Characterizing the relationships between soil organic matter components and microbial function and composition along a tillage disturbance gradient von Cookson, W. Richard, Murphy, Daniel V., Roper, Margaret M.

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Mitochondrial alterations in PINK1 deficient cells are influenced by calcineurin-dependent dephosphorylation of dynamin-related protein 1 von Sandebring, Anna, Thomas, Kelly Jean, Beilina, Alexandra, van der Brug, Marcel, Cleland, Megan M, Ahmad, Rili, Miller, David W, Zambrano, Ibardo, Cowburn, Richard F, Behbahani, Homira, Cedazo-Mínguez, Angel, Cookson, Mark R

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Airway mucins promote immunopathology in virus-exacerbated chronic obstructive pulmonary disease von Singanayagam, Aran, Footitt, Joseph, Marczynski, Matthias, Radicioni, Giorgia, Cross, Michael T, Finney, Lydia J, Trujillo-Torralbo, Maria-Belen, Calderazzo, Maria, Zhu, Jie, Aniscenko, Julia, Clarke, Thomas B, Molyneaux, Philip L, Bartlett, Nathan W, Moffatt, Miriam F, Cookson, William O, Wedzicha, Jadwiga, Evans, Christopher M, Boucher, Richard C, Kesimer, Mehmet, Lieleg, Oliver, Mallia, Patrick, Johnston, Sebastian L

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Genetic linkage of childhood atopic dermatitis to psoriasis susceptibility loci von Cookson, William O.C.M, Ubhi, Baljinder, Lawrence, Robert, Abecasis, Gonçalo R, Walley, Andrew J, Cox, Helen E, Coleman, Rosemary, Leaves, Nicholas I, Trembath, Richard C, Moffatt, Miriam F, Harper, John I

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Epichloë fungal endophyte interactions in perennial ryegrass (Lolium perenne L.) modified to accumulate foliar lipids for increased energy density von Richardson, Kim A, de Bonth, Anouck C M, Beechey-Gradwell, Zac, Kadam, Suhas, Cooney, Luke J, Nelson, Kelly A, Cookson, Ruth, Winichayakul, Somrutai, Reid, Michele, Anderson, Philip, Crowther, Tracey, Zou, Xiuying, Maher, Dorothy, Xue, Hong, Scott, Richard W, Allan, Anne, Johnson, Richard D, Card, Stuart D, Mace, Wade J, Roberts, Nicholas J, Bryan, Gregory

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Adult familial cryptogenic fibrosing alveolitis in the United Kingdom von Marshall, Richard P, Puddicombe, Anna, Cookson, William O C, Laurent, Geoffrey J

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Common genetic variants influence human subcortical brain structures von Hibar, Derrek P., Desrivières, Sylvane, Toro, Roberto, Wittfeld, Katharina, Abramovic, Lucija, Bernard, Manon, Chen, Qiang, Giddaluru, Sudheer, Janowitz, Deborah, Lee, Phil H., Ramasamy, Adaikalavan, Risacher, Shannon L., Rose, Emma J., Salami, Alireza, Schmaal, Lianne, Schork, Andrew J., Strike, Lachlan T., Walters, Raymond K., Winkler, Anderson M., Zwiers, Marcel P., Athanasiu, Lavinia, Hakobjan, Marina M. H., Hartberg, Cecilie B., Heister, Angelien J. G. A. M., Hoehn, David, Kasperaviciute, Dalia, Makkinje, Remco R. R., Reese McKay, D., Shen, Li, Walton, Esther, Ames, David, Corvin, Aiden, Curran, Joanne E., Dillman, Allissa, Erk, Susanne, Foroud, Tatiana M., Guelfi, Sebastian, Hegenscheid, Katrin, Hernandez, Dena G., Heslenfeld, Dirk J., Hottenga, Jouke-Jan, Jenkinson, Mark, Kanai, Ryota, Kent, Jack W., McMahon, Katie L., Meisenzahl, Eva, Mohnke, Sebastian, Mühleisen, Thomas W., Nalls, Michael A., Nichols, Thomas E., Potkin, Steven G., Reppermund, Simone, Rujescu, Dan, Schnell, Knut, Thalamuthu, Anbupalam, Turner, Jessica A., van 't Ent, Dennis, Wassink, Thomas H., Westman, Eric, Ashbrook, David G., Lu, Lu, Williams, Robert W., Buckner, Randy L., Calhoun, Vince D., Cavalleri, Gianpiero L., Dale, Anders M., Espeseth, Thomas, Hoffmann, Wolfgang, Le Hellard, Stephanie, Meyer-Lindenberg, Andreas, Müller-Myhsok, Bertram, Nyberg, Lars, Penninx, Brenda W. J. H., van Bokhoven, Hans, van Haren, Neeltje E. M., Völzke, Henry, Weiner, Michael W., White, Tonya, Agartz, Ingrid, Blangero, John, Boomsma, Dorret I., Fernández, Guillén, Fisher, Simon E., Francks, Clyde, Grabe, Hans J., Hashimoto, Ryota, Hulshoff Pol, Hilleke E., Jönsson, Erik G., McIntosh, Andrew M., Singleton, Andrew, Schmidt, Reinhold, Satizabal, Claudia L., Ebling, Maritza, Nyquist, Paul, Vinke, Louis N., Xue, Luting, Mazoyer, Bernard, Martin, Nicholas G., Wright, Margaret J., Schumann, Gunter

