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Number of items: 39.

Santiago, Enrique, Novo, Irene, Pardinas, Antonio F., Saura, María, Wang, Jinliang and Caballero, Armando 2020. Recent demographic history inferred by high-resolution analysis of linkage disequilibrium. Molecular Biology and Evolution 37 (12) , pp. 3642-3653. 10.1093/molbev/msaa169
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Alonso-Llamazares, Carmen, Blanco Márquez, Beatriz, Lopez, Belen and Pardinas, Antonio F. 2020. Assessing individual and population variability in degenerative joint disease prevalence using generalized linear mixed models. American Journal of Physical Anthropology 10.1002/ajpa.24195
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Hubbard, Leon, Rees, Elliott, Morris, Derek W., Lynham, Amy J., Richards, Alex L., Pardinas, Antonio F., Legge, Sophie E., Harold, Denise, Zammit, Stanley, Corvin, Aiden C., Gill, Michael G., Hall, Jeremy, Holmans, Peter, O'Donovan, Michael C., Owen, Michael J., Donohoe, Gary, Kirov, George, Pocklington, Andrew and Walters, James T.R. 2020. Rare copy number variations are associated with poorer cognition in schizophrenia. Biological Psychiatry 10.1016/j.biopsych.2020.11.025
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Kendall, Kimberley M., John, Ann, Lee, Sze Chim, Rees, Elliott, Pardiñas, Antonio F., Del Pozo Banos, Marcos, Owen, Michael J., O’Donovan, Michael C., Kirov, George, Lloyd, Keith, Jones, Ian, Legge, Sophie E. and Walters, James T. R. 2020. Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: a data linkage study. BJPsych Open 6 (6) , e139. 10.1192/bjo.2020.42

Legge, Sophie E., Christensen, Rune H., Petersen, Liselotte, Pardinas, Antonio F., Bracher-Smith, Matthew, Knapper, Steven, Bybjerg-Grauholm, Jonas, Baekvad-Hansen, Marie, Hougaard, David M., Werge, Thomas, Nordentoft, Merete, Mortensen, Preben Bo, Owen, Michael J., O'Donovan, Michael C., Benros, Michael E. and Walters, James T. R. 2020. The Duffy-null genotype and risk of infection. Human Molecular Genetics 29 (20) , pp. 3341-3349. 10.1093/hmg/ddaa208

Grama, Steluta, Willcocks, Isabella, Hubert, John, Pardiñas, Antonio, Legge, Sophie, Bracher-Smith, Matthew, Menzies, Georgina, Hall, Lynsey, Pocklington, Andrew, Anney, Richard, Bray, Nicholas, Escott-Price, Valentina and Caseras, Xavier 2020. Polygenic risk for schizophrenia and subcortical brain anatomy in the UK Biobank cohort. Translational Psychiatry 10 , 309. 10.1038/s41398-020-00940-0

Legge, Sophie, Dennison, Charlotte, Pardinas, Antonio, Rees, Elliott, Lynham, Amy, Hopkins, Lucinda, Bates, Lesley, Kirov, George, Owen, Michael, O'Donovan, Michael and Walters, James 2020. Clinical indicators of treatment-resistant psychosis. British Journal of Psychiatry 216 (5) , pp. 259-266. 10.1192/bjp.2019.120

Byrne, Enda, Zhu, Zhihong, Qi, Ting, Skene, Nathan, Bryois, Julien, Pardinas, Antonio, Stahl, Eli, Smoller, Jordon, Rietschel, Marcella, Owen, Michael, Walters, James, O'Donovan, Michael, McGarth, John, Hjerling-Leffler, Jens, Sullivan, Patrick, Goddard, Michael, Visscher, Peter, Yang, Jian and Wray, Naomi 2020. Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders. Molecular Psychiatry 10.1038/s41380-020-0705-9

