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BMC Medical Informatics and Decision Making|January 20, 2009
The SAIL databank: linking multiple health and social care datasetsRonan A Lyons, Kerina H Jones, Gareth John, et al.
World Journal of Hepatology|February 6, 2023
Rising incidence, progression and changing patterns of liver disease in Wales 1999-2019Thomas Peter Ignatius Pembroke, Gareth John, Berry Puyk, et al.
Oncogene|April 5, 2005
c-FMS chromatin structure and expression in normal and leukaemic myelopoiesisGeorge Alexander Follows, Hiromi Tagoh, Stephen John Richards, et al.
Journal of Public Health (Oxford, England)|May 19, 2009
Residential Anonymous Linking Fields (RALFs): a novel information infrastructure to study the interaction between the environment and individuals' healthSarah E Rodgers, Ronan A Lyons, Rohan Dsilva, et al.
Scientific Reports|July 4, 2023
Sensitivity of endogenous autofluorescence in HeLa cells to the application of external magnetic fieldsMariia Uzhytchak, Barbora Smolková, Adam Frtús, et al.
The Journal of Infection|February 11, 2023
Real-world effectiveness of molnupiravir, nirmatrelvir-ritonavir, and sotrovimab on preventing hospital admission among higher-risk patients with COVID-19 in Wales: A retrospective cohort studyAndrew Evans, Cathy Qi, Jubril Omololu Adebayo, et al.
Cell Cycle (Georgetown, Tex.)|March 17, 2022
POLG mutations lead to abnormal mitochondrial remodeling during neural differentiation of human pluripotent stem cells via SIRT3/AMPK pathway inhibitionAnbin Chen, Cecilie Katrin Kristiansen, Lena Elise Høyland, et al.
Experimental Neurology|December 2, 2020
N-acetylcysteine amide ameliorates mitochondrial dysfunction and reduces oxidative stress in hiPSC-derived dopaminergic neurons with POLG mutationKristina Xiao Liang, Guro Helén Vatne, Cecilie Katrin Kristiansen, et al.
Experimental Neurology|April 27, 2023
POLG genotype influences degree of mitochondrial dysfunction in iPSC derived neural progenitors, but not the parent iPSC or derived gliaYu Hong, Cecilie Katrin Kristiansen, Anbin Chen, et al.
Ophthalmology|July 2, 2010
Development of a diagnostic genetic test for simplex and autosomal recessive retinitis pigmentosaGraeme Richard Clark, Paul Crowe, Dorota Muszynska, et al.
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