Torthaí cuardaigh - Stitziel, Nathan O

Human genetic insights into lipoproteins and risk of cardiometabolic disease de réir Stitziel, Nathan O.

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

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Genetic association studies in cardiovascular diseases: do we have enough power? de réir Auer, Paul L., Stitziel, Nathan O.

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Computational and statistical approaches to analyzing variants identified by exome sequencing de réir Stitziel, Nathan O, Kiezun, Adam, Sunyaev, Shamil

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A Clinical Approach to Inherited Premature Coronary Artery Disease de réir Stitziel, Nathan O., MacRae, Calum A.

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Genetics of the Extracellular Matrix in Aortic Aneurysmal Diseases de réir Lin, Chien-Jung, Lin, Chieh-Yu, Stitziel, Nathan O.

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Emerging targets for cardiovascular disease prevention in diabetes de réir Stitziel, Nathan O., Kanter, Jenny E., Bornfeldt, Karin E.

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topoSNP: a topographic database of non-synonymous single nucleotide polymorphisms with and without known disease association de réir Stitziel, Nathan O., Binkowski, T. Andrew, Tseng, Yan Yuan, Kasif, Simon, Liang, Jie

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Intracellular retention of mutant lysyl oxidase leads to aortic dilation in response to increased hemodynamic stress de réir Lee, Vivian S., Halabi, Carmen M., Broekelmann, Thomas J., Trackman, Philip C., Stitziel, Nathan O., Mecham, Robert P.

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Non-parametric Polygenic Risk Prediction via Partitioned GWAS Summary Statistics de réir Chun, Sung, Imakaev, Maxim, Hui, Daniel, Patsopoulos, Nikolaos A., Neale, Benjamin M., Kathiresan, Sekar, Stitziel, Nathan O., Sunyaev, Shamil R.

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Functional Characterization of LIPA Variants associated with Coronary Artery Disease de réir Evans, Trent D., Zhang, Xiangyu, Clark, Reece E., Alisio, Arturo, Song, Eric, Zhang, Hanrui, Reilly, Muredach P., Stitziel, Nathan O., Razani, Babak

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SVEP1 is a human coronary artery disease locus that promotes atherosclerosis() de réir Jung, In-Hyuk, Elenbaas, Jared S., Alisio, Arturo, Santana, Katherine, Young, Erica P., Kang, Chul Joo, Kachroo, Puja, Lavine, Kory J., Razani, Babak, Mecham, Robert P., Stitziel, Nathan O.

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Loss of function mutation in LOX causes thoracic aortic aneurysm and dissection in humans de réir Lee, Vivian S., Halabi, Carmen M., Hoffman, Erin P., Carmichael, Nikkola, Leshchiner, Ignaty, Lian, Christine G., Bierhals, Andrew J., Vuzman, Dana, Mecham, Robert P., Frank, Natasha Y., Stitziel, Nathan O.

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Identification of Medically Actionable Secondary Findings in the 1000 Genomes de réir Olfson, Emily, Cottrell, Catherine E., Davidson, Nicholas O., Gurnett, Christina A., Heusel, Jonathan W., Stitziel, Nathan O., Chen, Li-Shiun, Hartz, Sarah, Nagarajan, Rakesh, Saccone, Nancy L., Bierut, Laura J.

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Polygenic risk score identifies subgroup with higher burden of atherosclerosis and greater relative benefit from statin therapy in the primary prevention setting de réir Natarajan, Pradeep, Young, Robin, Stitziel, Nathan O., Padmanabhan, Sandosh, Baber, Usman, Mehran, Roxana, Sartori, Samantha, Fuster, Valentin, Reilly, Dermot F., Butterworth, Adam, Rader, Daniel J., Ford, Ian, Sattar, Naveed, Kathiresan, Sekar

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Common and Rare Genetic Variation in CCR2, CCR5, or CX3CR1 and Risk of Atherosclerotic Coronary Heart Disease and Glucometabolic Traits de réir Golbus, Jessica R., Stitziel, Nathan O., Zhao, Wei, Xue, Chenyi, Farrall, Martin, McPherson, Ruth, Erdmann, Jeanette, Deloukas, Panos, Watkins, Hugh, Schunkert, Heribert, Samani, Nilesh J., Saleheen, Danish, Kathiresan, Sekar, Reilly, Muredach P.

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Coronary Artery Disease Risk and Lipidomic Profiles Are Similar in Hyperlipidemias With Family History and Population‐Ascertained Hyperlipidemias de réir Rämö, Joel T., Ripatti, Pietari, Tabassum, Rubina, Söderlund, Sanni, Matikainen, Niina, Gerl, Mathias J., Klose, Christian, Surma, Michal A., Stitziel, Nathan O., Havulinna, Aki S., Pirinen, Matti, Salomaa, Veikko, Freimer, Nelson B., Jauhiainen, Matti, Palotie, Aarno, Taskinen, Marja‐Riitta, Simons, Kai, Ripatti, Samuli

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High-protein diets increase cardiovascular risk by activating macrophage mTOR to suppress mitophagy de réir Zhang, Xiangyu, Sergin, Ismail, Evans, Trent D., Jeong, Se-Jin, Rodriguez-Velez, Astrid, Kapoor, Divya, Chen, Sunny, Song, Eric, Holloway, Karyn B., Crowley, Jan R., Epelman, Slava, Weihl, Conrad C., Diwan, Abhinav, Fan, Daping, Mittendorfer, Bettina, Stitziel, Nathan O., Schilling, Joel D., Lodhi, Irfan J., Razani, Babak

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Mapping and characterization of structural variation in 17,795 human genomes de réir Abel, Haley J., Larson, David E., Regier, Allison A., Chiang, Colby, Das, Indraniel, Kanchi, Krishna L., Layer, Ryan M., Neale, Benjamin M., Salerno, William J., Reeves, Catherine, Buyske, Steven, Matise, Tara C., Muzny, Donna M., Zody, Michael C., Lander, Eric S., Dutcher, Susan K., Stitziel, Nathan O., Hall, Ira M.

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Exome sequencing and the genetic basis of complex traits de réir Kiezun, Adam, Garimella, Kiran, Do, Ron, Stitziel, Nathan O., Neale, Benjamin M., McLaren, Paul J., Gupta, Namrata, Sklar, Pamela, Sullivan, Patrick F., Moran, Jennifer L., Hultman, Christina M., Lichtenstein, Paul, Magnusson, Patrik, Lehner, Thomas, Shugart, Yin Yao, Price, Alkes L., de Bakker, Paul I.W., Purcell, Shaun M., Sunyaev, Shamil R.

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