D G Evans

发表

Magnetic resonance imaging screening in women at genetic risk of breast cancer: imaging and analysis protocol for the UK multicentre study. UK MRI Breast Screening Study Advisory Group.

S F Keevil, A R Padhani, M O Leach, 2000, Magnetic resonance imaging.

A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severity.

D. Evans, T. Strachan, S. Huson, 1992, Journal of medical genetics.

Rationale for a national multi-centre study of magnetic resonance imaging screening in women at genetic risk of breast cancer.

M O Leach, A Coulthard, A K Dixon, 2000, Breast.

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

A Howell, A. Howell, D. Evans, 2003, Journal of medical genetics.

The accuracy of diagnoses as reported in families with cancer: a retrospective study

D. Evans, S. Lynch, D G Evans, 1999, Journal of medical genetics.

False-negative MRI breast screening in high-risk women.

A Howell, A. Howell, D. Evans, 2017, Clinical radiology.

Cost-effectiveness of screening with contrast enhanced magnetic resonance imaging vs X-ray mammography of women at a high familial risk of breast cancer

A R Padhani, M O Leach, F J Gilbert, 2006, British Journal of Cancer.

Probability of bilateral disease in people presenting with a unilateral vestibular schwannoma

R T Ramsden, D. Evans, T. Strachan, 1999, Journal of neurology, neurosurgery, and psychiatry.

A common MSH2 mutation in English and North American HNPCC families: origin, phenotypic expression, and sex specific differences in colorectal cancer

D. Evans, R. Kolodner, D. Bishop, 1999, Journal of medical genetics.

High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH.

D Pinkel, S. Pulst, D. Pinkel, 2001, Human molecular genetics.

The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions

H A Risch, J. Hopper, M. Southey, 2008, British Journal of Cancer.

Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA)

G Rennert, N Weerasooriya, K Offit, 2009, British Journal of Cancer.

Heritability of cellular radiosensitivity: a marker of low-penetrance predisposition genes in breast cancer?

D. Evans, S. Roberts, D. Scott, 1999, American journal of human genetics.

Germ-line mutations of TP53 in Li-Fraumeni families: an extended study of 39 families.

D. Evans, J. Varley, M. Santibanez-Koref, 1997, Cancer research.

False family history of breast cancer in the family cancer clinic.

D. Evans, S. Narod, C. Serruya, 1998, European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology.