Stephen E. Hamby

Groby Road LE39QP
Leicester, ENG LE39QP, United Kingdom

Last Updated: 09/26/2026

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Found 24 publications

Discovery of myosin light chain kinase gene variant in a patient with tetralogy of Fallot suffering aortic dissection: Implications for pathogenesis and the role of family and population screening.

Discovery of myosin light chain kinase gene variant in a patient with tetralogy of Fallot suffering aortic dissection: Implications for pathogenesis and the role of family and population screening.

Journal: International journal of cardiology. Congenital heart disease

Published: August 07, 2024

Aging-related defects in macrophage function are driven by MYC and USF1 transcriptional programs.

Aging-related defects in macrophage function are driven by MYC and USF1 transcriptional programs.

Journal: Cell reports

Published: October 27, 2023

Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation.

Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation.

Journal: Nature genetics

Published: June 13, 2022

Tribbles 3 deficiency promotes atherosclerotic fibrous cap thickening and macrophage-mediated extracellular matrix remodelling.

Tribbles 3 deficiency promotes atherosclerotic fibrous cap thickening and macrophage-mediated extracellular matrix remodelling.

Journal: Frontiers in cardiovascular medicine

Published: May 19, 2022

Exploring the Genetic Architecture of Spontaneous Coronary Artery Dissection Using Whole-Genome Sequencing.

Exploring the Genetic Architecture of Spontaneous Coronary Artery Dissection Using Whole-Genome Sequencing.

Journal: Circulation. Genomic and precision medicine

Published: May 18, 2022

TRIB1 regulates tumor growth via controlling tumor-associated macrophage phenotypes and is associated with breast cancer survival and treatment response.

TRIB1 regulates tumor growth via controlling tumor-associated macrophage phenotypes and is associated with breast cancer survival and treatment response.

Journal: Theranostics

Published: February 19, 2022

Whole blood transcriptomic profiling identifies molecular pathways related to cardiovascular mortality in heart failure.

Whole blood transcriptomic profiling identifies molecular pathways related to cardiovascular mortality in heart failure.

Journal: European journal of heart failure

Published: December 24, 2021

Contribution of NOTCH1 genetic variants to bicuspid aortic valve and other congenital lesions.

Contribution of NOTCH1 genetic variants to bicuspid aortic valve and other congenital lesions.

Journal: Heart (British Cardiac Society)

Published: October 10, 2021

Polygenic basis and biomedical consequences of telomere length variation.

Polygenic basis and biomedical consequences of telomere length variation.

Journal: Nature genetics

Published: March 21, 2021

Spontaneous Coronary Artery Dissection: Insights on Rare Genetic Variation From Genome Sequencing.

Spontaneous Coronary Artery Dissection: Insights on Rare Genetic Variation From Genome Sequencing.

Journal: Circulation. Genomic and precision medicine

Published: October 30, 2020

Novel loss of function mutation in NOTCH1 in a family with bicuspid aortic valve, ventricular septal defect, thoracic aortic aneurysm, and aortic valve stenosis.

Novel loss of function mutation in NOTCH1 in a family with bicuspid aortic valve, ventricular septal defect, thoracic aortic aneurysm, and aortic valve stenosis.

Journal: Molecular genetics & genomic medicine

Published: February 12, 2020

Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia.

Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia.

Journal: Cardiovascular research

Published: January 22, 2020

Showing 1-12 of 24

Last Updated: 09/26/2026