Activity of the leukotriene pathway in Barrett’s metaplasia and oesophageal adenocarcinoma von Shutt, James David, Boger, Philip, Neale, James Richard, Patel, Praful, Sampson, Anthony Peter

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Experimental and numerical investigation of noise generation from the expansion of high velocity HVAC flows on board ocean going fast ferries von Neale, James Richard

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Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis von Loh, Po-Ru, Bhatia, Gaurav, Gusev, Alexander, Finucane, Hilary K, Bulik-Sullivan, Brendan K, Pollack, Samuela J, de Candia, Teresa R, Lee, Sang Hong, Wray, Naomi R, Kendler, Kenneth S, O'Donovan, Michael C, Neale, Benjamin M, Patterson, Nick, Price, Alkes L

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LD Score regression distinguishes confounding from polygenicity in genome-wide association studies von Bulik-Sullivan, Brendan K, Loh, Po-Ru, Finucane, Hilary K, Ripke, Stephan, Yang, Jian, Patterson, Nick, Daly, Mark J, Price, Alkes L, Neale, Benjamin M

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A framework for the interpretation of de novo mutation in human disease von Samocha, Kaitlin E, Robinson, Elise B, Sanders, Stephan J, Stevens, Christine, Sabo, Aniko, McGrath, Lauren M, Kosmicki, Jack A, Rehnström, Karola, Mallick, Swapan, Kirby, Andrew, Wall, Dennis P, MacArthur, Daniel G, Gabriel, Stacey B, DePristo, Mark, Purcell, Shaun M, Palotie, Aarno, Boerwinkle, Eric, Buxbaum, Joseph D, Cook, Edwin H, Gibbs, Richard A, Schellenberg, Gerard D, Sutcliffe, James S, Devlin, Bernie, Roeder, Kathryn, Neale, Benjamin M, Daly, Mark J

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Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder von Demontis, Ditte, Walters, Raymond K., Martin, Joanna, Mattheisen, Manuel, Als, Thomas D., Agerbo, Esben, Baldursson, Gísli, Belliveau, Rich, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Dumont, Ashley, Eriksson, Nicholas, Gandal, Michael, Goldstein, Jacqueline I., Grasby, Katrina L., Grove, Jakob, Gudmundsson, Olafur O., Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Howrigan, Daniel P., Huang, Hailiang, Maller, Julian B., Martin, Alicia R., Martin, Nicholas G., Moran, Jennifer, Pallesen, Jonatan, Palmer, Duncan S., Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, Poterba, Timothy, Poulsen, Jesper Buchhave, Ripke, Stephan, Robinson, Elise B., Satterstrom, F. Kyle, Stefansson, Hreinn, Stevens, Christine, Turley, Patrick, Walters, G. Bragi, Won, Hyejung, Wright, Margaret J., Andreassen, Ole A., Asherson, Philip, Burton, Christie L., Boomsma, Dorret I., Cormand, Bru, Dalsgaard, Søren, Franke, Barbara, Gelernter, Joel, Geschwind, Daniel, Hakonarson, Hakon, Haavik, Jan, Kranzler, Henry R., Kuntsi, Jonna, Langley, Kate, Lesch, Klaus-Peter, Middeldorp, Christel, Reif, Andreas, Rohde, Luis Augusto, Roussos, Panos, Schachar, Russell, Sklar, Pamela, Sonuga-Barke, Edmund J. S., Sullivan, Patrick F., Thapar, Anita, Tung, Joyce Y., Waldman, Irwin D., Medland, Sarah E., Stefansson, Kari, Nordentoft, Merete, Hougaard, David M., Werge, Thomas, Mors, Ole, Mortensen, Preben Bo, Daly, Mark J., Faraone, Stephen V., Børglum, Anders D., Neale, Benjamin M.

