Matthew Wakeling

13PUBLICATIONS
71CO-AUTHORS
Peripheral nervous systemGene and molecular therapyInfant and child healthCancer geneticsGenome structure and regulation
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Publications (13)

|Apr 16, 2025
Complete Loss of PAX4 causes Transient Neonatal Diabetes in Humans.

James Russ-Silsby, Yunkyeong Lee, Varsha Rajesh

|Apr 14, 2025
REVEL Is Better at Predicting Pathogenicity of Loss-of-Function than Gain-of-Function Variants.

Jasmin J Hopkins, Matthew N Wakeling, Matthew B Johnson

|Apr 18, 2024
Human inherited PD-L1 deficiency is clinically and immunologically less severe than PD-1 deficiency.

Matthew B Johnson, Masato Ogishi, Clara Domingo-Vila

|Apr 11, 2024
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements.

Thomas W Laver, Matthew N Wakeling, Richard C Caswell

|Nov 17, 2023
Primate-specific ZNF808 is essential for pancreatic development in humans.

Elisa De Franco, Nick D L Owens, Hossam Montaser

|Oct 28, 2023
Paediatric diabetes subtypes in a consanguineous population: a single-centre cohort study from Kurdistan, Iraq.

Shenali A Amaratunga, Tara Hussein Tayeb, Rozhan N Muhamad Sediq

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