C. Crosby

A Comparison of Methods for EGFR Mutation Testing in Non–Small Cell Lung Cancer

S. Ellard, J. Knight, I. Cree, 2013, Diagnostic molecular pathology : the American journal of surgical pathology, part B.

Community‐onset methicillin‐resistant Staphylococcus aureus in an urban HIV clinic

D. Skiest, K. Brown, T. Cooper, 2006, HIV medicine.

Evidence for 28 genetic disorders discovered by combining healthcare and research data

Patrick J. Short, M. Hurles, L. Vissers, 2020, Nature.

The contribution of X-linked coding variation to severe developmental disorders

M. Hurles, R. Sandford, D. Baralle, 2020, Nature Communications.

IDH mutation analysis in gliomas as a diagnostic and prognostic biomarker

M. Williams, K. Hopkins, H. R. Haynes, 2013, British journal of neurosurgery.

Extending the phenotype associated with the CSNK2A1‐related Okur–Chung syndrome—A clinical study of 11 individuals

A. Green, M. Parker, B. Castle, 2018, American journal of medical genetics. Part A.

Biallelic DNAJC3 variants in a neuroendocrine developmental disorder with insulin dysregulation

I. C. Lloyd, D. Smedley, M. McEntagart, 2021, Clinical dysmorphology.

Variants of the EAAT2 Glutamate Transporter Gene Promoter Are Associated with Cerebral Palsy in Preterm Infants

E. Molnár, S. Rajatileka, A. Váradi, 2017, Molecular Neurobiology.

Quantifying prediction of pathogenicity for within-codon concordance (PM5) using 7541 functional classifications of BRCA1 and MSH2 missense variants

P. Tarpey, D. Baralle, J. Tolmie, 2021, Genetics in medicine : official journal of the American College of Medical Genetics.