Výsledky vyhledávání - Day-Williams, Aaron G

The effect of next-generation sequencing technology on complex trait research Autor Day-Williams, Aaron G, Zeggini, Eleftheria

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ARIEL and AMELIA: Testing for an Accumulation of Rare Variants Using Next-Generation Sequencing Data Autor Asimit, Jennifer L., Day-Williams, Aaron G., Morris, Andrew P., Zeggini, Eleftheria

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CCRaVAT and QuTie - enabling analysis of rare variants in large-scale case control and quantitative trait association studies Autor Lawrence, Robert, Day-Williams, Aaron G, Elliott, Katherine S, Morris, Andrew P, Zeggini, Eleftheria

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Linkage Analysis without Defined Pedigrees Autor Day-Williams, Aaron G., Blangero, John, Dyer, Thomas D., Lange, Kenneth, Sobel, Eric M.

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Genome-Wide Association Analysis of Imputed Rare Variants: Application to Seven Common Complex Diseases Autor Mägi, Reedik, Asimit, Jennifer L, Day-Williams, Aaron G, Zeggini, Eleftheria, Morris, Andrew P

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Unifying Ideas for Non-Parametric Linkage Analysis Autor Day-Williams, Aaron G., Blangero, John, Dyer, Thomas D., Lange, Kenneth, Sobel, Eric M.

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GLIDERS - A web-based search engine for genome-wide linkage disequilibrium between HapMap SNPs Autor Lawrence, Robert, Day-Williams, Aaron G, Mott, Richard, Broxholme, John, Cardon, Lon R, Zeggini, Eleftheria

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PINES: phenotype-informed tissue weighting improves prediction of pathogenic noncoding variants Autor Bodea, Corneliu A., Mitchell, Adele A., Bloemendal, Alex, Day-Williams, Aaron G., Runz, Heiko, Sunyaev, Shamil R.

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An Evaluation of Different Target Enrichment Methods in Pooled Sequencing Designs for Complex Disease Association Studies Autor Day-Williams, Aaron G., McLay, Kirsten, Drury, Eleanor, Edkins, Sarah, Coffey, Alison J., Palotie, Aarno, Zeggini, Eleftheria

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Genetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson’s disease Autor Leonard, Hampton, Blauwendraat, Cornelis, Krohn, Lynne, Faghri, Faraz, Iwaki, Hirotaka, Ferguson, Glen, Day-Williams, Aaron G., Stone, David J., Singleton, Andrew B., Nalls, Mike A., Gan-Or, Ziv

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Large-scale association analysis of TNF/LTA gene region polymorphisms in type 2 diabetes Autor Boraska, Vesna, Rayner, Nigel W, Groves, Christopher J, Frayling, Timothy M, Diakite, Mahamadou, Rockett, Kirk A, Kwiatkowski, Dominic P, Day-Williams, Aaron G, McCarthy, Mark I, Zeggini, Eleftheria

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Radiographic endophenotyping in hip osteoarthritis improves the precision of genetic association analysis Autor Panoutsopoulou, Kalliope, Thiagarajah, Shankar, Zengini, Eleni, Day-Williams, Aaron G, Ramos, Yolande FM, Meessen, Jennifer MTA, Huetink, Kasper, Nelissen, Rob GHH, Southam, Lorraine, Rayner, N William, Doherty, Michael, Meulenbelt, Ingrid, Zeggini, Eleftheria, Wilkinson, J Mark

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A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica Autor Estrada, Karol, Whelan, Christopher W., Zhao, Fengmei, Bronson, Paola, Handsaker, Robert E., Sun, Chao, Carulli, John P., Harris, Tim, Ransohoff, Richard M., McCarroll, Steven A., Day-Williams, Aaron G., Greenberg, Benjamin M., MacArthur, Daniel G.

