Deletion of the Caenorhabditis elegans homologues of the CLN3 gene, involved in human juvenile neuronal ceroid lipofuscinosis, causes a mild progeric phenotype von Voer, G., Bent, P., Rodrigues, A. J. G., Ommen, G.‐J. B., Peters, D. J. M., Taschner, P. E. M.

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Phenazine-1-carboxamide production in the biocontrol strain Pseudomonas chlororaphis PCL1391 is regulated by multiple factors secreted into the growth medium von CHIN-A-WOENG, Thomas F. C, VAN DEN BROEK, Daan, DE VOER, Gert, VAN DER DRIFT, Koen M. G. M, TUINMAN, Sietske, THOMAS-OATES, Jane E, LUGTENBERG, Ben J. J, BLOEMBERG, Guido V

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PND13 - Health Care Utilization and Costs of Multiple Sclerosis Patients in the Netherlands: A Health Care Claims Database Study von Buijs, S, Krol, M, Pescott, C, de Voer, G

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Health Care Utilization and Costs of Multiple Sclerosis Patients in the Netherlands: A Health Care Claims Database Study von Buijs, S, Krol, M, Pescott, C, de Voer, G

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Patient adherence to subcutaneous IFN beta-1a injections using the RebiSmart ® injection device: a retrospective real-world study among Dutch and German patients with multiple scle... von Krol, Marieke, de Voer, Gert, Osowski, Ulrike

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PND82 A DELPHI PANEL ON TREATMENT OF HIGH DISEASE ACTIVITY RELAPSING REMITTING MULTIPLE SCLEROSIS IN THE NETHERLANDS von Peters, M.L., Michels, R., Bouma, P., Hengstman, G., Hupperts, R., Van Munster, C.E., Zeinstra, E., de Voer, G., Krol, M., Schiffers, K.

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Caenorhabditis elegans homologues of the CLN3 gene,mutated in juvenile neuronal ceroid lipofuscinosis von De Voer, Gert, Jansen, Gert, Van Ommen, Gert-Jan B., Peters, Dorien J.M., Taschner, Peter E.M.

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The longitudinal relationship between fatigue, depression, anxiety, disability, and adherence with cognitive status in patients with early multiple sclerosis treated with interfero... von Ballegooijen, H. van, Hiele, K. van der, Enzinger, C., Voer, G. de, Visser, L.H.

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The cln-3 genes of Caenorhabditis elegans : making C. elegans models for Juvenile Neuronal Ceroid Lipofuscinosis von Voer, G. de

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Phenazine-1-carboxamide production in the biocontrol strain Pseudomonas chlororaphis PCL1391 is regulated by multiple factors secreted into the growth medium von Chin-A-Woeng, T.F.C., Broek, D. van den, Voer, G. de, Drift, K.M.G.M. van der, Tuinman, S., Thomas-Oates, J.E., Lugtenberg, EJ.J., Bloemberg, G.V.

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A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer von Weren, Robbert D A, Ligtenberg, Marjolijn J L, Kets, C Marleen, de Voer, Richarda M, Verwiel, Eugène T P, Spruijt, Liesbeth, van Zelst-Stams, Wendy A G, Jongmans, Marjolijn C, Gilissen, Christian, Hehir-Kwa, Jayne Y, Hoischen, Alexander, Shendure, Jay, Boyle, Evan A, Kamping, Eveline J, Nagtegaal, Iris D, Tops, Bastiaan B J, Nagengast, Fokko M, Geurts van Kessel, Ad, van Krieken, J Han J M, Kuiper, Roland P, Hoogerbrugge, Nicoline

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Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype von Grolleman, Judith E., de Voer, Richarda M., Elsayed, Fadwa A., Nielsen, Maartje, Weren, Robbert D.A., Palles, Claire, Ligtenberg, Marjolijn J.L., Vos, Janet R., ten Broeke, Sanne W., de Miranda, Noel F.C.C., Kuiper, Renske A., Kamping, Eveline J., Jansen, Erik A.M., Vink-Börger, M. Elisa, Popp, Isabell, Lang, Alois, Spier, Isabel, Hüneburg, Robert, James, Paul A., Li, Na, Staninova, Marija, Lindsay, Helen, Cockburn, David, Spasic-Boskovic, Olivera, Clendenning, Mark, Sweet, Kevin, Capellá, Gabriel, Sjursen, Wenche, Høberg-Vetti, Hildegunn, Jongmans, Marjolijn C., Neveling, Kornelia, Geurts van Kessel, Ad, Morreau, Hans, Hes, Frederik J., Sijmons, Rolf H., Schackert, Hans K., Ruiz-Ponte, Clara, Dymerska, Dagmara, Lubinski, Jan, Rivera, Barbara, Foulkes, William D., Tomlinson, Ian P., Valle, Laura, Buchanan, Daniel. D., Kenwrick, Sue, Adlard, Julian, Dimovski, Aleksandar J., Campbell, Ian G., Aretz, Stefan, Schindler, Detlev, van Wezel, Tom, Hoogerbrugge, Nicoline, Kuiper, Roland P.

