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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PARK7, a Novel Locus for Autosomal Recessive Early-Onset Parkinsonism, on Chromosome 1p36
van Duijn, C.M., Dekker, M.C.J., Bonifati, V., Galjaard, R.J., Houwing-Duistermaat, J.J., Snijders, P.J.L.M., Testers, L., Breedveld, G.J., Horstink, M., Sandkuijl, L.A., van Swieten, J.C., Oostra, B.A., Heutink, P.
Published in American journal of human genetics (01.09.2001)
Published in American journal of human genetics (01.09.2001)
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Association between an agouti-related protein gene polymorphism and anorexia nervosa
VINK, T, HINNEY, A, ADAN, R. A. H, VAN ELBURG, A. A, VAN GOOZEN, S. H. M, SANDKUIJL, L. A, SINKE, R. J, HERPERTZ-DAHLMANN, B-M, HEBEBRAND, J, REMSCHMIDT, H, VAN ENGELAND, H
Published in Molecular psychiatry (01.05.2001)
Published in Molecular psychiatry (01.05.2001)
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Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura
Terwindt, G M, Ophoff, R A, van Eijk, R, Vergouwe, M N, Haan, J, Frants, R R, Sandkuijl, L A, Ferrari, M D
Published in Neurology (24.04.2001)
Published in Neurology (24.04.2001)
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Frequency of glycogen storage disease type II in The Netherlands: implications for diagnosis and genetic counselling
Ausems, M G, Verbiest, J, Hermans, M P, Kroos, M A, Beemer, F A, Wokke, J H, Sandkuijl, L A, Reuser, A J, van der Ploeg, A T
Published in European journal of human genetics : EJHG (01.09.1999)
Published in European journal of human genetics : EJHG (01.09.1999)
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Clinical and genetic heterogeneity in benign hereditary chorea
Breedveld, G J, Percy, A K, MacDonald, M E, de Vries, B B A, Yapijakis, C, Dure, L S, Ippel, E F, Sandkuijl, L A, Heutink, P, Arts, W F M
Published in Neurology (27.08.2002)
Published in Neurology (27.08.2002)
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Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness
van den Ouweland, J M, Lemkes, H H, Ruitenbeek, W, Sandkuijl, L A, de Vijlder, M F, Struyvenberg, P A, van de Kamp, J J, Maassen, J A
Published in Nature genetics (01.08.1992)
Published in Nature genetics (01.08.1992)
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Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis
Baharloo, Siamak, Blankenship, Kathleen, Juyn, Jenneke, Raeymaekers, Peter, Houwen, Roderick H. J, Freimer, Nelson B, Sandkuijl, Lodewijk A
Published in Nature genetics (01.12.1994)
Published in Nature genetics (01.12.1994)
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A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis
Njajou, Omer T, Vaessen, Norbert, Joosse, Marijke, Berghuis, Bianca, van Dongen, Jeroen W.F, Breuning, Martijn H, Snijders, Pieter J.L.M, Rutten, Wim P.F, Sandkuijl, Lodewijk A, Oostra, Ben A, van Duijn, Cornelia M, Heutink, Peter
Published in Nature genetics (01.07.2001)
Published in Nature genetics (01.07.2001)
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Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds
Gruis, Nelleke A, van der Velden, Pieter A, Sandkuijl, Lodewijk A, Prins, Duncan E, Weaver-Feldhaus, Jane, Kamb, Alexander, Bergman, Wilma, Frants, Rune R
Published in Nature genetics (01.07.1995)
Published in Nature genetics (01.07.1995)
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Genetic mapping using haplotype, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22-q23
Batki, Steven, Tyler, David J, Blankenship, Kathleen, Leon, Pedro, Fournier, Eduardo, Smith, Lauren B, Spesny, Mitzi, Service, Susan K, Freimer, Nelson B, Reus, Victor I, Silva, Sandra, Gallegos, Alvaro, Sandkuijl, Lodewijk A, Escamilla, Michael A, Meza, Luis, Rojas, Eugenia, Baharloo, Siamak, Vinogradov, Sophia, Barondes, Samuel H, Weissenbach, Jean, Mclnnes, L. Alison
Published in Nature genetics (01.04.1996)
Published in Nature genetics (01.04.1996)
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An Apolipoprotein CIII Haplotype Protective Against Hypertriglyceridemia is Specified by Promoter and 3' Untranslated Region Polymorphisms
Dammerman, Marilyn, Sandkuijl, Lodewijk A., Halaas, Jeffrey L., Chung, Wendy, Breslow, Jan L.
Published in Proceedings of the National Academy of Sciences - PNAS (15.05.1993)
Published in Proceedings of the National Academy of Sciences - PNAS (15.05.1993)
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Defining the contribution of the HLA region to cis DQ2-positive coeliac disease patients
van Belzen, M J, Koeleman, B P C, Crusius, J B A, Meijer, J W R, Bardoel, A F J, Pearson, P L, Sandkuijl, L A, Houwen, R H J, Wijmenga, C
Published in Genes and immunity (01.05.2004)
Published in Genes and immunity (01.05.2004)
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A Gly15Arg mutation in the interleukin-10 gene reduces secretion of interleukin-10 in Crohn disease
van der Linde, K, Boor, P P C, Sandkuijl, L A, Meijssen, M A C, Savelkoul, H F J, Wilson, J H P, de Rooij, F W M
Published in Scandinavian journal of gastroenterology (01.01.2003)
Published in Scandinavian journal of gastroenterology (01.01.2003)
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The Gene for Leukoencephalopathy with Vanishing White Matter Is Located on Chromosome 3q27
Leegwater, Peter A.J., Könst, Andrea A.M., Kuyt, Bertus, Sandkuijl, Lodewijk A., Naidu, SakkuBai, Oudejans, Cees B.M., Schutgens, Ruud B.H., Pronk, Jan C., van der Knaap, Marjo S.
Published in American journal of human genetics (01.09.1999)
Published in American journal of human genetics (01.09.1999)
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A Genome-Wide Scan in Type 2 Diabetes Mellitus Provides Independent Replication of a Susceptibility Locus on 18p11 and Suggests the Existence of Novel Loci on 2q12 and 19q13
van Tilburg, J. H. O., Sandkuijl, L. A., Strengman, E., van Someren, H., Rigters-Aris, C. A. E., Pearson, P. L., van Haeften, T. W, Wijmenga, C.
Published in The journal of clinical endocrinology and metabolism (01.05.2003)
Published in The journal of clinical endocrinology and metabolism (01.05.2003)
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Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura
May, A, Ophoff, R A, Terwindt, G M, Urban, C, van Eijk, R, Haan, J, Diener, H C, Lindhout, D, Frants, R R, Sandkuijl, L A
Published in Human genetics (01.11.1995)
Published in Human genetics (01.11.1995)
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