Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis by Sawcer, Stephen, Hellenthal, Garrett, Pirinen, Matti, Spencer, Chris C A, Patsopoulos, Nikolaos A, Moutsianas, Loukas, Dilthey, Alexander, Su, Zhan, Freeman, Colin, Hunt, Sarah E, Edkins, Sarah, Gray, Emma, Booth, David R, Potter, Simon C, Goris, An, Band, Gavin, Oturai, Annette Bang, Strange, Amy, Saarela, Janna, Bellenguez, Céline, Fontaine, Bertrand, Gillman, Matthew, Hemmer, Bernhard, Gwilliam, Rhian, Zipp, Frauke, Jayakumar, Alagurevathi, Martin, Roland, Leslie, Stephen, Hawkins, Stanley, Giannoulatou, Eleni, D'alfonso, Sandra, Blackburn, Hannah, Martinelli Boneschi, Filippo, Liddle, Jennifer, Harbo, Hanne F, Perez, Marc L, Spurkland, Anne, Waller, Matthew J, Mycko, Marcin P, Ricketts, Michelle, Comabella, Manuel, Hammond, Naomi, Kockum, Ingrid, McCann, Owen T, Ban, Maria, Whittaker, Pamela, Kemppinen, Anu, Weston, Paul, Hawkins, Clive, Widaa, Sara, Zajicek, John, Dronov, Serge, Robertson, Neil, Bumpstead, Suzannah J, Barcellos, Lisa F, Ravindrarajah, Rathi, Abraham, Roby, Alfredsson, Lars, Ardlie, Kristin, Aubin, Cristin, Baker, Amie, Baker, Katharine, Baranzini, Sergio E, Bergamaschi, Laura, Bergamaschi, Roberto, Bernstein, Allan, Berthele, Achim, Boggild, Mike, Bradfield, Jonathan P, Brassat, David, Broadley, Simon A, Buck, Dorothea, Butzkueven, Helmut, Capra, Ruggero, Carroll, William M, Cavalla, Paola, Celius, Elisabeth G, Cepok, Sabine, Chiavacci, Rosetta, Clerget-Darpoux, Françoise, Clysters, Katleen, Comi, Giancarlo, Cossburn, Mark, Cournu-Rebeix, Isabelle, Cox, Mathew B, Cozen, Wendy, Cree, Bruce A C, Cross, Anne H, Cusi, Daniele, Daly, Mark J, Davis, Emma, de Bakker, Paul I W, Debouverie, Marc, D'hooghe, Marie Beatrice, Dixon, Katherine, Dobosi, Rita, Dubois, Bénédicte, Ellinghaus, David, Elovaara, Irina, Esposito, Federica

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Identification of 22 susceptibility loci associated with testicular germ cell tumors by Pluta, John, Pyle, Louise C., Nead, Kevin T., Wilf, Rona, Li, Mingyao, Mitra, Nandita, Weathers, Benita, D’Andrea, Kurt, Almstrup, Kristian, Anson-Cartwright, Lynn, Benitez, Javier, Brown, Christopher D., Chanock, Stephen, Chen, Chu, Cortessis, Victoria K., Ferlin, Alberto, Foresta, Carlo, Gamulin, Marija, Gietema, Jourik A., Grasso, Chiara, Greene, Mark H., Grotmol, Tom, Hamilton, Robert J., Haugen, Trine B., Hauser, Russ, Hildebrandt, Michelle A. T., Johnson, Matthew E., Karlsson, Robert, Kiemeney, Lambertus A., Lessel, Davor, Lothe, Ragnhild A., Loud, Jennifer T., Loveday, Chey, Martin-Gimeno, Paloma, Meijer, Coby, Nsengimana, Jérémie, Quinn, David I., Rafnar, Thorunn, Ramdas, Shweta, Richiardi, Lorenzo, Skotheim, Rolf I., Stefansson, Kari, Turnbull, Clare, Vaughn, David J., Wiklund, Fredrik, Wu, Xifeng, Yang, Daphne, Zheng, Tongzhang, Wells, Andrew D., Grant, Struan F. A., Rajpert-De Meyts, Ewa, Schwartz, Stephen M., Bishop, D. Timothy, McGlynn, Katherine A., Kanetsky, Peter A., Nathanson, Katherine L.

