Molecular prediction of disease risk and severity in a large Dutch Crohn’s disease cohort von Weersma, R K, Stokkers, P C F, van Bodegraven, A A, van Hogezand, R A, Verspaget, H W, de Jong, D J, van der Woude, C J, Oldenburg, B, Linskens, R K, Festen, E A M, van der Steege, G, Hommes, D W, Crusius, J B A, Wijmenga, C, Nolte, I M, Dijkstra, G

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Receptor for advanced glycation end products (RAGE) polymorphisms are associated with systemic lupus erythematosus and disease severity in lupus nephritis von Martens, HA, Nienhuis, HLA, Gross, S, der Steege, G van, Brouwer, E, Berden, JHM, Sévaux, RGL de, Derksen, RHWM, Voskuyl, AE, Berger, SP, Navis, GJ, Nolte, IM, Kallenberg, CGM, Bijl, M

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Susceptibility to Buruli ulcer is associated with the SLC11A1 (NRAMP1) D543N polymorphism von Stienstra, Y, van der Werf, T S, Oosterom, E, Nolte, I M, van der Graaf, W T A, Etuaful, S, Raghunathan, P L, Whitney, E A S, Ampadu, E O, Asamoa, K, Klutse, E Y, te Meerman, G J, Tappero, J W, Ashford, D A, van der Steege, G

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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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Association with HLA class I in Epstein-Barr-virus-positive and with HLA class III in Epstein-Barr-virus-negative Hodgkin's lymphoma von Diepstra, A, Niens, M, Vellenga, E, van Imhoff, GW, Nolte, IM, Schaapveld, M, van der Steege, G, van den Berg, A, Kibbelaar, RE, te Meerman, GJ, Poppema, S

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CARD15 in inflammatory bowel disease and Crohn's disease phenotypes: An association study and pooled analysis von Oostenbrug, L.E., Nolte, I.M., Oosterom, E., van der Steege, G., te Meerman, G.J., van Dullemen, H.M., Drenth, J.P.H., de Jong, D.J., van der Linde, K., Jansen, P.L.M., Kleibeuker, J.H.

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Analysis of C1q polymorphisms suggests association with systemic lupus erythematosus, serum C1q and CH50 levels and disease severity von Martens, H A, Zuurman, M W, de Lange, A H M, Nolte, I M, van der Steege, G, Navis, G J, Kallenberg, C G M, Seelen, M A, Bijl, M

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Review article: inflammatory bowel disease and genetics von WEERSMA, R. K., VAN DULLEMEN, H. M., VAN DER STEEGE, G., NOLTE, I. M., KLEIBEUKER, J. H., DIJKSTRA, G.

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Heme Oxygenase‐1 Genotype of the Donor Is Associated With Graft Survival After Liver Transplantation von Buis, C. I., van der Steege, G., Visser, D. S., Nolte, I. M., Hepkema, B. G., Nijsten, M., Slooff, M. J. H., Porte, R. J.

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Interleukin‐10 and Fas polymorphisms and susceptibility for (pre)neoplastic cervical disease von ZOODSMA, M., NOLTE, I.M., SCHIPPER, M., OOSTEROM, E., Van Der STEEGE, G., De VRIES, E.G.E., Te MEERMAN, G.J., Van Der ZEE, A.G.J.

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Analysis of the entire HLA region in susceptibility for cervical cancer: a comprehensive study von Zoodsma, M, Nolte, I M, Schipper, M, Oosterom, E, van der Steege, G, de Vries, E G E, te Meerman, G J, van der Zee, A G J

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Novel Association in Chromosome 4q27 Region with Rheumatoid Arthritis and Confirmation of Type 1 Diabetes Point to a General Risk Locus for Autoimmune Diseases von Zhernakova, Alexandra, Alizadeh, Behrooz Z., Bevova, Marianna, van Leeuwen, Miek A., Coenen, Marieke J.H., Franke, Barbara, Franke, Lude, Posthumus, Marcel D., van Heel, David A., van der Steege, Gerrit, Radstake, Timothy R.D.J., Barrera, Pilar, Roep, Bart O., Koeleman, Bobby P.C., Wijmenga, Cisca

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An extensive screen of the HLA region reveals an independent association of HLA class I and class II with susceptibility for systemic lupus erythematosus von Martens, H. A., Nolte, I. M., van der Steege, G., Schipper, M., Kallenberg, C. G. M., te Meerman, G. J., Bijl, M.

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Deletions of the survival motor neuron gene in unaffected siblings of patients with spinal muscular atrophy von COBBEN, J. M, VAN DER STEEGE, G, GROOTSCHOLTEN, P, DE VISSER, M, SCHEFFER, H, BUYS, C. H. C. M

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Apparent gene conversions involving the SMN gene in the region of the spinal muscular atrophy locus on chromosome 5 von VAN DER STEEGE, G, GROOTSCHOLTEN, P. M, COBBEN, J. M, ZAPPATA, S, SCHEFFER, H, DEN DUNNEN, J. T, VAN OMMEN, G.-J. B, BRAHE, C, BUYS, C. H. C. M

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Re-analysis of the Xq27–Xq28 region suggests a weak association of an X-linked gene with sporadic testicular germ cell tumour without cryptorchidism von Lutke Holzik, M.F., Hoekstra, H.J., Sijmons, R.H., Sonneveld, D.J.A., van der Steege, G., Sleijfer, D.Th, Nolte, I.M.

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Association Between Toll-like Receptor 4 and Inflammatory Bowel Disease von Oostenbrug, Liekele E, Drenth, Joost P. H., de Jong, Dirk J, Nolte, Ilja M, Oosterom, Elvira, van Dullemen, Hendrik M, van der Linde, Klaas, te Meerman, Gerard J, van der Steege, Gerrit, Kleibeuker, Jan H, Jansen, Peter L. M.

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Features of epidermolysis bullosa simplex due to mutations in the ectodomain of type XVII collagen von Pasmooij, A.M.G., Van Der Steege, G., Pas, H.H., Smitt, J.H.sillevis, Nijenhuis, A.M., Zuiderveen, J., Jonkman, M.F.

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Prothrombotic Gene Polymorphisms: Possible Contributors to Hepatic Artery Thrombosis After Orthotopic Liver Transplantation von PEREBOOM, Ilona T. A, ADELMEIJER, Jelle, DER STEEGE, Gerrit Van, VAN DEN BERG, Aad P, LISMAN, Ton, PORTE, Robert J

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Interleukin-10 and Fas polymorphisms and susceptibility for (pre)neoplastic cervical disease von Zoodsma, M., Nolte, I.M., Schipper, M., Oosterom, E., Van Der Steege, G., De Vries, E.G.E., Te Meerman, G.J., Van Der Zee, A.G.J.

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