Center-Authored Papers
Filters: Author is Samani, Nilesh J [Clear All Filters]
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2017.
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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2017.
Rare and low-frequency coding variants alter human adult height.. Nature. 542(7640):186-190. Abstract
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2017.
Discovery of novel heart rate-associated loci using the Exome Chip.. Human molecular genetics. Abstract
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2017.
Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals.. American journal of human genetics. Abstract
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2016.
Cystatin C and Cardiovascular Disease: A Mendelian Randomization Study.. Journal of the American College of Cardiology. 68(9):934-45. Abstract
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2016.
DCAF4, a novel gene associated with leucocyte telomere length.. Journal of medical genetics. 52(3):157-62. Abstract
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2015.
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.. Nature. 518(7537):102-6. Abstract
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2015.
Genetic studies of body mass index yield new insights for obesity biology.. Nature. 518(7538):197-206. Abstract
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2015.
New genetic loci link adipose and insulin biology to body fat distribution.. Nature. 518(7538):187-96. Abstract
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2015.
Defining the role of common variation in the genomic and biological architecture of adult human height.. Nature genetics. 46(11):1173-86. Abstract
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2014.
Loss-of-function mutations in APOC3, triglycerides, and coronary disease.. The New England journal of medicine. 371(1):22-31. Abstract
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2014.
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2014.
Mendelian randomization of blood lipids for coronary heart disease.. European heart journal. Abstract
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2014.
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2014.
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.
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2013.
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.
Loci influencing blood pressure identified using a cardiovascular gene-centric array.. Human molecular genetics. Abstract
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2013.
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.
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.. Nature genetics. 45(5):501-12. Abstract
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2013.
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.
Hypothesis-Based Analysis of Gene-Gene Interactions and Risk of Myocardial Infarction.. PloS one. 7(8):e41730. Abstract
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2012.
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.. Nature. 478(7367):103-9. Abstract
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