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Author Details

Mark J Caulfield
William Harvey Research Institute, Queen Mary University of London
1988
265
97
PMIDPaper TitleJournal TitlePublished Year
37793701UK Prescribing Safety Assessment (PSA): The development, implementation and outcomes of a national online prescribing assessment.Br J Clin Pharmacol2024
37793701UK Prescribing Safety Assessment (PSA): The development, implementation and outcomes of a national online prescribing assessment.Br J Clin Pharmacol2024
36808131Equal access to pharmacogenomics testing: The ethical imperative for population-wide access in the UK NHS.Br J Clin Pharmacol2023
37828025ADRA2A and IRX1 are putative risk genes for Raynaud's phenomenon.Nat Commun2023
37816352Functional filter for whole-genome sequencing data identifies HHT and stress-associated non-coding SMAD4 polyadenylation site variants >5 kb from coding DNA.Am J Hum Genet2023
37907686British South Asian ancestry participants views of pharmacogenomics clinical implementation and research: a thematic analysis.Pharmacogenomics J2023
37810217Factor V Leiden, estrogen, and multimorbidity association with venous thromboembolism in a British-South Asian cohort.iScience2023
37808344<i>CYP2C19</i> Genotype Prevalence and Association With Recurrent Myocardial Infarction in British-South Asians Treated With Clopidogrel.JACC Adv2023
36972688Genetic analyses identify brain structures related to cognitive impairment associated with elevated blood pressure.Eur Heart J2023
37211972Precision medicine in rare diseases: What is next?J Intern Med2023
37461547POPULATION FREQUENCY OF REPEAT EXPANSIONS INDICATES INCREASED DISEASE PREVALENCE ESTIMATES ACROSS DIFFERENT POPULATIONS.medRxiv2023
37143396CYP2C19 loss-of-function alleles are not associated with higher prevalence of gastrointestinal bleeds in those who have been prescribed antidepressants: Analysis in a British-South Asian cohort.Br J Clin Pharmacol2023
36808131Equal access to pharmacogenomics testing: The ethical imperative for population-wide access in the UK NHS.Br J Clin Pharmacol2023
36926444Poverty dynamics and the determining factors among East African smallholder farmers.Agric Syst2023
37221222SLCO1B1*5 is protective against non-senile cataracts in cohort prescribed statins: analysis in a British-South Asian cohort.Pharmacogenomics J2023
37808344<i>CYP2C19</i> Genotype Prevalence and Association With Recurrent Myocardial Infarction in British-South Asians Treated With Clopidogrel.JACC Adv2023
37907686British South Asian ancestry participants views of pharmacogenomics clinical implementation and research: a thematic analysis.Pharmacogenomics J2023
37828025ADRA2A and IRX1 are putative risk genes for Raynaud's phenomenon.Nat Commun2023
37816352Functional filter for whole-genome sequencing data identifies HHT and stress-associated non-coding SMAD4 polyadenylation site variants &gt;5 kb from coding DNA.Am J Hum Genet2023
37810217Factor V Leiden, estrogen, and multimorbidity association with venous thromboembolism in a British-South Asian cohort.iScience2023
37461547POPULATION FREQUENCY OF REPEAT EXPANSIONS INDICATES INCREASED DISEASE PREVALENCE ESTIMATES ACROSS DIFFERENT POPULATIONS.medRxiv2023
37221222SLCO1B1*5 is protective against non-senile cataracts in cohort prescribed statins: analysis in a British-South Asian cohort.Pharmacogenomics J2023
37211972Precision medicine in rare diseases: What is next?J Intern Med2023
37143396CYP2C19 loss-of-function alleles are not associated with higher prevalence of gastrointestinal bleeds in those who have been prescribed antidepressants: Analysis in a British-South Asian cohort.Br J Clin Pharmacol2023
36972688Genetic analyses identify brain structures related to cognitive impairment associated with elevated blood pressure.Eur Heart J2023
36926444Poverty dynamics and the determining factors among East African smallholder farmers.Agric Syst2023
34463331Challenges in cardiovascular pharmacogenomics implementation: a viewpoint from the European Society of Cardiology Working Group on Cardiovascular Pharmacotherapy.Eur Heart J Cardiovasc Pharmacother2022
36333502Whole-genome sequencing of chronic lymphocytic leukemia identifies subgroups with distinct biological and clinical features.Nat Genet2022
