Genome-Wide Association Study Reveals Multiple Loci Associated with Primary Tooth Development during Infancy: e1000856 by Pillas, Demetris, Hoggart, Clive J, Evans, David M, Sipilä, Kirsi, Lähdesmäki, Raija, Millwood, Iona Y, Kaakinen, Marika, Netuveli, Gopalakrishnan, Blane, David, Charoen, Pimphen, Sovio, Ulla, Pouta, Anneli, Freimer, Nelson, Hartikainen, Anna-Liisa, Laitinen, Jaana, Vaara, Sarianna, Glaser, Beate, Crawford, Peter, Timpson, Nicholas J, Ring, Susan M, Deng, Guohong, Zhang, Weihua, McCarthy, Mark I, Deloukas, Panos, Peltonen, Leena, Elliott, Paul, Coin, Lachlan JM, Smith, George Davey, Jarvelin, Marjo-Riitta

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Correction: Identification of PLCL1 Gene for Hip Bone Size Variation in Females in a Genome-Wide Association Study by Liu, Yao-Zhong, Wilson, Scott G., Wang, Liang, Liu, Xiao-Gang, Guo, Yan-Fang, Li, Jian, Yan, Han, Deloukas, Panos, Soranzo, Nicole, Chinappen-Horsley, Usha, Cervino, Alessandra, Williams, Frances M., Xiong, Dong-Hai, Zhang, Yin-Ping, Jin, Tian-Bo, Levy, Shawn, Papasian, Christopher J., Drees, Betty M., Hamilton, James J., Recker, Robert R., Spector, Tim D., Deng, Hong-Wen

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A Common Single Nucleotide Polymorphism in the Chromosome 7q22.3 Region, Which Is Frequently Deleted in Myeloid Malignancies, Is Associated with Mean Platelet Volume and Platelet F... by Soranzo, Nicole, Tijssen, Marloes R., Rendon, Augusto, Meisinger, Christine, Jones, Chris I., Gieger, Christian, Watkins, Nicholas A., Menzel, Stephan, Prokisch, Holger, Stephens, Jonathan, Doering, Angela, Erber, Wendy N., Potter, Simon C., Burns, Philippa, Jolley, Jennifer, Falchi, Mario, Garner, Stephen F., Rankin, Angela, Thein, Swee Lay, Wichmann, H-Erich, Goodall, Alison H., Illig, Thomas, Spector, Tim D., Deloukas, Panos, Ouwehand, Willem H.

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Thyroid function, pernicious anemia and erythropoiesis: a two-sample Mendelian randomization study by Kjaergaard, Alisa D, Teumer, Alexander, Marouli, Eirini, Deloukas, Panos, Kuś, Aleksander, Sterenborg, Rosalie, Åsvold, Bjørn Olav, Medici, Marco, Ellervik, Christina

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A Genome-Wide Association Study Reveals Variants in ARL15 that Influence Adiponectin Levels: e1000768 by Richards, J Brent, Waterworth, Dawn, Hivert, Marie-France, Loos, Ruth JF, Perry, John RB, Tanaka, Toshiko, Timpson, Nicholas John, Semple, Robert K, Soranzo, Nicole, Song, Kijoung, Rocha, Nuno, Grundberg, Elin, Dupuis, Josée, Florez, Jose C, Langenberg, Claudia, Prokopenko, Inga, Saxena, Richa, Sladek, Robert, Aulchenko, Yurii, Evans, David, Waeber, Gerard, Erdmann, Jeanette, Burnett, Mary-Susan, Sattar, Naveed, Devaney, Joseph, Willenborg, Christina, Hingorani, Aroon, Witteman, Jaquelin CM, Vollenweider, Peter, Glaser, Beate, Hengstenberg, Christian, Ferrucci, Luigi, Melzer, David, Stark, Klaus, Deanfield, John, Winogradow, Janina, Grassl, Martina, Hall, Alistair S, Egan, Josephine M, Thompson, John R, Ricketts, Sally L, König, Inke R, Reinhard, Wibke, Grundy, Scott, Wichmann, H-Erich, Barter, Phil, Mahley, Robert, Kesaniemi, Y Antero, Rader, Daniel J, Reilly, Muredach P, Epstein, Stephen E, Stewart, Alexandre FR, Duijn, Cornelia MVan, Schunkert, Heribert, Burling, Keith, Deloukas, Panos, Pastinen, Tomi, Samani, Nilesh J, McPherson, Ruth, Smith, George Davey, Frayling, Timothy M, Wareham, Nicholas J, Meigs, James B, Mooser, Vincent, Spector, Tim D, Consortium, GIANT

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Meta-Analysis of Genome-Wide Scans for Human Adult Stature Identifies Novel Loci and Associations with Measures of Skeletal Frame Size: e1000445 by Soranzo, Nicole, Rivadeneira, Fernando, Chinappen-Horsley, Usha, Malkina, Ida, Richards, J Brent, Hammond, Naomi, Stolk, Lisette, Nica, Alexandra, Inouye, Michael, Hofman, Albert, Stephens, Jonathan, Wheeler, Eleanor, Arp, Pascal, Gwilliam, Rhian, Jhamai, P Mila, Potter, Simon, Chaney, Amy, Ghori, Mohammed JR, Ravindrarajah, Radhi, Ermakov, Sergey, Estrada, Karol, Pols, Huibert AP, Williams, Frances M, McArdle, Wendy L, Meurs, Joyce Bvan, Loos, Ruth JF, Dermitzakis, Emmanouil T, Ahmadi, Kourosh R, Hart, Deborah J, Ouwehand, Willem H, Wareham, Nicholas J, Barroso, Inês, Sandhu, Manjinder S, Strachan, David P, Livshits, Gregory, Spector, Timothy D, Uitterlinden, André G, Deloukas, Panos

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Novel mutations in theZEB1 gene identified in Czech and British patients with posterior polymorphous corneal dystrophy by Liskova, Petra, Tuft, Stephen J., Gwilliam, Rhian, Ebenezer, Neil D., Jirsova, Katerina, Prescott, Quincy, Martincova, Radka, Pretorius, Marike, Sinclair, Neil, Boase, David L., Jeffrey, Margaret J., Deloukas, Panos, Hardcastle, Alison J., Filipec, Martin, Bhattacharya, Shomi S.

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The dopamine [beta]-hydroxylase -1021C/T polymorphism is associated with the risk of Alzheimer's disease in the Epistasis Project by Combarros, Onofre, Warden, Donald R, Hammond, Naomi, Cortina-Borja, Mario, Belbin, Olivia, Lehmann, Michael G, Wilcock, Gordon K, Brown, Kristelle, Kehoe, Patrick G, Barber, Rachel, Coto, Eliecer, Alvarez, Victoria, Deloukas, Panos, Gwilliam, Rhian, Heun, Reinhard, Kolsch, Heike, Mateo, Ignacio, Oulhaj, Abderrahim, Arias-Vasquez, Alejandro, Schuur, Maaike, Aulchenko, Yurii S, Ikram, M. Arfan, Breteler, Monique M, van Duijn, Cornelia M, Morgan, Kevin, Smith, A. David, Lehmann, Donald J

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Correction: Comprehensive Exploration of the Effects of miRNA SNPs on Monocyte Gene Expression by Nicolas Greliche, Tanja Zeller, Philipp S. Wild, Maxime Rotival, Arne Schillert, Andreas Ziegler, Panos Deloukas, Jeanette Erdmann, Christian Hengstenberg, Willem H. Ouwehand, Nilesh J. Samani, Heribert Schunkert, Thomas Munzel, Karl J. Lackner, François Cambien, Alison H. Goodall, Laurence Tiret, Stefan Blankenberg, David-Alexandre Trégouët

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An integrated cytogenetic, radiation-hybrid, and comparative map of dog chromosome 5 by Thomas, R, Breen, M, Deloukas, P, Holmes, N G, Binns, M M

