Výsledky vyhledávání - Guiducci, Candace

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 Autor Keebler, Mary E., Sanders, Christopher L., Surti, Aarti, Guiducci, Candace, Burtt, Noel P, Kathiresan, Sekar

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Fine-Mapping in African Americans of Eight Recently Discovered Genetic Loci for Plasma Lipids: The Jackson Heart Study Autor Keebler, Mary E., Deo, Rahul C., Surti, Aarti, Konieczkowski, David, Guiducci, Candace, Burtt, Noel, Buxbaum, Sarah G., Sarpong, Daniel F., Steffes, Michael W., Wilson, James G., Taylor, Herman A., Kathiresan, Sekar

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Comparing strategies to fine map the association of common SNPs on chromosome 9p21 to Type 2 Diabetes and Myocardial Infarction Autor Shea, Jessica, Agarwala, Vineeta, Philippakis, Anthony A., Maguire, Jared, Banks, Eric, DePristo, Mark, Thomson, Brian, Guiducci, Candace, Kathiresan, Sekar, Gabriel, Stacey, Burtt, Noël P, Daly, Mark J., Groop, Leif, Altshuler, David

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A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses Autor Ripatti, Samuli, Tikkanen, Emmi, Orho-Melander, Marju, Havulinna, Aki S, Silander, Kaisa, Sharma, Amitabh, Guiducci, Candace, Perola, Markus, Jula, Antti, Sinisalo, Juha, Lokki, Marja-Liisa, Nieminen, Markku S, Melander, Olle, Salomaa, Veikko, Peltonen, Leena, Kathiresan, Sekar

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The evolution of drug resistance in clinical isolates of Candida albicans Autor Ford, Christopher B, Funt, Jason M, Abbey, Darren, Issi, Luca, Guiducci, Candace, Martinez, Diego A, Delorey, Toni, Li, Bi yu, White, Theodore C, Cuomo, Christina, Rao, Reeta P, Berman, Judith, Thompson, Dawn A, Regev, Aviv

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Personalized Genetic Risk Counseling to Motivate Diabetes Prevention: A randomized trial Autor Grant, Richard W., O’Brien, Kelsey E., Waxler, Jessica L., Vassy, Jason L., Delahanty, Linda M., Bissett, Laurie G., Green, Robert C., Stember, Katherine G., Guiducci, Candace, Park, Elyse R., Florez, Jose C., Meigs, James B.

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A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study Autor Kathiresan, Sekar, Manning, Alisa K, Demissie, Serkalem, D'Agostino, Ralph B, Surti, Aarti, Guiducci, Candace, Gianniny, Lauren, Burtt, Nöel P, Melander, Olle, Orho-Melander, Marju, Arnett, Donna K, Peloso, Gina M, Ordovas, Jose M, Cupples, L Adrienne

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Association of Common Variants in NPPA and NPPB with Circulating Natriuretic Peptides and Blood Pressure Autor Newton-Cheh, Christopher, Larson, Martin G., Vasan, Ramachandran S., Levy, Daniel, Bloch, Kenneth D., Surti, Aarti, Guiducci, Candace, Kathiresan, Sekar, Benjamin, Emelia J., Struck, Joachim, Morgenthaler, Nils G., Bergmann, Andreas, Blankenberg, Stefan, Kee, Frank, Nilsson, Peter, Yin, Xiaoyan, Peltonen, Leena, Vartiainen, Erkki, Salomaa, Veikko, Hirschhorn, Joel N., Melander, Olle, Wang, Thomas J.

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High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency Autor Calvo, Sarah E, Tucker, Elena J, Compton, Alison G, Kirby, Denise M, Crawford, Gabriel, Burtt, Noel P, Rivas, Manuel A, Guiducci, Candace, Bruno, Damien L, Goldberger, Olga A, Redman, Michelle C, Wiltshire, Esko, Wilson, Callum J, Altshuler, David, Gabriel, Stacey B, Daly, Mark J, Thorburn, David R, Mootha, Vamsi K

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The Influence of Rare Genetic Variation in SLC30A8 on Diabetes Incidence and β-Cell Function Autor Billings, Liana K., Jablonski, Kathleen A., Ackerman, Rachel J., Taylor, Andrew, Fanelli, Rebecca R., McAteer, Jarred B., Guiducci, Candace, Delahanty, Linda M., Dabelea, Dana, Kahn, Steven E., Franks, Paul W., Hanson, Robert L., Maruthur, Nisa M., Shuldiner, Alan R., Mayer-Davis, Elizabeth J., Knowler, William C., Florez, Jose C.

