Tibben A - Search Results

1

Duchenne/Becker muscular dystrophy in the family: have potential carriers been tested at a molecular level?

Helderman-van den Enden AT, van den Bergen JC, Breuning MH, Verschuuren JJ, Tibben A, Bakker E, Ginjaar HB. Helderman-van den Enden AT, et al. Among authors: tibben a. Clin Genet. 2011 Mar;79(3):236-42. doi: 10.1111/j.1399-0004.2010.01579.x. Epub 2010 Nov 11. Clin Genet. 2011. PMID: 21070212

2

Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: a genetic and clinicopathological study of three Dutch families.

Heutink P, Stevens M, Rizzu P, Bakker E, Kros JM, Tibben A, Niermeijer MF, van Duijn CM, Oostra BA, van Swieten JC. Heutink P, et al. Among authors: tibben a. Ann Neurol. 1997 Feb;41(2):150-9. doi: 10.1002/ana.410410205. Ann Neurol. 1997. PMID: 9029063

3

DNA testing for fragile X syndrome: implications for parents and family.

van Rijn MA, de Vries BB, Tibben A, van den Ouweland AM, Halley DJ, Niermeijer MF. van Rijn MA, et al. Among authors: tibben a. J Med Genet. 1997 Nov;34(11):907-11. doi: 10.1136/jmg.34.11.907. J Med Genet. 1997. PMID: 9391884 Free PMC article.

4

New problems in testing for Huntington's disease: the issue of intermediate and reduced penetrance alleles.

Maat-Kievit A, Losekoot M, Van Den Boer-Van Den Berg H, Van Ommen GJ, Niermeijer M, Breuning M, Tibben A. Maat-Kievit A, et al. Among authors: tibben a. J Med Genet. 2001 Apr;38(4):E12. doi: 10.1136/jmg.38.4.e12. J Med Genet. 2001. PMID: 11283208 Free PMC article. No abstract available.

5

Testing the test--why pursue a better test for Huntington disease?

Timman R, Maat-Kievit A, Brouwer-DudokdeWit C, Zoeteweij M, Breuning MH, Tibben A. Timman R, et al. Among authors: tibben a. Am J Med Genet B Neuropsychiatr Genet. 2003 Feb;117B(1):79-85. doi: 10.1002/ajmg.b.10028. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12555240

6

Feeling at risk: how women interpret their familial breast cancer risk.

van Dijk S, Otten W, van Asperen CJ, Timmermans DR, Tibben A, Zoeteweij MW, Silberg S, Breuning MH, Kievit J. van Dijk S, et al. Among authors: tibben a. Am J Med Genet A. 2004 Nov 15;131(1):42-9. doi: 10.1002/ajmg.a.30322. Am J Med Genet A. 2004. PMID: 15382029

7

Variants of uncertain clinical significance as a result of BRCA1/2 testing: impact of an ambiguous breast cancer risk message.

van Dijk S, van Asperen CJ, Jacobi CE, Vink GR, Tibben A, Breuning MH, Otten W. van Dijk S, et al. Among authors: tibben a. Genet Test. 2004 Fall;8(3):235-9. doi: 10.1089/gte.2004.8.235. Genet Test. 2004. PMID: 15727245

8

What's the message? Interpretation of an uninformative BRCA1/2 test result for women at risk of familial breast cancer.

van Dijk S, Otten W, Timmermans DR, van Asperen CJ, Meijers-Heijboer H, Tibben A, Breuning MH, Kievit J. van Dijk S, et al. Among authors: tibben a. Genet Med. 2005 Apr;7(4):239-45. doi: 10.1097/01.gim.0000159902.34833.26. Genet Med. 2005. PMID: 15834241 Free article.

9

Family system characteristics and psychological adjustment to cancer susceptibility genetic testing: a prospective study.

van Oostrom I, Meijers-Heijboer H, Duivenvoorden HJ, Bröcker-Vriends AH, van Asperen CJ, Sijmons RH, Seynaeve C, van Gool AR, Klijn JG, Tibben A. van Oostrom I, et al. Among authors: tibben a. Clin Genet. 2007 Jan;71(1):35-42. doi: 10.1111/j.1399-0004.2007.00731.x. Clin Genet. 2007. PMID: 17204044

10

Genetic testing in familial melanoma: uptake and implications.

de Snoo FA, Riedijk SR, van Mil AM, Bergman W, ter Huurne JA, Timman R, Bertina W, Gruis NA, Vasen HF, van Haeringen A, Breuning MH, Tibben A. de Snoo FA, et al. Among authors: tibben a. Psychooncology. 2008 Aug;17(8):790-6. doi: 10.1002/pon.1377. Psychooncology. 2008. PMID: 18613292

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