Joe T.R. Clarke

Government of Northern Ireland — United Kingdom

Medicine · Health Sciences

38h-index4.0kcitations167works1.72yr avg
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Research Topics

Lysosomal Storage Disorders Research(77), Metabolism and Genetic Disorders(44), Trypanosoma species research and implications(18), Cellular transport and secretion(17), Carbohydrate Chemistry and Synthesis(16)

Publications167 total

No evidence of BoHV-1 exposure and low levels of pestivirus exposure in sera from 116 opportunistically sampled wild deer in Northern Ireland
Irish Veterinary Journal·2025Open Access
Determinants of SARS-CoV-2 within-host evolutionary rates in persistently infected individuals
2024· 4 citedOpen Access
Genotypic analysis of a localised hotspot of <i>Pestivirus A</i> (BVDV‐1) infections in Northern Ireland
Veterinary Record·2024· 1 citedOpen Access
The paradox of the darkening planet and the Earth’s climate sensitivity
2023Open Access
62 ‘Spending a penny, but keeping it clean’ – Reducing the rate of contaminated non-invasive urine samples in the paediatric department
2022· 1 citedOpen Access
Pestivirus apparent prevalence in sheep and goats in Northern Ireland: A serological survey
Veterinary Record·2021· 9 citedOpen Access
Identification of Dwelling-specific Energy Saving Benchmarks from Building Stock Models
Building Simulation Conference proceedings·2020Open Access
Conditions for the Compost Bomb Instability
2020Open Access
High-risk screening for Fabry disease in a Canadian cohort of chronic kidney disease patients
Clinica Chimica Acta·2019· 18 cited
Combined malonic and methylmalonic aciduria due to <i>ACSF3</i> mutations: Benign clinical course in an unselected cohort
Journal of Inherited Metabolic Disease·2019· 33 cited
Combined malonic and methylmalonic aciduria due to ACSF3 mutations: benign clinical course in an unselected cohort
Journal of Inherited Metabolic Disease·2018· 5 cited
P252 Clinical profile of infants with cystic fibrosis screen positive, inconclusive diagnosis (cfspid) in the west midlands
2017· 1 citedOpen Access
Managing sickle cell carrier results generated through newborn screening in Ontario: a precedent-setting policy story
Genetics in Medicine·2016· 7 citedOpen Access
Methylmalonyl-coA epimerase deficiency: A new case, with an acute metabolic presentation and an intronic splicing mutation in the MCEE gene
Molecular Genetics and Metabolism Reports·2016· 18 citedOpen Access
Hematological Disorders
2016
Validation of the finding of hypertrophy of the clava in infantile neuroaxonal dystrophy/PLA2G6 by biometric analysis
Neuroradiology·2016· 23 cited
UPLC-MS/MS detection of disaccharides derived from glycosaminoglycans as biomarkers of mucopolysaccharidoses
Analytica Chimica Acta·2016· 67 cited
determined by indicator amino acid oxidation Phenylalanine requirement in children with classical PKU
2016
Novel Microdeletions Affecting the GNAS Locus in Pseudohypoparathyroidism: Characterization of the Underlying Mechanisms
The Journal of Clinical Endocrinology & Metabolism·2015· 58 citedOpen Access
Urinary biomarker investigation in children with Fabry disease using tandem mass spectrometry
Clinica Chimica Acta·2014· 68 cited
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Frequent Co-authors

Christiane Auray‐Blais(8), Harold W. Cook(5), Matthew W. Spence(5), René Gagnon(4), Paméla Lavoie(4), Sarah P. Young(3), David S. Millington(3), B.‐A. Platt(3), Bruno Maranda(3), John W. Callahan(3), Susan Blasér(3), Nancy Braverman(2), Yan An(2), John Christodoulou(2), Aimé Ntwari(2), David G. Warnock(2), Daniel G. Bichet(2), Michael L. West(2), Michel Boutin(2), Leonhard S. Wolfe(2)