Cornelis RS - Search Results

1

The majority of 22 Dutch high-risk breast cancer families are due to either BRCA1 or BRCA2.

Peelen T, Cornelis RS, van Vliet M, Petrij-Bosch A, Cleton-Jansen AM, Meijers-Heijboer H, Klijn JG, Vasen HF, Cornelisse CJ, Devilee P. Peelen T, et al. Among authors: cornelis rs. Eur J Hum Genet. 1996;4(4):225-30. doi: 10.1159/000472203. Eur J Hum Genet. 1996. PMID: 8875189

2

Rapid detection of BRCA1 mutations by the protein truncation test.

Hogervorst FB, Cornelis RS, Bout M, van Vliet M, Oosterwijk JC, Olmer R, Bakker B, Klijn JG, Vasen HF, Meijers-Heijboer H, et al. Hogervorst FB, et al. Among authors: cornelis rs. Nat Genet. 1995 Jun;10(2):208-12. doi: 10.1038/ng0695-208. Nat Genet. 1995. PMID: 7663517

3

Age at diagnosis as an indicator of eligibility for BRCA1 DNA testing in familial breast cancer.

Cornelis RS, Vasen HF, Meijers-Heijboer H, Ford D, van Vliet M, van Tilborg AA, Cleton FJ, Klijn JG, Menko FH, Meera Khan P, et al. Cornelis RS, et al. Hum Genet. 1995 May;95(5):539-44. doi: 10.1007/BF00223866. Hum Genet. 1995. PMID: 7759075

4

Linkage to markers for the chromosome region 17q12-q21 in 13 Dutch breast cancer kindreds.

Devilee P, Cornelis RS, Bootsma A, Bardoel A, van Vliet M, van Leeuwen I, Cleton FJ, de Klein A, Lindhout D, Vasen HF, et al. Devilee P, et al. Among authors: cornelis rs. Am J Hum Genet. 1993 Apr;52(4):730-5. Am J Hum Genet. 1993. PMID: 8096358 Free PMC article.

5

Genes responsible for familial breast cancer.

Cornelisse CJ, Cornelis RS, Devilee P. Cornelisse CJ, et al. Among authors: cornelis rs. Pathol Res Pract. 1996 Jul;192(7):684-93. doi: 10.1016/S0344-0338(96)80090-2. Pathol Res Pract. 1996. PMID: 8880869 Review.

6

Three germline mutations in the TP53 gene.

Cornelis RS, van Vliet M, van de Vijver MJ, Vasen HF, Voute PA, Top B, Khan PM, Devilee P, Cornelisse CJ. Cornelis RS, et al. Hum Mutat. 1997;9(2):157-63. doi: 10.1002/(SICI)1098-1004(1997)9:2<157::AID-HUMU8>3.0.CO;2-6. Hum Mutat. 1997. PMID: 9067756

7

Evidence for a gene on 17p13.3, distal to TP53, as a target for allele loss in breast tumors without p53 mutations.

Cornelis RS, van Vliet M, Vos CB, Cleton-Jansen AM, van de Vijver MJ, Peterse JL, Khan PM, Børresen AL, Cornelisse CJ, Devilee P. Cornelis RS, et al. Cancer Res. 1994 Aug 1;54(15):4200-6. Cancer Res. 1994. PMID: 8033152

8

Allele loss patterns on chromosome 17q in 109 breast carcinomas indicate at least two distinct target regions.

Cornelis RS, Devilee P, van Vliet M, Kuipers-Dijkshoorn N, Kersenmaeker A, Bardoel A, Khan PM, Cornelisse CJ. Cornelis RS, et al. Oncogene. 1993 Mar;8(3):781-5. Oncogene. 1993. PMID: 8437862

9

Selection of families for predictive testing for breast cancer.

Cornelis RS, Cornelisse CJ, Devilee P. Cornelis RS, et al. Lancet. 1994 Oct 22;344(8930):1151. doi: 10.1016/s0140-6736(94)90654-8. Lancet. 1994. PMID: 7934504 No abstract available.

10

High allele loss rates at 17q12-q21 in breast and ovarian tumors from BRCAl-linked families. The Breast Cancer Linkage Consortium.

Cornelis RS, Neuhausen SL, Johansson O, Arason A, Kelsell D, Ponder BA, Tonin P, Hamann U, Lindblom A, Lalle P, et al. Cornelis RS, et al. Genes Chromosomes Cancer. 1995 Jul;13(3):203-10. doi: 10.1002/gcc.2870130310. Genes Chromosomes Cancer. 1995. PMID: 7669740

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