D. Shields

发表

Applied Computational Genomics

J. Beckmann, H. Deng, C. Baumgartner, 2018, Translational Bioinformatics.

Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

Matti Pirinen, David M. Herrington, Alex Doney, 2014, Nature Communications.

The Impact on Coronary Artery Disease of Common Polymorphisms Known to Modulate Responses to Pathogens

A. Stanton, A. O’Halloran, E. O’Brien, 2006, Annals of human genetics.

The future of genomics in Ireland – focus on genomics for health

C. Steward, D. Morris, W. Kolch, 2020, HRB open research.

Raised plasma homocysteine as a risk factor for retinal vascular occlusive disease

M. Cahill, P. Ueland, H. Refsum, 2000, The British journal of ophthalmology.

Genome-Wide Analysis of Blood Pressure Variability and Ischemic Stroke Clinical Sciences

M. Nalls, L. Ferrucci, P. Munroe, 2013 .

G‐protein β3 subunit polymorphism and bleeding in the orbofiban in patients with unstable coronary syndromes–thrombolysis in myocardial infarction 16 trial

C. Cannon, H. Jneid, A. Maree, 2010, Journal of thrombosis and haemostasis : JTH.

Impact of genetic variation in the 5-HT transporter and receptor on platelet function in patients with stable CAD taking aspirin.

A. Maree, D. Fitzgerald, C. Vangjeli, 2016, Thrombosis research.

Homocysteine and risk of premature coronary heart disease. Evidence for a common gene mutation.

A. Evans, R. Rozen, D. Shields, 1996, Circulation.

Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function

Jie Huang, Uwe Völker, Ming-Huei Chen, 2017, The Journal of clinical investigation.

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

May E. Montasser, H. M. Draisma, K. Lunetta, 2014 .

Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney

Andrew D. Johnson, Lorna M. Lopez, P. O’Reilly, 2017, Hypertension.

Genetic analysis of over one million people identifies 535 novel loci for blood pressure

Christian Gieger, Gonçalo Abecasis, He Gao, 2017, bioRxiv.

A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects.

D C Shields, A M Molloy, D. Shields, 1995, QJM : monthly journal of the Association of Physicians.

Meta-analysis of genome-wide association studies of HDL cholesterol response to statins

Joshua C Denny, Wei-Qi Wei, Fredrik Nyberg, 2016, Journal of Medical Genetics.

Serum amyloid A in the assessment of early inflammatory arthritis.

B. Bresnihan, D. Shields, O. FitzGerald, 2000, The Journal of rheumatology.

Genetic variation in glycoprotein IIb/IIIa (GPIIb/IIIa) as a determinant of the responses to an oral GPIIb/IIIa antagonist in patients with unstable coronary syndromes

C. Cannon, E. Braunwald, D. Fitzgerald, 2001 .

Integration of Proteomics and Genomics in Platelets

Dermot F. Reilly, D. Reilly, Stephen D. E. Park, 2004, Molecular & Cellular Proteomics.

Genetic analysis of the thermolabile variant of 5, 10-methylenetetrahydrofolate reductase as a risk factor for ischemic stroke.

D. Coakley, D. Shields, I. Graham, 1999, Arteriosclerosis, thrombosis, and vascular biology.

Cyclooxygenase‐1 haplotype modulates platelet response to aspirin

A. Maree, D. Shields, D. Fitzgerald, 2005, Journal of thrombosis and haemostasis : JTH.

The contribution of genetic factors to thrombotic and bleeding outcomes in coronary patients randomised to IIb/IIIa antagonists

C. Cannon, D. Shields, D. Fitzgerald, 2002, The Pharmacogenomics Journal.

Preliminary evidence of an association between bipolar disorder in females and the catechol‐O‐methyltransferase gene

D. Shields, E. Claffey, P. Mckeon, 1998, Psychiatric genetics.

Comparative RNA expression analyses from small‐scale, single‐donor platelet samples 1

S. Harmon, Stephen D. E. Park, D. Shields, 2006, Journal of thrombosis and haemostasis : JTH.

The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother.

D. Shields, J. Mills, A. Whitehead, 1999, American journal of human genetics.

Bmc Medical Genetics Elevated White Cell Count in Acute Coronary Syndromes: Relationship to Variants in Inflammatory and Thrombotic Genes Inflammationacute Coronary Syndromeswhite Cell Countinterleukin 1 Receptor Antagonistinterleukin 6

J. Todd, S. Nutland, N. Walker, 2004 .

MTHFR thermolabile genotype frequencies and longevity in Northern Ireland.

D. Shields, A. Whitehead, I. Rea, 1997, Atherosclerosis.

Raised plasma homocysteine as a risk factor for retinal vascular occlusive disease

M. Cahill, P. Ueland, H. Refsum, 2000, The British journal of ophthalmology.

Clinical Observations, Interventions, and Therapeutic Trials There Was a Significant Interaction between Treatment (placebo and Orbofiban) and the Pl a Polymorphism for Bleeding

E. Braunwald, C. Cannon, E. Braunwald, 2022 .