Bulman M - Search Results

1

Phenocopies in BRCA1 and BRCA2 families: evidence for modifier genes and implications for screening.

Smith A, Moran A, Boyd MC, Bulman M, Shenton A, Smith L, Iddenden R, Woodward ER, Lalloo F, Maher ER, Evans DG. Smith A, et al. Among authors: bulman m. J Med Genet. 2007 Jan;44(1):10-15. doi: 10.1136/jmg.2006.043091. Epub 2006 Nov 1. J Med Genet. 2007. PMID: 17079251 Free PMC article.

2

Prevalence of germline pathogenic BRCA1/2 variants in sequential epithelial ovarian cancer cases.

Morgan RD, Burghel GJ, Flaum N, Bulman M, Clamp AR, Hasan J, Mitchell CL, Schlecht H, Woodward ER, Lallo FI, Crosbie EJ, Edmondson RJ, Wallace AJ, Jayson GC, Evans DGR. Morgan RD, et al. Among authors: bulman m. J Med Genet. 2019 May;56(5):301-307. doi: 10.1136/jmedgenet-2018-105792. Epub 2019 Jan 25. J Med Genet. 2019. PMID: 30683677

3

BRCA1/2 mutation analysis in male breast cancer families from North West England.

Evans DG, Bulman M, Young K, Howard E, Bayliss S, Wallace A, Lalloo F. Evans DG, et al. Among authors: bulman m. Fam Cancer. 2008;7(2):113-7. doi: 10.1007/s10689-007-9153-9. Epub 2007 Jul 17. Fam Cancer. 2008. PMID: 17636422

4

Sensitivity of BRCA1/2 mutation testing in 466 breast/ovarian cancer families.

Evans DG, Bulman M, Young K, Gokhale D, Lalloo F. Evans DG, et al. Among authors: bulman m. J Med Genet. 2003 Sep;40(9):e107. doi: 10.1136/jmg.40.9.e107. J Med Genet. 2003. PMID: 12960223 Free PMC article. No abstract available.

5

High detection rate for BRCA2 mutations in male breast cancer families from North West England.

Evans DG, Bulman M, Young K, Gokhale D, Lalloo F. Evans DG, et al. Among authors: bulman m. Fam Cancer. 2001;1(3-4):131-3. doi: 10.1023/a:1021165031643. Fam Cancer. 2001. PMID: 14574168

6

Haplotype and cancer risk analysis of two common mutations, BRCA1 4184del4 and BRCA2 2157delG, in high risk northwest England breast/ovarian families.

Evans DG, Neuhausen SL, Bulman M, Young K, Gokhale D, Lalloo F. Evans DG, et al. Among authors: bulman m. J Med Genet. 2004 Feb;41(2):e21. doi: 10.1136/jmg.2003.012104. J Med Genet. 2004. PMID: 14757871 Free PMC article. No abstract available.

7

A new scoring system for the chances of identifying a BRCA1/2 mutation outperforms existing models including BRCAPRO.

Evans DG, Eccles DM, Rahman N, Young K, Bulman M, Amir E, Shenton A, Howell A, Lalloo F. Evans DG, et al. Among authors: bulman m. J Med Genet. 2004 Jun;41(6):474-80. doi: 10.1136/jmg.2003.017996. J Med Genet. 2004. PMID: 15173236 Free PMC article.

8

Probability of BRCA1/2 mutation varies with ovarian histology: results from screening 442 ovarian cancer families.

Evans DG, Young K, Bulman M, Shenton A, Wallace A, Lalloo F. Evans DG, et al. Among authors: bulman m. Clin Genet. 2008 Apr;73(4):338-45. doi: 10.1111/j.1399-0004.2008.00974.x. Epub 2008 Feb 26. Clin Genet. 2008. PMID: 18312450

9

Risk of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers: a 30-year semi-prospective analysis.

Basu NN, Ingham S, Hodson J, Lalloo F, Bulman M, Howell A, Evans DG. Basu NN, et al. Among authors: bulman m. Fam Cancer. 2015 Dec;14(4):531-8. doi: 10.1007/s10689-015-9825-9. Fam Cancer. 2015. PMID: 26239694

10

Mainstreaming germline BRCA1/2 testing in non-mucinous epithelial ovarian cancer in the North West of England.

Flaum N, Morgan RD, Burghel GJ, Bulman M, Clamp AR, Hasan J, Mitchell CL, Badea D, Moon S, Hogg M, Hadjiyiannakis D, Clancy T, Schlecht H, Woodward ER, Crosbie EJ, Edmondson RJ, Wallace AJ, Jayson GC, Lalloo FI, Harkness EF, Evans DGR. Flaum N, et al. Among authors: bulman m. Eur J Hum Genet. 2020 Nov;28(11):1541-1547. doi: 10.1038/s41431-020-0692-y. Epub 2020 Jul 10. Eur J Hum Genet. 2020. PMID: 32651552 Free PMC article.

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