Rahman N - Search Results

1

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

2

Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12-q21.

Rahman N, Arbour L, Tonin P, Renshaw J, Pelletier J, Baruchel S, Pritchard-Jones K, Stratton MR, Narod SA. Rahman N, et al. Nat Genet. 1996 Aug;13(4):461-3. doi: 10.1038/ng0896-461. Nat Genet. 1996. PMID: 8696342

3

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

4

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.

5

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

6

The gene for cherubism maps to chromosome 4p16.3.

Mangion J, Rahman N, Edkins S, Barfoot R, Nguyen T, Sigurdsson A, Townend JV, Fitzpatrick DR, Flanagan AM, Stratton MR. Mangion J, et al. Among authors: rahman n. Am J Hum Genet. 1999 Jul;65(1):151-7. doi: 10.1086/302454. Am J Hum Genet. 1999. PMID: 10364527 Free PMC article.

7

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.

8

Evidence for susceptibility genes to familial Wilms tumour in addition to WT1, FWT1 and FWT2.

Rapley EA, Barfoot R, Bonaïti-Pellié C, Chompret A, Foulkes W, Perusinghe N, Reeve A, Royer-Pokora B, Schumacher V, Shelling A, Skeen J, de Tourreil S, Weirich A, Pritchard-Jones K, Stratton MR, Rahman N. Rapley EA, et al. Among authors: rahman n. Br J Cancer. 2000 Jul;83(2):177-83. doi: 10.1054/bjoc.2000.1283. Br J Cancer. 2000. PMID: 10901367 Free PMC article.

9

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

10

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.

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