Jansen JC - Search Results

1

Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma.

Bayley JP, van Minderhout I, Weiss MM, Jansen JC, Oomen PH, Menko FH, Pasini B, Ferrando B, Wong N, Alpert LC, Williams R, Blair E, Devilee P, Taschner PE. Bayley JP, et al. Among authors: jansen jc. BMC Med Genet. 2006 Jan 11;7:1. doi: 10.1186/1471-2350-7-1. BMC Med Genet. 2006. PMID: 16405730 Free PMC article.

2

First experiences with genetic counselling based on predictive DNA diagnosis in hereditary glomus tumours (paragangliomas).

Oosterwijk JC, Jansen JC, van Schothorst EM, Oosterhof AW, Devilee P, Bakker E, Zoeteweij MW, van der Mey AG. Oosterwijk JC, et al. Among authors: jansen jc. J Med Genet. 1996 May;33(5):379-83. doi: 10.1136/jmg.33.5.379. J Med Genet. 1996. PMID: 8733047 Free PMC article.

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: jansen jc. 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: jansen jc. 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

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: jansen jc. Genes Chromosomes Cancer. 2001 Jul;31(3):274-81. doi: 10.1002/gcc.1144. Genes Chromosomes Cancer. 2001. PMID: 11391798

6

Carotid body tumors in humans caused by a mutation in the gene for succinate dehydrogenase D (SDHD).

Dahan A, Taschner PE, Jansen JC, van der Mey A, Teppema LJ, Cornelisse CJ. Dahan A, et al. Among authors: jansen jc. Adv Exp Med Biol. 2004;551:71-6. doi: 10.1007/0-387-27023-x_12. Adv Exp Med Biol. 2004. PMID: 15602946 No abstract available.

7

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: jansen jc. Eur J Endocrinol. 2005 Jan;152(1):87-94. doi: 10.1530/eje.1.01833. Eur J Endocrinol. 2005. PMID: 15762191

8

Malignant paragangliomas associated with mutations in the succinate dehydrogenase D gene.

Havekes B, Corssmit EP, Jansen JC, van der Mey AG, Vriends AH, Romijn JA. Havekes B, et al. Among authors: jansen jc. J Clin Endocrinol Metab. 2007 Apr;92(4):1245-8. doi: 10.1210/jc.2006-1993. Epub 2007 Jan 16. J Clin Endocrinol Metab. 2007. PMID: 17227803

9

Pheochromocytomas and extra-adrenal paragangliomas detected by screening in patients with SDHD-associated head-and-neck paragangliomas.

Havekes B, van der Klaauw AA, Weiss MM, Jansen JC, van der Mey AG, Vriends AH, Bonsing BA, Romijn JA, Corssmit EP. Havekes B, et al. Among authors: jansen jc. Endocr Relat Cancer. 2009 Jun;16(2):527-36. doi: 10.1677/ERC-09-0024. Epub 2009 Mar 16. Endocr Relat Cancer. 2009. PMID: 19289533 Clinical Trial.

10

The first Dutch SDHB founder deletion in paraganglioma-pheochromocytoma patients.

Bayley JP, Grimbergen AE, van Bunderen PA, van der Wielen M, Kunst HP, Lenders JW, Jansen JC, Dullaart RP, Devilee P, Corssmit EP, Vriends AH, Losekoot M, Weiss MM. Bayley JP, et al. Among authors: jansen jc. BMC Med Genet. 2009 Apr 15;10:34. doi: 10.1186/1471-2350-10-34. BMC Med Genet. 2009. PMID: 19368708 Free PMC article.

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