Carcinoma of unknown primary – rare but ripe for help from genomics?
Guccione L, Mileshkin L, Schofield P, Bowtell D.. Carcinoma of unknown primary – rare but ripe for help from genomics?. Cancer Forum. 2015. 39 (1) : 44-46.

Dynamic consent: a patient interface for twenty-first century research networks
Kaye J, Whitley EA, Lund D, Morrison M, Teare H, Melham K. Dynamic consent: a patient interface for twenty-first century research networks. European Journal of Human Genetics. 2015. 23 (2) : 141—6.

ClinGen-the Clinical Genome Resource
Rehm H.L, Berg J.S, Brooks L.D, Bustamante C.D, Evans J.P, Landrum M.J, et al. ClinGen-the Clinical Genome Resource. New England Journal of Medicine. 2015. 372 (23) : 2235-42.

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, et al. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genetics in Medicine. 2015. 17 (5) : 405—24.

The Matchmaker Exchange: a platform for rare disease gene discovery
Philippakis A.A, Azzariti D.R, Beltran S, Brookes A.J, Brownstein C.A, Brudno M, et al. The Matchmaker Exchange: a platform for rare disease gene discovery. Human Mutation. 2015. 36 (10) : 915—21.