Mark T. Ross

Granta Park
Cambridge, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 44 publications

Whole-genome sequencing implicates rare, low-frequency and structural non-coding variation at the SCN5A locus in Brugada syndrome.

Whole-genome sequencing implicates rare, low-frequency and structural non-coding variation at the SCN5A locus in Brugada syndrome.

Journal: medRxiv : the preprint server for health sciences

Published: July 17, 2026

Blood-based RNA-Seq of 5412 individuals with rare disease identifies new candidate diagnoses in the National Genomic Research Library.

Blood-based RNA-Seq of 5412 individuals with rare disease identifies new candidate diagnoses in the National Genomic Research Library.

Journal: medRxiv : the preprint server for health sciences

Published: April 03, 2026

High-depth whole genome sequencing of premalignant breast lesions reveals rearrangement hotspots and personalized management opportunities.

High-depth whole genome sequencing of premalignant breast lesions reveals rearrangement hotspots and personalized management opportunities.

Journal: Nature communications

Published: October 13, 2025

Benchmarking the paediatric T-cell ALL subtype classifier, TALLSorts.

Benchmarking the paediatric T-cell ALL subtype classifier, TALLSorts.

Journal: British journal of haematology

Published: June 02, 2025

Seasonal variation in vascular function: a systematic review and recommendations for future research.

Seasonal variation in vascular function: a systematic review and recommendations for future research.

Journal: International journal of environmental health research

Published: November 24, 2024

A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in Thailand.

A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in Thailand.

Journal: Circulation

Published: October 11, 2024

Clinical utility of 'Shaken' biopsies for whole-genome sequencing.

Clinical utility of 'Shaken' biopsies for whole-genome sequencing.

Journal: Journal of clinical pathology

Published: August 27, 2024

An ultra-endurance event leads to changes in circulating regulatory T-cells, CD4+ naïve and CD8+ effector memory T-cells in the 48 h post-race recovery period.

An ultra-endurance event leads to changes in circulating regulatory T-cells, CD4+ naïve and CD8+ effector memory T-cells in the 48 h post-race recovery period.

Journal: European journal of applied physiology

Published: July 24, 2024

Centenarians-the way to healthy vascular ageing and longevity: a review from VascAgeNet.

Centenarians-the way to healthy vascular ageing and longevity: a review from VascAgeNet.

Journal: GeroScience

Published: July 04, 2024

The association between circulating CD34+CD133+ endothelial progenitor cells and reduced risk of Alzheimer's disease in the Framingham Heart Study.

The association between circulating CD34+CD133+ endothelial progenitor cells and reduced risk of Alzheimer's disease in the Framingham Heart Study.

Journal: Exploration of medicine

Published: June 10, 2024

A dedicated caller for DUX4 rearrangements from whole-genome sequencing data.

A dedicated caller for DUX4 rearrangements from whole-genome sequencing data.

Journal: BMC medical genomics

Published: June 06, 2024

Identifying barriers and opportunities to facilitate the uptake of whole genome sequencing in paediatric haematology and oncology practice.

Identifying barriers and opportunities to facilitate the uptake of whole genome sequencing in paediatric haematology and oncology practice.

Journal: BMC medical education

Published: December 21, 2023

Showing 1-12 of 44

Last Updated: 09/26/2026