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Schizophrenia risk from complex variation of complement component 4 von Sekar, Aswin, Bialas, Allison R., de Rivera, Heather, Davis, Avery, Hammond, Timothy R., Kamitaki, Nolan, Tooley, Katherine, Presumey, Jessy, Baum, Matthew, Van Doren, Vanessa, Genovese, Giulio, Rose, Samuel A., Handsaker, Robert E., Daly, Mark J., Carroll, Michael C., Stevens, Beth, McCarroll, Steven A.

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Family-Based Genome-Wide Association Scan of Attention-Deficit/Hyperactivity Disorder von Mick, Eric, Sc.D, Todorov, Alexandre, Ph.D, Smalley, Susan, Ph.D, Hu, Xiaolan, Ph.D, Loo, Sandra, Ph.D, Todd, Richard D., M.D, Biederman, Joseph, M.D, Byrne, Deirdre, B.S, Dechairo, Bryan, Ph.D, Guiney, Allan, B.A, McCracken, James, M.D, McGough, James, M.D, Nelson, Stanley F., M.D, Reiersen, Angela M., M.D, Wilens, Timothy E., M.D, Wozniak, Janet, M.D, Neale, Benjamin M., Ph.D, Faraone, Stephen V., Ph.D

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The DOE E3SM Coupled Model Version 1: Overview and Evaluation at Standard Resolution von Golaz, Jean‐Christophe, Caldwell, Peter M., Van Roekel, Luke P., Petersen, Mark R., Tang, Qi, Wolfe, Jonathan D., Abeshu, Guta, Anantharaj, Valentine, Asay‐Davis, Xylar S., Bader, David C., Baldwin, Sterling A., Bisht, Gautam, Bogenschutz, Peter A., Branstetter, Marcia, Brunke, Michael A., Brus, Steven R., Burrows, Susannah M., Cameron‐Smith, Philip J., Donahue, Aaron S., Deakin, Michael, Easter, Richard C., Evans, Katherine J., Feng, Yan, Flanner, Mark, Foucar, James G., Fyke, Jeremy G., Griffin, Brian M., Hannay, Cécile, Harrop, Bryce E., Hoffman, Mattthew J., Hunke, Elizabeth C., Jacob, Robert L., Jacobsen, Douglas W., Jeffery, Nicole, Jones, Philip W., Keen, Noel D., Klein, Stephen A., Larson, Vincent E., Leung, L. Ruby, Li, Hong‐Yi, Lin, Wuyin, Lipscomb, William H., Ma, Po‐Lun, Mahajan, Salil, Maltrud, Mathew E., Mametjanov, Azamat, McClean, Julie L., McCoy, Renata B., Neale, Richard B., Price, Stephen F., Qian, Yun, Rasch, Philip J., Reeves Eyre, J. E. Jack, Riley, William J., Ringler, Todd D., Roberts, Andrew F., Roesler, Erika L., Salinger, Andrew G., Shaheen, Zeshawn, Shi, Xiaoying, Singh, Balwinder, Tang, Jinyun, Taylor, Mark A., Thornton, Peter E., Turner, Adrian K., Veneziani, Milena, Wan, Hui, Wang, Hailong, Wang, Shanlin, Williams, Dean N., Wolfram, Phillip J., Worley, Patrick H., Xie, Shaocheng, Yang, Yang, Yoon, Jin‐Ho, Zelinka, Mark D., Zender, Charles S., Zeng, Xubin, Zhang, Chengzhu, Zhang, Kai, Zhang, Yuying, Zheng, Xue, Zhou, Tian, Zhu, Qing

