Davina J. Moss-Hensman

London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 17 publications

Genetic testing for Huntington's disease: Past, present and future. How could genetic data be used to improve clinical practice?

Genetic testing for Huntington's disease: Past, present and future. How could genetic data be used to improve clinical practice?

Journal: Journal of Huntington's disease

Published: December 23, 2025

Huntington disease: somatic expansion, pathobiology and therapeutics.

Huntington disease: somatic expansion, pathobiology and therapeutics.

Journal: Nature reviews. Neurology

Published: October 03, 2025

Toward the clinical application of long-read sequencing in repeat-expansion disorders.

Toward the clinical application of long-read sequencing in repeat-expansion disorders.

Journal: Nature genetics

Published: September 03, 2025

Huntington's disease phenocopy syndromes revisited: a clinical comparison and next-generation sequencing exploration.

Huntington's disease phenocopy syndromes revisited: a clinical comparison and next-generation sequencing exploration.

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: February 26, 2024

Increased frequency of repeat expansion mutations across different populations.

Increased frequency of repeat expansion mutations across different populations.

Journal: medRxiv : the preprint server for health sciences

Published: July 18, 2023

Increased frequency of repeat expansion mutations across different populations.

Increased frequency of repeat expansion mutations across different populations.

Journal: Nature medicine

Published: June 22, 2023

Genetic modifiers of repeat expansion disorders.

Genetic modifiers of repeat expansion disorders.

Journal: Emerging topics in life sciences

Published: May 19, 2023

Intellectual enrichment and genetic modifiers of cognition and brain volume in Huntington's disease.

Intellectual enrichment and genetic modifiers of cognition and brain volume in Huntington's disease.

Journal: Brain communications

Published: April 04, 2022

Expanding the Spectrum of Movement Disorders Associated With C9orf72 Hexanucleotide Expansions.

Expanding the Spectrum of Movement Disorders Associated With C9orf72 Hexanucleotide Expansions.

Journal: Neurology. Genetics

Published: November 02, 2020

A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes.

A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes.

Journal: EBioMedicine

Published: August 23, 2019

MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1.

MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1.

Journal: Brain : a journal of neurology

Published: October 29, 2018

Quantification of huntingtin protein species in Huntington's disease patient leukocytes using optimised electrochemiluminescence immunoassays.

Quantification of huntingtin protein species in Huntington's disease patient leukocytes using optimised electrochemiluminescence immunoassays.

Journal: PloS one

Published: July 26, 2017

Showing 1-12 of 17

Last Updated: 09/26/2026