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Publications

Rethinking the Ethical Principles of Genomic Medicine Services

JOHNSON S. et al, (2019), European Journal of Human Genetics

Evaluating the integration of genomics into cancer screening programmes: challenges and opportunities

Briggs S. and Slade I., (2019), Current Genetic Medicine Reports, 7, 63 - 74

Understanding and using patient experiences as evidence in healthcare priority setting.

Rand L. et al, (2019), Cost Eff Resour Alloc, 17

Genomics education for medical professionals - the current UK landscape.

Slade I. et al, (2016), Clin Med (Lond), 16, 347 - 352

Implementing rapid, robust, cost-effective, patient-centred, routine genetic testing in ovarian cancer patients.

George A. et al, (2016), Sci Rep, 6

A cost analysis of a cancer genetic service model in the UK.

Slade I. et al, (2016), J Community Genet, 7, 185 - 194

Preparing clinicians for genomic medicine.

Slade I. and Burton H., (2016), Postgrad Med J, 92, 369 - 371

Development of cancer genetic services in the UK: A national consultation.

Slade I. et al, (2015), Genome Med, 7

A genome-wide association study identifies susceptibility loci for Wilms tumor.

Turnbull C. et al, (2012), Nat Genet, 44, 681 - 684

Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma.

Slade I. et al, (2011), Fam Cancer, 10, 337 - 342

DICER1 syndrome: clarifying the diagnosis, clinical features and management implications of a pleiotropic tumour predisposition syndrome.

Slade I. et al, (2011), J Med Genet, 48, 273 - 278

DICER1 syndrome - a pleiotropic tumor predisposition syndrome

Slade I. et al, (2010), JOURNAL OF MEDICAL GENETICS, 47, S115 - S115

Constitutional translocation breakpoint mapping by genome-wide paired-end sequencing identifies HACE1 as a putative Wilms tumour susceptibility gene.

Slade I. et al, (2010), J Med Genet, 47, 342 - 347

Include forthcoming?