C. Dunlop

Not All Next Generation Sequencing Diagnostics are Created Equal: Understanding the Nuances of Solid Tumor Assay Design for Somatic Mutation Detection

A. Elliott, Charles L M Dunlop, Aaron M. Elliott, 2015, Cancers.

Enhanced utility of family-centered diagnostic exome sequencing with inheritance model–based analysis: results from 500 unselected families with undiagnosed genetic conditions

Xiang Li, Aaron Elliott, Xiang Li, 2014, Genetics in Medicine.

Association of Breast and Ovarian Cancers With Predisposition Genes Identified by Large-Scale Sequencing

Sitao Wu, Jefferey Chen, M. Black, 2019, JAMA Oncology.

Hereditary predisposition to ovarian cancer, looking beyond BRCA1/BRCA2.

B. Monk, E. Chao, D. Chase, 2014, Gynecologic oncology.

Comprehensive genetic analysis of the cystic fibrosis transmembrane conductance regulator from dried blood specimens – Implications for newborn screening

S. Keiles, Charles L M Dunlop, A. Kammesheidt, 2006, Genetics in Medicine.

Diagnostic testing by CFTR gene mutation analysis in a large group of Hispanics: novel mutations and assessment of a population-specific mutation spectrum.

I. Schrijver, J. Oehlert, R. Moss, 2005, The Journal of molecular diagnostics : JMD.