Bilaketaren emaitzak - Kathiresan, Sekar

2018 Curt Stern Award Address nork Kathiresan, Sekar

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HapMap and mapping genes for cardiovascular disease nork Musunuru, Kiran, Kathiresan, Sekar

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Genetics of Human Cardiovascular Disease nork Kathiresan, Sekar, Srivastava, Deepak

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Genetics of Lipid Disorders nork Pirruccello, James, Kathiresan, Sekar

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Surprises From Genetic Analyses of Lipid Risk Factors for Atherosclerosis nork Musunuru, Kiran, Kathiresan, Sekar

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Leveraging Human Genetics to Guide Drug Target Discovery nork Stitziel, Nathan O., Kathiresan, Sekar

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Is Coronary Atherosclerosis One Disease or Many?: Setting Realistic Expectations for Precision Medicine nork Khera, Amit V., Kathiresan, Sekar

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Genetics of coronary artery disease: discovery, biology and clinical translation nork Khera, Amit V., Kathiresan, Sekar

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Clonal Hematopoiesis: Somatic Mutations in Blood Cells and Atherosclerosis nork Natarajan, Pradeep, Siddhartha, Jaiswal, Kathiresan, Sekar

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Genetic determinants of plasma triglycerides nork Johansen, Christopher T., Kathiresan, Sekar, Hegele, Robert A.

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Exome sequencing and complex disease: practical aspects of rare variant association studies nork Do, Ron, Kathiresan, Sekar, Abecasis, Gonçalo R.

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The Future of LDL-Cholesterol Lowering Therapy: An End to Statin Exceptionalism? nork Khera, Amit V., Natarajan, Pradeep, Kathiresan, Sekar

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On the Significance of Linkage Studies of Complex Traits nork Newton-Cheh, Christopher, Larson, Martin, Kathiresan, Sekar, O’Donnell, Christopher

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Genetic Analysis of Venous Thromboembolism in UK Biobank Identifies the ZFPM2 Locus and Implicates Obesity as a Causal Risk Factor nork Klarin, Derek, Emdin, Connor A., Natarajan, Pradeep, Conrad, Mark F., Kathiresan, Sekar

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Response to Letter Regarding Article, “Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery” nork Aragam, Krishna G., Chaffin, Mark, Ellinor, Patrick T., Kathiresan, Sekar, Lubitz, Steven A.

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Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study nork Yang, Qiong, Kathiresan, Sekar, Lin, Jing-Ping, Tofler, Geoffrey H, O'Donnell, Christopher J

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Multiple associated variants increase the heritability explained for plasma lipids and coronary artery disease nork Tada, Hayato, Won, Hong-Hee, Melander, Olle, Yang, Jian, Peloso, Gina M, Kathiresan, Sekar

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Association of Blood Lipids with Common DNA Sequence Variants at Nineteen Genetic Loci in the Multiethnic United States National Health and Nutrition Examination Survey III nork Keebler, Mary E., Sanders, Christopher L., Surti, Aarti, Guiducci, Candace, Burtt, Noel P, Kathiresan, Sekar

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Genetic Variation at the Sulfonylurea Receptor, Type 2 Diabetes, and Coronary Heart Disease nork Emdin, Connor A., Klarin, Derek, Natarajan, Pradeep, Florez, Jose C., Kathiresan, Sekar, Khera, Amit V.

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Phenotypic extremes in rare variant study designs nork Peloso, Gina M, Rader, Daniel J, Gabriel, Stacey, Kathiresan, Sekar, Daly, Mark J, Neale, Benjamin M

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