Meijers-Heijboer H - Search Results

1

Uptake of prenatal diagnostic testing for retinoblastoma compared to other hereditary cancer syndromes in the Netherlands.

Dommering CJ, Henneman L, van der Hout AH, Jonker MA, Tops CM, van den Ouweland AM, van der Luijt RB, Mensenkamp AR, Hogervorst FB, Redeker EJ, de Die-Smulders CE, Moll AC, Meijers-Heijboer H. Dommering CJ, et al. Fam Cancer. 2017 Apr;16(2):271-277. doi: 10.1007/s10689-016-9943-z. Fam Cancer. 2017. PMID: 27826806 Free PMC article.

2

Long term follow-up of HNPCC gene mutation carriers: compliance with screening and satisfaction with counseling and screening procedures.

Wagner A, van Kessel I, Kriege MG, Tops CM, Wijnen JT, Vasen HF, van der Meer CA, van Oostrom II, Meijers-Heijboer H. Wagner A, et al. Fam Cancer. 2005;4(4):295-300. doi: 10.1007/s10689-005-0658-9. Fam Cancer. 2005. PMID: 16341806

3

IVF and retinoblastoma revisited.

Dommering CJ, van der Hout AH, Meijers-Heijboer H, Marees T, Moll AC. Dommering CJ, et al. Fertil Steril. 2012 Jan;97(1):79-81. doi: 10.1016/j.fertnstert.2011.10.035. Epub 2011 Nov 23. Fertil Steril. 2012. PMID: 22112645 Free article.

4

RB1 mutations and second primary malignancies after hereditary retinoblastoma.

Dommering CJ, Marees T, van der Hout AH, Imhof SM, Meijers-Heijboer H, Ringens PJ, van Leeuwen FE, Moll AC. Dommering CJ, et al. Fam Cancer. 2012 Jun;11(2):225-33. doi: 10.1007/s10689-011-9505-3. Fam Cancer. 2012. PMID: 22205104 Free PMC article.

5

RB1 mutation spectrum in a comprehensive nationwide cohort of retinoblastoma patients.

Dommering CJ, Mol BM, Moll AC, Burton M, Cloos J, Dorsman JC, Meijers-Heijboer H, van der Hout AH. Dommering CJ, et al. J Med Genet. 2014 Jun;51(6):366-74. doi: 10.1136/jmedgenet-2014-102264. Epub 2014 Mar 31. J Med Genet. 2014. PMID: 24688104

6

High resolution SNP array profiling identifies variability in retinoblastoma genome stability.

Mol BM, Massink MP, van der Hout AH, Dommering CJ, Zaman JM, Bosscha MI, Kors WA, Meijers-Heijboer HE, Kaspers GJ, Riele Ht, Moll AC, Cloos J, Dorsman JC. Mol BM, et al. Genes Chromosomes Cancer. 2014 Jan;53(1):1-14. doi: 10.1002/gcc.22111. Epub 2013 Nov 5. Genes Chromosomes Cancer. 2014. PMID: 24249257

7

A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting.

van der Hout AH, van den Ouweland AM, van der Luijt RB, Gille HJ, Bodmer D, Brüggenwirth H, Mulder IM, van der Vlies P, Elfferich P, Huisman MT, ten Berge AM, Kromosoeto J, Jansen RP, van Zon PH, Vriesman T, Arts N, Lange MB, Oosterwijk JC, Meijers-Heijboer H, Ausems MG, Hoogerbrugge N, Verhoef S, Halley DJ, Vos YJ, Hogervorst F, Ligtenberg M, Hofstra RM. van der Hout AH, et al. Hum Mutat. 2006 Jul;27(7):654-66. doi: 10.1002/humu.20340. Hum Mutat. 2006. PMID: 16683254

8

TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes.

Ruijs MW, Verhoef S, Rookus MA, Pruntel R, van der Hout AH, Hogervorst FB, Kluijt I, Sijmons RH, Aalfs CM, Wagner A, Ausems MG, Hoogerbrugge N, van Asperen CJ, Gomez Garcia EB, Meijers-Heijboer H, Ten Kate LP, Menko FH, van 't Veer LJ. Ruijs MW, et al. J Med Genet. 2010 Jun;47(6):421-8. doi: 10.1136/jmg.2009.073429. J Med Genet. 2010. PMID: 20522432 Free article.

9

CHEK2*1100delC homozygosity is associated with a high breast cancer risk in women.

Adank MA, Jonker MA, Kluijt I, van Mil SE, Oldenburg RA, Mooi WJ, Hogervorst FB, van den Ouweland AM, Gille JJ, Schmidt MK, van der Vaart AW, Meijers-Heijboer H, Waisfisz Q. Adank MA, et al. J Med Genet. 2011 Dec;48(12):860-3. doi: 10.1136/jmedgenet-2011-100380. Epub 2011 Nov 5. J Med Genet. 2011. PMID: 22058428

10

Somatic genomic alterations in retinoblastoma beyond RB1 are rare and limited to copy number changes.

Kooi IE, Mol BM, Massink MP, Ameziane N, Meijers-Heijboer H, Dommering CJ, van Mil SE, de Vries Y, van der Hout AH, Kaspers GJ, Moll AC, Te Riele H, Cloos J, Dorsman JC. Kooi IE, et al. Sci Rep. 2016 Apr 29;6:25264. doi: 10.1038/srep25264. Sci Rep. 2016. PMID: 27126562 Free PMC article.

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