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Mark J Caulfield

Showing results (31-40 of 162) with videos related to

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BMC Medicine|May 15, 2026
Survey to inform personalised prescribing in a British South Asian community: pharmacogenomics and traditional medicine useEmma F Magavern, Gabriel Marengo, Stavroula Kanoni, et al.
Nature|October 5, 2022
Nuclear-embedded mitochondrial DNA sequences in 66,083 human genomesWei Wei, Katherine R Schon, Greg Elgar, et al.
British Journal of Clinical Pharmacology|October 4, 2023
UK Prescribing Safety Assessment (PSA): The development, implementation and outcomes of a national online prescribing assessmentEmma F Magavern, Andrew Hitchings, Lynne Bollington, et al.
Human Molecular Genetics|July 29, 2016
A blood pressure-associated variant of the SLC39A8 gene influences cellular cadmium accumulation and toxicityRuoxin Zhang, Kate Witkowska, José Afonso Guerra-Assunção, et al.
Human Molecular Genetics|October 29, 2009
Replication of the five novel loci for uric acid concentrations and potential mediating mechanismsPim van der Harst, Stephan J L Bakker, Rudolf A de Boer, et al.
Nature Communications|October 12, 2023
ADRA2A and IRX1 are putative risk genes for Raynaud's phenomenonSylvia Hartmann, Summaira Yasmeen, Benjamin M Jacobs, et al.
Journal of Public Health (Oxford, England)|June 20, 2020
Greater risk of severe COVID-19 in Black, Asian and Minority Ethnic populations is not explained by cardiometabolic, socioeconomic or behavioural factors, or by 25(OH)-vitamin D status: study of 1326 cases from the UK BiobankZahra Raisi-Estabragh, Celeste McCracken, Mae S Bethell, et al.
Journal of Hypertension|October 14, 2004
Haplotypes of the beta2-adrenergic receptor gene are associated with essential hypertension in a Singaporean Chinese populationYee-Wei Lee, Vernon M S Oh, Edwin Garcia, et al.
Atherosclerosis|February 1, 2020
Effect of a coronary-heart-disease-associated variant of ADAMTS7 on endothelial cell angiogenesisXiangyuan Pu, Kenneth Chan, Wei Yang, et al.
Human Molecular Genetics|June 19, 2012
Functional analyses of coronary artery disease associated variation on chromosome 9p21 in vascular smooth muscle cellsAnna Motterle, Xiangyuan Pu, Harriet Wood, et al.
Pageof 17

Showing results (31-40 of 162) with videos related to

Sort By:
Pageof 17
BMC Medicine|May 15, 2026
Survey to inform personalised prescribing in a British South Asian community: pharmacogenomics and traditional medicine useEmma F Magavern, Gabriel Marengo, Stavroula Kanoni, et al.
Nature|October 5, 2022
Nuclear-embedded mitochondrial DNA sequences in 66,083 human genomesWei Wei, Katherine R Schon, Greg Elgar, et al.
British Journal of Clinical Pharmacology|October 4, 2023
UK Prescribing Safety Assessment (PSA): The development, implementation and outcomes of a national online prescribing assessmentEmma F Magavern, Andrew Hitchings, Lynne Bollington, et al.
Human Molecular Genetics|July 29, 2016
A blood pressure-associated variant of the SLC39A8 gene influences cellular cadmium accumulation and toxicityRuoxin Zhang, Kate Witkowska, José Afonso Guerra-Assunção, et al.
Human Molecular Genetics|October 29, 2009
Replication of the five novel loci for uric acid concentrations and potential mediating mechanismsPim van der Harst, Stephan J L Bakker, Rudolf A de Boer, et al.
Nature Communications|October 12, 2023
ADRA2A and IRX1 are putative risk genes for Raynaud's phenomenonSylvia Hartmann, Summaira Yasmeen, Benjamin M Jacobs, et al.
Journal of Public Health (Oxford, England)|June 20, 2020
Greater risk of severe COVID-19 in Black, Asian and Minority Ethnic populations is not explained by cardiometabolic, socioeconomic or behavioural factors, or by 25(OH)-vitamin D status: study of 1326 cases from the UK BiobankZahra Raisi-Estabragh, Celeste McCracken, Mae S Bethell, et al.
Journal of Hypertension|October 14, 2004
Haplotypes of the beta2-adrenergic receptor gene are associated with essential hypertension in a Singaporean Chinese populationYee-Wei Lee, Vernon M S Oh, Edwin Garcia, et al.
Atherosclerosis|February 1, 2020
Effect of a coronary-heart-disease-associated variant of ADAMTS7 on endothelial cell angiogenesisXiangyuan Pu, Kenneth Chan, Wei Yang, et al.
Human Molecular Genetics|June 19, 2012
Functional analyses of coronary artery disease associated variation on chromosome 9p21 in vascular smooth muscle cellsAnna Motterle, Xiangyuan Pu, Harriet Wood, et al.
Pageof 17