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Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index by Hinney, A, Kesselmeier, M, Jall, S, Volckmar, A-L, Föcker, M, Antel, J, Heid, I M, Winkler, T W, Guo, Y, Bergen, A W, Kaye, W, Berrettini, W, Hakonarson, H, Herpertz-Dahlmann, B, de Zwaan, M, Herzog, W, Ehrlich, S, Zipfel, S, Egberts, K M, Adan, R, Brandys, M, van Elburg, A, Boraska Perica, V, Franklin, C S, Tschöp, M H, Zeggini, E, Bulik, C M, Collier, D, Scherag, A, Müller, T D, Hebebrand, J

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Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci by Saxena, Richa, Guo, Yiran, Peter, Inga, Gaunt, Tom R., Mega, Jessica L., Li, Yun R., Johnson, Toby, Bruinenberg, Marcel, Gilbert-Diamond, Diane, Rajagopalan, Ramakrishnan, Voight, Benjamin F., Barnard, John, Bauer, Florianne, Bhangale, Tushar, Burton, Paul R., Clarke, Robert, Cooper-DeHoff, Rhonda M., Crook, Errol D., Davey-Smith, George, Day, Ian N., Drenos, Fotios, Furlong, Clement E., Gibson, Quince, Gieger, Christian, Goel, Anuj, Gong, Yan, Hastie, Claire, Humphries, Steve E., Kim, Cecilia E., Kleber, Marcus, Kumari, Meena, Langaee, Taimour Y., Lawlor, Debbie A., Li, Mingyao, Lobmeyer, Maximilian T., Maitland-van der Zee, Anke-Hilse, Meijs, Matthijs F.L., Molony, Cliona M., Musani, Solomon K., Nelson, Christopher P., Newhouse, Stephen J., O'Connell, Jeffery R., Palmen, Jutta, Patel, Sanjey R., Pepine, Carl J., Pettinger, Mary, Price, Thomas S., Rafelt, Suzanne, Ranchalis, Jane, Rasheed, Asif, Rosenthal, Elisabeth, Ruczinski, Ingo, Shen, Haiqing, Spijkerman, Annemieke W.M., Stanton, Alice, Steffes, Michael W., Thorand, Barbara, van der Harst, Pim, van Iperen, Erik P.A., van Vliet-Ostaptchouk, Jana V., Verweij, Niek, Wolffenbuttel, Bruce H.R., Young, Taylor, Zafarmand, M. Hadi, Zmuda, Joseph M., Altshuler, David, Kao, W.H. Linda, Poulter, Neil, Caulfield, Mark, Bhatt, Deepak L., Curtis, Sean P., Danesh, John, Onland-Moret, N. Charlotte, Doevendans, Pieter A., Dorn, Gerald W., Farrall, Martin, FitzGerald, Garret A., Hamsten, Anders, Hofker, Marten H., Jarvik, Gail P., Klungel, Olaf H., Knowler, William C., März, Winfried, Munroe, Patricia B., Bielinski, Susan J., Rader, Daniel J., Reilly, Muredach P., Rich, Stephen S., Rotter, Jerome I., Saleheen, Danish, Schadt, Eric E., Shuldiner, Alan R., Talmud, Philippa J., de Bakker, Paul I.W., McCaffery, Jeanne, Wijmenga, Cisca, Wilson, James G., Bowden, Donald W., Siscovick, David S., Keating, Brendan J.

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Dissecting heterogeneity in paediatric Type 1 diabetes: association of TCF7L2 rs7903146 TT and low‐risk human leukocyte antigen (HLA) genotypes by Redondo, M. J., Grant, S. F. A., Davis, A., Greenbaum, C.

