Peter N Ray

Whole Genome Scanning: Resolving Clinical Diagnosis and Management Amidst Complex Data

Stephen W Scherer, Abdallah S Daar, S. Scherer, 2009, Pediatric Research.

The Genome Clinic: A Multidisciplinary Approach to Assessing the Opportunities and Challenges of Integrating Genomic Analysis into Clinical Care

S. Bowdin, M. Meyn, P. Ray, 2014, Human mutation.

Strategy for comprehensive molecular testing for Duchenne and Becker muscular dystrophies.

T. Stockley, P. Ray, N. Bulgin, 2006, Genetic testing.

Cloning and characterization of human CADPS and CADPS2, new members of the Ca2+-dependent activator for secretion protein family.

Stephen W Scherer, S. Scherer, J. Vincent, 2003, Genomics.

Recurrent focal copy-number changes and loss of heterozygosity implicate two noncoding RNAs and one tumor suppressor gene at chromosome 3q13.31 in osteosarcoma.

David Malkin, Ana Novokmet, Adam Shlien, 2010, Cancer research.

PhenoTips: Patient Phenotyping Software for Clinical and Research Use

Michael Brudno, Sergiu Dumitriu, Marc Fiume, 2013, Human mutation.

Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test

Daniele Merico, Raveen Basran, Christian R Marshall, 2017, Genetics in Medicine.

Whole-genome sequencing expands diagnostic utility and improves clinical management in paediatric medicine

Michael Brudno, Daniele Merico, Christian R Marshall, 2016, npj Genomic Medicine.