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Chris Clarkson is an expert in Genetics at Queen Mary University of London (United Kingdom). Chris Clarkson has authored 21 publications, the most recent in 2025. SLR score: 66 (community average: 125). How the SLR is computed.

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Chris Clarkson Queen Mary University of London United Kingdom
66 ScienceLeadR Reputation 66

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Genetics

Subspecialties: Biochemistry - Neurology - Public Health

Full career – Last 3 years

Main Topics

Publications and Clinical Studies

Publications – Clinical Studies

Profile data updated on

Organizations

Career arc: 2017 - 2025
Source: PubMed

Queen Mary University of London

Publications Synthesis

Sources: PubMed, OpenAlex

Number : 21

Citations

Citations: 708 1st author: 3 Last author: 6 Unique author: 0

Main journals

J COSMOL ASTROPART P 4
Mon Not R Astron Soc 2
Mov Disord 2
PHYS DARK UNIVERSE 2
Physical review. D. Particles, fields, gravitation, and cosmology/Physical review. D, Particles, fields, gravitation, and cosmology 2

Best Journals

Nat Med 1

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Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
A Population-Wide Exploration of the THAP11 CAG Repeat Size and Structure in the 100,000 Genomes Project and UK Biobank.
PMID 39651830 — genome, movement disorders, ataxia		Mov Disord20240
Analysis of Short Tandem Repeat Expansions in a Cohort of 12,496 Exomes from Patients with Neurological Diseases Reveals Variable Genotyping Rate Dependent on Exome Capture Kits.
PMID 40004498 — genomics, microsatellite repeats, myotonic dystrophy, spinocerebellar ataxias, ataxia, exome, tandem repeat sequences		Genes (Basel)20250
Increased frequency of repeat expansion mutations across different populations.
PMID 39354197 — molecular biology, prevalence, diagnosis, mutation		Nat Med Top journal202412
Apparent Parity Violation in the Observed Galaxy Trispectrum.
PMID 39373453 — physics, parity		Phys Rev Lett20241
Adaptive Long-Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4.
PMID 38197134 — spinocerebellar ataxias, movement disorders, ataxia, genome		Mov Disord202431

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Sources: PubMed, OpenAlex, ClinicalTrials, EU CTIS