Harry Costello

A Nonsense Mutation in COQ9 Causes Autosomal-Recessive Neonatal-Onset Primary Coenzyme Q10 Deficiency: A Potentially Treatable Form of Mitochondrial Disease

Andrew Duncan, Maria Bitner‐Glindzicz, Brigitte Meunier et al. · The American Journal of Human Genetics · 2009 · 216 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +9

Persistent psychotic symptoms following COVID-19 infection

Soon Tjin Lim, Benjamin Janaway, Harry Costello et al. · BJPsych Open · 2020 · 65 citations · Full text

A Clinical, Neuropathological and Genetic Study of Homozygous A467T POLG-Related Mitochondrial Disease

Sanjeev Rajakulendran, Robert D. S. Pitceathly, Jan‐Willem Taanman et al. · PLoS ONE · 2016 · 51 citations · Full text

Genetics, Pathology, Dna Polymerase Gamma +17

Hearing in 44–45 year olds with m.1555A>G, a genetic mutation predisposing to aminoglycoside-induced deafness: a population based cohort study

Shamima Rahman, Russell Ecob, Harry Costello et al. · BMJ Open · 2012 · 45 citations · Full text

Genetic Testing, Genetics, Genetic Epidemiology +19

Burnout in UK care home staff and its effect on staff turnover: MARQUE English national care home longitudinal survey

Harry Costello, Claudia Cooper, Louise Marston et al. · Age and Ageing · 2019 · 45 citations · Full text