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A Proposal for an Individualized Pharmacogenetics-Based Warfarin Initiation Dose Regimen for Patients Commencing Anticoagulation Therapy

Clinical pharmacology and therapeutics, 2011-11, Vol.90 (5), p.701-706

2011

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The VKORC1 and CYP2C9 genotypes are associated with over‐anticoagulation during initiation of warfarin therapy in children

Journal of thrombosis and haemostasis, 2013-02, Vol.11 (2), p.373-375

2013

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Regional variations and drivers of mercury and selenium concentrations in Steller sea lions

The Science of the total environment, 2020-11, Vol.744, p.140787, Article 140787

2020

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Heritability estimates for beta cell function and features of the insulin resistance syndrome in UK families with an increased susceptibility to Type 2 diabetes

Diabetologia, 2004-04, Vol.47 (4), p.732-738

2004

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Novel genetic variants linked to coronary artery disease by genome-wide association are not associated with carotid artery intima-media thickness or intermediate risk phenotypes

Atherosclerosis, 2009-03, Vol.203 (1), p.41-44

2009

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Common variation in the adiponectin gene has an effect on systolic blood pressure

Journal of human hypertension, 2011-12, Vol.25 (12), p.719-724

2011

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The clinical implications of metal debris release from the taper junctions and bearing surfaces of metal-on-metal hip arthroplasty: joint fluid and blood metal ion concentrations

The bone & joint journal, 2016-07, Vol.98-B (7), p.925-933

2016

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Local vessel injury following percutaneous coronary intervention does not promote early mobilisation of endothelial progenitor cells in the absence of myocardial necrosis

Heart (British Cardiac Society), 2009-04, Vol.95 (7), p.555-558

2009

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Common genetic variation in the type A endothelin-1 receptor is associated with ambulatory blood pressure: a family study

Journal of human hypertension, 2008-04, Vol.22 (4), p.282-288

2008

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Tumour necrosis factor-alpha gene promoter polymorphism and decreased insulin resistance

Diabetologia, 1998-04, Vol.41 (4), p.430-434

1998

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Reduced beta cell function in offspring of mothers with young-onset type 2 diabetes

Diabetologia, 2006-08, Vol.49 (8), p.1876-1880

2006

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Predicting macular hole closure with ocriplasmin based on spectral domain optical coherence tomography

Eye (London), 2016-05, Vol.30 (5), p.740-745

2016

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The effect of surgical factors on early patient-reported outcome measures (PROMS) following total knee replacement

Journal of bone and joint surgery. British volume, 2012-08, Vol.94 (8), p.1058-1066

2012

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Comparison of ‘time within therapeutic INR range’ with ‘percentage INR within therapeutic range’ for assessing long‐term anticoagulation control in children

Journal of thrombosis and haemostasis, 2011-05, Vol.9 (5), p.1090-1092

2011

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Comparison of time within therapeutic INR range with percentage INR within therapeutic range for assessing long‐term anticoagulation control in children: reply to a rebuttal

Journal of thrombosis and haemostasis, 2011-11, Vol.9 (11), p.2332-2333

2011

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Multiple metabolic abnormalities in normal glucose tolerant relatives of NIDDM families

Diabetologia, 1997-10, Vol.40 (10), p.1185-1190

1997

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Warfarin treatment outcomes in children monitored at home with a point-of-care device

Thrombosis and haemostasis, 2011-06, Vol.105 (6), p.1103-1105

2011

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Vitamin K epoxide reductase complex subunit 1 (VKORC1 ) polymorphism influences the anticoagulation response subsequent to vitamin K intake: a pilot study

Journal of thrombosis and haemostasis, 2008-07, Vol.6 (7), p.1226-1228

2008

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Comparison of patient-reported outcome measures following total and unicondylar knee replacement

Journal of bone and joint surgery. British volume, 2012-07, Vol.94 (7), p.919-927

