The emerging landscape of dynamic DNA methylation in early childhood von Xu, Cheng-Jian, Bonder, Marc Jan, Söderhäll, Cilla, Bustamante, Mariona, Baïz, Nour, Gehring, Ulrike, Jankipersadsing, Soesma A, van der Vlies, Pieter, van Diemen, Cleo C, van Rijkom, Bianca, Just, Jocelyne, Kull, Inger, Kere, Juha, Antó, Josep Maria, Bousquet, Jean, Zhernakova, Alexandra, Wijmenga, Cisca, Annesi-Maesano, Isabella, Sunyer, Jordi, Melén, Erik, Li, Yang, Postma, Dirkje S, Koppelman, Gerard H

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Combining genomewide association study and lung eQTL analysis provides evidence for novel genes associated with asthma von Nieuwenhuis, M. A., Siedlinski, M., Berge, M., Granell, R., Li, X., Niens, M., Vlies, P., Altmüller, J., Nürnberg, P., Kerkhof, M., Schayck, O. C., Riemersma, R. A., Molen, T., Monchy, J. G., Bossé, Y., Sandford, A., Bruijnzeel‐Koomen, C. A., Gerth van Wijk, R., Hacken, N. H., Timens, W., Boezen, H. M., Henderson, J., Kabesch, M., Vonk, J. M., Postma, D. S., Koppelman, G. H.

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PCR-based DNA test to confirm clinical diagnosis of autosomal recessive spinal muscular atrophy von van der Steege, G., Grootscholten, P.M., van der Vlies, P., Draaijers, T.G., Osinga, J., Cobben, J.M., Scheffer, H., Buys, C.H.C.M.

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450: The consequence of SETD2 mutation in clear cell renal cell carcinoma progenitor cells von Li, J, Osinga, J, Ferronika, P, Van Werkhoven, M.B, Terpstra, M.M, Van der Vlies, P, Duns, G, Westers, H, Sijmons, R.H, Kok, K

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DNA methylation in childhood asthma: an epigenome-wide meta-analysis von Xu, Cheng-Jian, Söderhäll, Cilla, Bustamante, Mariona, Baïz, Nour, Gruzieva, Olena, Gehring, Ulrike, Mason, Dan, Chatzi, Leda, Basterrechea, Mikel, Llop, Sabrina, Torrent, Maties, Forastiere, Francesco, Fantini, Maria Pia, Carlsen, Karin C Lødrup, Haahtela, Tari, Morin, Andréanne, Kerkhof, Marjan, Merid, Simon Kebede, van Rijkom, Bianca, Jankipersadsing, Soesma A, Bonder, Marc Jan, Ballereau, Stephane, Vermeulen, Cornelis J, Aguirre-Gamboa, Raul, de Jongste, Johan C, Smit, Henriette A, Kumar, Ashish, Pershagen, Göran, Guerra, Stefano, Garcia-Aymerich, Judith, Greco, Dario, Reinius, Lovisa, McEachan, Rosemary R C, Azad, Raf, Hovland, Vegard, Mowinckel, Petter, Alenius, Harri, Fyhrquist, Nanna, Lemonnier, Nathanaël, Pellet, Johann, Auffray, Charles, van der Vlies, Pieter, van Diemen, Cleo C, Li, Yang, Wijmenga, Cisca, Netea, Mihai G, Moffatt, Miriam F, Cookson, William O C M, Anto, Josep M, Bousquet, Jean, Laatikainen, Tiina, Laprise, Catherine, Carlsen, Kai-Håkon, Gori, Davide, Porta, Daniela, Iñiguez, Carmen, Bilbao, Jose Ramon, Kogevinas, Manolis, Wright, John, Brunekreef, Bert, Kere, Juha, Nawijn, Martijn C, Annesi-Maesano, Isabella, Sunyer, Jordi, Melén, Erik, Koppelman, Gerard H

