Houwen RH - Search Results

1

A genomewide screen in a four-generation Dutch family with celiac disease: evidence for linkage to chromosomes 6 and 9.

van Belzen MJ, Vrolijk MM, Meijer JW, Crusius JB, Pearson PL, Sandkuijl LA, Houwen RH, Wijmenga C. van Belzen MJ, et al. Among authors: houwen rh. Am J Gastroenterol. 2004 Mar;99(3):466-71. doi: 10.1111/j.1572-0241.2004.04072.x. Am J Gastroenterol. 2004. PMID: 15056087

2

Defining the contribution of the HLA region to cis DQ2-positive coeliac disease patients.

van Belzen MJ, Koeleman BP, Crusius JB, Meijer JW, Bardoel AF, Pearson PL, Sandkuijl LA, Houwen RH, Wijmenga C. van Belzen MJ, et al. Among authors: houwen rh. Genes Immun. 2004 May;5(3):215-20. doi: 10.1038/sj.gene.6364061. Genes Immun. 2004. PMID: 15014431

3

A major non-HLA locus in celiac disease maps to chromosome 19.

Van Belzen MJ, Meijer JW, Sandkuijl LA, Bardoel AF, Mulder CJ, Pearson PL, Houwen RH, Wijmenga C. Van Belzen MJ, et al. Among authors: houwen rh. Gastroenterology. 2003 Oct;125(4):1032-41. doi: 10.1016/s0016-5085(03)01205-8. Gastroenterology. 2003. PMID: 14517787

4

CTLA4 +49 A/G and CT60 polymorphisms in Dutch coeliac disease patients.

van Belzen MJ, Mulder CJ, Zhernakova A, Pearson PL, Houwen RH, Wijmenga C. van Belzen MJ, et al. Among authors: houwen rh. Eur J Hum Genet. 2004 Sep;12(9):782-5. doi: 10.1038/sj.ejhg.5201165. Eur J Hum Genet. 2004. PMID: 15199380

5

The interferon gamma gene in celiac disease: augmented expression correlates with tissue damage but no evidence for genetic susceptibility.

Wapenaar MC, van Belzen MJ, Fransen JH, Sarasqueta AF, Houwen RH, Meijer JW, Mulder CJ, Wijmenga C. Wapenaar MC, et al. Among authors: houwen rh. J Autoimmun. 2004 Sep;23(2):183-90. doi: 10.1016/j.jaut.2004.05.004. J Autoimmun. 2004. PMID: 15324937

6

The tissue transglutaminase gene is not a primary factor predisposing to celiac disease.

van Belzen MJ, Mulder CJ, Pearson PL, Houwen RH, Wijmenga C. van Belzen MJ, et al. Among authors: houwen rh. Am J Gastroenterol. 2001 Dec;96(12):3337-40. doi: 10.1111/j.1572-0241.2001.05335.x. Am J Gastroenterol. 2001. PMID: 11774946

7

Autosomal-recessive inheritance of benign recurrent intrahepatic cholestasis.

De Koning TJ, Sandkuijl LA, De Schryver JE, Hennekam EA, Beemer FA, Houwen RH. De Koning TJ, et al. Among authors: houwen rh. Am J Med Genet. 1995 Jul 3;57(3):479-82. doi: 10.1002/ajmg.1320570324. Am J Med Genet. 1995. PMID: 7677155

8

Endemic Tyrolean infantile cirrhosis is not an allelic variant of Wilson's disease.

Wijmenga C, Müller T, Murli IS, Brunt T, Feichtinger H, Schönitzer D, Houwen RH, Müller W, Sandkuijl LA, Pearson PL. Wijmenga C, et al. Among authors: houwen rh. Eur J Hum Genet. 1998 Nov-Dec;6(6):624-8. doi: 10.1038/sj.ejhg.5200235. Eur J Hum Genet. 1998. PMID: 9887382

9

Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis.

Houwen RH, Baharloo S, Blankenship K, Raeymaekers P, Juyn J, Sandkuijl LA, Freimer NB. Houwen RH, et al. Nat Genet. 1994 Dec;8(4):380-6. doi: 10.1038/ng1294-380. Nat Genet. 1994. PMID: 7894490

10

Benign recurrent intrahepatic cholestasis (BRIC): evidence of genetic heterogeneity and delimitation of the BRIC locus to a 7-cM interval between D18S69 and D18S64.

Sinke RJ, Carlton VE, Juijn JA, Delhaas T, Bull L, van Berge Henegouwen GP, van Hattum J, Keller KM, Sinaasappel M, Bijleveld CM, Knol IE, Ploos van Amstel HK, Pearson PL, Berger R, Freimer NB, Houwen RH. Sinke RJ, et al. Among authors: houwen rh. Hum Genet. 1997 Sep;100(3-4):382-7. doi: 10.1007/s004390050520. Hum Genet. 1997. PMID: 9272159 Free article.

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