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Biological insights from 108 schizophrenia-associated genetic loci von Neale, Benjamin M, Pers, Tune H, Agartz, Ingrid, Agerbo, Esben, Amin, Farooq, Bergen, Sarah E, Bigdeli, Tim B, Buckner, Randy L, Cai, Guiqing, Catts, Stanley V, Chan, Raymond C. K, Chen, Eric Y. H, Cheng, Wei, Cheung, Eric F. C, Ann Chong, Siow, Robert Cloninger, C, Cohen, Nadine, Crowley, James J, Davidson, Michael, Davis, Kenneth L, Del Favero, Jurgen, Demontis, Ditte, Dinan, Timothy, Djurovic, Srdjan, Drapeau, Elodie, Eriksson, Johan, Escott-Price, Valentina, Friedl, Marion, Fromer, Menachem, Genovese, Giulio, Georgieva, Lyudmila, Giusti-Rodriguez, Paola, Gopal, Srihari, Gratten, Jacob, Hammer, Christian, Hofman, Andrea, Hougaard, David M, Julia, Antonio, Klovins, Janis, Ausrele Kucinskiene, Zita, Hong Lee, S, Lerer, Bernard, Limborska, Svetlana, Lubinski, Jan, Macek Jr, Milan, Magnusson, Patrik K. E, Mattheisen, Manuel, McDonald, Colm, Michie, Patricia T, Milanova, Vihra, Mokrab, Younes, Muller-Myhsok, Bertram, Nenadic, Igor, Nordin, Annelie, Van Os, Jim, Endophenotypes International Consortium, Psychosis, Parkhomenko, Elena, Pejovic-Milovancevic, Milica, Pimm, Jonathan, Price, Alkes, Purcell, Shaun M, Quested, Digby, Rasmussen, Henrik B, Roffman, Joshua L, Schubert, Christian R, Schwab, Sibylle G, Scott, Rodney J, Seidman, Larry J, Silverman, Jeremy M, Smoller, Jordan W, Steinberg, Stacy, Strengman, Eric, Strohmaier, Jana, Svrakic, Dragan M, Soderman, Erik, Thirumalai, Srinivas, Toncheva, Draga, Tosato, Sarah, Veijola, Juha, Walsh, Dermot, Weiser, Mark, Wolen, Aaron R, Zheng, Xuebin, Wray, Naomi R, Visscher, Peter M, Trust Case-Control Consortium, Wellcome, Andreassen, Ole A, Blackwood, Douglas H. R, Esko, Tonu, Gill, Michael, Jablensky, Assen V, McCarroll, Steven A, Mowry, Bryan J, Owen, Michael J, Pato, Carlos N, Posthuma, Danielle, Rujescu, Dan, Sham, Pak C, Sklar, Pamela, St Clair, David

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Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores von Gusev, Alexander, Ripke, Stephan, Walters, James T.R., Agartz, Ingrid, Albus, Margot, Bene, Judit, Bevilacqua, Elizabeth, Bigdeli, Tim B., Bruggeman, Richard, Buckner, Randy L., Carr, Vaughan J., Catts, Stanley V., Chan, Raymond C.K., Cheng, Wei, Cohen, Nadine, Curtis, David, Dikeos, Dimitris, Dinan, Timothy, Eriksson, Johan, Escott-Price, Valentina, Franke, Lude, Godard, Stephanie, Goldstein, Jacqueline I., de Haan, Lieuwe, Hartmann, Annette M., Hoffmann, Per, Hofman, Andrea, Hollegaard, Mads V., Hougaard, David M., Ikeda, Masashi, Kim, Yunjung, Kucinskas, Vaidutis, Laurent, Claudine, Limborska, Svetlana, Loughland, Carmel M., Macek, Milan, Marsal, Sara, Mattheisen, Manuel, Milanova, Vihra, Mors, Ole, Mortensen, Preben B., Olsen, Line, Parkhomenko, Elena, Paunio, Tiina, Pimm, Jonathan, Purcell, Shaun M., Reichenberg, Abraham, Reimers, Mark A., Richards, Alexander L., Roussos, Panos, Ruderfer, Douglas M., Sigurdsson, Engilbert, Silverman, Jeremy M., So, Hon-Cheong, Spencer, Chris C.A., Stefansson, Hreinn, Straub, Richard E., Strengman, Eric, Strohmaier, Jana, Svrakic, Dragan M., Tosato, Sarah, Veijola, Juha, Walsh, Dermot, Wang, Dai, Weiser, Mark, Wolen, Aaron R., Wong, Emily H.M., Stefansson, Kari, Andreassen, Ole A., Ehrenreich, Hannelore, Gill, Michael, Hultman, Christina M., Jablensky, Assen V., McQuillin, Andrew, Pato, Carlos N., Rietschel, Marcella, Sham, Pak C., Sklar, Pamela, Weinberger, Daniel R., Daly, Mark J., Crisponi, Laura, Figueroa, Jonine, Gaudet, Mia M., Hall, Per, Hein, Rebecca, Irwanto, Astrid, Johansson, Mattias, Lund, Eiliv, Peto, Julian, Rahman, Nazneen, Southey, Melissa C., Travis, Ruth, Waisfisz, Quinten, Pato, Carlos, Stahl, Eli, Belbin, Gillian, Kenny, Eimear E., Purcell, Shaun, Chasman, Daniel, Neale, Benjamin