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Investigation of Association Between Hip Osteoarthritis Susceptibility Loci and Radiographic Proximal Femur Shape Autor Lindner, Claudia, Thiagarajah, Shankar, Wilkinson, J. Mark, Panoutsopoulou, Kalliope, Day‐Williams, Aaron G., Cootes, Timothy F., Wallis, Gillian A., Loughlin, John, Arden, Nigel, Birrell, Fraser, Carr, Andrew, Chapman, Kay, Deloukas, Panos, Doherty, Michael, McCaskie, Andrew, Ollier, William E. R., Rai, Ashok, Ralston, Stuart H., Spector, Timothy D., Valdes, Ana M., Wallis, Gillian A., Mark Wilkinson, J., Zeggini, Eleftheria

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Phenome-wide association studies across large population cohorts support drug target validation Autor Diogo, Dorothée, Tian, Chao, Franklin, Christopher S., Alanne-Kinnunen, Mervi, March, Michael, Spencer, Chris C. A., Vangjeli, Ciara, Weale, Michael E., Mattsson, Hannele, Kilpeläinen, Elina, Sleiman, Patrick M. A., Reilly, Dermot F., McElwee, Joshua, Maranville, Joseph C., Chatterjee, Arnaub K., Bhandari, Aman, Nguyen, Khanh-Dung H., Estrada, Karol, Reeve, Mary-Pat, Hutz, Janna, Bing, Nan, John, Sally, MacArthur, Daniel G., Salomaa, Veikko, Ripatti, Samuli, Hakonarson, Hakon, Daly, Mark J., Palotie, Aarno, Hinds, David A., Donnelly, Peter, Fox, Caroline S., Day-Williams, Aaron G., Plenge, Robert M., Runz, Heiko

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Diagnosis of Parkinson’s disease on the basis of clinical–genetic classification: a population-based modelling study Autor Nalls, Mike A., McLean, Cory Y., Rick, Jacqueline, Eberly, Shirley, Hutten, Samantha J., Gwinn, Katrina, Sutherland, Margaret, Martinez, Maria, Heutink, Peter, Williams, Nigel, Hardy, John, Gasser, Thomas, Brice, Alexis, Price, T. Ryan, Nicolas, Aude, Keller, Margaux F., Molony, Cliona, Gibbs, J. Raphael, Chen-Plotkin, Alice, Suh, Eunran, Letson, Christopher, Fiandaca, Massimo S., Mapstone, Mark, Federoff, Howard J., Noyce, Alastair J, Morris, Huw, Van Deerlin, Vivianna M., Weintraub, Daniel, Zabetian, Cyrus, Hernandez, Dena G., Lesage, Suzanne, Mullins, Meghan, Conley, Emily Drabant, Northover, Carrie, Frasier, Mark, Marek, Ken, Day-Williams, Aaron G., Stone, David J., Ioannidis, John P. A., Singleton, Andrew B.

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A Variant in MCF2L Is Associated with Osteoarthritis Autor Day-Williams, Aaron G., Southam, Lorraine, Panoutsopoulou, Kalliope, Rayner, Nigel W., Esko, Tonu, Estrada, Karol, Helgadottir, Hafdis T., Hofman, Albert, Ingvarsson, Throvaldur, Jonsson, Helgi, Keis, Aime, Kerkhof, Hanneke J.M., Thorleifsson, Gudmar, Arden, Nigel K., Carr, Andrew, Chapman, Kay, Deloukas, Panos, Loughlin, John, McCaskie, Andrew, Ollier, William E.R., Ralston, Stuart H., Spector, Timothy D., Wallis, Gillian A., Wilkinson, J. Mark, Aslam, Nadim, Birell, Fraser, Carluke, Ian, Joseph, John, Rai, Ashok, Reed, Mike, Walker, Kirsten, Doherty, Sally A., Jonsdottir, Ingileif, Maciewicz, Rose A., Muir, Kenneth R., Metspalu, Andres, Rivadeneira, Fernando, Stefansson, Kari, Styrkarsdottir, Unnur, Uitterlinden, Andre G., van Meurs, Joyce B.J., Zhang, Weiya, Valdes, Ana M., Doherty, Michael, Zeggini, Eleftheria

