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Functional analyses of coronary artery disease associated variation on chromosome 9p21 in vascular smooth muscle cells

Human molecular genetics, 2012-09, Vol.21 (18), p.4021-4029

2012

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Investigation and management of adult hypertension

Heart (British Cardiac Society), 2018-09, Vol.104 (18), p.1543-1551

2018

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Coronary-Heart-Disease-Associated Genetic Variant at the COL4A1/COL4A2 Locus Affects COL4A1/COL4A2 Expression, Vascular Cell Survival, Atherosclerotic Plaque Stability and Risk of Myocardial Infarction

PLoS genetics, 2016-07, Vol.12 (7), p.e1006127-e1006127

2016

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ADAMTS7 Cleavage and Vascular Smooth Muscle Cell Migration Is Affected by a Coronary-Artery-Disease-Associated Variant

American journal of human genetics, 2013-03, Vol.92 (3), p.366-374

2013

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Expression and function of the K+ channel KCNQ genes in human arteries

British journal of pharmacology, 2011-01, Vol.162 (1), p.42-53

2011

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UK survey of non-medical use of prescription drugs (NMURx) as a valuable source of general population illicit drug use data

Postgraduate medical journal, 2018-11, Vol.94 (1117), p.627-633

2018

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Exploring hypertension genome-wide association studies findings and impact on pathophysiology, pathways, and pharmacogenetics

Wiley interdisciplinary reviews. Mechanisms of disease, 2015-03, Vol.7 (2), p.73-90

2015

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Attenuation of Splanchnic Autotransfusion Following Noninvasive Ultrasound Renal Denervation: A Novel Marker of Procedural Success

Journal of the American Heart Association, 2018-06, Vol.7 (12)

2018

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Candidates registered for reasonable adjustments underperform compared to other candidates in the national undergraduate Prescribing Safety Assessment: Retrospective cohort analysis (2014–2018)

British journal of clinical pharmacology, 2021-03, Vol.87 (3), p.946-954

2021

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Black renal transplant recipients have poorer long-term graft survival than CYP3A5 expressers from other ethnic groups

Nephrology, dialysis, transplantation, 2010-02, Vol.25 (2), p.628-634

2010

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Over 1000 genetic loci influencing blood pressure with multiple systems and tissues implicated

Human molecular genetics, 2019-11, Vol.28 (R2), p.R151-R161

2019

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A retrospective cohort study of risk factors and outcomes in older patients admitted to an inner-city geriatric unit in London during first peak of COVID-19 pandemic

Irish journal of medical science, 2022-06, Vol.191 (3), p.1037-1045

2022

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HYPERTENSIVE PATIENTS WITH GREATER GENETIC RISK RESPOND LESS EFFECTIVELY TO TREATMENT AND ARE MORE LIKELY TO BE TREATMENT RESISTANT

Journal of hypertension, 2021-04, Vol.39 (Supplement 1), p.e359

2021

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Status and future of genomics in blood pressure

European heart journal, 2017-04, Vol.38 (14), p.1011-1013

2017

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A blood pressure-associated variant of the SLC39A8 gene influences cellular cadmium accumulation and toxicity

Human molecular genetics, 2016-09, Vol.25 (18), p.4117-4126

2016

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LBOS 02-04 BLOOD PRESSURE-ASSOCIATED POLYMORPHISMS IN SLC4A7 (SODIUM/BICARBONATE CO-TRANSPORTER NBCn1) ARE LINKED TO GENE EXPRESSION AND INTRACELLULAR pH REGULATION

Journal of hypertension, 2016-09, Vol.34 Suppl 1 - ISH 2016 Abstract Book (Supplement 1), p.e549-e550

2016

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Increased NBCn1 expression, Na+/HCO3- co-transport and intracellular pH in human vascular smooth muscle cells with a risk allele for hypertension

Human molecular genetics, 2017-03, Vol.26 (5), p.989-1002

2017

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The biological impact of blood pressure-associated genetic variants in the natriuretic peptide receptor C gene on human vascular smooth muscle

Human molecular genetics, 2018-01, Vol.27 (1), p.199-210

2018

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Hypertension genomics and cardiovascular prevention

Annals of translational medicine, 2018-08, Vol.6 (15), p.291-291

2018

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Increased NBCn1 expression, Na + /HCO 3 - co-transport and intracellular pH in human vascular smooth muscle cells with a risk allele for hypertension