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IFITM3 restricts the morbidity and mortality associated with influenza von Everitt, Aaron R., Clare, Simon, Pertel, Thomas, John, Sinu P., Wash, Rachael S., Smith, Sarah E., Chin, Christopher R., Feeley, Eric M., Sims, Jennifer S., Adams, David J., Wise, Helen M., Kane, Leanne, Goulding, David, Digard, Paul, Anttila, Verneri, Baillie, J. Kenneth, Walsh, Tim S., Hume, David A., Palotie, Aarno, Xue, Yali, Colonna, Vincenza, Tyler-Smith, Chris, Dunning, Jake, Gordon, Stephen B., Smyth, Rosalind L., Openshaw, Peter J., Dougan, Gordon, Brass, Abraham L., Kellam, Paul

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Twelve Years of Drug Prioritization to Help Accelerate Disease Modification Trials in Parkinson’s Disease: The International Linked Clinical Trials Initiative von Wyse, Richard K., Isaacs, Tom, Barker, Roger A., Cookson, Mark R., Dawson, Ted M., Devos, David, Dexter, David T., Duffen, Joy, Federoff, Howard, Fiske, Brian, Foltynie, Thomas, Fox, Susan, Greenamyre, J. Timothy, Kieburtz, Karl, Kordower, Jeffrey H., Krainc, Dimitri, Matthews, Helen, Moore, Darren J., Mursaleen, Leah, Schwarzschild, Michael A., Stott, Simon R.W., Sulzer, David, Svenningsson, Per, Tanner, Caroline M., Carroll, Camille, Simon, David K., Brundin, Patrik

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Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease von Beilina, Alexandria, Rudenko, Iakov N., Kaganovich, Alice, Civiero, Laura, Chau, Hien, Kalia, Suneil K., Kalia, Lorraine V., Lobbestael, Evy, Chia, Ruth, Ndukwe, Kelechi, Ding, Jinhui, Nalls, Mike A., Olszewski, Maciej, Hauser, David N., Kumaran, Ravindran, Lozano, Andres M., Baekelandt, Veerle, Greene, Lois E., Taymans, Jean-Marc, Greggio, Elisa, Cookson, Mark R.

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Genome-wide association study of Tourette's syndrome von Scharf, J M, Yu, D, Mathews, C A, Neale, B M, Stewart, S E, Fagerness, J A, Evans, P, Gamazon, E, Edlund, C K, Service, S K, Tikhomirov, A, Osiecki, L, Illmann, C, Pluzhnikov, A, Konkashbaev, A, Davis, L K, Han, B, Crane, J, Moorjani, P, Crenshaw, A T, Parkin, M A, Reus, V I, Lowe, T L, Rangel-Lugo, M, Chouinard, S, Dion, Y, Girard, S, Cath, D C, Smit, J H, King, R A, Fernandez, T V, Leckman, J F, Kidd, K K, Kidd, J R, Pakstis, A J, State, M W, Herrera, L D, Romero, R, Fournier, E, Sandor, P, Barr, C L, Phan, N, Gross-Tsur, V, Benarroch, F, Pollak, Y, Budman, C L, Bruun, R D, Erenberg, G, Naarden, A L, Lee, P C, Weiss, N, Kremeyer, B, Berrío, G B, Campbell, D D, Cardona Silgado, J C, Ochoa, W C, Mesa Restrepo, S C, Muller, H, Valencia Duarte, A V, Lyon, G J, Leppert, M, Morgan, J, Weiss, R, Grados, M A, Anderson, K, Davarya, S, Singer, H, Walkup, J, Jankovic, J, Tischfield, J A, Heiman, G A, Gilbert, D L, Hoekstra, P J, Robertson, M M, Kurlan, R, Liu, C, Gibbs, J R, Singleton, A, Hardy, J, Strengman, E, Ophoff, R A, Wagner, M, Moessner, R, Mirel, D B, Posthuma, D, Sabatti, C, Eskin, E, Conti, D V, Knowles, J A, Ruiz-Linares, A, Rouleau, G A, Purcell, S, Heutink, P, Oostra, B A, McMahon, W M, Freimer, N B, Cox, N J, Pauls, D L