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Rare Complete Knockouts in Humans: Population Distribution and Significant Role in Autism Spectrum Disorders von Lim, Elaine T., Raychaudhuri, Soumya, Sanders, Stephan J., Stevens, Christine, Sabo, Aniko, MacArthur, Daniel G., Neale, Benjamin M., Kirby, Andrew, Ruderfer, Douglas M., Fromer, Menachem, Lek, Monkol, Liu, Li, Flannick, Jason, Ripke, Stephan, Nagaswamy, Uma, Muzny, Donna, Reid, Jeffrey G., Hawes, Alicia, Newsham, Irene, Wu, Yuanqing, Lewis, Lora, Dinh, Huyen, Gross, Shannon, Wang, Li-San, Lin, Chiao-Feng, Valladares, Otto, Gabriel, Stacey B., dePristo, Mark, Altshuler, David M., Purcell, Shaun M., State, Matthew W., Boerwinkle, Eric, Buxbaum, Joseph D., Cook, Edwin H., Gibbs, Richard A., Schellenberg, Gerard D., Sutcliffe, James S., Devlin, Bernie, Roeder, Kathryn, Daly, Mark J.

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Complement genes contribute sex-biased vulnerability in diverse disorders von Kamitaki, Nolan, Sekar, Aswin, Handsaker, Robert E., de Rivera, Heather, Tooley, Katherine, Morris, David L., Taylor, Kimberly E., Whelan, Christopher W., Tombleson, Philip, Loohuis, Loes M. Olde, Boehnke, Michael, Kimberly, Robert P., Kaufman, Kenneth M., Harley, John B., Langefeld, Carl D., Seidman, Christine E., Pato, Michele T., Pato, Carlos N., Ophoff, Roel A., Graham, Robert R., Criswell, Lindsey A., Vyse, Timothy J., McCarroll, Steven A.

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Exome resequencing and GWAS for growth, ecophysiology, and chemical and metabolomic composition of wood of Populus trichocarpa von Guerra, Fernando P, Suren, Haktan, Holliday, Jason, Richards, James H, Fiehn, Oliver, Famula, Randi, Stanton, Brian J, Shuren, Richard, Sykes, Robert, Davis, Mark F, Neale, David B

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A novel retinoblastoma therapy from genomic and epigenetic analyses von Zhang, Jinghui, Benavente, Claudia A., McEvoy, Justina, Flores-Otero, Jacqueline, Ding, Li, Chen, Xiang, Ulyanov, Anatoly, Wu, Gang, Wilson, Matthew, Wang, Jianmin, Brennan, Rachel, Rusch, Michael, Manning, Amity L., Ma, Jing, Easton, John, Shurtleff, Sheila, Mullighan, Charles, Pounds, Stanley, Mukatira, Suraj, Gupta, Pankaj, Neale, Geoff, Zhao, David, Lu, Charles, Fulton, Robert S., Fulton, Lucinda L., Hong, Xin, Dooling, David J., Ochoa, Kerri, Naeve, Clayton, Dyson, Nicholas J., Mardis, Elaine R., Bahrami, Armita, Ellison, David, Wilson, Richard K., Downing, James R., Dyer, Michael A.

