Darroch Hall
Newcastle Upon Tyne, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 10 publications
Exogenous Transforming Growth Factor-β1 and Its Helminth-Derived Mimic Attenuate the Heart's Inflammatory Response to Ischemic Injury and Reduce Mature Scar Size.
Journal: The American journal of pathology
Published: July 12, 2023
Cardiosphere-Derived Cells Require Endoglin for Paracrine-Mediated Angiogenesis.
Journal: Stem cell reports
Published: January 17, 2017
Functionally significant, rare transcription factor variants in tetralogy of Fallot.
Journal: PloS one
Published: October 01, 2013
Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls.
Journal: Circulation. Cardiovascular genetics
Published: July 24, 2013
Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot.
Journal: Human molecular genetics
Published: January 09, 2013
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.
Journal: Nature genetics
Published: November 20, 2012
Common variation neighbouring micro-RNA 22 is associated with increased left ventricular mass.
Journal: PloS one
Published: August 02, 2012
A common variant in the PTPN11 gene contributes to the risk of tetralogy of Fallot.
Journal: Circulation. Cardiovascular genetics
Published: April 17, 2012
Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease.
Journal: American journal of human genetics
Published: February 24, 2012
Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls.
Journal: Human molecular genetics
Published: December 27, 2011
Showing 1-10 of 10
Last Updated: 09/26/2026