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Erratum: Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index by Hinney, A, Kesselmeier, M, Jall, S, Volckmar, A-L, Föcker, M, Antel, J, Heid, I M, Winkler, T W, Guo, Y, Bergen, A W, Kaye, W, Berrettini, W, Hakonarson, H, Herpertz-Dahlmann, B, de Zwaan, M, Herzog, W, Ehrlich, S, Zipfel, S, Egberts, K M, Adan, R, Brandys, M, van Elburg, A, Boraska Perica, V, Franklin, C S, Tschöp, M H, Zeggini, E, Bulik, C M, Collier, D, Scherag, A, Müller, T D, Hebebrand, J

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A novel common variant in DCST2 is associated with length in early life and height in adulthood by van der Valk, Ralf J P, Kreiner-Møller, Eskil, Kooijman, Marjolein N, Guxens, Mònica, Stergiakouli, Evangelia, Sääf, Annika, Bradfield, Jonathan P, Geller, Frank, Hayes, M Geoffrey, Cousminer, Diana L, Körner, Antje, Thiering, Elisabeth, Curtin, John A, Myhre, Ronny, Huikari, Ville, Joro, Raimo, Kerkhof, Marjan, Warrington, Nicole M, Pitkänen, Niina, Ntalla, Ioanna, Horikoshi, Momoko, Veijola, Riitta, Freathy, Rachel M, Teo, Yik-Ying, Barton, Sheila J, Evans, David M, Kemp, John P, St Pourcain, Beate, Ring, Susan M, Davey Smith, George, Bergström, Anna, Kull, Inger, Hakonarson, Hakon, Mentch, Frank D, Bisgaard, Hans, Chawes, Bo, Stokholm, Jakob, Waage, Johannes, Eriksen, Patrick, Sevelsted, Astrid, Melbye, Mads, van Duijn, Cornelia M, Medina-Gomez, Carolina, Hofman, Albert, de Jongste, Johan C, Taal, H Rob, Uitterlinden, André G, Armstrong, Loren L, Eriksson, Johan, Palotie, Aarno, Bustamante, Mariona, Estivill, Xavier, Gonzalez, Juan R, Llop, Sabrina, Kiess, Wieland, Mahajan, Anubha, Flexeder, Claudia, Tiesler, Carla M T, Murray, Clare S, Simpson, Angela, Magnus, Per, Sengpiel, Verena, Hartikainen, Anna-Liisa, Keinanen-Kiukaanniemi, Sirkka, Lewin, Alexandra, Da Silva Couto Alves, Alexessander, Blakemore, Alexandra I, Buxton, Jessica L, Kaakinen, Marika, Rodriguez, Alina, Sebert, Sylvain, Vaarasmaki, Marja, Lakka, Timo, Lindi, Virpi, Gehring, Ulrike, Postma, Dirkje S, Ang, Wei, Newnham, John P, Lyytikäinen, Leo-Pekka, Pahkala, Katja, Raitakari, Olli T, Panoutsopoulou, Kalliope, Zeggini, Eleftheria, Boomsma, Dorret I, Groen-Blokhuis, Maria, Ilonen, Jorma, Franke, Lude, Hirschhorn, Joel N, Pers, Tune H, Liang, Liming, Huang, Jinyan, Hocher, Berthold, Knip, Mikael, Saw, Seang-Mei, Holloway, John W, Melén, Erik, Grant, Struan F A, Feenstra, Bjarke, Lowe, William L, Widén, Elisabeth

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GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI by Couto Alves, Alexessander, De Silva, N Maneka G, Karhunen, Ville, Sovio, Ulla, Das, Shikta, Taal, H Rob, Warrington, Nicole M, Lewin, Alexandra M, Kaakinen, Marika, Cousminer, Diana L, Thiering, Elisabeth, Timpson, Nicholas J, Bond, Tom A, Lowry, Estelle, Brown, Christopher D, Estivill, Xavier, Lindi, Virpi, Bradfield, Jonathan P, Geller, Frank, Speed, Doug, Coin, Lachlan J M, Loh, Marie, Barton, Sheila J, Beilin, Lawrence J, Bisgaard, Hans, Bønnelykke, Klaus, Alili, Rohia, Hatoum, Ida J, Schramm, Katharina, Cartwright, Rufus, Charles, Marie-Aline, Salerno, Vincenzo, Clément, Karine, Claringbould, Annique A J, van Duijn, Cornelia M, Moltchanova, Elena, Eriksson, Johan G, Elks, Cathy, Feenstra, Bjarke, Flexeder, Claudia, Franks, Stephen, Frayling, Timothy M, Freathy, Rachel M, Elliott, Paul, Widén, Elisabeth, Hakonarson, Hakon, Hattersley, Andrew T, Rodriguez, Alina, Banterle, Marco, Heinrich, Joachim, Heude, Barbara, Holloway, John W, Hofman, Albert, Hyppönen, Elina, Inskip, Hazel, Kaplan, Lee M, Hedman, Asa K, Läärä, Esa, Prokisch, Holger, Grallert, Harald, Lakka, Timo A, Lawlor, Debbie A, Melbye, Mads, Ahluwalia, Tarunveer S, Marinelli, Marcella, Millwood, Iona Y, Palmer, Lyle J, Pennell, Craig E, Perry, John R, Ring, Susan M, Savolainen, Markku J, Rivadeneira, Fernando, Standl, Marie, Sunyer, Jordi, Tiesler, Carla M T, Uitterlinden, Andre G, Schierding, William, O'Sullivan, Justin M, Prokopenko, Inga, Herzig, Karl-Heinz, Smith, George Davey, O'Reilly, Paul, Felix, Janine F, Buxton, Jessica L, Blakemore, Alexandra I F, Ong, Ken K, Jaddoe, Vincent W V, Grant, Struan F A, Sebert, Sylvain, McCarthy, Mark I, Järvelin, Marjo-Riitta

