ study—a national prospective cohort study of clinical and metabolic phenotyping of individuals with long-standi... von Aanstoot, Henk-Jan, Varkevisser, Rita D M, Mul, Dick, Dekker, Pim, Birnie, Erwin, Boesten, Lianne S M, Brugts, Michael P, van Dijk, Peter R, Duijvestijn, Petronella H L M, Dutta, Sanjoy, Fransman, Christine, Gonera, Rob K, Hoogenberg, Klaas, Kooy, Adriaan, Latres, Esther, Loves, Sandra, Nefs, Giesje, Sas, Theo, Vollenbrock, Charlotte E, Vosjan-Noeverman, Marleen J, de Vries-Velraeds, Martine M C, Veeze, Henk J, Wolffenbuttel, Bruce H R, van der Klauw, Melanie M, Aanstoot, Henk-Jan, Varkevisser, Rita DM, Mul, Dick, Dekker, Pim, Birnie, Erwin, Boesten, Lianne SM, Brugts, Michael P, Dijk, Peter R van, Duijvestijn, Petronella HLM, Dutta, Sanjoy, Fransman, Christine, Gonera, Rob K, Hoogenberg, Klaas, Kooy, Adriaan, Latres, Esther, Loves, Sandra, Nefs, Giesje, Sas, Theo, Vollenbrock, Charlotte E, Vosjan-Noeverman, Marleen J, Vries-Velraeds, Martine MC de, Veeze, Henk J, Wolffenbuttel, Bruce HR, Klauw, Melanie M van der

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A randomized phase 3 study on the effect of thalidomide combined with adriamycin, dexamethasone, and high-dose melphalan, followed by thalidomide maintenance in patients with multi... von Lokhorst, Henk M., van der Holt, Bronno, Zweegman, Sonja, Vellenga, Edo, Croockewit, Sandra, van Oers, Marinus H., von dem Borne, Peter, Wijermans, Pierre, Schaafsma, Ron, de Weerdt, Okke, Wittebol, Shulamiet, Delforge, Michel, Berenschot, Henriëtte, Bos, Gerard M., Jie, Kon-Siong G., Sinnige, Harm, van Marwijk-Kooy, Marinus, Joosten, Peter, Minnema, Monique C., van Ammerlaan, Rianne, Sonneveld, Pieter

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The Compassionate Side of Neuroscience: Tony Sermone’s Undiagnosed Genetic Journey—ADNP Mutation von Gozes, Illana, Helsmoortel, Celine, Vandeweyer, Geert, Van der Aa, Nathalie, Kooy, Frank, Sermone, Sandra Bedrosian

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Correction to: The Compassionate Side of Neuroscience: Tony Sermone’s Undiagnosed Genetic Journey—ADNP Mutation von Gozes, Illana, Helsmoortel, Celine, Vandeweyer, Geert, Van der Aa, Nathalie, Kooy, Frank, Bedrosian-Sermone, Sandra

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Implementation of genomic arrays in prenatal diagnosis: The Belgian approach to meet the challenges von Vanakker, Olivier, Vilain, Catheline, Janssens, Katrien, Van der Aa, Nathalie, Smits, Guillaume, Bandelier, Claude, Blaumeiser, Bettina, Bulk, Saskia, Caberg, Jean-Hubert, De Leener, Anne, De Rademaeker, Marjan, de Ravel, Thomy, Desir, Julie, Destree, Anne, Dheedene, Annelies, Gaillez, Stéphane, Grisart, Bernard, Hellin, Ann-Cécile, Janssens, Sandra, Keymolen, Kathelijn, Menten, Björn, Pichon, Bruno, Ravoet, Marie, Revencu, Nicole, Rombout, Sonia, Staessens, Catherine, Van Den Bogaert, Ann, Van Den Bogaert, Kris, Vermeesch, Joris R, Kooy, Frank, Sznajer, Yves, Devriendt, Koen

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Thalidomide in induction treatment increases the very good partial response rate before and after high-dose therapy in previously untreated multiple myeloma von Lokhorst, Henk M, Schmidt-Wolf, Ingo, Sonneveld, Pieter, van der Holt, Bronno, Martin, Hans, Barge, Rene, Bertsch, Uta, Schlenzka, Jana, Bos, Gerard M.J, Croockewit, Sandra, Zweegman, Sonja, Breitkreutz, Iris, Joosten, Peter, Scheid, Christof, van Marwijk-Kooy, Marinus, Salwender, Hans-Juergen, van Oers, Marinus H.J, Schaafsma, Ron, Naumann, Ralph, Sinnige, Harm, Blau, Igor, Delforge, Michel, de Weerdt, Okke, Wijermans, Pierre, Wittebol, Shulamiet, Duersen, Ulrich, Vellenga, Edo, Goldschmidt, Hartmut, for Dutch-Belgian HOVON and German GMMG

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Erratum to: The Compassionate Side of Neuroscience: Tony Sermone’s Undiagnosed Genetic Journey—ADNP Mutation von Gozes, Illana, Helsmoortel, Celine, Vandeweyer, Geert, Van der Aa, Nathalie, Kooy, Frank, Sermone, Sandra Bedrosian

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Haploinsufficiency of CMIP in a Girl With Autism Spectrum Disorder and Developmental Delay due to a De Novo Deletion on Chromosome 16q23.2 von Van der Aa, Nathalie, Vandeweyer, Geert, Reyniers, Edwin, Kenis, Sandra, Dom, Lina, Mortier, Geert, Rooms, Liesbeth, Kooy, R. Frank

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Adhesion Is Prerequisite, But Alone Insufficient, to Elicit Stem Cell Pluripotency von Karpowicz, Phillip, Inoue, Tomoyuki, Runciman, Sue, Deveale, Brian, Seaberg, Raewyn, Gertsenstein, Marina, Byers, Lois, Yamanaka, Yojiro, Tondat, Sandra, Slevin, John, Hitoshi, Seiji, Rossant, Janet, van der Kooy, Derek

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Influence of Renal Function on Outcome of VAD or Bortezomib, Doxorubicin, Dexamethasone (PAD) Induction Treatment Followed by High-Dose Melphalan (HDM): A Subgroup Analysis From th... von Scheid, Christof, Sonneveld, Pieter, Schmidt-Wolf, Ingo, van der Holt, Bronno, Hielscher, Thomas, el Jarari, Laila, Bertsch, Uta, Salwender, Hans, Zweegman, Sonja, Hänel, Mathias, Vellenga, Edo, Schubert, Joerg, Blau, Igor Wolfgang, Jie, Asiong, Van de elde, Helgi, Peter, Norma, Schaafsma, Martijn, Lindemann, Walter, Kersten, Marie Jose, Duehrsen, Ulrich, Delforge, Michel, Weisel, Katja, Croockewit, Sandra, Martin, Hans, Wittebol, Shulamit, Schouten, Harry, van Marwijk-Kooy, Marinus, Wijermans, Pierre, Lokhorst, Henk M, Goldschmidt, Hartmut

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