Evans DGR - Search Results

1

A Dominantly Inherited 5' UTR Variant Causing Methylation-Associated Silencing of BRCA1 as a Cause of Breast and Ovarian Cancer.

Evans DGR, van Veen EM, Byers HJ, Wallace AJ, Ellingford JM, Beaman G, Santoyo-Lopez J, Aitman TJ, Eccles DM, Lalloo FI, Smith MJ, Newman WG. Evans DGR, et al. Am J Hum Genet. 2018 Aug 2;103(2):213-220. doi: 10.1016/j.ajhg.2018.07.002. Am J Hum Genet. 2018. PMID: 30075112 Free PMC article.

2

Uptake of screening and prevention in women at very high risk of breast cancer.

Evans D, Lalloo F, Shenton A, Boggis C, Howell A. Evans D, et al. Lancet. 2001 Sep 15;358(9285):889-90. doi: 10.1016/S0140-6736(01)06039-1. Lancet. 2001. PMID: 11567707

3

Predictors of the risk of mortality in neurofibromatosis 2.

Baser ME, Friedman JM, Aeschliman D, Joe H, Wallace AJ, Ramsden RT, Evans DG. Baser ME, et al. Am J Hum Genet. 2002 Oct;71(4):715-23. doi: 10.1086/342716. Epub 2002 Aug 22. Am J Hum Genet. 2002. PMID: 12235555 Free PMC article.

4

Prediction of pathogenic mutations in patients with early-onset breast cancer by family history.

Lalloo F, Varley J, Ellis D, Moran A, O'Dair L, Pharoah P, Evans DG; Early Onset Breast Cancer Study Group. Lalloo F, et al. Lancet. 2003 Mar 29;361(9363):1101-2. doi: 10.1016/S0140-6736(03)12856-5. Lancet. 2003. PMID: 12672316

5

Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility.

Astuti D, Hart-Holden N, Latif F, Lalloo F, Black GC, Lim C, Moran A, Grossman AB, Hodgson SV, Freemont A, Ramsden R, Eng C, Evans DG, Maher ER. Astuti D, et al. Clin Endocrinol (Oxf). 2003 Dec;59(6):728-33. doi: 10.1046/j.1365-2265.2003.01914.x. Clin Endocrinol (Oxf). 2003. PMID: 14974914

6

Genotype-phenotype correlations for nervous system tumors in neurofibromatosis 2: a population-based study.

Baser ME, Kuramoto L, Joe H, Friedman JM, Wallace AJ, Gillespie JE, Ramsden RT, Evans DG. Baser ME, et al. Am J Hum Genet. 2004 Aug;75(2):231-9. doi: 10.1086/422700. Epub 2004 Jun 9. Am J Hum Genet. 2004. PMID: 15190457 Free PMC article.

7

Screening for familial ovarian cancer: failure of current protocols to detect ovarian cancer at an early stage according to the international Federation of gynecology and obstetrics system.

Stirling D, Evans DG, Pichert G, Shenton A, Kirk EN, Rimmer S, Steel CM, Lawson S, Busby-Earle RM, Walker J, Lalloo FI, Eccles DM, Lucassen AM, Porteous ME. Stirling D, et al. J Clin Oncol. 2005 Aug 20;23(24):5588-96. doi: 10.1200/JCO.2005.05.097. J Clin Oncol. 2005. PMID: 16110018

8

BRCA1, BRCA2 and TP53 mutations in very early-onset breast cancer with associated risks to relatives.

Lalloo F, Varley J, Moran A, Ellis D, O'dair L, Pharoah P, Antoniou A, Hartley R, Shenton A, Seal S, Bulman B, Howell A, Evans DG. Lalloo F, et al. Eur J Cancer. 2006 May;42(8):1143-50. doi: 10.1016/j.ejca.2005.11.032. Epub 2006 Apr 27. Eur J Cancer. 2006. PMID: 16644204

9

Optimal selection of individuals for BRCA mutation testing.

Evans DG, Lalloo F, Eccles D. Evans DG, et al. J Clin Oncol. 2006 Jul 10;24(20):3311; author reply 3311-2. doi: 10.1200/JCO.2006.06.6134. J Clin Oncol. 2006. PMID: 16829657 No abstract available.

10

Mosaicism in neurofibromatosis type 2: an update of risk based on uni/bilaterality of vestibular schwannoma at presentation and sensitive mutation analysis including multiple ligation-dependent probe amplification.

Evans DG, Ramsden RT, Shenton A, Gokhale C, Bowers NL, Huson SM, Pichert G, Wallace A. Evans DG, et al. J Med Genet. 2007 Jul;44(7):424-8. doi: 10.1136/jmg.2006.047753. Epub 2007 Feb 16. J Med Genet. 2007. PMID: 17307835 Free PMC article.

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