35363781Heteroplasmic mitochondrial DNA variants in cardiovascular diseases.PLoS Genet2022
36198798Nuclear-embedded mitochondrial DNA sequences in 66,083 human genomes.Nature2022
33638977The role of pharmacogenomics in contemporary cardiovascular therapy: a position statement from the European Society of Cardiology Working Group on Cardiovascular Pharmacotherapy.Eur Heart J Cardiovasc Pharmacother2022
34463331Challenges in cardiovascular pharmacogenomics implementation: a viewpoint from the European Society of Cardiology Working Group on Cardiovascular Pharmacotherapy.Eur Heart J Cardiovasc Pharmacother2022
34904380Identification and validation of a novel pathogenic variant in GDF2 (BMP9) responsible for hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations.Am J Med Genet A2022
35162696Factors Affecting Citizen Trust and Public Engagement Relating to the Generation and Use of Real-World Evidence in Healthcare.Int J Environ Res Public Health2022
35069183The Pharmacogenetics of Statin Therapy on Clinical Events: No Evidence that Genetic Variation Affects Statin Response on Myocardial Infarction.Front Pharmacol2022
35363781Heteroplasmic mitochondrial DNA variants in cardiovascular diseases.PLoS Genet2022
36333502Whole-genome sequencing of chronic lymphocytic leukemia identifies subgroups with distinct biological and clinical features.Nat Genet2022
36198798Nuclear-embedded mitochondrial DNA sequences in 66,083 human genomes.Nature2022
33638977The role of pharmacogenomics in contemporary cardiovascular therapy: a position statement from the European Society of Cardiology Working Group on Cardiovascular Pharmacotherapy.Eur Heart J Cardiovasc Pharmacother2022
35162696Factors Affecting Citizen Trust and Public Engagement Relating to the Generation and Use of Real-World Evidence in Healthcare.Int J Environ Res Public Health2022
35069183The Pharmacogenetics of Statin Therapy on Clinical Events: No Evidence that Genetic Variation Affects Statin Response on Myocardial Infarction.Front Pharmacol2022
34904380Identification and validation of a novel pathogenic variant in GDF2 (BMP9) responsible for hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations.Am J Med Genet A2022
33350578An online compendium of treatable genetic disorders.Am J Med Genet C Semin Med Genet2021
34231218Adverse Cardiovascular Outcomes and Antihypertensive Treatment: A Genome-Wide Interaction Meta-Analysis in the International Consortium for Antihypertensive Pharmacogenomics Studies.Clin Pharmacol Ther2021
33958779Uncovering genetic mechanisms of hypertension through multi-omic analysis of the kidney.Nat Genet2021
34115965Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals.Am J Hum Genet2021
33727701Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.Nat Genet2021
33977903The Barts Health NHS Trust COVID-19 cohort: characteristics, outcomes and risk scoring of patients in East London.Int J Tuberc Lung Dis2021
34329581Scaling national and international improvement in virtual gene panel curation via a collaborative approach to discordance resolution.Am J Hum Genet2021
33307546Genetic mechanisms of critical illness in COVID-19.Nature2021
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Collaborators

Co-authored papers 123
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King's College London
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University of Oxford
Co-authored papers 40
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 38
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Lee Kong Chian School of Medicine, Nanyang Technological University
Co-authored papers 38
London NorthWest Healthcare NHS Trust
Co-authored papers 38
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National Institute on Aging
Co-authored papers 37
Baylor College of Medicine
Co-authored papers 36
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Harvard Medical School, Harvard University
Co-authored papers 36
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Co-authored papers 34
German Research Center for Cardiovascular Disease (DZHK)
Co-authored papers 34
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