Suchergebnisse - Day-Williams, Aaron G

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

Volltext Volltext Volltext

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

Volltext Volltext Volltext

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

Volltext Volltext Volltext

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

Volltext Volltext Volltext

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

Volltext Volltext Volltext

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

Volltext Volltext Volltext

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

Volltext Volltext Volltext

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

Volltext Volltext Volltext

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

Volltext Volltext Volltext

Genetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson’s disease von 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

Volltext Volltext Volltext

Large-scale association analysis of TNF/LTA gene region polymorphisms in type 2 diabetes von 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

Volltext Volltext Volltext

Radiographic endophenotyping in hip osteoarthritis improves the precision of genetic association analysis von 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

Volltext Volltext Volltext

A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica von 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.

Volltext Volltext Volltext

Investigation of Association Between Hip Osteoarthritis Susceptibility Loci and Radiographic Proximal Femur Shape von 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

Volltext Volltext Volltext

Phenome-wide association studies across large population cohorts support drug target validation von 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

Volltext Volltext Volltext

Diagnosis of Parkinson’s disease on the basis of clinical–genetic classification: a population-based modelling study von 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.

Volltext Volltext Volltext

A Variant in MCF2L Is Associated with Osteoarthritis von 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

Volltext Volltext Volltext

Genetic risk of Parkinson disease and progression:: An analysis of 13 longitudinal cohorts von 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.

Volltext Volltext Volltext

Genomewide Association Study of Parkinson’s Disease Clinical Biomarkers in 12 Longitudinal Patients’ Cohorts von 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.

Volltext Volltext Volltext

Differences in the Presentation and Progression of Parkinson’s Disease by Sex von 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.

Volltext Volltext Volltext