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Medulloblastoma: clinicopathological correlates of SHH, WNT, and non-SHH/WNT molecular subgroups von Ellison, David W., Dalton, James, Kocak, Mehmet, Nicholson, Sarah Leigh, Fraga, Charles, Neale, Geoff, Kenney, Anna M., Brat, Dan J., Perry, Arie, Yong, William H., Taylor, Roger E., Bailey, Simon, Clifford, Steven C., Gilbertson, Richard J.

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A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts von Ni, Guiyan, Wang, Ying, Ge, Tian, Smoller, Jordan W., Ripke, Stephan, Farh, Kai-How, Holmans, Peter A., Agartz, Ingrid, Belliveau, Richard A., Bigdeli, Tim B., Black, Donald W., Buckner, Randy L., Cheng, Wei, Degenhardt, Franziska, Dudbridge, Frank, Eichhammer, Peter, Farrell, Martilias S., Frank, Josef, Freedman, Robert, Friedl, Marion, Giegling, Ina, Giusti-Rodríguez, Paola, Gratten, Jacob, Hartmann, Annette M., Hollegaard, Mads V., Kahn, René S., Karachanak-Yankova, Sena, Kavanagh, David, Keller, Matthew C., Kennedy, James L., Knowles, James A., Kucinskiene, Zita Ausrele, Li, Tao, Loughland, Carmel M., Lubinski, Jan, Maier, Wolfgang, Mallet, Jacques, Michie, Patricia T., Myin-Germeys, Inez, Nertney, Deborah A., Nicodemus, Kristin K., Nikitina-Zake, Liene, O’Callaghan, Eadbhard, O’Dushlaine, Colm, Pejovic-Milovancevic, Milica, Pocklington, Andrew J., Powell, John, Pulver, Ann E., Ruderfer, Douglas M., Salomaa, Veikko, Shi, Jianxin, Sim, Kang, Slominsky, Petr, Spencer, Chris C.A., Stahl, Eli A., Steinberg, Stacy, Stogmann, Elisabeth, Suvisaari, Jaana, Williams, Nigel M., Witt, Stephanie H., Wormley, Brandon K., Blackwood, Douglas H.R., Bramon, Elvira, Buxbaum, Joseph D., Esko, Tõnu, Gurling, Hugh, Moran, Jennifer L., Mowry, Bryan J., Owen, Michael J., Petryshen, Tracey L., Weinberger, Daniel R., Byrne, Enda M., Abdellaoui, Abdel, Andlauer, Till F.M., Castelao, Enrique, Derks, Eske M., Foo, Jerome C., Forstner, Andreas J., Hall, Lynsey S., Homuth, Georg, Jansen, Rick, Jones, Ian, Jones, Lisa A., Kretzschmar, Warren W., McGuffin, Peter, Mihailov, Evelin, Mostafavi, Sara, Nivard, Michel G., O’Reilly, Paul F., Quiroz, Jorge A., Smith, Daniel J., Thompson, Wesley, Treutlein, Jens, Umbricht, Daniel, Wu, Yang, Zhang, Futao, Grabe, Hans J., Hayward, Caroline, Lewis, Glyn, Wray, Naomi R.

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Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles von Goldstein, Jacqueline I., Fredrik Jarskog, L., Hilliard, Chris, Alfirevic, Ana, Duncan, Laramie, Fourches, Denis, Huang, Hailiang, Lek, Monkol, Neale, Benjamin M., Ripke, Stephan, Shianna, Kevin, Szatkiewicz, Jin P., Tropsha, Alexander, van den Oord, Edwin JCG, Cascorbi, Ingolf, Dettling, Michael, Gazit, Ephraim, Goff, Donald C., Holden, Arthur L., Kelly, Deanna L., Malhotra, Anil K., Nielsen, Jimmi, Pirmohamed, Munir, Rujescu, Dan, Werge, Thomas, Levy, Deborah L., Josiassen, Richard C., Kennedy, James L., Lieberman, Jeffrey A., Daly, Mark J., Sullivan, Patrick F.