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Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants by Aragam, Krishna G, Jiang, Tao, Goel, Anuj, Kanoni, Stavroula, Wolford, Brooke N, Atri, Deepak S, Weeks, Elle M, Wang, Minxian, Hindy, George, Zhou, Wei, Grace, Christopher, Roselli, Carolina, Marston, Nicholas A, Kamanu, Frederick K, Surakka, Ida, Venegas, Loreto Muñoz, Sherliker, Paul, Koyama, Satoshi, Ishigaki, Kazuyoshi, Åsvold, Bjørn Olav, Brown, Michael R, Brumpton, Ben Michael, de Vries, Paul S, Giannakopoulou, Olga, Giardoglou, Panagiota, Gudbjartsson, Daniel F, Güldener, Ulrich, Haider, Syed M. Ijlal, Helgadottir, Anna, Ibrahim, Maysson, Kastrati, Adnan, Kessler, Thorsten, Kyriakou, Theodosios, Konopka, Tomasz, Li, Ling, Ma, Lijiang, Meitinger, Thomas, Mucha, Sören, Munz, Matthias, Murgia, Federico, Nielsen, Jonas Bille, Nöthen, Markus M, Pang, Shichao, Reinberger, Tobias, Schnitzler, Gavin, Smedley, Damian, Thorleifsson, Gudmar, von Scheidt, Moritz, Ulirsch, Jacob C, Danesh, John, Arnar, David O, Burtt, Noël P, Costanzo, Maria C, Flannick, Jason, Ito, Kaoru, Jang, Dong-Keun, Kamatani, Yoichiro, Khera, Amit V, Komuro, Issei, Kullo, Iftikhar J, Lotta, Luca A, Nelson, Christopher P, Roberts, Robert, Thorgeirsson, Gudmundur, Thorsteinsdottir, Unnur, Webb, Thomas R, Baras, Aris, Björkegren, Johan L. M, Boerwinkle, Eric, Dedoussis, George, Holm, Hilma, Hveem, Kristian, Melander, Olle, Morrison, Alanna C, Orho-Melander, Marju, Rallidis, Loukianos S, Ruusalepp, Arno, Sabatine, Marc S, Stefansson, Kari, Zalloua, Pierre, Ellinor, Patrick T, Farrall, Martin, Ruff, Christian T, Finucane, Hilary K, Hopewell, Jemma C, Clarke, Robert, Gupta, Rajat M, Erdmann, Jeanette, Samani, Nilesh J, Schunkert, Heribert, Watkins, Hugh, Willer, Cristen J, Deloukas, Panos, Kathiresan, Sekar, Butterworth, Adam S

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A Detailed Physical and Transcriptional Map of the Region of Chromosome 20 That Is Deleted in Myeloproliferative Disorders and Refinement of the Common Deleted Region by Bench, Anthony J., Aldred, Micheala A., Humphray, Sean J., Champion, Kim M., Gilbert, James G.R., Asimakopoulos, Fotios A., Deloukas, Panos, Gwilliam, Rhian, Bentley, David R., Green, Anthony R.

