Cornelisse CJ - Search Results

1

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

2

The Dutch founder mutation SDHD.D92Y shows a reduced penetrance for the development of paragangliomas in a large multigenerational family.

Hensen EF, Jansen JC, Siemers MD, Oosterwijk JC, Vriends AH, Corssmit EP, Bayley JP, van der Mey AG, Cornelisse CJ, Devilee P. Hensen EF, et al. Among authors: cornelisse cj. Eur J Hum Genet. 2010 Jan;18(1):62-6. doi: 10.1038/ejhg.2009.112. Eur J Hum Genet. 2010. PMID: 19584903 Free PMC article.

3

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

4

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

5

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

6

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.

7

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

8

Estimation of growth rate in patients with head and neck paragangliomas influences the treatment proposal.

Jansen JC, van den Berg R, Kuiper A, van der Mey AG, Zwinderman AH, Cornelisse CJ. Jansen JC, et al. Among authors: cornelisse cj. Cancer. 2000 Jun 15;88(12):2811-6. Cancer. 2000. PMID: 10870065

9

SDHD mutations in head and neck paragangliomas result in destabilization of complex II in the mitochondrial respiratory chain with loss of enzymatic activity and abnormal mitochondrial morphology.

Douwes Dekker PB, Hogendoorn PC, Kuipers-Dijkshoorn N, Prins FA, van Duinen SG, Taschner PE, van der Mey AG, Cornelisse CJ. Douwes Dekker PB, et al. Among authors: cornelisse cj. J Pathol. 2003 Nov;201(3):480-6. doi: 10.1002/path.1461. J Pathol. 2003. PMID: 14595761

10

Increased prevalence of catecholamine excess and phaeochromocytomas in a well-defined Dutch population with SDHD-linked head and neck paragangliomas.

van Houtum WH, Corssmit EP, Douwes Dekker PB, Jansen JC, van der Mey AG, Bröcker-Vriends AH, Taschner PE, Losekoot M, Frölich M, Stokkel MP, Cornelisse CJ, Romijn JA. van Houtum WH, et al. Among authors: cornelisse cj. Eur J Endocrinol. 2005 Jan;152(1):87-94. doi: 10.1530/eje.1.01833. Eur J Endocrinol. 2005. PMID: 15762191

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