Candidate gene association study in type 2 diabetes indicates a role for genes involved in beta-cell function as well as insulin action by Barroso, Inês, Luan, Jian'an, Middelberg, Rita P S, Harding, Anne-Helen, Franks, Paul W, Jakes, Rupert W, Clayton, D, Schafer, Alan J, O'Rahilly, Stephen, Wareham, Nicholas J

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DNA variation and the future of human genetics by Schafer, Alan J, Hawkins, J. Ross

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A Family with Severe Insulin Resistance and Diabetes Due to a Mutation in AKT2 by George, Stella, Rochford, Justin J., Wolfrum, Christian, Gray, Sarah L., Schinner, Sven, Wilson, Jenny C., Soos, Maria A., Murgatroyd, Peter R., Williams, Rachel M., Acerini, Carlo L., Dunger, David B., Barford, David, Umpleby, A. Margot, Wareham, Nicholas J., Davies, Huw Alban, Schafer, Alan J., Stoffel, Markus, O'Rahilly, Stephen, Barroso, Inês

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Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY -related gene by Foster, Jamie W, Dominguez-Steglich, Marina A, Guioli, Silvana, Kwok, Cheni, Weller, Polly A, Stevanovi, Milena, Weissenbach, Jean, Mansour, Sahar, Young, Ian D, Goodfellow, Peter N, Brook, J. David, Schafer, Alan J

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Compound Effects of Point Mutations Causing Campomelic Dysplasia/Autosomal Sex Reversal upon SOX9 Structure, Nuclear Transport, DNA Binding, and Transcriptional Activation by Preiss, S, Argentaro, A, Clayton, A, John, A, Jans, D A, Ogata, T, Nagai, T, Barroso, I, Schafer, A J, Harley, V R

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Association study of candidate genes for the prevalence and progression of knee osteoarthritis by Valdes, Ana M., Hart, Deborah J., Jones, Karen A., Surdulescu, Gabriela, Swarbrick, Peter, Doyle, David V., Schafer, Alan J., Spector, Tim D.

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Differentiating campomelic dysplasia from Cumming syndrome by Watiker, Valerie, Lachman, Ralph S., Wilcox, William R., Barroso, Inês, Schafer, Alan J., Scherer, Gerd

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In PLoS Biology, volume 1, issue 1: Candidate Gene Association Study in Type 2 Diabetes Indicates a Role for Genes Involved in β-Cell Function as Well as Insulin Action by Barroso, Inês, Luan, Jian'an, Middelberg, Rita P. S, Harding, Anne-Helen, Franks, Paul W, Jakes, Rupert W, Clayton, David, Schafer, Alan J, O'Rahilly, Stephen, Wareham, Nicholas J

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Campomelic Dysplasia with XY Sex Reversal: Diverse Phenotypes Resulting from Mutations in a Single Gene by Schafer, Alan J., Foster, Jamie W., Kwok, Cheni, Weller, Polly A., Guioli, Silvana, Goodfellow, Peter N.

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The Role of SOX9 in Autosomal Sex Reversal and Campomelic Dysplasia [and Discussion] by Schafer, Alan J., Dominguez-Steglich, Marina A., Guioli, Silvana, Kwok, Cheni, Weller, Polly A., Stevanovic, Milena, Weissenbach, Jean, Mansour, Sahar, Young, Ian D., Goodfellow, Peter N., Brook, J. David, Foster, Jamie W., Burgoyne, P., Graves, J. A. M.

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Mutations in SOX9, the gene responsible for campomelic dysplasia and autosomal sex reversal by CHENI KWOK, WELLER, P. A, GOODFELLOW, P. N, SCHAFER, A. J, GUIOLI, S, FOSTER, J. W, SAHAR MANSOUR, ZUFFARDI, O, PUNNETT, H. H, DOMINGUEZ-STEGLICH, M. A, BROOK, J. D, YOUNG, I. D