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Immunity against Neisseria meningitidis serogroup C in the Dutch population before and after introduction of the meningococcal c conjugate vaccine von de Voer, Richarda M, Mollema, Liesbeth, Schepp, Rutger M, de Greeff, Sabine C, van Gageldonk, Pieter G M, de Melker, Hester E, Sanders, Elisabeth A M, Berbers, Guy A M, van der Klis, Fiona R M

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Clonal Hematopoiesis Is Associated With Low CD4 Nadir and Increased Residual HIV Transcriptional Activity in Virally Suppressed Individuals With HIV von van der Heijden, Wouter A, van Deuren, Rosanne C, van de Wijer, Lisa, van den Munckhof, Inge C L, Steehouwer, Marloes, Riksen, Niels P, Netea, Mihai G, de Mast, Quirijn, Vandekerckhove, Linos, de Voer, Richarda M, van der Ven, Andre J, Hoischen, Alexander

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Germline MBD4 deficiency causes a multi-tumor predisposition syndrome von Palles, Claire, West, Hannah D., Chew, Edward, Galavotti, Sara, Flensburg, Christoffer, Grolleman, Judith E., Jansen, Erik A.M., Curley, Helen, Chegwidden, Laura, Arbe-Barnes, Edward H., Lander, Nicola, Truscott, Rebekah, Pagan, Judith, Bajel, Ashish, Sherwood, Kitty, Martin, Lynn, Thomas, Huw, Georgiou, Demetra, Fostira, Florentia, Goldberg, Yael, Adams, David J., van der Biezen, Simone A.M., Christie, Michael, Clendenning, Mark, Thomas, Laura E., Deltas, Constantinos, Dimovski, Aleksandar J., Dymerska, Dagmara, Lubinski, Jan, Mahmood, Khalid, van der Post, Rachel S., Sanders, Mathijs, Weitz, Jürgen, Taylor, Jenny C., Turnbull, Clare, Vreede, Lilian, van Wezel, Tom, Whalley, Celina, Arnedo-Pac, Claudia, Caravagna, Giulio, Cross, William, Chubb, Daniel, Frangou, Anna, Gruber, Andreas J., Kinnersley, Ben, Noyvert, Boris, Church, David, Graham, Trevor, Houlston, Richard, Lopez-Bigas, Nuria, Sottoriva, Andrea, Wedge, David, Jenkins, Mark A., Kuiper, Roland P., Roberts, Andrew W., Cheadle, Jeremy P., Ligtenberg, Marjolijn J.L., Hoogerbrugge, Nicoline, Koelzer, Viktor H., Rivas, Andres Dacal, Winship, Ingrid M., Ponte, Clara Ruiz, Buchanan, Daniel D., Power, Derek G., Green, Andrew, Tomlinson, Ian P.M., Sampson, Julian R., Majewski, Ian J., de Voer, Richarda M.

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Immunological and Genomic Analysis Reveals Clinically Relevant Distinctions between Angiosarcoma Subgroups von van Ravensteijn, Stefan G, Versleijen-Jonkers, Yvonne M H, Hillebrandt-Roeffen, Melissa H S, Weidema, Marije E, Nederkoorn, Maikel J L, Bol, Kalijn F, Gorris, Mark A J, Verrijp, Kiek, Kroeze, Leonie I, de Bitter, Tessa J J, de Voer, Richarda M, Flucke, Uta E, Desar, Ingrid M E

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Somatic Nonepigenetic Mismatch Repair Gene Aberrations Underly Most Mismatch Repair–Deficient Lynch-Like Tumors von Elze, Lisa, Mensenkamp, Arjen R., Nagtegaal, Iris D., van Zelst-Stams, Wendy A.G., Dommering, Charlotte J., Hoogerbrugge, Nicoline, de Jong, Mirjam M., Bleeker, Fonnet E., Leter, Edward M., Letteboer, Tom G.W., Nielsen, Maartje, van der Post, Rachel S., Wapstra, Brigit, de Voer, Richarda M., Ligtenberg, Marjolijn J.L.

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Germline mutations in the spindle assembly checkpoint genes BUB1 and BUB3 are infrequent in familial colorectal cancer and polyposis von Mur, Pilar, De Voer, Richarda M, Olivera-Salguero, Rubén, Rodríguez-Perales, Sandra, Pons, Tirso, Setién, Fernando, Aiza, Gemma, Valdés-Mas, Rafael, Bertini, Angelo, Pineda, Marta, Vreede, Lilian, Navarro, Matilde, Iglesias, Silvia, González, Sara, Brunet, Joan, Valencia, Alfonso, Esteller, Manel, Lázaro, Conxi, Kops, Geert J P L, Urioste, Miguel, Puente, Xose S, Capellá, Gabriel, Valle, Laura

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Correction: Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples von Wijngaard, Robin, Demidov, German, O'Gorman, Luke, Corominas-Galbany, Jordi, Yaldiz, Burcu, Steyaert, Wouter, de Boer, Elke, Vissers, Lisenka E L M, Kamsteeg, Erik-Jan, Pfundt, Rolph, Swinkels, Hilde, den Ouden, Amber, Te Paske, Iris B A W, de Voer, Richarda M, Faivre, Laurence, Denommé-Pichon, Anne-Sophie, Duffourd, Yannis, Vitobello, Antonio, Chevarin, Martin, Straub, Volker, Töpf, Ana, van der Kooi, Anneke J, Magrinelli, Francesca, Rocca, Clarissa, Hanna, Michael G, Vandrovcova, Jana, Ossowski, Stephan, Laurie, Steven, Gilissen, Christian

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Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples von Wijngaard, Robin, Demidov, German, O'Gorman, Luke, Corominas-Galbany, Jordi, Yaldiz, Burcu, Steyaert, Wouter, de Boer, Elke, Vissers, Lisenka E L M, Kamsteeg, Erik-Jan, Pfundt, Rolph, Swinkels, Hilde, den Ouden, Amber, Te Paske, Iris B A W, de Voer, Richarda M, Faivre, Laurence, Denommé-Pichon, Anne-Sophie, Duffourd, Yannis, Vitobello, Antonio, Chevarin, Martin, Straub, Volker, Töpf, Ana, van der Kooi, Anneke J, Magrinelli, Francesca, Rocca, Clarissa, Hanna, Michael G, Vandrovcova, Jana, Ossowski, Stephan, Laurie, Steven, Gilissen, Christian

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