Davina J. Hensman Moss

发表

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

S. Tabrizi, R. Scahill, E. Wild, 2017, PloS one.

Expanding the Spectrum of Movement Disorders Associated With C9orf72 Hexanucleotide Expansions

S. Tabrizi, K. Bhatia, H. Houlden, 2021, Neurology: Genetics.

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

P. Holmans, S. Tabrizi, D. Langbehn, 2022, Brain communications.

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

P. Holmans, R. Roos, S. Tabrizi, 2019, EBioMedicine.

Huntington’s disease blood and brain show a common gene expression pattern and share an immune signature with Alzheimer’s disease

P. Holmans, S. Tabrizi, D. Langbehn, 2017, Scientific Reports.

C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies

P. McColgan, S. Tabrizi, H. Houlden, 2014, Neurology.

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

Nick C Fox, T. Heskes, C. Kennard, 2019, Brain : a journal of neurology.

RNA-Seq of Huntington’s disease patient myeloid cells reveals innate transcriptional dysregulation associated with proinflammatory pathway activation

P. Holmans, S. Tabrizi, V. Plagnol, 2016, Human molecular genetics.

Genetic modifiers of repeat expansion disorders

M. Flower, Davina J. Hensman Moss, Jasmine Donaldson, 2023, Emerging topics in life sciences.