A microarray screen for novel candidate genes in coeliac disease pathogenesis
Diosdado, B, Wapenaar, M C, Franke, L, Duran, K J, Goerres, M J, Hadithi, M, Crusius, J B A, Meijer, J W R, Duggan, D J, Mulder, C J J, Holstege, F C P, Wijmenga, C
Published in Gut (01.07.2004)
Published in Gut (01.07.2004)
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Journal Article
Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications
DEN DUNNEN, J. T, GROOTSCHOLTEN, P. M, BAKKER, E, BLONDEN, L. A. J, GINJAAR, H. B, WAPENAAR, M. C, VAN PAASSEN, H. M. B, VAN BROECKHOVEN, C, PEARSON, P. L, VAN OMMEN, G. J. B
Published in American journal of human genetics (01.12.1989)
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Published in American journal of human genetics (01.12.1989)
Journal Article
Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitis
Wapenaar, M C, Monsuur, A J, van Bodegraven, A A, Weersma, R K, Bevova, M R, Linskens, R K, Howdle, P, Holmes, G, Mulder, C J, Dijkstra, G, van Heel, D A, Wijmenga, C
Published in Gut (01.04.2008)
Published in Gut (01.04.2008)
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Characterization of Cxorf5 (71-7A), a novel human cDNA mapping to Xp22 and encoding a protein containing coiled-coil α-helical domains
DE CONCILIIS, L, MARCHITIELLO, A, BANFI, S, WAPENAAR, M. C, BORSANI, G, GIGLIO, S, MARIANI, M, CONSALEZ, G. G, ZUFFARDI, O, FRANCO, B, BALLABIO, A
Published in Genomics (San Diego, Calif.) (15.07.1998)
Published in Genomics (San Diego, Calif.) (15.07.1998)
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Journal Article
A gene from the Xp22.3 region shares homology with voltage-gated chloride channels
van Slegtenhorst, M A, Bassi, M T, Borsani, G, Wapenaar, M C, Ferrero, G B, de Conciliis, L, Rugarli, E I, Grillo, A, Franco, B, Zoghbi, H Y, Ballabio, A
Published in Human molecular genetics (01.04.1994)
Published in Human molecular genetics (01.04.1994)
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Journal Article
Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy
Hofker, M H, Wapenaar, M C, Goor, N, Bakker, E, van Ommen, G J, Pearson, P L
Published in Human genetics (01.01.1985)
Published in Human genetics (01.01.1985)
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The genes for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects (MLS): cloning and characterization of the critical regions
Wapenaar, M C, Bassi, M T, Schaefer, L, Grillo, A, Ferrero, G B, Chinault, A C, Ballabio, A, Zoghbi, H Y
Published in Human molecular genetics (01.07.1993)
Published in Human molecular genetics (01.07.1993)
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The X chromosome shows less genetic variation at restriction sites than the autosomes
HOFKER, M. H, SKRAASTAD, M. I, BERGEN, A. A. B, WAPENAAR, M. C, BAKKER, E, MILLINGTON-WARD, A, VAN OMMEN, G. J. B, PEARSON, P. L
Published in American journal of human genetics (01.10.1986)
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Published in American journal of human genetics (01.10.1986)
Journal Article
Generation and fluorescent in situ hybridization mapping of yeast artificial chromosomes of 1p, 17p, 17q, and 19q from a hybrid cell line by high-density screening of an amplified library
Driesen, M.S., Dauwerse, J.G., Wapenaar, M.C., Meershoek, E.J., Mollevanger, P., Chen, K.L., Fischbeck, K.H., van Ommen, G.J.B.
Published in Genomics (San Diego, Calif.) (01.12.1991)
Published in Genomics (San Diego, Calif.) (01.12.1991)
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Journal Article
A CA-repeat polymorphism near DXS418 (P122)
Van De Vosse, E, Booms, P F, Vossen, R H, Wapenaar, M C, Van Ommen, G J, Den Dunnen, J T
Published in Human molecular genetics (01.12.1993)
Published in Human molecular genetics (01.12.1993)
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Journal Article
Association Analysis of MYO9B Gene Polymorphisms with Celiac Disease in a Swedish/Norwegian Cohort
Amundsen, Silja S., Monsuur, Alienke J., Wapenaar, Martin C., Lie, Benedicte A., Ek, Johan, Gudjónsdóttir, Audur H., Ascher, Henry, Wijmenga, Cisca, Sollid, Ludvig M.
Published in Human Immunology (01.04.2006)
Published in Human Immunology (01.04.2006)
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Journal Article
Physical mapping of 14 new DNA markers isolated from the human distal Xp region
Wapenaar, M.C., Petit, C., Basler, E., Ballabio, A., Henke, A., Rappold, G.A., van Paassen, H.M.B., Blonden, L.A.J., van Ommen, G.J.B.
Published in Genomics (San Diego, Calif.) (01.05.1992)
Published in Genomics (San Diego, Calif.) (01.05.1992)
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Journal Article
The interferon gamma gene in celiac disease: augmented expression correlates with tissue damage but no evidence for genetic susceptibility
Wapenaar, Martin C., van Belzen, Martine J., Fransen, Justin H., Fariña Sarasqueta, Aranzazu, Houwen, Roderick H.J., Meijer, Jos W.R., Mulder, Chris J.J., Wijmenga, Cisca
Published in Journal of autoimmunity (01.09.2004)
Published in Journal of autoimmunity (01.09.2004)
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Journal Article
Detection of a new submicroscopic Norrie disease deletion interval with a novel DNA probe isolated by differential Alu PCR fingerprint cloning
Bergen, A A, Wapenaar, M C, Schuurman, E J, Diergaarde, P J, Lerach, H, Monaco, A P, Bakker, E, Bleeker-Wagemakers, E M, van Ommen, G J
Published in Cytogenetics and cell genetics (01.01.1993)
Published in Cytogenetics and cell genetics (01.01.1993)
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Journal Article
A submicroscopic deletion in a patient with isolated X-linked ocular albinism (OA1)
Bassi, M T, Bergen, A A, Wapenaar, M C, Schiaffino, M V, van Schooneveld, M, Yates, J R, Charles, S J, Meitinger, T, Ballabio, A
Published in Human molecular genetics (01.04.1994)
Published in Human molecular genetics (01.04.1994)
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Journal Article
Duchenne muscular dystrophy: high frequency of deletions
Bartlett, R J, Pericak-Vance, M A, Koh, J, Yamaoka, L H, Chen, J C, Hung, W Y, Speer, M C, Wapenaar, M C, Van Ommen, G J, Bakker, E
Published in Neurology (01.01.1988)
Published in Neurology (01.01.1988)
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Isolation and characterization of cell hybrids containing human Xp-chromosome fragments
Wapenaar, M C, Kievits, T, Meera Khan, P, Pearson, P L, Van Ommen, G J
Published in Cytogenetics and cell genetics (01.01.1990)
Published in Cytogenetics and cell genetics (01.01.1990)
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