Thimet oligopeptidase: site-directed mutagenesis disproves previous assumptions about the nature of the catalytic site von Chen, Jinq-May, Stevens, Richard A.E., Wray, Paul W., Rawlings, Neil D., Barrett, Alan J.

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Erratum: The DNA sequence and biological annotation of human chromosome 1 von Kaul, R., Dunham, A., Woodfine, K., Jones, M. C., McDonald, L., Evans, R., Phillips, K., Atkinson, A., Cooper, R., Hall, R. E., Andrews, T. D., Lloyd, C., Ambrose, K. D., Anderson, F., Andrew, R. W., Ashwell, R. I. S., Aubin, K., Babbage, A. K., Bagguley, C. L., Bailey, J., Banerjee, R., Beasley, H., Bird, C. P., Bray-Allen, S., Brown, J. Y., Brown, A. J., Bryant, S. P., Buckley, D., Burton, J., Chapman, J. C., Clarke, G., Clee, C., Clegg, S. M., Cobley, V., Collier, R. E., Corby, N., Deadman, R., Dhami, P., Dunn, M., Ellington, A. G., Errington, H., Faulkner, L. M., Frankish, A., French, L., Garner, P., Garnett, J., Ghori, M. R. J., Gibson, R., Gillett, W., Grafham, D. V., Griffiths, C., Grocock, R., Harrison, E. S. I., Heath, P. D., Holmes, S., Hunt, S. E., Hunter, G., Isherwood, J., James, R., Johnson, C., Johnson, D., Joy, A., Kimberley, A. M., King, A., Langford, C. F., Lawlor, S., Leongamornlert, D. A., Lloyd, D. M., Loveland, J., Lovell, J., Lush, M. J., Lyne, R., Martin, S., Matthews, N. S. W., McLaren, S., oore, M. J. F. M., O'Dell, C. N., Patel, D., Peck, A. I., Pelan, S., Phillimore, B. J., Plumb, R., Raymond, C., Saenphimmachak, C., Shownkeen, R., Sims, S., Skuce, C. D., Smith, M., White, S., Williams, H., Wilming, L., Wray, P. W., Wu, Z., Vaudin, M., Durbin, R., Hubbard, T., Carter, N. P., McVean, G., Beck, S., Bentley, D. R.

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A direct test of the diathesis–stress model for depression von Colodro-Conde, L, Couvy-Duchesne, B, Zhu, G, Coventry, W L, Byrne, E M, Gordon, S, Wright, M J, Montgomery, G W, Madden, P A F, Ripke, S, Eaves, L J, Heath, A C, Wray, N R, Medland, S E, Martin, N G

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The evolution of transcriptional regulation in eukaryotes von Wray, Gregory A., Hahn, Matthew W., Abouheif, Ehab, Balhoff, James P., Pizer, Margaret, Rockman, Matthew V., Romano, Laura A.

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Dynamics and universal scaling law in geometrically-controlled sessile drop evaporation von Sáenz, P. J., Wray, A. W., Che, Z., Matar, O. K., Valluri, P., Kim, J., Sefiane, K.

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GWAS on family history of Alzheimer’s disease von Marioni, Riccardo E., Harris, Sarah E., Zhang, Qian, McRae, Allan F., Hagenaars, Saskia P., Hill, W. David, Davies, Gail, Ritchie, Craig W., Gale, Catharine R., Starr, John M., Goate, Alison M., Porteous, David J., Yang, Jian, Evans, Kathryn L., Deary, Ian J., Wray, Naomi R., Visscher, Peter M.