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Shared DNA methylation signatures in childhood allergy: The MeDALL study von Xu, Cheng-Jian, Gruzieva, Olena, Qi, Cancan, Esplugues, Ana, Gehring, Ulrike, Bergström, Anna, Mason, Dan, Chatzi, Leda, Porta, Daniela, Lodrup Carlsen, Karin C., Baïz, Nour, Madore, Anne-Marie, Alenius, Harri, van Rijkom, Bianca, Jankipersadsing, Soesma A., van der Vlies, Pieter, Kull, Inger, van Hage, Marianne, Bustamante, Mariona, Lertxundi, Aitana, Torrent, Matias, Santorelli, Gillian, Fantini, Maria Pia, Hovland, Vegard, Pesce, Giancarlo, Fyhrquist, Nanna, Laatikainen, Tiina, Nawijn, Martijn C., Li, Yang, Wijmenga, Cisca, Netea, Mihai G., Bousquet, Jean, Anto, Josep M., Laprise, Catherine, Haahtela, Tari, Annesi-Maesano, Isabella, Carlsen, Kai-Håkon, Gori, Davide, Kogevinas, Manolis, Wright, John, Söderhäll, Cilla, Vonk, Judith M., Sunyer, Jordi, Melén, Erik, Koppelman, Gerard H.

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Three novel KCNA1 mutations in episodic ataxia type I families von Scheffer, H, Brunt, E R, Mol, G J, van der Vlies, P, Stulp, R P, Verlind, E, Mantel, G, Averyanov, Y N, Hofstra, R M, Buys, C H

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Genetic regulation of IL1RL1 methylation and IL1RL1-a protein levels in asthma von Dijk, F Nicole, Xu, Chengjian, Melén, Erik, Carsin, Anne-Elie, Kumar, Asish, Nolte, Ilja M, Gruzieva, Olena, Pershagen, Goran, Grotenboer, Neomi S, Savenije, Olga E M, Antó, Josep Maria, Lavi, Iris, Dobaño, Carlota, Bousquet, Jean, van der Vlies, Pieter, van der Valk, Ralf J P, de Jongste, Johan C, Nawijn, Martijn C, Guerra, Stefano, Postma, Dirkje S, Koppelman, Gerard H

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Genetic and epigenetic regulation of YKL-40 in childhood von Guerra, Stefano, Melén, Erik, Sunyer, Jordi, Xu, Cheng-Jian, Lavi, Iris, Benet, Marta, Bustamante, Mariona, Carsin, Anne-Elie, Dobaño, Carlota, Guxens, Mònica, Tischer, Christina, Vrijheid, Martine, Kull, Inger, Bergström, Anna, Kumar, Ashish, Söderhäll, Cilla, Gehring, Ulrike, Dijkstra, Dorieke J., van der Vlies, Pieter, Wickman, Magnus, Bousquet, Jean, Postma, Dirkje S., Anto, Josep M., Koppelman, Gerard H.

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Improvements in gel composition and electrophoretic conditions for broad-range mutation analysis by denaturing gradient gel electrophoresis von Hayes, V M, Wu, Y, Osinga, J, Mulder, I M, van der Vlies, P, Elfferich, P, Buys, C H, Hofstra, R M

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Two novel germline mutations of the retinoblastoma gene (RB1) that show incomplete penetrance, one splice site and one missense von SCHEFFER, H, VAN DER VLIES, P, BURTON, M, VERLIND, E, MOLL, A C, IMHOF, S M, BUYS, C H C M

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High expression of calcium‐binding proteins, S100A10, S100A11 and CALM2 in anaplastic large cell lymphoma von Rust, Renata, Visser, Lydia, Leij, Judith, Harms, Geert, Blokzijl, Tjasso, Deloulme, Jean C., Vlies, Pieter, Kamps, Willem, Kok, Klaas, Lim, Megan, Poppema, Sibrand, Berg, Anke

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B59 ASTHMA-LIKE PHENOTYPE: EMERGENCE OF (EPI)GENETICS AND TARGETED TRANSGENESIS: (epi)genetic Regulation Of Expression Of Il1rl1 Mrna And Il1rl1-A Protein Levels In Asthma von Dijk, F, Grotenboer, N S, Xu, C, Kumar, A, Soderhall, C, Melen, E, Lavi, I, Dobano, C, Guerra, S, Savenije, O, Nolte, I, Der Vlies, P Van, Smit, H, Brunekreef, B, Der Valk, R Van, Jongste, J De, Kerkhof, M, Nawijn, M C, Postma, D S, Koppelman, G H