Richards, Alexander, Pardinas, Antonio, Frizzati, Aura, Tansey, Katherine, Lynham, Amy, Holmans, Peter, Legge, Sophie, Savage, Jeanna, Agartz, Ingrid, Andreassen, Ole, Blokland, Gabriella, Corvin, Aiden, Cosgrove, Donna, Degenhardt, Franzoska, Djurovic, Srdjan, Espeseth, Thomas, Ferraro, Laura, Gayer-Anderson, Charlotte, Giegking, Ina, van Haren, Neeltje, Hartmann, Annette, Hubert, John, Jonsson, Erik, Konte, Bettina, Lennertz, Leonhard, Olde Loohuis, Loes, Melle, Ingrid, Morgan, Craig, Morris, Derek, Murray, Robin, Nyman, Håkan, Ophoff, Roel, van Os, Jim, Petryshen, Tracey, Quattrone, Diego, Rietschel, Marcella, Rujescu, Dan, Ruttan, Bart, Streit, Fabin, Strohmaier, Janna, Sullivan, Patrick, Sundet, Kjetil, Wagner, MIchael, Escott-Price, Valentina, Owen, Michael, Donohoe, Gary, O'Donovan, Michael, Walters, James, Schizophrenia Working Group of the Psychiatric Genomics Consorti, and EUGEI WP Group, 2020. The relationship between polygenic risk scores and cognition in schizophrenia. Schizophrenia Bulletin 46 (2) , -. 10.1093/schbul/sbz061

Dennison, Charlotte A., Legge, Sophie E., Pardinas, Antonio F. and Walters, James T.R. 2020. Genome-wide association studies in schizophrenia: Recent advances, challenges and future perspective. Schizophrenia Research 217 , pp. 4-12. 10.1016/j.schres.2019.10.048

Rees, Elliott, Han, Jun, Morgan, Joanne, Carrera, Noa, Escott-Price, Valentina, Pocklington, Andrew J., Duffield, Madeleine, Hall, Lynsey S., Legge, Sophie E., Pardinas, Antonio F., Richards, Alexander L., Roth, Julian, Lezheiko, Tatyana, Kondratyev, Nikolay, Golimbat, Vera, Parellada, Mara, González-Peñas, Javier, Arango, Celso, Gawlik, Micha, Kirov, George, Walters, James T. R., Holmans, Peter, O'Donovan, Michael C. and Owen, Michael J. 2020. De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia. Nature Neuroscience 23 (2) , pp. 179-184. 10.1038/s41593-019-0565-2

Cleynen, Isabelle, Engchuan, Worrawat, Hestand, Matthew S., Heung, Tracy, Holleman, Aaron M., Johnston, H. Richard, Monfeuga, Thomas, Monfeuga, Thomas, McDonald-McGinn, Donna M., Gur, Raquel E., Morrow, Bernice E., Swillen, Ann, Vorstman, Jacob A.S., Bearden, Carrie E., Chow, Eva W. C., Van den Bree, Marianne, Emanuel, Beverley S., Vermeesch, Joris R., Warren, Stephen T., Owen, Michael J., Chopra, Pankaj, Cutler, David J., Duncan, Richard, Kotlar, Alex V., Mulle, Jennifer G., Voss, Anna J., Zwick, Michael E., Diacou, Alexander, Golden, Aaron, Guo, Tingwei, Lin, Jhih-Rong, Wang, Tao, Zhang, Zhengdong, Zhao, Yingjie, Marshall, Christian, Merico, Daniele, Jin, Andrea, Lilley, Brenna, Salmons, Harold I., Tran, Oanh, Holmans, Peter, Pardinas, Antonio, Walters, James T. R., Demaeral, Wolfman, Boot, Erik, Butcher, Nancy J., Costain, Gregory A., Lowther, Chelsea, Evers, Rens, van Amelsvoort, Therese A. M. J., van Duin, Esther, Vingerhoets, Claudia, Breckpot, Jeroen, Devriendt, Koren, Vergaelen, Elfi, Vogels, Annick, Crowley, Blaine, McGinn, Daniel E., Moss, Edward M., Sharkus, Robert J., Unolt, Marta, Zackai, Elaine H., Calkins, Monica E., Gallagher, Robert S., Gur, Ruben C., Tang, Sunny X., Fritsch, Rosemarie, Ornstein, Claudia, Repetto, Gabriela M., Breetvelt, Elemi, Duijff, Sasja N., Fiksinski, Ania, Moss, Hayley, Niarchou, Maria, Murphy, Kieran C., Prasad, Sarah E., Daly, Eileen M., Gudbrandsen, Maria, Murphy, Clodagh M., Murphy, Declan C., Buzzanca, Antonio, Fabio, Fabio Di, Digilio, Maria C., Pontillo, Maria, Marino, Bruno, Vicari, Stefano, Coleman, Karlene, Cubells, Joseph F., Ousley, Opal Y., Carmel, Miri, Gothelf, Doron, Mekori-Domachevsky, Ehud, Michaelovsky, Elena, Weinberger, Ronnie, Weizman, Abraham, Kushan, Leila, Jalbrzikowski, Maria, Armando, Marco, Eliez, Stephan, Sandini, Corrado, Schneider, Maude, Bena, Frederique Sloan, Antshel, Kevin M., Fremont, Wanda, Kates, Wendy R., Belzeaux, Raoul, Busa, Tiffany, Philip, Nicole, Campbell, Linda E., McCabe, Kathryn L., Hooper, Stephen R., Schoch, Kelly, Shashi, Vandana, Simon, Tony J., Tassone, Flora, Arango, Celso, Fraguas, David, Garcia-Miñaur, Sixto, Morey-Canyelles, Jaume, Rosell, Jordi, Suner, Damia H., Raventos-Simic, Jasna, Epstein, Michael, Williams, Nigel M. and Bassett, Anne S. 2020. Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. Molecular Psychiatry 10.1038/s41380-020-0654-3

