Center-Authored Papers
Filters: Author is Reilly, Muredach P [Clear All Filters]
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.. American journal of human genetics. 94(2):223-32. Abstract
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2014.
Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease.. The American journal of clinical nutrition. Abstract
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2013.
Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population.. PLoS genetics. 10(7):e1004494. Abstract
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2014.
Exome sequencing and directed clinical phenotyping diagnose cholesterol ester storage disease presenting as autosomal recessive hypercholesterolemia.. Arteriosclerosis, thrombosis, and vascular biology. 33(12):2909-14. Abstract
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2013.
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.. Nature. 518(7537):102-6. Abstract
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2015.
Gene-centric Meta-analysis in 87,736 Individuals of European Ancestry Identifies Multiple Blood-Pressure-Related Loci.. American journal of human genetics. Abstract
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2014.
Genetic association of long-chain acyl-CoA synthetase 1 variants with fasting glucose, diabetes, and subclinical atherosclerosis.. Journal of lipid research. 57(3):433-42. Abstract
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2016.
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.. Nature. 478(7367):103-9. Abstract
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2011.
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.. Nature genetics. 41(3):334-41. Abstract
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2009.
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2012.
Genome-Wide Association Study for Circulating Tissue Plasminogen Activator Levels and Functional Follow-Up Implicates Endothelial STXBP5 and STX2.. Arteriosclerosis, thrombosis, and vascular biology. Abstract
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2014.
A Genome-Wide Association Study Identifies LIPA as a Susceptibility Gene for Coronary Artery Disease.. Circulation. Cardiovascular genetics. 4(4):403-12. Abstract
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2011.
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.. Nature genetics. 41(11):1182-90. Abstract
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2009.
Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies.. Journal of the American College of Cardiology. 56(19):1552-63. Abstract
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2010.
Large-Scale Gene-Centric Meta-analysis across 32 Studies Identifies Multiple Lipid Loci.. American journal of human genetics. 91(5):823-38. Abstract
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2012.
Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci.. American journal of human genetics. 90(3):410-25. Abstract
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2012.
Loci influencing blood pressure identified using a cardiovascular gene-centric array.. Human molecular genetics. Abstract
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2013.
Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height.. American journal of human genetics. 88(1):6-18. Abstract
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2011.
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2013.
A second independent locus within DMRT1 is associated with testicular germ cell tumor susceptibility.. Human molecular genetics. 20(15):3109-17. Abstract
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2011.
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease.. Journal of the American College of Cardiology. 69(7):823-836. Abstract
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