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The Diabetes Syndrome - A Collection of Conditions with Common, Interrelated Pathophysiologic Mechanisms by Rachfal, Amy W, Grant, Struan F A, Schwartz, Stanley S

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Association between the Gene Encoding 5-Lipoxygenase–Activating Protein and Stroke Replicated in a Scottish Population by Helgadottir, A., Gretarsdottir, S., St. Clair, D., Manolescu, A., Cheung, J., Thorleifsson, G., Pasdar, A., Grant, S.F.A., Whalley, L.J., Hakonarson, H., Thorsteinsdottir, U., Kong, A., Gulcher, J., Stefansson, K., MacLeod, M.J.

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Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height by Lanktree, Matthew B., Guo, Yiran, Murtaza, Muhammed, Bailey, Swneke D., Ongen, Halit, Rajagopalan, Ramakrishnan, Shen, Haiqing, Padmanabhan, Sandosh, Pankratz, Nathan, Pankow, James S., Shah, Sonia, Barnard, John, M. Maloney, Cliona, Lobmeyer, Maximilian T., Stanton, Alice, Mehta, Amar, Smith, Erin N., Li, Yun R., Asselbergs, Folkert W., Bailey, Kristian M., Bauer, Florianne, Behr, Elijah R., Bhangale, Tushar, Boehm, Bernhard O., Bradfield, Jonathan P., Brown, Morris, Braund, Peter S., Chen, Wei, Connell, John, Dalgeorgou, Chrysoula, Drenos, Fotios, Fang, James C., Fox, Caroline S., Frackelton, Edward C., Fuchs, Barry, Furlong, Clement E., Gibson, Quince, Goel, Anuj, Grobbee, Diederik E., Huang, Guan-Hua, Kooperberg, Charles, Ky, Bonnie, LaCroix, Andrea, Li, Mingyao, Marshall, Vanessa, Melander, Olle, Murugesan, Gurunathan, Nondahl, Dave, Newhouse, Stephen J., Patel, Sanjey R., Sivapalaratnam, Suthesh, Srinivasan, Sathanur R., Swergold, Gary, Sweitzer, Nancy K., Thomas, Kelly A., Timpson, Nicholas J., Tischfield, Sam, Tobin, Martin, Verschuren, W.M. Monique, Wallace, Chris, Winkelmann, Bernhard, Zhang, Haitao, Zmuda, Joseph M., Clarke, Robert, Balmforth, Anthony J., Danesh, John, Day, Ian N., Hingorani, Aroon D., Lawlor, Debbie A., Kottke-Marchant, Kandice, Mega, Jessica L., Mitchell, Braxton D., Redline, Susan, Shields, Denis C., Smith, George Davey, Farrall, Martin, Christiani, David C., Hall, Alistair S., Doevendans, Pieter A., D. Christie, Jason, Berenson, Gerald S., Illig, Thomas, Dorn, Gerald W., Cappola, Thomas P., Sever, Peter, Caulfield, Mark, Curtis, Sean P., Sabatine, Marc S., Trip, Mieke, O'Connell, Jeffrey R., Maitland-van der Zee, Anke Hilse, Schadt, Eric E., Johnson, Julie A., Jarvik, Gail P., Munroe, Patricia B., Gaunt, Tom R., Anand, Sonia S., FitzGerald, Garret A., Hegele, Robert A., Keating, Brendan J.

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The Early Growth Genetics (EGG) and EArly Genetics and Lifecourse Epidemiology (EAGLE) consortia: design, results and future prospects by Middeldorp, Christel M., Felix, Janine F., Mahajan, Anubha, McCarthy, Mark I.

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Disease-associated loci are significantly over-represented among genes bound by transcription factor 7-like 2 (TCF7L2) in vivo by Zhao, J., Schug, J., Li, M., Kaestner, K. H., Grant, S. F. A.

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Linkage of osteoporosis to chromosome 20p12 and association to BMP2 by Styrkarsdottir, Unnur, Cazier, Jean-Baptiste, Kong, Augustine, Rolfsson, Ottar, Larsen, Helene, Bjarnadottir, Emma, Johannsdottir, Vala D, Sigurdardottir, Margret S, Bagger, Yu, Christiansen, Claus, Reynisdottir, Inga, Grant, Struan F A, Jonasson, Kristjan, Frigge, Michael L, Gulcher, Jeffrey R, Sigurdsson, Gunnar, Stefansson, Kari

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A COL1A1 Sp1 binding site polymorphism predisposes to osteoporotic fracture by affecting bone density and quality by Mann, V, Hobson, E E, Li, B, Stewart, T L, Grant, S F, Robins, S P, Aspden, R M, Ralston, S H

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Genetic Discrimination between LADA and Type 1 Diabetes within the MHC by Mishra, R, Bradfield, JP, Cousminer, DL, Chesi, A, Hodge, KM, Hakonarson, H, Mauricio, D, Schloot, NC, Yderstræde, KB, Voight, B, Schwartz, S, Boehm, BO, Leslie, RDG, Grant, SFA

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Localization of a Susceptibility Gene for Type 2 Diabetes to Chromosome 5q34–q35.2 by Reynisdottir, Inga, Thorleifsson, Gudmar, Benediktsson, Rafn, Sigurdsson, Gunnar, Emilsson, Valur, Einarsdottir, Anna Sigurlin, Hjorleifsdottir, Eyrun Edda, Orlygsdottir, Gudbjorg Th, Bjornsdottir, Gudrun Thora, Saemundsdottir, Jona, Halldorsson, Skarphedinn, Hrafnkelsdottir, Soffia, Sigurjonsdottir, Steinunn Bjorg, Steinsdottir, Svana, Martin, Mitchell, Kochan, Jarema P., Rhees, Brian K., Grant, Struan F.A., Frigge, Michael L., Kong, Augustine, Gudnason, Vilmundur, Stefansson, Kari, Gulcher, Jeffrey R.

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Transferability and fine-mapping of glucose and insulin quantitative trait loci across populations: CARe, the Candidate Gene Association Resource by Liu, C. -T., Ng, M. C. Y., Rybin, D., Adeyemo, A., Bielinski, S. J., Boerwinkle, E., Borecki, I., Cade, B., Chen, Y. D. I., Djousse, L., Fornage, M., Goodarzi, M. O., Grant, S. F. A., Guo, X., Harris, T., Kabagambe, E., Kizer, J. R., Liu, Y., Lunetta, K. L., Mukamal, K., Nettleton, J. A., Pankow, J. S., Patel, S. R., Ramos, E., Rasmussen-Torvik, L., Rich, S. S., Rotimi, C. N., Sarpong, D., Shriner, D., Sims, M., Zmuda, J. M., Redline, S., Kao, W. H., Siscovick, D., Florez, J. C., Rotter, J. I., Dupuis, J., Wilson, J. G., Bowden, D. W., Meigs, J. B.

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Lack of relationship between mitochondrial heteroplasmy or variation and childhood obesity by Grant, S F A, Glessner, J T, Bradfield, J P, Zhao, J, Tirone, J E, Berkowitz, R I, Hakonarson, H, Sondheimer, N

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Influence of SNPSNP interaction on BMI in European American adolescents: findings from the National Longitudinal Study of Adolescent Health by Young, K. L., Graff, M., North, K. E., Richardson, A. S., Bradfield, J. P., Grant, S. F. A., Lange, L. A., Lange, E. M., Harris, K. M., Gordon-Larsen, P.

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