2012

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Genome-wide linkage analysis of electrocardiographic and echocardiographic left ventricular hypertrophy in families with hypertension

European heart journal, 2008-02, Vol.29 (4), p.525-530

2008

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Apolipoprotein E and familial non-insulin-dependent diabetes mellitus

The Lancet (British edition), 1994-08, Vol.344 (8919), p.406-406

1994

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Variation in the ADIPOQ gene promoter is associated with carotid intima media thickness independent of plasma adiponectin levels in healthy subjects

European heart journal, 2008-02, Vol.29 (3), p.386-393

2008

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Scandinavian and Dutch lessons in childhood road traffic accident prevention

BMJ, 1982-08, Vol.285 (6342), p.621-626

1982

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The C-532T polymorphism of the angiotensinogen gene is associated with pulse pressure: A possible explanation for heterogeneity in genetic association studies of AGT and hypertension

International journal of epidemiology, 2007-12, Vol.36 (6), p.1356-1362

2007

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Genotype at the - 174G/C polymorphism of the interleukin-6 gene is associated with common carotid artery intimal-medial thickness : Family study and meta-analysis

Stroke (1970), 2005-10, Vol.36 (10), p.2215-2219

2005

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A Proposal for an Individualized Pharmacogenetics-Based Warfarin Initiation Dose Regimen for Patients Commencing Anticoagulation Therapy

The VKORC1 and CYP2C9 genotypes are associated with over‐anticoagulation during initiation of warfarin therapy in children

Regional variations and drivers of mercury and selenium concentrations in Steller sea lions

Heritability estimates for beta cell function and features of the insulin resistance syndrome in UK families with an increased susceptibility to Type 2 diabetes

Novel genetic variants linked to coronary artery disease by genome-wide association are not associated with carotid artery intima-media thickness or intermediate risk phenotypes

Common variation in the adiponectin gene has an effect on systolic blood pressure

The clinical implications of metal debris release from the taper junctions and bearing surfaces of metal-on-metal hip arthroplasty: joint fluid and blood metal ion concentrations

Local vessel injury following percutaneous coronary intervention does not promote early mobilisation of endothelial progenitor cells in the absence of myocardial necrosis

Common genetic variation in the type A endothelin-1 receptor is associated with ambulatory blood pressure: a family study

Tumour necrosis factor-alpha gene promoter polymorphism and decreased insulin resistance

Reduced beta cell function in offspring of mothers with young-onset type 2 diabetes

Predicting macular hole closure with ocriplasmin based on spectral domain optical coherence tomography

The effect of surgical factors on early patient-reported outcome measures (PROMS) following total knee replacement

Comparison of ‘time within therapeutic INR range’ with ‘percentage INR within therapeutic range’ for assessing long‐term anticoagulation control in children

Comparison of time within therapeutic INR range with percentage INR within therapeutic range for assessing long‐term anticoagulation control in children: reply to a rebuttal

Multiple metabolic abnormalities in normal glucose tolerant relatives of NIDDM families

Warfarin treatment outcomes in children monitored at home with a point-of-care device

Vitamin K epoxide reductase complex subunit 1 (VKORC1 ) polymorphism influences the anticoagulation response subsequent to vitamin K intake: a pilot study

Comparison of patient-reported outcome measures following total and unicondylar knee replacement

Genome-wide linkage analysis of electrocardiographic and echocardiographic left ventricular hypertrophy in families with hypertension

Apolipoprotein E and familial non-insulin-dependent diabetes mellitus

Variation in the ADIPOQ gene promoter is associated with carotid intima media thickness independent of plasma adiponectin levels in healthy subjects

Scandinavian and Dutch lessons in childhood road traffic accident prevention

The C-532T polymorphism of the angiotensinogen gene is associated with pulse pressure: A possible explanation for heterogeneity in genetic association studies of AGT and hypertension

Genotype at the - 174G/C polymorphism of the interleukin-6 gene is associated with common carotid artery intimal-medial thickness : Family study and meta-analysis

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