Rhian L Clissold (Rhian Clissold, Lorna W Harries)

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 7

Top Topics

Skeletal Muscle

Glycemic Control

Top Venues

Journal of diabetes investigation

Clinical epigenetics

This page only lists publications with an associated author ORCID identifier.

Publications

Rhian L Clissold, Coralie Bingham, Andrew Hattersley
Comment on a recent article titled 'Hepatocyte nuclear factor 1B deletion, but not intragenic mutation, might be more susceptible to hypomagnesemia'. Journal of diabetes investigation 15 (6) (2023)
Rhian L Clissold, Coralie Bingham, Andrew Hattersley
Comment on a recent article titled 'Hepatocyte nuclear factor 1B deletion, but not intragenic mutation, might be more susceptible to hypomagnesemia'. Journal of diabetes investigation 15 (6) (2023)
Rhian L Clissold, Coralie Bingham, Andrew Hattersley
Comment on a recent article titled 'Hepatocyte nuclear factor 1B deletion, but not intragenic mutation, might be more susceptible to hypomagnesemia'. Journal of diabetes investigation 15 (6) (2023)
Rhian L Clissold, Coralie Bingham, Andrew Hattersley
Comment on a recent article titled 'Hepatocyte nuclear factor 1B deletion, but not intragenic mutation, might be more susceptible to hypomagnesemia'. Journal of diabetes investigation (2023)
Rhian L Clissold, Coralie Bingham, Andrew Hattersley
Comment on a recent article titled 'Hepatocyte nuclear factor 1B deletion, but not intragenic mutation, might be more susceptible to hypomagnesemia'. Journal of diabetes investigation 15 (6) (2023)
Rhian L Clissold, Rhian L Clissold, Sian Ellard, Coralie Bingham, Andrew T Hattersley
Comment on Dubois-Laforgue et al. Diabetes, Associated Clinical Spectrum, Long-term Prognosis, and Genotype/Phenotype Correlations in 201 Adult Patients With Hepatocyte Nuclear Factor 1B (HNF1B) Molecular Defects. Diabetes Care 2017;40:1436-1443. Diabetes care 41 (1) (2018)
Rhian L Clissold, Beth Ashfield, Joe Burrage, Eilis Hannon, Coralie Bingham, Jonathan Mill, Andrew Hattersley, Emma L Dempster
Genome-wide methylomic analysis in individuals with HNF1B intragenic mutation and 17q12 microdeletion. Clinical epigenetics 10 (1) (2018)