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The efficacy of detecting variants with small effects on the Affymetrix 6.0 platform using pooled DNA Autor Chiang, Charleston W. K., Gajdos, Zofia K. Z., Korn, Joshua M., Butler, Johannah L., Hackett, Rachel, Guiducci, Candace, Nguyen, Thutrang T., Wilks, Rainford, Forrester, Terrence, Henderson, Katherine D., Le Marchand, Loic, Henderson, Brian E., Haiman, Christopher A., Cooper, Richard S., Lyon, Helen N., Zhu, Xiaofeng, McKenzie, Colin A., Palmer, Mark R., Hirschhorn, Joel N.

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Genetic Variants Near TNFAIP3 on 6q23 are Associated with Systemic Lupus Erythematosus (SLE) Autor Graham, Robert R., Cotsapas, Chris, Davies, Leela, Hackett, Rachel, Lessard, Christopher J., Leon, Joanlise M., Burtt, Noel P., Guiducci, Candace, Parkin, Melissa, Gates, Casey, Plenge, Robert M., Behrens, Timothy W., Wither, Joan E., Rioux, John D., Fortin, Paul R., Graham, Deborah Cunninghame, Wong, Andrew K., Vyse, Timothy J., Daly, Mark J., Altshuler, David, Moser, Kathy L., Gaffney, Patrick M.

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Rapid Assessment of Genetic Ancestry in Populations of Unknown Origin by Genome-Wide Genotyping of Pooled Samples Autor Chiang, Charleston W. K., Gajdos, Zofia K. Z., Korn, Joshua M., Kuruvilla, Finny G., Butler, Johannah L., Hackett, Rachel, Guiducci, Candace, Nguyen, Thutrang T., Wilks, Rainford, Forrester, Terrence, Haiman, Christopher A., Henderson, Katherine D., Le Marchand, Loic, Henderson, Brian E., Palmert, Mark R., McKenzie, Colin A., Lyon, Helen N., Cooper, Richard S., Zhu, Xiaofeng, Hirschhorn, Joel N.

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Genome-wide association of anthropometric traits in African- and African-derived populations Autor Kang, Sun J., Chiang, Charleston W.K., Palmer, Cameron D., Tayo, Bamidele O., Lettre, Guillaume, Butler, Johannah L., Hackett, Rachel, Adeyemo, Adebowale A., Guiducci, Candace, Berzins, Ilze, Nguyen, Thutrang T., Feng, Tao, Luke, Amy, Shriner, Daniel, Ardlie, Kristin, Rotimi, Charles, Wilks, Rainford, Forrester, Terrence, McKenzie, Colin A., Lyon, Helen N., Cooper, Richard S., Zhu, Xiaofeng, Hirschhorn, Joel N.

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Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans Autor Kathiresan, Sekar, Melander, Olle, Guiducci, Candace, Surti, Aarti, Burtt, Noël P, Rieder, Mark J, Cooper, Gregory M, Roos, Charlotta, Voight, Benjamin F, Havulinna, Aki S, Wahlstrand, Björn, Hedner, Thomas, Corella, Dolores, Tai, E Shyong, Ordovas, Jose M, Berglund, Göran, Vartiainen, Erkki, Jousilahti, Pekka, Hedblad, Bo, Taskinen, Marja-Riitta, Newton-Cheh, Christopher, Salomaa, Veikko, Peltonen, Leena, Groop, Leif, Altshuler, David M, Orho-Melander, Marju

