Lalloo F - Search Results

1

Clinical practice guidelines for the diagnosis and surveillance of BAP1 tumour predisposition syndrome.

Lalloo F, Kulkarni A, Chau C, Nielsen M, Sheaff M, Steele J, van Doorn R, Wadt K, Hamill M, Torr B, Tischkowitz M; Delphi respondents; Hanson H. Lalloo F, et al. Eur J Hum Genet. 2023 Nov;31(11):1261-1269. doi: 10.1038/s41431-023-01448-z. Epub 2023 Aug 22. Eur J Hum Genet. 2023. PMID: 37607989 Free PMC article.

2

An evaluation of common breast cancer gene mutations in a population of Ashkenazi Jews.

Lalloo F, Cochrane S, Bulman B, Varley J, Elles R, Howell A, Evans DG. Lalloo F, et al. J Med Genet. 1998 Jan;35(1):10-2. doi: 10.1136/jmg.35.1.10. J Med Genet. 1998. PMID: 9475087 Free PMC article.

3

The pathology of familial breast cancer: Clinical and genetic counselling implications of breast cancer pathology.

Lalloo F, Evans DG. Lalloo F, et al. Breast Cancer Res. 1999;1(1):48-51. doi: 10.1186/bcr13. Epub 1999 Oct 27. Breast Cancer Res. 1999. PMID: 11250683 Free PMC article. Review.

4

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: lalloo f. Fam Cancer. 2001;1(3-4):131-3. doi: 10.1023/a:1021165031643. Fam Cancer. 2001. PMID: 14574168

5

Evaluation of breast cancer risk assessment packages in the family history evaluation and screening programme.

Amir E, Evans DG, Shenton A, Lalloo F, Moran A, Boggis C, Wilson M, Howell A. Amir E, et al. Among authors: lalloo f. J Med Genet. 2003 Nov;40(11):807-14. doi: 10.1136/jmg.40.11.807. J Med Genet. 2003. PMID: 14627668 Free PMC article.

6

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: lalloo f. 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.

7

Parity and breast cancer risk among BRCA1 and BRCA2 mutation carriers.

Antoniou AC, Shenton A, Maher ER, Watson E, Woodward E, Lalloo F, Easton DF, Evans DG. Antoniou AC, et al. Among authors: lalloo f. Breast Cancer Res. 2006;8(6):R72. doi: 10.1186/bcr1630. Breast Cancer Res. 2006. PMID: 17187672 Free PMC article.

8

Screening for familial ovarian cancer: poor survival of BRCA1/2 related cancers.

Evans DG, Gaarenstroom KN, Stirling D, Shenton A, Maehle L, Dørum A, Steel M, Lalloo F, Apold J, Porteous ME, Vasen HF, van Asperen CJ, Moller P. Evans DG, et al. Among authors: lalloo f. J Med Genet. 2009 Sep;46(9):593-7. doi: 10.1136/jmg.2008.058248. Epub 2008 Apr 15. J Med Genet. 2009. PMID: 18413372

9

Penetrance estimates for BRCA1 and BRCA2 based on genetic testing in a Clinical Cancer Genetics service setting: risks of breast/ovarian cancer quoted should reflect the cancer burden in the family.

Evans DG, Shenton A, Woodward E, Lalloo F, Howell A, Maher ER. Evans DG, et al. Among authors: lalloo f. BMC Cancer. 2008 May 30;8:155. doi: 10.1186/1471-2407-8-155. BMC Cancer. 2008. PMID: 18513387 Free PMC article.

10

Colorectal cancer in HNPCC: cumulative lifetime incidence, survival and tumour distribution. A report of 121 families with proven mutations.

Barrow E, Alduaij W, Robinson L, Shenton A, Clancy T, Lalloo F, Hill J, Evans DG. Barrow E, et al. Among authors: lalloo f. Clin Genet. 2008 Sep;74(3):233-42. doi: 10.1111/j.1399-0004.2008.01035.x. Epub 2008 Jun 28. Clin Genet. 2008. PMID: 18554281

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