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Correction: Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease by Lesley Jones, Peter A. Holmans, Marian L. Hamshere, Denise Harold, Valentina Moskvina, Dobril Ivanov, Andrew Pocklington, Richard Abraham, Paul Hollingworth, Rebecca Sims, Amy Gerrish, Jaspreet Singh Pahwa, Nicola Jones, Alexandra Stretton, Angharad R. Morgan, Simon Lovestone, John Powell, Petroula Proitsi, Michelle K. Lupton, Carol Brayne, David C. Rubinsztein, Michael Gill, Brian Lawlor, Aoibhinn Lynch, Kevin Morgan, Kristelle S. Brown, Peter A. Passmore, David Craig, Bernadette McGuinness, Stephen Todd, Clive Holmes, David Mann, A. David Smith, Seth Love, Patrick G. Kehoe, Simon Mead, Nick Fox, Martin Rossor, John Collinge, Wolfgang Maier, Frank Jessen, Britta Schürmann, Hendrik van den Bussche, Isabella Heuser, Oliver Peters, Johannes Kornhuber, Jens Wiltfang, Martin Dichgans, Lutz Frölich, Harald Hampel, Michael Hüll, Dan Rujescu, Alison M. Goate, John S. K. Kauwe, Carlos Cruchaga, Petra Nowotny, John C. Morris, Kevin Mayo, Gill Livingston, Nicholas J. Bass, Hugh Gurling, Andrew McQuillin, Rhian Gwilliam, Panos Deloukas, Ammar Al-Chalabi, Christopher E. Shaw, Andrew B. Singleton, Rita Guerreiro, Thomas W. Mühleisen, Markus M. Nöthen, Susanne Moebus, Karl-Heinz Jöckel, Norman Klopp, H.-Erich Wichmann, Eckhard Rüther, Minerva M. Carrasquillo, V. Shane Pankratz, Steven G. Younkin, John Hardy, Michael C. O'Donovan, Michael J. Owen, Julie Williams

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Comparison of human genetic and sequence-based physical maps : The human genome by ADONG YU, CHENGFENG ZHAO, WEBER, James L, YING FAN, WONHEE JANG, MUNGALL, Andrew J, DELOUKAS, Panos, OLSEN, Anne, DOGGETT, Norman A, GHEBRANIOUS, Nader, BROMAN, Karl W

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Correction: Identification of Gene for Hip Bone Size Variation in Females in a Genome-Wide Association Study by Yao-Zhong Liu, Scott G. Wilson, Liang Wang, Xiao-Gang Liu, Yan-Fang Guo, Jian Li, Han Yan, Panos Deloukas, Nicole Soranzo, Usha Chinappen-Horsley, Alessandra Cervino, Frances M. Williams, Dong-Hai Xiong, Yin-Ping Zhang, Tian-Bo Jin, Shawn Levy, Christopher J. Papasian, Betty M. Drees, James J. Hamilton, Robert R. Recker, Tim D. Spector, Hong-Wen Deng

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Localization of HuC (ELAVL3) to chromosome 19p13.2 by fluorescence in situ hybridization utilizing a novel tyramide labeling technique by VAN TINE, B. A, KNOPS, J. F, BUTLER, A, DELOUKAS, P, SHAW, G. M, KING, P. H

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Localization ofHuC(ELAVL3) to Chromosome 19p13.2 by Fluorescencein SituHybridization Utilizing a Novel Tyramide Labeling Technique by Van Tine, Brian A., Knops, Judith F., Butler, Adam, Deloukas, Panos, Shaw, George M., King, Peter H.

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Predicting genome-wide DNA methylation using methylation marks, genomic position, and DNA regulatory elements by Zhang, Weiwei, Spector, Tim D, Deloukas, Panos, Bell, Jordana T, Engelhardt, Barbara E

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Interaction of insulin and PPAR-[alpha] genes in Alzheimer's disease: the Epistasis Project by Kölsch, Heike, Lehmann, Donald J, Ibrahim-verbaas, Carla A, Combarros, Onofre, van Duijn, Cornelia M, Hammond, Naomi, Belbin, Olivia, Cortina-borja, Mario, Lehmann, Michael G, Aulchenko, Yurii S, Schuur, Maaike, Breteler, Monique, Wilcock, Gordon K, Brown, Kristelle, Kehoe, Patrick G, Barber, Rachel, Coto, Eliecer, Alvarez, Victoria, Deloukas, Panos, Mateo, Ignacio, Maier, Wolfgang, Morgan, Kevin, Warden, Donald R, Smith, A David, Heun, Reinhard

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Does a short breastfeeding period protect from FTO-induced adiposity in children? by Dedoussis, George V. Z., Yannakoulia, Mary, Timpson, Nicholas J., Manios, Yannis, Kanoni, Stavroula, Scott, Robert A., Papoutsakis, Constantina, Deloukas, Panos, Pitsiladis, Yannis P., Davey-Smith, George, Hirschhorn, Joel N., Lyon, Helen N.

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