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Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis von Johnson, Janel O, Pioro, Erik P, Boehringer, Ashley, Chia, Ruth, Feit, Howard, Renton, Alan E, Pliner, Hannah A, Abramzon, Yevgeniya, Marangi, Giuseppe, Winborn, Brett J, Gibbs, J Raphael, Nalls, Michael A, Morgan, Sarah, Shoai, Maryam, Hardy, John, Pittman, Alan, Orrell, Richard W, Malaspina, Andrea, Sidle, Katie C, Fratta, Pietro, Harms, Matthew B, Baloh, Robert H, Pestronk, Alan, Weihl, Conrad C, Rogaeva, Ekaterina, Zinman, Lorne, Drory, Vivian E, Borghero, Giuseppe, Mora, Gabriele, Calvo, Andrea, Rothstein, Jeffrey D, Drepper, Carsten, Sendtner, Michael, Singleton, Andrew B, Taylor, J Paul, Cookson, Mark R, Restagno, Gabriella, Sabatelli, Mario, Bowser, Robert, Chiò, Adriano, Traynor, Bryan J

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Genome-wide meta-analysis identifies new susceptibility loci for migraine von Anttila, Verneri, Winsvold, Bendik S, Gormley, Padhraig, Kurth, Tobias, Bettella, Francesco, McMahon, George, Kallela, Mikko, Malik, Rainer, de Vries, Boukje, Terwindt, Gisela, Medland, Sarah E, Todt, Unda, McArdle, Wendy L, Quaye, Lydia, Koiranen, Markku, Ikram, M Arfan, Lehtimäki, Terho, Stam, Anine H, Ligthart, Lannie, Wedenoja, Juho, Dunham, Ian, Neale, Benjamin M, Palta, Priit, Hamalainen, Eija, Schürks, Markus, Rose, Lynda M, Buring, Julie E, Ridker, Paul M, Steinberg, Stacy, Stefansson, Hreinn, Jakobsson, Finnbogi, Lawlor, Debbie A, Evans, David M, Ring, Susan M, Färkkilä, Markus, Artto, Ville, Kaunisto, Mari A, Freilinger, Tobias, Schoenen, Jean, Frants, Rune R, Pelzer, Nadine, Weller, Claudia M, Zielman, Ronald, Heath, Andrew C, Madden, Pamela A F, Montgomery, Grant W, Martin, Nicholas G, Borck, Guntram, Göbel, Hartmut, Heinze, Axel, Heinze-Kuhn, Katja, Williams, Frances M K, Hartikainen, Anna-Liisa, Pouta, Anneli, van den Ende, Joyce, Uitterlinden, Andre G, Hofman, Albert, Amin, Najaf, Hottenga, Jouke-Jan, Vink, Jacqueline M, Heikkilä, Kauko, Alexander, Michael, Muller-Myhsok, Bertram, Schreiber, Stefan, Meitinger, Thomas, Wichmann, Heinz Erich, Aromaa, Arpo, Eriksson, Johan G, Traynor, Bryan J, Trabzuni, Daniah, Rossin, Elizabeth, Lage, Kasper, Jacobs, Suzanne B R, Gibbs, J Raphael, Birney, Ewan, Kaprio, Jaakko, Penninx, Brenda W, Boomsma, Dorret I, van Duijn, Cornelia, Raitakari, Olli, Jarvelin, Marjo-Riitta, Zwart, John-Anker, Cherkas, Lynn, Strachan, David P, Kubisch, Christian, Ferrari, Michel D, van den Maagdenberg, Arn M J M, Dichgans, Martin, Wessman, Maija, Smith, George Davey, Stefansson, Kari, Daly, Mark J

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Worldwide trends in the prevalence of asthma symptoms: phase III of the International Study of Asthma and Allergies in Childhood (ISAAC) von Pearce, Neil, Aït-Khaled, Nadia, Beasley, Richard, Mallol, Javier, Keil, Ulrich, Mitchell, Ed, Robertson, Colin

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A protocol for high-throughput phenotyping, suitable for quantitative trait analysis in mice von Solberg, Leah C, Valdar, William, Gauguier, Dominique, Nunez, Graciela, Taylor, Amy, Burnett, Stephanie, Arboledas-Hita, Carmen, Hernandez-Pliego, Polinka, Davidson, Stuart, Burns, Peter, Bhattacharya, Shoumo, Hough, Tertius, Higgs, Douglas, Klenerman, Paul, Cookson, William O, Zhang, Youming, Deacon, Robert M, Rawlins, J Nicholas P, Mott, Richard, Flint, Jonathan

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Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study von Pichler, Irene, Del Greco M, Fabiola, Gögele, Martin, Lill, Christina M, Bertram, Lars, Do, Chuong B, Eriksson, Nicholas, Foroud, Tatiana, Myers, Richard H, Nalls, Michael, Keller, Margaux F, Benyamin, Beben, Whitfield, John B, Pramstaller, Peter P, Hicks, Andrew A, Thompson, John R, Minelli, Cosetta

