Garan Jones

Common conditions associated with hereditary haemochromatosis genetic variants: cohort study in UK Biobank

Luke C. Pilling, Jone Tamosauskaite, Garan Jones et al. · BMJ · 2019 · 186 citations · Full text

Dominant ER Stress–Inducing <i>WFS1</i> Mutations Underlie a Genetic Syndrome of Neonatal/Infancy-Onset Diabetes, Congenital Sensorineural Deafness, and Congenital Cataracts

Elisa De Franco, Sarah E. Flanagan, Takuya Yagi et al. · Diabetes · 2017 · 107 citations · Full text

Diagnosis of lethal or prenatal‐onset autosomal recessive disorders by parental exome sequencing

Karen Stals, Matthew N. Wakeling, Júlia Baptista et al. · Prenatal Diagnosis · 2017 · 76 citations · Full text

Comparison of the Legionella pneumophila population structure as determined by sequence-based typing and whole genome sequencing

Anthony Underwood, Garan Jones, M. Mentasti et al. · BMC Microbiology · 2013 · 48 citations · Full text

Sarcopenia and Variation in the Human Leukocyte Antigen Complex

Garan Jones, Luke C. Pilling, Chia‐Ling Kuo et al. · The Journals of Gerontology Series A · 2019 · 34 citations · Full text