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International network of cancer genome projects by Hudson, Thomas J., Anderson, Warwick, Artez, Axel, Barker, Anna D., Bell, Cindy, Bernabé, Rosa R., Bhan, M. K., Calvo, Fabien, Eerola, Iiro, Gerhard, Daniela S., Guttmacher, Alan, Guyer, Mark, Hemsley, Fiona M., Jennings, Jennifer L., Kerr, David, Klatt, Peter, Kolar, Patrik, Kusuda, Jun, Lane, David P., Laplace, Frank, Lu, Youyong, Nettekoven, Gerd, Ozenberger, Brad, Peterson, Jane, Rao, T.S., Remacle, Jacques, Schafer, Alan J., Shibata, Tatsuhiro, Stratton, Michael R., Vockley, Joseph G, Watanabe, Koichi, Yang, Huanming, Yuen, Matthew M. F., Knoppers, Bartha Maria Bm, Bobrow, Martin, Cambon-Thomsen, Anne, Dressler, Lynn G, Dyke, Stephanie O. M., Joly, Yann, Kato, Kazuto, Kennedy, Karen L., Nicolás, Pilar, Parker, Michael J., Rial-Sebbag, Emmanuelle, Romeo-Casabona, Carlos M, Shaw, Kenna M., Wallace, Susan, Wiesner, Georgia L, Zeps, Nikolajs, Lichter, Peter, Biankin, Andrew V, Chabannon, Christian, Chin, Lynda, Clément, Bruno, de Alava, Enrique, Degos, Françoise, Ferguson, Martin L., Geary, Peter, Hayes, D. Neil, Johns, Amber L., Kasprzyk, Arek, Nakagawa, Hidewaki, Penny, Robert, Piris, Miguel A., Sarin, Rajiv, Scarpa, Aldo, van de Vijver, Marc, Aburatani, Hiroyuki, Bayés, Mónica, Bowtell, David D L, Campbell, Peter J., Estivill, Xavier, Futreal, P Andrew, Gerhard, Daniela S, Grimmond, Sean M, Gut, Ivo G, Hirst, Martin, López-Otín, Carlos, Majumder, Partha, Marra, Marco, Mcpherson, John D, Ning, Zemin, Puente, Xose S, Ruan, Yijun, Stunnenberg, Hendrik G, Swerdlow, Harold, Velculescu, Victor E, Wilson, Richard K., Xue, Hong H., Yang, Liu, Spellman, Paul T, Bader, Gary D., Boutros, Paul C, Flicek, Paul, Getz, Gad, Guigo, Roderic, Guo, Guangwu, Haussler, David, Heath, Simon, Hubbard, Tim J.

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Correction: Candidate Gene Association Study in Type 2 Diabetes Indicates a Role for Genes Involved in [beta]-Cell Function as Well as Insulin Action: e92 by Barroso, Inês, Luan, an, Middelberg, Rita PS, Harding, Anne-Helen, Jakes, Rupert W, Clayton, David, Schafer, Alan J, Wareham, Nicholas J

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Candidate Gene Association Study in Type 2 Diabetes Indicates a Role for Genes Involved in [beta]-Cell Function as Well as Insulin Action: e20 by Barroso, Inês, Luan, an, Middelberg, Rita PS, Harding, Anne-Helen, Franks, Paul W, Jakes, Rupert W, Clayton, David, Schafer, Alan J, Wareham, Nicholas J

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Correction: Candidate Gene Association Study in Type 2 Diabetes Indicates a Role for Genes Involved in β-Cell Function as Well as Insulin Action by Barroso, Inês, Luan, Jian'an, Middelberg, Rita P. S, Harding, Anne-Helen, Jakes, Rupert W, Clayton, David, Schafer, Alan J, O'Rahilly, Stephen, Wareham, Nicholas J

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PGC-1alpha genotype modifies the association of volitional energy expenditure with [OV0312]O2max by Franks, Paul W, Barroso, Inês, Luan, Jian'an, Ekelund, Ulf, Crowley, Vivion E F, Brage, Søren, Sandhu, Manjinder S, Jakes, Rupert W, Middelberg, Rita P S, Harding, Anne-Helen, Schafer, Alan J, O'Rahilly, Stephen, Wareham, Nicholas J

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A Family with Severe Insulin Resistance and Diabetes Mellitus due to a Missense Mutation in AKT2 by George, Stella, Rochford, Justin J., Wolfrum, Christian, Gray, Sarah L., Schinner, Sven, Wilson, Jenny C., Soos, Maria A., Murgatroyd, Peter R., Williams, Rachel M., Acerini, Carlo L., Dunger, David B., Barford, David, Umpleby, A. Margot, Wareham, Nicholas J., Davies, Huw Alban, Schafer, Alan J., Stoffel, Markus, O’Rahilly, Stephen, Barroso, Ines

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PGC-1α genotype modifies the association of volitional energy expenditure with VO2max by FRANKS, Paul W, BARROSO, Inês, SCHAFER, Alan J, O'RAHILLY, Stephen, WAREHAM, Nicholas J, LUAN, Jian'An, EKELUND, U. L. F, CROWLEY, Vivion E. F, BRAGE, Siren, SANDHU, Manjinder S, JAKES, Rupert W, MIDDELBERG, Rita P. S, HARDING, Anne-Helen

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PGC-1?? Genotype Modifies the Association of Volitional Energy Expenditure with O2max by FRANKS, PAUL W., BARROSO, IN??S, LUAN, JIAN???AN, EKELUND, ULF, CROWLEY, VIVION E. F., BRAGE, S??REN, SANDHU, MANJINDER S., JAKES, RUPERT W., S. MIDDELBERG, RITA P., HARDING, ANNE-HELEN, SCHAFER, ALAN J., O???RAHILLY, STEPHEN, WAREHAM, NICHOLAS J.

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Detection of polymorphism in the RING3 gene by high-throughput fluorescent SSCP analysis by Thorpe, K L, Schafer, A J, Génin, E, Trowsdale, J, Beck, S

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