G. Bayly | Researchain

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Featured researches published by G. Bayly.

Annals of Clinical Biochemistry | 2002

HDL-cholesterol and cardiac disease: which table to use?

G. Bayly

Atherosclerosis Supplements | 2018

The impact of socio-economic status on case finding for familial hypercholesterolaemia.

L. Gritzmacher; K. Haralambos; P. Downie; G. Bayly

Atherosclerosis | 2018

A comparison of Simon Broome and welsh criteria for selecting patients for familial hypercholesterolaemia (FH) genetic testing

Pauline Annie L. Ashfield-Watt; Lisa Gritzmacher; Ian McDowell; G. Bayly; K. Haralambos

Atherosclerosis | 2018

Assessment of Lp(a) and detection of monogenic and polygenic hypercholesterolaemia in a cohort of patients presenting with an acute coronary syndrome

Paul Downie; L. Hirt; Lisa Gritzmacher; T. Johnson; G. Bayly

Atherosclerosis Supplements | 2017

Genetic testing for Familial Hypercholesterolaemia in the genomic era. The utility of an NGS test for monogenic and polygenic hypercholesterolaemia

E. Watson; J. Honeychurch; A. Hills; P. Dean; L. Yarram-Smith; G. Woodward; M. Wadsley; R. Moore; S. Humphries; G. Bayly; Maggie Williams

Atherosclerosis Supplements | 2017

Standardising genetic variant classification for FH – application of the ACMG guidelines

C. Dent; A. Hills; J. Honeychurch; E. Watson; P. Dean; G. Woodward; M. Wadsley; J. Davies; L. Yarram-Smith; S. Humphries; S. Leigh; K. Haralambos; G. Bayly; Maggie Williams

Atherosclerosis Supplements | 2017

Development of a multigene panel screening test for hypertriglyceridaemia using next generation sequencing

P. Downie; J. Honeychurch; P. Dean; R. Whittington; G. Woodward; R. Moore; A. Day; Maggie Williams; G. Bayly

Atherosclerosis | 2016

Validation and utility of a new NGS assay for familial hypercholesterolaemia incorporating 12 LDL-C-raising SNPs

J. Honeychurch; E. Watson; Alison Hills; P. Dean; G. Woodward; M. Wadsley; J. Davies; S. Humphries; G. Bayly; Maggie Williams

Atherosclerosis | 2016

Homozygous Familial Hypercholesterolaemia – Summary of cases detected at the Bristol Genetics Laboratory

A. Hills; Julie Honeychurch; P. Dean; G. Dennis; M. Greenslade; M. Barbir; Jane B. Breen; C. Dawson; N. El-Farhan; R. Ayling; A. Sharma; G. Bayly; Maggie Williams

Atherosclerosis | 2013

Implementation of a comprehensive gene screening test for familial hypercholesterolaemia using next generation sequencing

P. Dean; L. Yarram; G. Dennis; G. Bayly; Andrew Taylor; A. Day; K. Haralambos; Sharon D. Whatley; Ian McDowell; E. Roberts; M. Greenslade; Maggie Williams

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