Vink GR - Search Results

1

A scenario-drafting study to explore potential future implementation pathways of circulating tumor DNA testing in oncology.

Kramer A, Rubio-Alarcón C, van den Broek D, Vessies DCL, Van't Erve I, Meijer GA, Vink GR, Schuuring E, Fijneman RJA, Coupé VMH, Retèl VP. Kramer A, et al. Among authors: vink gr. Mol Oncol. 2024 Nov;18(11):2730-2742. doi: 10.1002/1878-0261.13562. Epub 2024 Jan 11. Mol Oncol. 2024. PMID: 38060377 Free PMC article.

2

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: vink gr. Genet Test. 2004 Fall;8(3):235-9. doi: 10.1089/gte.2004.8.235. Genet Test. 2004. PMID: 15727245

3

Intronic variants in BRCA1 and BRCA2 that affect RNA splicing can be reliably selected by splice-site prediction programs.

Vreeswijk MP, Kraan JN, van der Klift HM, Vink GR, Cornelisse CJ, Wijnen JT, Bakker E, van Asperen CJ, Devilee P. Vreeswijk MP, et al. Among authors: vink gr. Hum Mutat. 2009 Jan;30(1):107-14. doi: 10.1002/humu.20811. Hum Mutat. 2009. PMID: 18693280

4

Two-color multiplex ligation-dependent probe amplification: detecting genomic rearrangements in hereditary multiple exostoses.

White SJ, Vink GR, Kriek M, Wuyts W, Schouten J, Bakker B, Breuning MH, den Dunnen JT. White SJ, et al. Among authors: vink gr. Hum Mutat. 2004 Jul;24(1):86-92. doi: 10.1002/humu.20054. Hum Mutat. 2004. PMID: 15221792

5

Genotype-phenotype correlation in patients suspected of having Sotos syndrome.

de Boer L, Kant SG, Karperien M, van Beers L, Tjon J, Vink GR, van Tol D, Dauwerse H, le Cessie S, Beemer FA, van der Burgt I, Hamel BC, Hennekam RC, Kuhnle U, Mathijssen IB, Veenstra-Knol HE, Stumpel CT, Breuning MH, Wit JM. de Boer L, et al. Among authors: vink gr. Horm Res. 2004;62(4):197-207. doi: 10.1159/000081063. Epub 2004 Sep 24. Horm Res. 2004. PMID: 15452385 Free article.

6

Unclassified variants in disease-causing genes: nonuniformity of genetic testing and counselling, a proposal for guidelines.

Vink GR, van Asperen CJ, Devilee P, Breuning MH, Bakker E. Vink GR, et al. Eur J Hum Genet. 2005 May;13(5):525-7. doi: 10.1038/sj.ejhg.5201379. Eur J Hum Genet. 2005. PMID: 15741995 No abstract available.

7

Efficacy of screening women at high risk of hereditary ovarian cancer: results of an 11-year cohort study.

Gaarenstroom KN, van der Hiel B, Tollenaar RA, Vink GR, Jansen FW, van Asperen CJ, Kenter GG. Gaarenstroom KN, et al. Among authors: vink gr. Int J Gynecol Cancer. 2006 Jan-Feb;16 Suppl 1:54-9. doi: 10.1111/j.1525-1438.2006.00480.x. Int J Gynecol Cancer. 2006. PMID: 16515568

8

Mutation screening of EXT1 and EXT2 by direct sequence analysis and MLPA in patients with multiple osteochondromas: splice site mutations and exonic deletions account for more than half of the mutations.

Vink GR, White SJ, Gabelic S, Hogendoorn PC, Breuning MH, Bakker E. Vink GR, et al. Eur J Hum Genet. 2005 Apr;13(4):470-4. doi: 10.1038/sj.ejhg.5201343. Eur J Hum Genet. 2005. PMID: 15586175

9

Impulse oscillometry: a measure for airway obstruction.

Vink GR, Arets HG, van der Laag J, van der Ent CK. Vink GR, et al. Pediatr Pulmonol. 2003 Mar;35(3):214-9. doi: 10.1002/ppul.10235. Pediatr Pulmonol. 2003. PMID: 12567390

10

Prospective Dutch colorectal cancer cohort: an infrastructure for long-term observational, prognostic, predictive and (randomized) intervention research.

Burbach JP, Kurk SA, Coebergh van den Braak RR, Dik VK, May AM, Meijer GA, Punt CJ, Vink GR, Los M, Hoogerbrugge N, Huijgens PC, Ijzermans JN, Kuipers EJ, de Noo ME, Pennings JP, van der Velden AM, Verhoef C, Siersema PD, van Oijen MG, Verkooijen HM, Koopman M. Burbach JP, et al. Among authors: vink gr. Acta Oncol. 2016 Nov;55(11):1273-1280. doi: 10.1080/0284186X.2016.1189094. Epub 2016 Aug 25. Acta Oncol. 2016. PMID: 27560599

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