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DNA methylation in childhood asthma: an epigenome-wide meta-analysis von Xu, C-J, Soderhall, C, Bustamante, M, Baiz, N, Gruzieva, O, Gehring, U, Mason, D, Chatzi, L, Basterrechea, M, Llop, S, Torrent, M, Forastiere, F, Fantini, MP, Carlsen, KCL, Haahtela, T, Morin, A, Kerkhof, M, Merid, SK, Van Rijkom, B, Jankipersadsing, SA, Bonder, MJ, Ballereau, S, Vermeulen, CJ, Aguirre-Gamboa, R, De Jongste, JC, Smit, HA, Kumar, A, Pershagen, G, Guerra, S, Garcia-Aymerich, J, Greco, D, Reinius, L, McEachan, RRC, Azad, R, Hovland, V, Mowinckel, P, Alenius, H, Fyhrquist, N, Lemonnier, N, Pellet, J, Auffray, C, Van der Vlies, P, Van Diemen, CC, Li, Y, Wijmenga, C, Netea, MG, Moffatt, MF, Cookson, WOCM, Anto, JM, Bousquet, J, Laatikainen, T, Laprise, C, Carlsen, K-H, Gori, D, Porta, D, Iniguez, C, Bilbao, JR, Kogevinas, M, Wright, J, Brunekreef, B, Kere, J, Nawijn, MC, Annesi-Maesano, I, Sunyer, J, Melen, E, Koppelman, GH

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Loss of heterozygosity at the short arm of chromosome 3 in renal‐cell cancer correlates with the cytological tumour type von Van Hout, A. H. Der, Van Berg, E. Den, Van Vlies, P. Der, Dijkhuizen, T., Störkel, S., Oosterhuis, J. W., De Jong, B., Buys, C. H. C. M.

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Translocations involving 6p22 in acute myeloid leukaemia at relapse: breakpoint characterization using microarray‐based comparative genomic hybridization von Tchinda, Joëlle, Dijkhuizen, Trijnie, Vlies, Pieter van der, Kok, Klaas, Horst, Jürgen

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37: A FIRST GENOME-WIDE ASSOCIATION STUDY IN DUPUYTRENʼS DISEASE IDENTIFIES 9 SUSCEPTIBILITY LOCI AND SUGGESTS A MAJOR ROLE FOR WNT-SIGNALLING von Dolmans, GH, Werker, PM, Hennies, HC, Furniss, D, Festen, EA, Franke, L, van der Vlies, P, Wolffenbuttel, BH, Giele, H, Ophoff, RA, Wijmenga, C

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(epi)genetic Regulation Of Expression Of Il1rl1 Mrna And Il1rl1-A Protein Levels In Asthma von Dijk, F, Grotenboer, NS, Xu, C, Kumar, A, Soderhall, C, Melen, E, Lavi, I, Dobano, C, Guerra, S, Savenije, O, Nolte, I, Van der Vlies, P, Smit, H, Brunekreef, B, Van der Valk, R, De Jongste, J, Kerkhof, M, Nawijn, MC, Postma, DS, Koppelman, GH

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Application of a comprehensive subtelomere array in clinical diagnosis of mental retardation von Kok, Klaas, Dijkhuizen, Trijnie, Swart, Yolanthe E., Zorgdrager, Hanny, van der Vlies, Pieter, Fehrmann, Rudolf, te Meerman, Gerard J., Gerssen-Schoorl, Klasien B.J., van Essen, Ton, Sikkema-Raddatz, Birgit, Buys, Charles H.C.M.

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Detection of point mutation in dystrophin gene reveals somatic and germline mosaicism in the mother of a patient with Duchenne muscular dystrophy von Essen, Anthonie J. van, Mulder, Inge M., Vlies, Pieter van der, Hout, Annemarie H. van der, Buys, Charles H.C.M., Hofstra, Robert M.W., Dunnen, Johan T. den

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