Wijmenga C - Search Results

1

Isochromosome 1q as the sole chromosomal abnormality in two fetal teratomas. Possible trisomic or tetrasomic zygote rescue in fetal teratoma with an additional isochromosome 1q.

Scheres JM, de Pater JM, Stoutenbeek P, Wijmenga C, Rosenberg C, Pearson PL. Scheres JM, et al. Among authors: wijmenga c. Cancer Genet Cytogenet. 1999 Nov;115(1):1-10. doi: 10.1016/s0165-4608(99)00049-7. Cancer Genet Cytogenet. 1999. PMID: 10565292

2

Polymorphic detection of a parthenogenetic maternal and double paternal contribution to a 46,XX/46,XY hermaphrodite.

Giltay JC, Brunt T, Beemer FA, Wit JM, van Amstel HK, Pearson PL, Wijmenga C. Giltay JC, et al. Among authors: wijmenga c. Am J Hum Genet. 1998 Apr;62(4):937-40. doi: 10.1086/301796. Am J Hum Genet. 1998. PMID: 9529354 Free PMC article.

3

Genetic mapping of the copper toxicosis locus in Bedlington terriers to dog chromosome 10, in a region syntenic to human chromosome region 2p13-p16.

van de Sluis BJ, Breen M, Nanji M, van Wolferen M, de Jong P, Binns MM, Pearson PL, Kuipers J, Rothuizen J, Cox DW, Wijmenga C, van Oost BA. van de Sluis BJ, et al. Among authors: wijmenga c. Hum Mol Genet. 1999 Mar;8(3):501-7. doi: 10.1093/hmg/8.3.501. Hum Mol Genet. 1999. PMID: 9949209

4

Characterization and chromosomal localization of five canine ATOX1 pseudogenes.

van de Sluis B, Nanji MS, Breen M, Pearson PL, Oost BA, Cox DW, Wijmenga C. van de Sluis B, et al. Among authors: wijmenga c. Cytogenet Cell Genet. 2001;93(1-2):105-8. doi: 10.1159/000056959. Cytogenet Cell Genet. 2001. PMID: 11474190

5

Defining the genetic contribution of type 2 diabetes mellitus.

van Tilburg J, van Haeften TW, Pearson P, Wijmenga C. van Tilburg J, et al. Among authors: wijmenga c. J Med Genet. 2001 Sep;38(9):569-78. doi: 10.1136/jmg.38.9.569. J Med Genet. 2001. PMID: 11546824 Free PMC article. Review.

6

Localization of the ICF syndrome to chromosome 20 by homozygosity mapping.

Wijmenga C, van den Heuvel LP, Strengman E, Luyten JA, van der Burgt IJ, de Groot R, Smeets DF, Draaisma JM, van Dongen JJ, De Abreu RA, Pearson PL, Sandkuijl LA, Weemaes CM. Wijmenga C, et al. Am J Hum Genet. 1998 Sep;63(3):803-9. doi: 10.1086/302021. Am J Hum Genet. 1998. PMID: 9718351 Free PMC article.

7

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: wijmenga c. Am J Gastroenterol. 2001 Dec;96(12):3337-40. doi: 10.1111/j.1572-0241.2001.05335.x. Am J Gastroenterol. 2001. PMID: 11774946

8

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 JH, Sandkuijl LA, Strengman E, van Someren H, Rigters-Aris CA, Pearson PL, van Haeften TW, Wijmenga C. van Tilburg JH, et al. Among authors: wijmenga c. J Clin Endocrinol Metab. 2003 May;88(5):2223-30. doi: 10.1210/jc.2002-021252. J Clin Endocrinol Metab. 2003. PMID: 12727978

9

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. Eur J Hum Genet. 1998 Nov-Dec;6(6):624-8. doi: 10.1038/sj.ejhg.5200235. Eur J Hum Genet. 1998. PMID: 9887382

10

Genome-wide screen in obese pedigrees with type 2 diabetes mellitus from a defined Dutch population.

van Tilburg JH, Sandkuijl LA, Franke L, Strengman E, Pearson PL, van Haeften TW, Wijmenga C. van Tilburg JH, et al. Among authors: wijmenga c. Eur J Clin Invest. 2003 Dec;33(12):1070-4. doi: 10.1111/j.1365-2362.2003.01276.x. Eur J Clin Invest. 2003. PMID: 14636289

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