Cornelisse CJ - Search Results

1

A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter.

Heutink P, van der Mey AG, Sandkuijl LA, van Gils AP, Bardoel A, Breedveld GJ, van Vliet M, van Ommen GJ, Cornelisse CJ, Oostra BA, et al. Heutink P, et al. Among authors: cornelisse cj. Hum Mol Genet. 1992 Apr;1(1):7-10. doi: 10.1093/hmg/1.1.7. Hum Mol Genet. 1992. PMID: 1301144

2

Further localization of the gene for hereditary paragangliomas and evidence for linkage in unrelated families.

Heutink P, van Schothorst EM, van der Mey AG, Bardoel A, Breedveld G, Pertijs J, Sandkuijl LA, van Ommen GJ, Cornelisse CJ, Oostra BA, et al. Heutink P, et al. Among authors: cornelisse cj. Eur J Hum Genet. 1994;2(3):148-58. doi: 10.1159/000472358. Eur J Hum Genet. 1994. PMID: 7834274

3

Confinement of PGL, an imprinted gene causing hereditary paragangliomas, to a 2-cM interval on 11q22-q23 and exclusion of DRD2 and NCAM as candidate genes.

van Schothorst EM, Jansen JC, Bardoel AF, van der Mey AG, James MJ, Sobol H, Weissenbach J, van Ommen GJ, Cornelisse CJ, Devilee P. van Schothorst EM, et al. Among authors: cornelisse cj. Eur J Hum Genet. 1996;4(5):267-73. doi: 10.1159/000472213. Eur J Hum Genet. 1996. PMID: 8946172

4

Founder effect at PGL1 in hereditary head and neck paraganglioma families from the Netherlands.

van Schothorst EM, Jansen JC, Grooters E, Prins DE, Wiersinga JJ, van der Mey AG, van Ommen GJ, Devilee P, Cornelisse CJ. van Schothorst EM, et al. Among authors: cornelisse cj. Am J Hum Genet. 1998 Aug;63(2):468-73. doi: 10.1086/301951. Am J Hum Genet. 1998. PMID: 9683583 Free PMC article.

5

Paragangliomas of the head and neck region show complete loss of heterozygosity at 11q22-q23 in chief cells and the flow-sorted DNA aneuploid fraction.

van Schothorst EM, Beekman M, Torremans P, Kuipers-Dijkshoorn NJ, Wessels HW, Bardoel AF, van der Mey AG, van der Vijver MJ, van Ommen GJ, Devilee P, Cornelisse CJ. van Schothorst EM, et al. Among authors: cornelisse cj. Hum Pathol. 1998 Oct;29(10):1045-9. doi: 10.1016/s0046-8177(98)90411-7. Hum Pathol. 1998. PMID: 9781639

6

Allelotype of head and neck paragangliomas: allelic imbalance is confined to the long arm of chromosome 11, the site of the predisposing locus PGL.

Devilee P, van Schothorst EM, Bardoel AF, Bonsing B, Kuipers-Dijkshoorn N, James MR, Fleuren G, van der Mey AG, Cornelisse CJ. Devilee P, et al. Among authors: cornelisse cj. Genes Chromosomes Cancer. 1994 Oct;11(2):71-8. doi: 10.1002/gcc.2870110202. Genes Chromosomes Cancer. 1994. PMID: 7529551

7

Allele loss patterns on chromosome 17q in 109 breast carcinomas indicate at least two distinct target regions.

Cornelis RS, Devilee P, van Vliet M, Kuipers-Dijkshoorn N, Kersenmaeker A, Bardoel A, Khan PM, Cornelisse CJ. Cornelis RS, et al. Among authors: cornelisse cj. Oncogene. 1993 Mar;8(3):781-5. Oncogene. 1993. PMID: 8437862

8

The majority of 22 Dutch high-risk breast cancer families are due to either BRCA1 or BRCA2.

Peelen T, Cornelis RS, van Vliet M, Petrij-Bosch A, Cleton-Jansen AM, Meijers-Heijboer H, Klijn JG, Vasen HF, Cornelisse CJ, Devilee P. Peelen T, et al. Among authors: cornelisse cj. Eur J Hum Genet. 1996;4(4):225-30. doi: 10.1159/000472203. Eur J Hum Genet. 1996. PMID: 8875189

9

Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene.

Taschner PE, Jansen JC, Baysal BE, Bosch A, Rosenberg EH, Bröcker-Vriends AH, van Der Mey AG, van Ommen GJ, Cornelisse CJ, Devilee P. Taschner PE, et al. Among authors: cornelisse cj. Genes Chromosomes Cancer. 2001 Jul;31(3):274-81. doi: 10.1002/gcc.1144. Genes Chromosomes Cancer. 2001. PMID: 11391798

10

Frequent somatic imbalance of marker alleles for chromosome 1 in human primary breast carcinoma.

Devilee P, van Vliet M, Bardoel A, Kievits T, Kuipers-Dijkshoorn N, Pearson PL, Cornelisse CJ. Devilee P, et al. Among authors: cornelisse cj. Cancer Res. 1991 Feb 1;51(3):1020-5. Cancer Res. 1991. PMID: 1670997

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