Rahman N - Search Results

1

Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer.

Peto J, Collins N, Barfoot R, Seal S, Warren W, Rahman N, Easton DF, Evans C, Deacon J, Stratton MR. Peto J, et al. Among authors: rahman n. J Natl Cancer Inst. 1999 Jun 2;91(11):943-9. doi: 10.1093/jnci/91.11.943. J Natl Cancer Inst. 1999. PMID: 10359546

2

Heterozygosity for mutations in the ataxia telangiectasia gene is not a major cause of radiotherapy complications in breast cancer patients.

Shayeghi M, Seal S, Regan J, Collins N, Barfoot R, Rahman N, Ashton A, Moohan M, Wooster R, Owen R, Bliss JM, Stratton MR, Yarnold J. Shayeghi M, et al. Among authors: rahman n. Br J Cancer. 1998 Oct;78(7):922-7. doi: 10.1038/bjc.1998.602. Br J Cancer. 1998. PMID: 9764584 Free PMC article. Clinical Trial.

3

The genetics of breast cancer susceptibility.

Rahman N, Stratton MR. Rahman N, et al. Annu Rev Genet. 1998;32:95-121. doi: 10.1146/annurev.genet.32.1.95. Annu Rev Genet. 1998. PMID: 9928476 Review.

4

Lobular carcinoma in situ of the breast is not caused by constitutional mutations in the E-cadherin gene.

Rahman N, Stone JG, Coleman G, Gusterson B, Seal S, Marossy A, Lakhani SR, Ward A, Nash A, McKinna A, A'Hern R, Stratton MR, Houlston RS. Rahman N, et al. Br J Cancer. 2000 Feb;82(3):568-70. doi: 10.1054/bjoc.1999.0965. Br J Cancer. 2000. PMID: 10682667 Free PMC article.

5

Penetrance of mutations in the familial Wilms tumor gene FWT1.

Rahman N, Arbour L, Houlston R, Bonaïti-Pellié C, Abidi F, Tranchemontagne J, Ford D, Narod S, Pritchard-Jones K, Foulkes WD, Schwartz C, Stratton MR. Rahman N, et al. J Natl Cancer Inst. 2000 Apr 19;92(8):650-2. doi: 10.1093/jnci/92.8.650. J Natl Cancer Inst. 2000. PMID: 10772684 No abstract available.

6

Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22.

Rahman N, Teare MD, Seal S, Renard H, Mangion J, Cour C, Thompson D, Shugart Y, Eccles D, Devilee P, Meijers H, Nathanson KL, Neuhausen SL, Weber B, Chang-Claude J, Easton DF, Goldgar D, Stratton MR. Rahman N, et al. Oncogene. 2000 Aug 24;19(36):4170-3. doi: 10.1038/sj.onc.1203735. Oncogene. 2000. PMID: 10962578

7

The familial Wilms' tumour susceptibility gene, FWT1, may not be a tumour suppressor gene.

Rahman N, Arbour L, Tonin P, Baruchel S, Pritchard-Jones K, Narod SA, Stratton MR. Rahman N, et al. Oncogene. 1997 Jun 26;14(25):3099-102. doi: 10.1038/sj.onc.1201107. Oncogene. 1997. PMID: 9223674

8

A missense mutation in the BRCA2 gene in three siblings with ovarian cancer.

Roth S, Kristo P, Auranen A, Shayehgi M, Seal S, Collins N, Barfoot R, Rahman N, Klemi PJ, Grénman S, Sarantaus L, Nevanlinna H, Butzow R, Ashworth A, Stratton MR, Aaltonen LA. Roth S, et al. Among authors: rahman n. Br J Cancer. 1998 Apr;77(8):1199-202. doi: 10.1038/bjc.1998.202. Br J Cancer. 1998. PMID: 9579822 Free PMC article.

9

Inherited susceptibility to colorectal adenomas and carcinomas: evidence for a new predisposition gene on 15q14-q22.

Tomlinson I, Rahman N, Frayling I, Mangion J, Barfoot R, Hamoudi R, Seal S, Northover J, Thomas HJ, Neale K, Hodgson S, Talbot I, Houlston R, Stratton MR. Tomlinson I, et al. Among authors: rahman n. Gastroenterology. 1999 Apr;116(4):789-95. doi: 10.1016/s0016-5085(99)70061-2. Gastroenterology. 1999. PMID: 10092300

10

Low frequency of germline E-cadherin mutations in familial and nonfamilial gastric cancer.

Stone J, Bevan S, Cunningham D, Hill A, Rahman N, Peto J, Marossy A, Houlston RS. Stone J, et al. Among authors: rahman n. Br J Cancer. 1999 Apr;79(11-12):1935-7. doi: 10.1038/sj.bjc.6690308. Br J Cancer. 1999. PMID: 10206317 Free PMC article.

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