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Exome Sequencing, ANGPTL3 Mutations, and Familial Combined Hypolipidemia Autor Musunuru, Kiran, Pirruccello, James P., Do, Ron, Peloso, Gina M., Guiducci, Candace, Sougnez, Carrie, Garimella, Kiran V., Fisher, Sheila, Abreu, Justin, Barry, Andrew J., Fennell, Tim, Banks, Eric, Ambrogio, Lauren, Cibulskis, Kristian, Kernytsky, Andrew, Gonzalez, Elena, Rudzicz, Nicholas, Engert, James C., DePristo, Mark A., Daly, Mark J., Cohen, Jonathan C., Hobbs, Helen H., Altshuler, David, Schonfeld, Gustav, Gabriel, Stacey B., Yue, Pin, Kathiresan, Sekar

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Rare, Low-Frequency, and Common Variants in the Protein-Coding Sequence of Biological Candidate Genes from GWASs Contribute to Risk of Rheumatoid Arthritis Autor Diogo, Dorothée, Kurreeman, Fina, Stahl, Eli A., Liao, Katherine P., Gupta, Namrata, Greenberg, Jeffrey D., Rivas, Manuel A., Hickey, Brendan, Flannick, Jason, Thomson, Brian, Guiducci, Candace, Ripke, Stephan, Adzhubey, Ivan, Barton, Anne, Kremer, Joel M., Alfredsson, Lars, Sunyaev, Shamil, Martin, Javier, Zhernakova, Alexandra, Bowes, John, Eyre, Steve, Siminovitch, Katherine A., Gregersen, Peter K., Worthington, Jane, Klareskog, Lars, Padyukov, Leonid, Raychaudhuri, Soumya, Plenge, Robert M.

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Identification of ten loci associated with height highlights new biological pathways in human growth Autor Lettre, Guillaume, Jackson, Anne U, Gieger, Christian, Schumacher, Fredrick R, Berndt, Sonja I, Sanna, Serena, Eyheramendy, Susana, Voight, Benjamin F, Butler, Johannah L, Guiducci, Candace, Illig, Thomas, Hackett, Rachel, Heid, Iris M, Jacobs, Kevin B, Lyssenko, Valeriya, Uda, Manuela, Boehnke, Michael, Chanock, Stephen J, Groop, Leif C, Hu, Frank B, Isomaa, Bo, Kraft, Peter, Peltonen, Leena, Salomaa, Veikko, Schlessinger, David, Hunter, David J, Hayes, Richard B, Abecasis, Gonçalo R, Wichmann, H-Erich, Mohlke, Karen L, Hirschhorn, Joel N

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A common variant of HMGA2 is associated with adult and childhood height in the general population Autor Weedon, Michael N, Lettre, Guillaume, Freathy, Rachel M, Lindgren, Cecilia M, Voight, Benjamin F, Perry, John R B, Elliott, Katherine S, Hackett, Rachel, Guiducci, Candace, Shields, Beverley, Zeggini, Eleftheria, Lango, Hana, Lyssenko, Valeriya, Timpson, Nicholas J, Burtt, Noel P, Rayner, Nigel W, Saxena, Richa, Ardlie, Kristin, Tobias, Jonathan H, Ness, Andrew R, Ring, Susan M, Palmer, Colin N A, Morris, Andrew D, Peltonen, Leena, Salomaa, Veikko, Smith, George Davey, Groop, Leif C, Hattersley, Andrew T, McCarthy, Mark I, Hirschhorn, Joel N, Frayling, Timothy M

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Exome and whole genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity Autor Dulak, Austin M., Stojanov, Petar, Peng, Shouyong, Lawrence, Michael S., Fox, Cameron, Stewart, Chip, Bandla, Santhoshi, Imamura, Yu, Schumacher, Steven E., Shefler, Erica, McKenna, Aaron, Cibulskis, Kristian, Sivachenko, Andrey, Carter, Scott L., Saksena, Gordon, Voet, Douglas, Ramos, Alex H., Auclair, Daniel, Thompson, Kristin, Sougnez, Carrie, Onofrio, Robert C., Guiducci, Candace, Beroukhim, Rameen, Zhou, David, Lin, Lin, Lin, Jules, Reddy, Rishindra, Chang, Andrew, Luketich, James D., Pennathur, Arjun, Ogino, Shuji, Golub, Todd R., Gabriel, Stacey B., Lander, Eric S., Beer, David G., Godfrey, Tony E., Getz, Gad, Bass, Adam J.

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