Kevin Colclough

14PUBLICATIONS
108CO-AUTHORS
Cell and nuclear divisionEpigenetics (incl. genome methylation and epigenomics)Molecular targetsMolecular evolutionMedical biotechnology diagnostics (incl. biosensors)
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Publications (14)

|Aug 25, 2026
Identification of Nuclear Genetic Loci Linked to Clinical Features of the m.3243A>G Mitochondrial DNA Variant.

|Mar 18, 2026
Polygenic background contributes to GCK-MODY clinical presentation and glycaemic variability.

Jacques Murray Leech, Ankit M Arni, V Kartik Chundru

|Mar 18, 2026
Familial medullary thyroid carcinoma secondary to an SLC30A9 intragenic deletion and translation reinitiation.

Donato Iacovazzo, Federica Begalli, Oniz Suleyman

|Nov 25, 2025
MODY Is Prevalent in Later-Onset Diabetes and Has Potential for Targeted Therapy but Is Challenging to Identify.

Luke N Sharp, Uyenlinh L Mirshahi, Kevin Colclough

|Oct 14, 2025
Updating a Clinical Prediction Model for Identifying Monogenic Diabetes to Include Both Clinical Features and Biomarkers.

Julieanne Knupp, Pedro Cardoso, Katherine G Young

|Aug 08, 2025
Rare Variants in NEUROD1 and PDX1 Are Low-Penetrance Causes of MODY, Whereas Those in APPL1 and WFS1 Are Not Associated With MODY.

Aparajita Sriram, Matthew N Wakeling, Andrew T Hattersley

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Frequent Collaborators

9 joint publications

Kashyap Patel

8 joint publications

Andrew T Hattersley

5 joint publications

Michael N Weedon

3 joint publications

Beverley Shields