An association screen of myelin-related genes implicates the chromosome 22q11 PIK4CA gene in schizophrenia
JUNGERIUS, B. J, HOOGENDOORN, M. L. C, BAKKER, S. C, VAN'T SLOT, R, BARDOEL, A. F, OPHOFF, R. A, WIJMENGA, C, KAHN, R. S, SINKE, R. J
Published in Molecular psychiatry (01.11.2008)
Published in Molecular psychiatry (01.11.2008)
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A Whole-Genome Scan in 164 Dutch Sib Pairs with Attention-Deficit/Hyperactivity Disorder: Suggestive Evidence for Linkage on Chromosomes 7p and 15q
Bakker, S.C., Meulen, E. M. van der, Buitelaar, J.K., Sandkuijl, L.A., Pauls, D.L., Monsuur, A.J., Slot, R. van ‘t, Minderaa, R.B., Gunning, W.B., Pearson, P.L., Sinke, R.J.
Published in American journal of human genetics (01.05.2003)
Published in American journal of human genetics (01.05.2003)
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Copy number changes of the microcephalin 1 gene (MCPH1) in patients with autism spectrum disorders
Ozgen, HM, Van Daalen, E, Bolton, PF, Maloney, VK, Huang, S, Cresswell, L, Van Den Boogaard, MJ, Eleveld, MJ, Van‘t Slot, R, Hochstenbach, R, Beemer, FA, Barrow, M, Barber, JCK, Poot, M
Published in Clinical genetics (01.10.2009)
Published in Clinical genetics (01.10.2009)
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Survival of autoreactive T lymphocytes by microRNA-mediated regulation of apoptosis through TRAIL and Fas in type 1 diabetes
de Jong, V M, van der Slik, A R, Laban, S, van 't Slot, R, Koeleman, B P C, Zaldumbide, A, Roep, B O
Published in Genes and immunity (01.09.2016)
Published in Genes and immunity (01.09.2016)
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Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect
Wijmenga, Cisca, Monsuur, Alienke J, Bakker, Paul I W de, Alizadeh, Behrooz Z, Zhernakova, Alexandra, Bevova, Marianna R, Strengman, Eric, Franke, Lude, Slot, Ruben van't, Belzen, Martine J van, Lavrijsen, Ineke C M, Diosdado, Begoña, Daly, Mark J, Mulder, Chris J J, Mearin, M Luisa, Meijer, Jos W R, Meijer, Gerrit A, Oort, Erica van, Wapenaar, Martin C, Koeleman, Bobby P C
Published in Nature genetics (01.12.2005)
Published in Nature genetics (01.12.2005)
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Association of the TGF-β receptor genes with abdominal aortic aneurysm
BAAS, A. F, MEDIC, J, WIJMENGA, C, BLANKENSTEIJN, J. D, RUIGROK, Y. M, VAN 'T SLOT, R, DE KOVEL, C. G, ZHERNAKOVA, A, GEELKERKEN, R. H, KRANENDONK, S. E, VAN STERKENBURG, S. M, GROBBEE, D. E, BOLL, A. P
Published in European journal of human genetics : EJHG (01.02.2010)
Published in European journal of human genetics : EJHG (01.02.2010)
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Genetic variations in regulatory pathways of fatty acid and glucose metabolism are associated with obesity phenotypes: a population-based cohort study
Berg, S.W. van den, Dolle, M.E.T, Imholz, S, A, D.L. van der, Slot, R. van't, Wijmenga, C, Verschuren, W.M.M, Strien, C, Siezen, C.L.E, Hoebee, B, Feskens, E.J.M, Boer, J.M.A
Published in International Journal of Obesity (01.10.2009)
Published in International Journal of Obesity (01.10.2009)
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Reliable high-throughput genotyping and loss-of-heterozygosity detection in formalin-fixed, paraffin-embedded tumors using single nucleotide polymorphism arrays
LIPS, Esther H, DIERSSEN, Jan Willem F, VAN WEZEL, Tom, VAN EIJK, Ronald, OOSTING, Jan, EILERS, Paul H. C, TOLLENAAR, Rob A. E. M, DE GRAAF, Eelco J, VAN'T SLOT, Ruben, WIJMENGA, Cisca, MORREAU, Hans
Published in Cancer research (Chicago, Ill.) (15.11.2005)
Published in Cancer research (Chicago, Ill.) (15.11.2005)
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Multiple independent variants in 6q21-22 associated with susceptibility to celiac disease in the Dutch, Finnish and Hungarian populations
EINARSDOTTIR, Elisabet, BEVOVA, Marianna R, KURPPA, Kalle, KERE, Juha, MÄKI, Markku, WIJMENGA, Cisca, SAAVALAINEN, Päivi, ZHERNAKOVA, Alexandra, MONSUUR, Alienke, KOSKINEN, Lotta Le, VAN'T SLOT, Ruben, MULDER, Chris, MEARIN, M. Luisa, KORPONAY-SZABO, Ilma R, KAUKINEN, Katri
Published in European journal of human genetics : EJHG (01.06.2011)
Published in European journal of human genetics : EJHG (01.06.2011)
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Gain of FAM123B and ARHGEF9 in an Obese Man with Intellectual Disability, Congenital Heart Defects and Multiple Supernumerary Ring Chromosomes
Hochstenbach, R., van Gijn, M.E., Krijtenburg, P.-J., Raemakers, R., van ’t Slot, R., Renkens, I., Eleveld, M.J., van der Smagt, J.J., Poot, M.
Published in Molecular syndromology (2013)
Published in Molecular syndromology (2013)
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The cps locus of Streptococcus suis serotype 2: genetic determinant for the synthesis of sialic acid
Smith, Hilde E, de Vries, Ruth, Slot, Ruben van»t, Smits, Mari A
Published in Microbial pathogenesis (01.08.2000)
Published in Microbial pathogenesis (01.08.2000)
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