Resultados da busca - Stitziel, Nathan O

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

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

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

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

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

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

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Emerging targets for cardiovascular disease prevention in diabetes por 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 por 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 por 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 por 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 por 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() por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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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