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Genetic risk of Parkinson disease and progression:: An analysis of 13 longitudinal cohorts Autor Iwaki, Hirotaka, Blauwendraat, Cornelis, Leonard, Hampton L., Liu, Ganqiang, Maple-Grødem, Jodi, Corvol, Jean-Christophe, Pihlstrøm, Lasse, van Nimwegen, Marlies, Hutten, Samantha J., Nguyen, Khanh-Dung H., Rick, Jacqueline, Eberly, Shirley, Faghri, Faraz, Auinger, Peggy, Scott, Kirsten M., Wijeyekoon, Ruwani, Van Deerlin, Vivianna M., Hernandez, Dena G., Day-Williams, Aaron G., Brice, Alexis, Alves, Guido, Noyce, Alastair J., Tysnes, Ole-Bjørn, Evans, Jonathan R., Breen, David P., Estrada, Karol, Wegel, Claire E., Danjou, Fabrice, Simon, David K., Ravina, Bernard, Toft, Mathias, Heutink, Peter, Bloem, Bastiaan R., Weintraub, Daniel, Barker, Roger A., Williams-Gray, Caroline H., van de Warrenburg, Bart P., Van Hilten, Jacobus J., Scherzer, Clemens R., Singleton, Andrew B., Nalls, Mike A.

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Genomewide Association Study of Parkinson’s Disease Clinical Biomarkers in 12 Longitudinal Patients’ Cohorts Autor Iwaki, Hirotaka, Blauwendraat, Cornelis, Leonard, Hampton L., Kim, Jonggeol J., Liu, Ganqiang, Maple-Grødem, Jodi, Corvol, Jean-Christophe, Pihlstrøm, Lasse, van Nimwegen, Marlies, Hutten, Samantha J., Nguyen, Khanh-Dung H., Rick, Jacqueline, Eberly, Shirley, Faghri, Faraz, Auinger, Peggy, Scott, Kirsten M., Wijeyekoon, Ruwani, Van Deerlin, Vivianna M., Hernandez, Dena G., Gibbs, J. Raphael, Chitrala, Kumaraswamy Naidu, Day-Williams, Aaron G., Brice, Alexis, Alves, Guido, Noyce, Alastair J., Tysnes, Ole-Bjørn, Evans, Jonathan R., Breen, David P., Estrada, Karol, Wegel, Claire E., Danjou, Fabrice, Simon, David K., Andreassen, Ole, Ravina, Bernard, Toft, Mathias, Heutink, Peter, Bloem, Bastiaan R., Weintraub, Daniel, Barker, Roger A., Williams-Gray, Caroline H., van de Warrenburg, Bart P., Van Hilten, Jacobus J., Scherzer, Clemens R., Singleton, Andrew B., Nalls, Mike A.

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Differences in the Presentation and Progression of Parkinson’s Disease by Sex Autor Iwaki, Hirotaka, Blauwendraat, Cornelis, Leonard, Hampton L., Makarious, Mary B., Kim, Jonggeol J., Liu, Ganqiang, Maple-Grødem, Jodi, Corvol, Jean-Christophe, Pihlstrøm, Lasse, van Nimwegen, Marlies, Smolensky, Luba, Amondikar, Ninad, Hutten, Samantha J., Frasier, Mark, Nguyen, Khanh-Dung H., Rick, Jacqueline, Eberly, Shirley, Faghri, Faraz, Auinger, Peggy, Scott, Kirsten M., Wijeyekoon, Ruwani, Van Deerlin, Vivianna M., Hernandez, Dena G., Gibbs, Raphael J., Day-Williams, Aaron G., Brice, Alexis, Alves, Guido, Noyce, Alastair J., Tysnes, Ole-Bjørn, Evans, Jonathan R., Breen, David P., Estrada, Karol, Wegel, Claire E., Danjou, Fabrice, Simon, David K., Andreassen, Ole A., Ravina, Bernard, Toft, Mathias, Heutink, Peter, Bloem, Bastiaan R., Weintraub, Daniel, Barker, Roger A., Williams-Gray, Caroline H., van de Warrenburg, Bart P., Van Hilten, Jacobus J., Scherzer, Clemens R., Singleton, Andrew B., Nalls, Mike A.

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