van Ommen GJ - Search Results

1

BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients.

Petrij-Bosch A, Peelen T, van Vliet M, van Eijk R, Olmer R, Drüsedau M, Hogervorst FB, Hageman S, Arts PJ, Ligtenberg MJ, Meijers-Heijboer H, Klijn JG, Vasen HF, Cornelisse CJ, van 't Veer LJ, Bakker E, van Ommen GJ, Devilee P. Petrij-Bosch A, et al. Among authors: van t veer lj, van eijk r, van ommen gj, van vliet m. Nat Genet. 1997 Nov;17(3):341-5. doi: 10.1038/ng1197-341. Nat Genet. 1997. PMID: 9354803 Free article.

2

Screening for BRCA2 mutations in 81 Dutch breast-ovarian cancer families.

Peelen T, van Vliet M, Bosch A, Bignell G, Vasen HF, Klijn JG, Meijers-Heijboer H, Stratton M, van Ommen GJ, Cornelisse CJ, Devilee P. Peelen T, et al. Among authors: van ommen gj, van vliet m. Br J Cancer. 2000 Jan;82(1):151-6. doi: 10.1054/bjoc.1999.0892. Br J Cancer. 2000. PMID: 10638982 Free PMC article.

3

Genetic analysis of a breast-ovarian cancer family, with 7 cases of colorectal cancer linked to BRCA1, fails to support a role for BRCA1 in colorectal tumorigenesis.

Peelen T, de Leeuw W, van Lent K, Morreau H, van Eijk R, van Vliet M, Wijnen J, Ligtenberg M, Ginjaar HB, Zweemer R, Menko F, Fodde R, van Ommen GJ, Vasen HF, Cornelisse CJ, Devilee P. Peelen T, et al. Among authors: van eijk r, van lent k, van ommen gj, van vliet m. Int J Cancer. 2000 Dec 1;88(5):778-82. doi: 10.1002/1097-0215(20001201)88:5<778::aid-ijc15>3.0.co;2-n. Int J Cancer. 2000. PMID: 11072248

4

A partial BRCA1 sequence homology mapping to 4q28.

Stec I, van Vliet M, van Eijk R, Meijers H, Kroeze KH, Dauwerse JG, van Ommen GJ, Cornelisse CJ, den Dunnen JT, Devilee P. Stec I, et al. Among authors: van eijk r, van ommen gj, van vliet m. Cytogenet Cell Genet. 2001;94(1-2):26-9. doi: 10.1159/000048777. Cytogenet Cell Genet. 2001. PMID: 11701949

5

Germline mosaicism and Duchenne muscular dystrophy mutations.

Bakker E, Van Broeckhoven C, Bonten EJ, van de Vooren MJ, Veenema H, Van Hul W, Van Ommen GJ, Vandenberghe A, Pearson PL. Bakker E, et al. Among authors: van de vooren mj, van ommen gj, van broeckhoven c, van hul w. Nature. 1987 Oct 8-14;329(6139):554-6. doi: 10.1038/329554a0. Nature. 1987. PMID: 2889144

6

Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gels.

den Dunnen JT, Bakker E, Breteler EG, Pearson PL, van Ommen GJ. den Dunnen JT, et al. Among authors: van ommen gj. Nature. 1987 Oct 15-21;329(6140):640-2. doi: 10.1038/329640a0. Nature. 1987. PMID: 2889148

7

Dynamic mutation in Dutch Huntington's disease patients: increased paternal repeat instability extending to within the normal size range.

De Rooij KE, De Koning Gans PA, Skraastad MI, Belfroid RD, Vegter-Van Der Vlis M, Roos RA, Bakker E, Van Ommen GJ, Den Dunnen JT, Losekoot M. De Rooij KE, et al. Among authors: van ommen gj. J Med Genet. 1993 Dec;30(12):996-1002. doi: 10.1136/jmg.30.12.996. J Med Genet. 1993. PMID: 8133511 Free PMC article.

8

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: van der mey ag, van ommen gj. Eur J Hum Genet. 1996;4(5):267-73. doi: 10.1159/000472213. Eur J Hum Genet. 1996. PMID: 8946172

9

Splicing mutations in DMD/BMD detected by RT-PCR/PTT: detection of a 19AA insertion in the cysteine rich domain of dystrophin compatible with BMD.

Roest PA, Bout M, van der Tuijn AC, Ginjaar IB, Bakker E, Hogervorst FB, van Ommen GJ, den Dunnen JT. Roest PA, et al. Among authors: van der tuijn ac, van ommen gj. J Med Genet. 1996 Nov;33(11):935-9. doi: 10.1136/jmg.33.11.935. J Med Genet. 1996. PMID: 8950674 Free PMC article.

10

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: van der mey ag, van ommen gj. Am J Hum Genet. 1998 Aug;63(2):468-73. doi: 10.1086/301951. Am J Hum Genet. 1998. PMID: 9683583 Free PMC article.

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