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Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls von Liu, Li, Sabo, Aniko, Neale, Benjamin M, Nagaswamy, Uma, Stevens, Christine, Lim, Elaine, Bodea, Corneliu A, Muzny, Donna, Reid, Jeffrey G, Banks, Eric, Coon, Hillary, Depristo, Mark, Dinh, Huyen, Fennel, Tim, Flannick, Jason, Gabriel, Stacey, Garimella, Kiran, Gross, Shannon, Hawes, Alicia, Lewis, Lora, Makarov, Vladimir, Maguire, Jared, Newsham, Irene, Poplin, Ryan, Ripke, Stephan, Shakir, Khalid, Samocha, Kaitlin E, Wu, Yuanqing, Boerwinkle, Eric, Buxbaum, Joseph D, Cook, Jr, Edwin H, Devlin, Bernie, Schellenberg, Gerard D, Sutcliffe, James S, Daly, Mark J, Gibbs, Richard A, Roeder, Kathryn

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Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases von Trynka, Gosia, Stahl, Eli, Neale, Benjamin M., Farh, Kai-How, Pers, Tune H., Albus, Margot, Cahn, Wiepke, Cai, Guiqing, Carr, Vaughan J., Carrera, Noa, Cheng, Wei, Cheung, Eric F.C., Cohen, David, Cormican, Paul, Craddock, Nick, Demontis, Ditte, Djurovic, Srdjan, Donohoe, Gary, Dudbridge, Frank, Durmishi, Naser, Eriksson, Johan, Farrell, Martilias S., Freimer, Nelson B., Fromer, Menachem, Godard, Stephanie, Goldstein, Jacqueline I., Grove, Jakob, Hartmann, Annette M., Henskens, Frans A., Herms, Stefan, Hirschhorn, Joel N., Hoffmann, Per, Hougaard, David M., Ikeda, Masashi, Julià, Antonio, Kelly, Brian J., Kennedy, James L., Kucinskas, Vaidutis, Kuzelova-Ptackova, Hana, Laurent, Claudine, Lee, S. Hong, Li, Tao, Lieberman, Jeffrey, Limborska, Svetlana, Loughland, Carmel M., Lnnqvist, Jouko, Marsal, Sara, McCarley, Robert W., Meijer, Carin J., Melegh, Bela, Melle, Ingrid, Milani, Lili, Mors, Ole, Myin-Germeys, Inez, Nikitina-Zake, Liene, O’Callaghan, Eadbhard, O’Dushlaine, Colm, O’Neill, F. Anthony, Oh, Sang-Yun, Pantelis, Christos, Parkhomenko, Elena, Perkins, Diana O., Powell, John, Quested, Digby, Salomaa, Veikko, Schubert, Christian R., Shi, Jianxin, Sigurdsson, Engilbert, Sim, Kang, Stogmann, Elisabeth, Strengman, Eric, Suvisaari, Jaana, Thirumalai, Srinivas, Veijola, Juha, Walsh, Dermot, Weiser, Mark, Witt, Stephanie H., Wong, Emily H.M., Wu, Jing Qin, Stefansson, Kari, Blackwood, Douglas H.R., Ehrenreich, Hannelore, Gurling, Hugh, Hultman, Christina M., Kirov, George, Malhotra, Anil K., McCarroll, Steven A., McQuillin, Andrew, Palotie, Aarno, Rietschel, Marcella, Sham, Pak C., O’Donovan, Michael C., Bergen, Sarah, Magnusson, Patrik K.E., Scolnick, Edward, Purcell, Shaun M., Pasaniuc, Bogdan, Sullivan, Patrick F., Raychaudhuri, Soumya, Price, Alkes L.

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