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Estimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip data von Chen, Guo-Bo, Lee, Sang Hong, Brion, Marie-Jo A, Montgomery, Grant W, Wray, Naomi R, Radford-Smith, Graham L, Visscher, Peter M

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Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned von Wray, N R, Pergadia, M L, Blackwood, D H R, Penninx, B W J H, Gordon, S D, Nyholt, D R, Ripke, S, MacIntyre, D J, McGhee, K A, Maclean, A W, Smit, J H, Hottenga, J J, Willemsen, G, Middeldorp, C M, de Geus, E J C, Lewis, C M, McGuffin, P, Hickie, I B, van den Oord, E J C G, Liu, J Z, Macgregor, S, McEvoy, B P, Byrne, E M, Medland, S E, Statham, D J, Henders, A K, Heath, A C, Montgomery, G W, Martin, N G, Boomsma, D I, Madden, P A F, Sullivan, P F

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Evaluation of chromatin accessibility in prefrontal cortex of individuals with schizophrenia von Bryois, Julien, Garrett, Melanie E., Song, Lingyun, Safi, Alexias, Giusti-Rodriguez, Paola, Johnson, Graham D., Shieh, Annie W., Buil, Alfonso, Fullard, John F., Roussos, Panos, Sklar, Pamela, Akbarian, Schahram, Haroutunian, Vahram, Stockmeier, Craig A., Wray, Gregory A., White, Kevin P., Liu, Chunyu, Reddy, Timothy E., Ashley-Koch, Allison, Sullivan, Patrick F., Crawford, Gregory E.

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Genetic predisposition to schizophrenia associated with increased use of cannabis von Power, R A, Verweij, K J H, Zuhair, M, Montgomery, G W, Henders, A K, Heath, A C, Madden, P A F, Medland, S E, Wray, N R, Martin, N G

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Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis von Lee, S Hong, Harold, Denise, Nyholt, Dale R, Goddard, Michael E, Zondervan, Krina T, Williams, Julie, Montgomery, Grant W, Wray, Naomi R, Visscher, Peter M

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DNA methylation age of blood predicts all-cause mortality in later life von Marioni, Riccardo E, Shah, Sonia, McRae, Allan F, Chen, Brian H, Colicino, Elena, Harris, Sarah E, Gibson, Jude, Henders, Anjali K, Redmond, Paul, Cox, Simon R, Pattie, Alison, Corley, Janie, Murphy, Lee, Martin, Nicholas G, Montgomery, Grant W, Feinberg, Andrew P, Fallin, M Daniele, Multhaup, Michael L, Jaffe, Andrew E, Joehanes, Roby, Schwartz, Joel, Just, Allan C, Lunetta, Kathryn L, Murabito, Joanne M, Starr, John M, Horvath, Steve, Baccarelli, Andrea A, Levy, Daniel, Visscher, Peter M, Wray, Naomi R, Deary, Ian J

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Remote system administration using command line environment von WRAY DARYL W.,SNOVER JEFFREY P.,CHANDRASCHEKARAN RAJESH,SHASTRY M. C. SHANKARA

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Genetic risk profiles for depression and anxiety in adult and elderly cohorts von Demirkan, A, Penninx, B W J H, Hek, K, Wray, N R, Amin, N, Aulchenko, Y S, van Dyck, R, de Geus, E J C, Hofman, A, Uitterlinden, A G, Hottenga, J-J, Nolen, W A, Oostra, B A, Sullivan, P F, Willemsen, G, Zitman, F G, Tiemeier, H, Janssens, A C J W, Boomsma, D I, van Duijn, C M, Middeldorp, C M

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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder von Purcell, Shaun M, Wray, Naomi R, Stone, Jennifer L, Visscher, Peter M, O'Donovan, Michael C, Sullivan, Patrick F, Sklar, Pamela

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Lithium carbonate in amyotrophic lateral sclerosis patients homozygous for the C-allele at SNP rs12608932 in UNC13A: protocol for a confirmatory, randomized, group-sequential, even... von Willemse, Sean W, Roes, Kit C B, Van Damme, Philip, Hardiman, Orla, Ingre, Caroline, Povedano, Monica, Wray, Naomi R, Gijzen, Marleen, de Pagter, Mirjam S, Demaegd, Koen C, Janse, Annemarie F C, Vink, Roel G, Sleutjes, Boudewijn T H M, Chiò, Adriano, Corcia, Philippe, Reviers, Evy, Al-Chalabi, Ammar, Kiernan, Matthew C, van den Berg, Leonard H, van Es, Michael A, van Eijk, Ruben P A