Human molecular genetics, 2017-01, p.ddx015

2017

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Abstract P048: Blood-Pressure Associated Variants in Natriuretic Peptide Receptor C Affect Human Vascular Smooth Muscle Cells Proliferation and Calcium Flux in Response to Angiotensin II

Hypertension (Dallas, Tex. 1979), 2015-09, Vol.66 (suppl_1)

2015

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PD.06. Hypertension related variant of SLC39A8 gene influences cadmium uptake and cell toxicity

Journal of human hypertension, 2015-10, Vol.29 (10), p.645

2015

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3A.03. Blood-pressure associated variants in NPR3 affect human vascular smooth muscle cells proliferation and calcium response to angiotensin II

Journal of human hypertension, 2015-10, Vol.29 (10), p.624

2015

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189Genetic Variation in ADAMTS7 is Associated with Severity of Coronary Artery Disease

Heart (British Cardiac Society), 2015-06, Vol.101 (Suppl 4), p.A105-A106

2015

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189 Genetic Variation in ADAMTS7 is Associated with Severity of Coronary Artery Disease

Heart (British Cardiac Society), 2015-06, Vol.101 (Suppl 4), p.A105-A106

2015

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Functional analyses of coronary artery disease associated variation on chromosome 9p21 in vascular smooth muscle cells

Investigation and management of adult hypertension

Coronary-Heart-Disease-Associated Genetic Variant at the COL4A1/COL4A2 Locus Affects COL4A1/COL4A2 Expression, Vascular Cell Survival, Atherosclerotic Plaque Stability and Risk of Myocardial Infarction

ADAMTS7 Cleavage and Vascular Smooth Muscle Cell Migration Is Affected by a Coronary-Artery-Disease-Associated Variant

Expression and function of the K+ channel KCNQ genes in human arteries

UK survey of non-medical use of prescription drugs (NMURx) as a valuable source of general population illicit drug use data

Exploring hypertension genome-wide association studies findings and impact on pathophysiology, pathways, and pharmacogenetics

Attenuation of Splanchnic Autotransfusion Following Noninvasive Ultrasound Renal Denervation: A Novel Marker of Procedural Success

Candidates registered for reasonable adjustments underperform compared to other candidates in the national undergraduate Prescribing Safety Assessment: Retrospective cohort analysis (2014–2018)

Black renal transplant recipients have poorer long-term graft survival than CYP3A5 expressers from other ethnic groups

Over 1000 genetic loci influencing blood pressure with multiple systems and tissues implicated

A retrospective cohort study of risk factors and outcomes in older patients admitted to an inner-city geriatric unit in London during first peak of COVID-19 pandemic

HYPERTENSIVE PATIENTS WITH GREATER GENETIC RISK RESPOND LESS EFFECTIVELY TO TREATMENT AND ARE MORE LIKELY TO BE TREATMENT RESISTANT

Status and future of genomics in blood pressure

A blood pressure-associated variant of the SLC39A8 gene influences cellular cadmium accumulation and toxicity

LBOS 02-04 BLOOD PRESSURE-ASSOCIATED POLYMORPHISMS IN SLC4A7 (SODIUM/BICARBONATE CO-TRANSPORTER NBCn1) ARE LINKED TO GENE EXPRESSION AND INTRACELLULAR pH REGULATION

Increased NBCn1 expression, Na+/HCO3- co-transport and intracellular pH in human vascular smooth muscle cells with a risk allele for hypertension

The biological impact of blood pressure-associated genetic variants in the natriuretic peptide receptor C gene on human vascular smooth muscle

Hypertension genomics and cardiovascular prevention

Increased NBCn1 expression, Na + /HCO 3 - co-transport and intracellular pH in human vascular smooth muscle cells with a risk allele for hypertension

Abstract P048: Blood-Pressure Associated Variants in Natriuretic Peptide Receptor C Affect Human Vascular Smooth Muscle Cells Proliferation and Calcium Flux in Response to Angiotensin II

PD.06. Hypertension related variant of SLC39A8 gene influences cadmium uptake and cell toxicity

3A.03. Blood-pressure associated variants in NPR3 affect human vascular smooth muscle cells proliferation and calcium response to angiotensin II

189Genetic Variation in ADAMTS7 is Associated with Severity of Coronary Artery Disease

189 Genetic Variation in ADAMTS7 is Associated with Severity of Coronary Artery Disease

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