Hall, Lynsey S, Medway, Christopher W, Pain, Oliver, Pardinas, Antonio F, Rees, Elliott G, Escott-Price, Valentina, Pocklington, Andrew, Bray, Nicholas J, Holmans, Peter A, Walters, James T R, Owen, Michael and O'Donovan, Michael 2020. A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia. Human Molecular Genetics 29 (1) , pp. 159-167. 10.1093/hmg/ddz253

Konte, Bettina, Walters, James, Gieglin, Ina, Legge, Sophie, Pardinas, Antonio, Cohen, Dan, Pirmohamed, Munir, Tiihonen, Jari, Hartmann, Annette, Bogers, Jan, van der Weide, Jan, van der Weide, Karen, Putkonen, Anu, Repo-Tiihonen, Eila, Hallikainen, Tero, Silva, Ed, Ingimarsson, Oddur, Sigurdsson, Engilbert, Kennedy, James, Sullivan, Patrick, Rietschel, Marcella, Breen, Gerome, Stefansson, Hreinn, Stefansson, Kari, Stefansson, Hreinn, Collier, David, O'Donovan, Michael and Rujescu, Dan 2020. HLA-DQB1 6672G>C (rs113332494) is associated with clozapine-induced neutropenia and agranulocytosis in individuals of European ancestry. Translational Psychiatry
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Legge, Sophie E., Jones, Hannah J., Kendall, Kimberley M., Pardinas, Antonio F., Menzies, Georgina, Bracher-Smith, Matthew, Escott-Price, Valentina, Rees, Elliott, Davis, Katrina A., Hotopf, Matthew, Savage, Jeanne E., Posthuma, Danielle, Holmans, Peter, Kirov, George, Owen, Michael J., O'Donovan, Michael C., Zammit, Stanley and Walters, James T. R. 2019. Association of genetic liability to psychotic experiences with neuropsychotic disorders and traits. JAMA Psychiatry 76 (12) , pp. 1256-1265. 10.1001/jamapsychiatry.2019.2508

Chapman, Ria M, Tinsley, Caroline L, Hill, Matthew J, Forrest, Marc P, Tansey, Katherine E, Pardinas, Antonio F., Rees, Elliott, Doyle, A. Michelle, Wilkinson, Lawrence S., Owen, Michael J., O'Donovan, Michael and Blake, Derek J. 2019. Convergent evidence that ZNF804A is a regulator of pre-messenger RNA processing and gene expression. Schizophrenia Bulletin 45 (6) , pp. 1267-1278. 10.1093/schbul/sby183