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Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis von Dekker, Annelot M., Diekstra, Frank P., van der Spek, Rick A. A., Võsa, Urmo, Yang, Jian, Vajda, Alice, Lin, Kuang, Vrabec, Katarina, Koritnik, Blaž, Zidar, Janez, de Visser, Marianne, Leonardis, Lea, Millecamps, Stéphanie, Meininger, Vincent, Mora, Jesus S., Colville, Shuna, Morrison, Karen E., Shaw, Pamela J., Hardy, John, Pittman, Alan, Sidle, Katie, Malaspina, Andrea, Petri, Susanne, Drepper, Carsten, Meyer, Thomas, Ophoff, Roel A., Staats, Kim A., Van Deerlin, Vivianna M., Trojanowski, John Q., Elman, Lauren, McCluskey, Leo, Basak, A Nazli, Hamzeiy, Hamid, Parman, Yesim, Meitinger, Thomas, Smith, Bradley N., Lichtner, Peter, Radivojkov-Blagojevic, Milena, Andres, Christian R., Maurel, Cindy, Landwehrmeyer, Bernhard, Brice, Alexis, Payan, Christine A. M., Saker-Delye, Safaa, Tittmann, Lukas, Rietschel, Marcella, Cichon, Sven, Nöthen, Markus M., Tzourio, Christophe, Dartigues, Jean-François, Cereda, Cristina, Uitterlinden, Andre G., Estrada, Karol, Hofman, Albert, Curtis, Charles, Comi, Giacomo P., D'Alfonso, Sandra, Fogh, Isabella, Bertolin, Cinzia, Sorarù, Gianni, Tiloca, Cinzia, Ratti, Antonia, Calvo, Andrea, Brunetti, Maura, van Doormaal, Perry T. C., Arcuti, Simona, Capozzo, Rosa, Lunetta, Christian, Riva, Nilo, Filosto, Massimiliano, Muller, Bernard, Tazelaar, Gijs H. P., Zhang, Katharine, McCann, Emily P., Rowe, Dominic B., Grosskreutz, Julian, Ringer, Thomas, Prell, Tino, Stubendorff, Beatrice, Beghi, Ettore, Pupillo, Elisabetta, Blokhuis, Anna M., Tortelli, Rosanna, Powell, John, Ludolph, Albert C., Van Damme, Philip, Franke, Lude, Brown, Robert H., Sproviero, William, Andersen, Peter M., Silani, Vincenzo, Jones, Ashley R., Pasterkamp, R Jeroen, Breen, Gerome, Al-Chalabi, Ammar, Veldink, Jan H., Kenna, Kevin P., Harschnitz, Oliver, Schellevis, Raymond D., Brands, William J.

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Identification of common genetic risk variants for autism spectrum disorder von Grove, Jakob, Ripke, Stephan, Als, Thomas D., Mattheisen, Manuel, Walters, Raymond K., Won, Hyejung, Pallesen, Jonatan, Agerbo, Esben, Andreassen, Ole A., Anney, Richard, Awashti, Swapnil, Belliveau, Rich, Bettella, Francesco, Buxbaum, Joseph D., Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Christensen, Jane H., Churchhouse, Claire, Dellenvall, Karin, Demontis, Ditte, De Rubeis, Silvia, Devlin, Bernie, Djurovic, Srdjan, Dumont, Ashley L., Goldstein, Jacqueline I., Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Hope, Sigrun, Howrigan, Daniel P., Huang, Hailiang, Hultman, Christina M., Klei, Lambertus, Maller, Julian, Martin, Joanna, Martin, Alicia R., Moran, Jennifer L., Nyegaard, Mette, Nærland, Terje, Palmer, Duncan S., Palotie, Aarno, Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, dPoterba, Timothy, Poulsen, Jesper Buchhave, Pourcain, Beate St, Qvist, Per, Rehnström, Karola, Reichenberg, Abraham, Reichert, Jennifer, Robinson, Elise B., Roeder, Kathryn, Roussos, Panos, Saemundsen, Evald, Sandin, Sven, Satterstrom, F. Kyle, Davey Smith, George, Stefansson, Hreinn, Steinberg, Stacy, Stevens, Christine R., Sullivan, Patrick F., Turley, Patrick, Walters, G. Bragi, Xu, Xinyi, Stefansson, Kari, Geschwind, Daniel H., Nordentoft, Merete, Hougaard, David M., Werge, Thomas, Mors, Ole, Mortensen, Preben Bo, Neale, Benjamin M., Daly, Mark J., Børglum, Anders D.