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Encapsulation of sodium alkyl sulfates by the cyclotriveratrylene-based, [Pd(6)L(8)](12+) stella octangula cage von Cookson, Nikki J, Henkelis, James J, Ansell, Richard J, Fishwick, Colin W G, Hardie, Michaele J, Fisher, Julie

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Initial Assessment of the Pathogenic Mechanisms of the Recently Identified Alzheimer Risk Loci von Holton, Patrick, Ryten, Mina, Nalls, Michael, Trabzuni, Daniah, Weale, Michael E., Hernandez, Dena, Crehan, Helen, Gibbs, J. Raphael, Mayeux, Richard, Haines, Jonathan L., Farrer, Lindsay A., Pericak‐Vance, Margaret A., Schellenberg, Gerard D., Ramirez‐Restrepo, Manuel, Engel, Anzhelika, Myers, Amanda J., Corneveaux, Jason J., Huentelman, Matthew J., Dillman, Allissa, Cookson, Mark R., Reiman, Eric M., Singleton, Andrew, Hardy, John, Guerreiro, Rita

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Autoimmunity Is a Significant Feature of Idiopathic Pulmonary Arterial Hypertension von Jones, Rowena J, De Bie, Eckart M D D, Groves, Emily, Zalewska, Kasia I, Swietlik, Emilia M, Treacy, Carmen M, Martin, Jennifer M, Polwarth, Gary, Li, Wei, Guo, Jingxu, Baxendale, Helen E, Coleman, Stephen, Savinykh, Natalia, Coghlan, J Gerry, Corris, Paul A, Howard, Luke S, Johnson, Martin K, Church, Colin, Kiely, David G, Lawrie, Allan, Lordan, James L, Mackenzie Ross, Robert V, Pepke Zaba, Joanna, Wilkins, Martin R, Wort, S John, Fiorillo, Edoardo, Orrù, Valeria, Cucca, Francesco, Rhodes, Christopher J, Gräf, Stefan, Morrell, Nicholas W, McKinney, Eoin F, Wallace, Chris, Toshner, Mark

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Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes von West, Hannah, Carss, Keren, Shakeel, Hassan, Adlard, Julian, Cole, Trevor, Kwong, Ava, Paterson, Joan, Searle, Claire, Skytte, Anne-Bine, Aitman, Timothy, Ambegaonkar, Gautum, Antrobus, Richard, Arno, Gavin, Astle, William, Attwood, Antony, Austin, Steve, Bakchoul, Tamam, Bennett, David, Bitner-Glindzicz, Maria, Bleda, Marta, Bolton-Maggs, Paula, Booth, Claire, Clements-Brod, Naomi, Clowes, Virginia, Collins, Peter, Cookson, Victoria, Creaser-Myers, Amanda, DaCosta, Rosa, Davies, Sophie, Deegan, Patrick, Dewhurst, Eleanor, Doffinger, Rainer, Drewe, Elizabeth, Favier, Remi, Firth, Helen, Furie, Bruce, Furnell, Abigail, Gardham, Alice, Gissen, Paul, Gomez, Keith, Graf, Stefan, Gräf, Stefan, Greenhalgh, Alan, Hackett, Scott, Haimel, Matthias, Herwadkar, Archana, Holder, Muriel, Huissoon, Aarnoud, James, Roger, Kennedy, Fiona, Kingston, Nathalie, Kuijpers, Taco, Lawrie, Allan, Lentaigne, Claire, Machado, Rajiv, Maher, Eamonn, Mangles, Sarah, Manson, Ania, Matser, Vera, McDermott, Elizabeth, Megy, Karyn, Millar, Carolyn M., Morrell, Nicholas, Ouwehand, Willem H., Papadia, Sofia, Payne, Jeanette, Peacock, Andrew, Pollock, Val, Quinti, Isabella, Rayner-Matthews, Paula, Rehnstrom, Karola, Rhodes, Christopher J., Richardson, Sylvia, Richter, Alex, Rondina, Matthew, Rosser, Elisabeth, Rue-Albrecht, Kevin, Sargur, Ravishankar, Savic, Sinisa, Schotte, Gwen, Schulze, Harald, Seneviratne, Suranjith, Shamardina, Olga, Simeoni, Ilenia, Staines, Simon, Stark, Hannah, Stock, Sophie, Thaventhiran, James, Thompson, Dorothy, Toh, Cheng-Hock, Turek, Wojciech, Wassmer, Evangeline, Watt, Christopher, Wharton, John, Williamson, Catherine, Woods, Geoff, Wort, John, Yeatman, Nigel, Tischkowitz, Marc D., Maher, Eamonn R.

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