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Author Details

Steve E Humphries
1981
913
121
PMIDPaper TitleJournal TitlePublished Year
36493747Causal analysis of plasma IL-8 on carotid intima media thickness, a measure of subclinical atherosclerosis.2023
37924278Alternative cascade-testing protocols for identifying and managing patients with familial hypercholesterolaemia: systematic reviews, qualitative study and cost-effectiveness analysis.2023
38060059Should Familial Hypercholesterolaemia Be Included in the UK Newborn Whole Genome Sequencing Programme?2023
37409534Prevalence of FH-Causing Variants and Impact on LDL-C Concentration in European, South Asian, and African Ancestry Groups of the UK Biobank-Brief Report.2023
37021583Cross-Sectional Gene-Smoking Interaction Analysis in Relation to Subclinical Atherosclerosis-Results From the IMPROVE Study.2023
36642658How does cholesterol burden change the case for investing in familial hypercholesterolaemia? A cost-effectiveness analysis.2023
34809444Posttranscriptional Regulation of the Human LDL Receptor by the U2-Spliceosome.Circulation Research2022
35432461LDL-C Concentrations and the 12-SNP LDL-C Score for Polygenic Hypercholesterolaemia in Self-Reported South Asian, Black and Caribbean Participants of the UK Biobank.Frontiers in Genetics2022
35292153How should public health recommendations address Lp(a) measurement, a causative risk factor for cardiovascular disease (CVD)?Atherosclerosis2022
34906454The Clinical Genome Resource (ClinGen) Familial Hypercholesterolemia Variant Curation Expert Panel consensus guidelines for LDLR variant classification.Genet Med2022
35330330Cost-Effectiveness of Screening Algorithms for Familial Hypercholesterolaemia in Primary Care.Journal of Personalized Medicine2022
34635577Comparing the performance of the novel FAMCAT algorithms and established case-finding criteria for familial hypercholesterolaemia in primary care.Open Heart2021
33517400Genome-wide association study of circulating interleukin 6 levels identifies novel loci.Hum Mol Genet2021
33508743Comparison of the mutation spectrum and association with pre and post treatment lipid measures of children with heterozygous familial hypercholesterolaemia (FH) from eight European countries.Atherosclerosis2021
34194581Lack of Association of Gene Polymorphisms with Coronary Artery Disease in Pakistani Subjects.Disease Markers2021
33436761The overlap of genetic susceptibility to schizophrenia and cardiometabolic disease can be used to identify metabolically different groups of individuals.Scientific Reports2021
34521694Case-finding and genetic testing for familial hypercholesterolaemia in primary care.Heart2021
34666015Genetic testing for familial hypercholesterolemia-past, present, and future.Journal of Lipid Research2021
32833799Management of familial hypercholesterolaemia in childhood.Current Opinion in Pediatrics2020
31893970PCSK6 Is a Key Protease in the Control of Smooth Muscle Cell Function in Vascular Remodeling.Circ Res2020
31893465The familial hypercholesterolaemia phenotype: Monogenic familial hypercholesterolaemia, polygenic hypercholesterolaemia and other causes.Clinical Genetics2020
31996015Triglyceride-containing lipoprotein sub-fractions and risk of coronary heart disease and stroke: A prospective analysis in 11,560 adults.Eur J Prev Cardiol2020
32396387Metabolic Dysregulation of the Lysophospholipid/Autotaxin Axis in the Chromosome 9p21 Gene SNP rs10757274.Circ Genom Precis Med2020
31809987Comparison of the characteristics at diagnosis and treatment of children with heterozygous familial hypercholesterolaemia (FH) from eight European countries.Atherosclerosis2020
32443900Higher Responsiveness to Rosuvastatin in Polygenic versus Monogenic Hypercholesterolaemia: A Propensity Score Analysis.Life2020
33187671Sex differences in cardiovascular morbidity associated with familial hypercholesterolaemia: A retrospective cohort study of the UK Simon Broome register linked to national hospital records.Atherosclerosis2020
32618729Non-HDL or LDL cholesterol in heterozygous familial hypercholesterolaemia: findings of the Simon Broome Register.Current Opinion in Lipidology2020
31536851Current management of children and young people with heterozygous familial hypercholesterolaemia - HEART UK statement of care.Atherosclerosis2019
31746944Familial hypercholesterolaemia workshop for leveraging point-of-care testing and personalised medicine in association with the Lipid and Atherosclerosis Society of Southern Africa.2019
31696945Statins for children with familial hypercholesterolemia.2019
28705542Effect of Coronary Artery Disease risk SNPs on serum cytokine levels and cytokine imbalance in Premature Coronary Artery Disease.Cytokine2019
30458964Coronary heart disease mortality in severe vs. non-severe familial hypercholesterolaemia in the Simon Broome Register.Atherosclerosis2019
30545617A priori-defined Mediterranean-like dietary pattern predicts cardiovascular events better in north Europe than in Mediterranean countries.International Journal of Cardiology2019
30056760Estimation of the prevalence of cholesteryl ester storage disorder in a cohort of patients with clinical features of familial hypercholesterolaemia.Annals of Clinical Biochemistry2019
31089183Genetic variation in CADM2 as a link between psychological traits and obesity.Scientific Reports2019
31181417Risk of cardiovascular disease outcomes in primary care subjects with familial hypercholesterolaemia: A cohort study.Atherosclerosis2019
31011892Polygenic Hypercholesterolemia and Cardiovascular Disease Risk.Current Cardiology Reports2019
31372435Data on the association between a simplified Mediterranean diet score and the incidence of combined, cardio and cerebro vascular events.Data in Brief2019
29188294Genetic Association of Lipids and Lipid Drug Targets With Abdominal Aortic Aneurysm: A Meta-analysis.JAMA Cardiol2018
30270085Clinical utility of the polygenic LDL-C SNP score in familial hypercholesterolemia.Atherosclerosis2018
30510157GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes.Nat Commun2018
30311388ClinVar database of global familial hypercholesterolemia-associated DNA variants.Hum Mutat2018
29879685Cost-utility analysis of searching electronic health records and cascade testing to identify and diagnose familial hypercholesterolaemia in England and Wales.Atherosclerosis2018
29872056Association of circulating metabolites with healthy diet and risk of cardiovascular disease: analysis of two cohort studies.Sci Rep2018
29937236Universal screening at age 1-2 years as an adjunct to cascade testing for familial hypercholesterolaemia in the UK: A cost-utility analysis.Atherosclerosis2018
29673405GWAS implicated risk variants in different genes contribute additively to increase the risk of coronary artery disease (CAD) in the Pakistani subjects.Lipids in Health and Disease2018
29353228Association of lifelong occupation and educational level with subclinical atherosclerosis in different European regions. Results from the IMPROVE study.Atherosclerosis2018
29304826The SNP rs10911021 is associated with oxidative stress in coronary heart disease patients from Pakistan.Lipids in Health and Disease2018
29751283Coronary heart disease mortality in treated familial hypercholesterolaemia: Update of the UK Simon Broome FH register.Atherosclerosis2018
29208363The UK Paediatric Familial Hypercholesterolaemia Register: Statin-related safety and 1-year growth data.Journal of Clinical Lipidology2018
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