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Autism-related dietary preferences mediate autism-gut microbiome associations von Yap, Chloe X., Henders, Anjali K., Alvares, Gail A., Wood, David L.A., Krause, Lutz, Tyson, Gene W., Restuadi, Restuadi, Wallace, Leanne, McLaren, Tiana, Hansell, Narelle K., Cleary, Dominique, Grove, Rachel, Hafekost, Claire, Harun, Alexis, Holdsworth, Helen, Jellett, Rachel, Khan, Feroza, Lawson, Lauren P., Leslie, Jodie, Frenk, Mira Levis, Masi, Anne, Mathew, Nisha E., Muniandy, Melanie, Nothard, Michaela, Miller, Jessica L., Nunn, Lorelle, Holtmann, Gerald, Strike, Lachlan T., de Zubicaray, Greig I., Thompson, Paul M., McMahon, Katie L., Wright, Margaret J., Visscher, Peter M., Dawson, Paul A., Dissanayake, Cheryl, Eapen, Valsamma, Heussler, Helen S., McRae, Allan F., Whitehouse, Andrew J.O., Wray, Naomi R., Gratten, Jacob

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Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression von Ripke, Stephan, Trzaskowski, Maciej, Byrne, Enda M., Adams, Mark J., Andlauer, Till M. F., Bacanu, Silviu-Alin, Beekman, Aartjan F. T., Bigdeli, Tim B., Binder, Elisabeth B., Blackwood, Douglas R. H., Bybjerg-Grauholm, Jonas, Castelao, Enrique, Couvy-Duchesne, Baptiste, Craddock, Nick, Deary, Ian J., Finucane, Hilary K., Forstner, Andreas J., Frank, Josef, Gill, Michael, Goes, Fernando S., Grove, Jakob, Hall, Lynsey S., Hannon, Eilis, Hansen, Thomas F., Hickie, Ian B., Hoffmann, Per, Horn, Carsten, Hougaard, David M., Hyde, Craig L., Jorgenson, Eric, Knowles, James A., Kraft, Julia, Krogh, Jesper, Kutalik, Zoltán, Lane, Jacqueline M., Li, Yihan, Li, Yun, Liu, Xiaoxiao, Lu, Leina, MacIntyre, Donald J., MacKinnon, Dean F., Maier, Robert M., Marchini, Jonathan, Mbarek, Hamdi, McGrath, Patrick, Mehta, Divya, Montgomery, Grant W., Nauck, Matthias, Nivard, Michel G., Pedersen, Carsten Bøcker, Posthuma, Danielle, Purcell, Shaun M., Quiroz, Jorge A., Saeed Mirza, Saira, Schoevers, Robert, Schulte, Eva C., Shi, Jianxin, Shyn, Stanley I., Smit, Johannes H., Smith, Daniel J., Stockmeier, Craig A., Teumer, Alexander, Thompson, Wesley, Thomson, Pippa A., Thorgeirsson, Thorgeir E., Tian, Chao, Treutlein, Jens, van Hemert, Albert M., Viktorin, Alexander, Visscher, Peter M., Wang, Yunpeng, Weinsheimer, Shantel Marie, Wellmann, Jürgen, Witt, Stephanie H., Wu, Yang, Xi, Hualin S., Yang, Jian, Zhang, Futao, Baune, Bernhard T., Berger, Klaus, de Geus, E. C. J., Domschke, Katharina, Esko, Tõnu, Hinds, David A., Li, Qingqin S., McIntosh, Andrew M., Metspalu, Andres, Mors, Ole, Müller-Myhsok, Bertram, O’Donovan, Michael C., Paciga, Sara A., Pedersen, Nancy L., Perlis, Roy H., Potash, James B., Schaefer, Catherine, Schulze, Thomas G., Uher, Rudolf, Völzke, Henry, Winslow, Ashley R., Børglum, Anders D.

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