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Scientific Reports|December 4, 2025
Dysglycaemia and the interaction of chronic and acute glycaemia with mortality post cardiac surgeryJenny Shi, Mark Plummer, Luke Perry, et al.ERJ Open Research|October 15, 2025
Quality standards for paediatric bronchiectasis care in the UK, a national studySiobhán B Carr, Priti Kenia, Ross Langley, et al.Neuromuscular Disorders : NMD|June 24, 2025
Multi-omics approach identifies a novel recessive pathogenic variant in the TNNT3 gene in two siblings with congenital myopathyJuliane S Müller, Shira Rabinowicz, Irina Zaharieva, et al.BMJ Open|February 23, 2020
Adding evidence of the effects of treatments into relevant Wikipedia pages: a randomised trialClive E Adams, Alan A Montgomery, Tony Aburrow, et al.Annals of Clinical and Translational Neurology|July 23, 2022
GGPS1-associated muscular dystrophy with and without hearing lossRauan Kaiyrzhanov, Luke Perry, Clarissa Rocca, et al.Genome Research|March 26, 2025
Unraveling undiagnosed rare disease cases by HiFi long-read genome sequencingWouter Steyaert, Lydia Sagath, German Demidov, et al.Medrxiv : the Preprint Server for Health Sciences|May 15, 2024
Unravelling undiagnosed rare disease cases by HiFi long-read genome sequencingWouter Steyaert, Lydia Sagath, German Demidov, et al.Journal of Cachexia, Sarcopenia and Muscle|April 25, 2025
Myo-Guide: A Machine Learning-Based Web Application for Neuromuscular Disease Diagnosis With MRIJose Verdu-Diaz, Carla Bolano-Díaz, Alejandro Gonzalez-Chamorro, et al.Pageof 3