D'Ambrosio, Enrico, Dahoun, Tarik, Pardinas, Antonio F., Veronese, Mattia, Bloomfield, Michael A.P., Jauhar, Sameer, Bonoldi, Ilaria, Rogdaki, Maria, Froudist-Walsh, Sean, Walters, James T. R. and Howes, Oliver D. 2019. The effect of a genetic variant at the schizophrenia associated AS3MT/BORCS7 locus on striatal dopamine function: A PET imaging study. Psychiatry Research: Neuroimaging 291 , pp. 34-41. 10.1016/j.pscychresns.2019.07.005

Pain, Oliver, Pocklington, Andrew J., Holmans, Peter A., Bray, Nichloas J., O'Brian, Heath E., Hall, Lynsey S., Pardinas, Antonio F., O'Donovan, Michael C., Owen, Michael J. and Anney, Richard 2019. Novel insight into the etiology of autism spectrum disorder gained by integrating expression data with genome-wide association statistics. Biological Psychiatry 86 (4) , pp. 265-273. 10.1016/j.biopsych.2019.04.034

Escott-Price, Valentina, Pardinas, Antonio F., Santiago, Enrique, Walters, James, Kirov, George, Owen, Michael J. and O'Donovan, Michael C. 2019. The relationship between common variant schizophrenia liability and number of offspring in the UK Biobank. American Journal of Psychiatry 176 (8) , pp. 661-666. 10.1176/appi.ajp.2018.18020140

Pardinas, Antonio F., Nalmpanti, Mariana, Pocklington, Andrew J., Legge, Sophie E., Medway, Christopher, King, Adrian, Jansen, John, Helthuis, Marinka, Zammit, Stanley, MacCabe, James, Owen, Michael J., O'Donovan, Michael C. and Walters, James T. R 2019. Pharmacogenomic variants and drug interactions identified through the genetic analysis of clozapine metabolism. American Journal of Psychiatry 176 (6) , pp. 477-486. 10.1176/appi.ajp.2019.18050589

Pettersson, E., Lichtenstein, P., Larsson, H., Song, J., Agrawal, A., Børglum, A. D., Bulik, C. M., Daly, M. J., Davis, L. K., Demontis, D., Edenberg, H. J., Grove, J., Gelernter, J., Neale, B. M., Pardinas, A. F., Stahl, E., Walters, J. T. R., Walters, R., Sullivan, P. F., Posthuma, D. and Polderman, T. J. C. 2019. Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls. Psychological Medicine 49 (7) , pp. 1166-1173. 10.1017/S0033291718002039

Huckins, Laura M., Dobbyn, Amanda, Ruderfer, Douglas M., Hoffman, Gabriel, Wang, Weiqing, Pardinas, Antonio F., Rajagopal, Veera M., Als, Thomas D., Tan Hoang, Hoang T., Girdhar, Kiran, Boocock, James, Roussos, Panagiotis, Fromer, Menachem, Kramer, Robin, Domenici, Enrico, Gamazon, Eric R., Purcell, Shaun, Demontis, Ditte, Borglum, Anders, Walters, James T. R., O'Donovan, Michael C., Sullivan, Patrick, Owen, Michael J., Devlin, Bernie, Sieberts, Solveig K., Cox, Nancy J., Kyung Im, Hae, Sklar, Pamela and Ayumi Stahl, Eli A. 2019. Gene expression imputation across multiple brain regions provides insights into schizophrenia risk. Nature Genetics 51 , pp. 659-674. 10.1038/s41588-019-0364-4

Rees, Elliott, Carrera, Noa, Morgan, Joanne, Hambridge, Kirsty, Escott-Price, Valentina, Pocklington, Andrew J., Richards, Alexander L., Pardinas, Antonio F., McDonald, Colm, Donohoe, Gary, Morris, Derek W., Kenny, Elaine, Kelleher, Eric, Gill, Michael, Corvin, Aiden, Kirov, George, Walters, James T. R., Holmans, Peter, Owen, Michael J. and O'Donovan, Michael C. 2019. Targeted sequencing of 10,198 samples confirms abnormalities in neuronal activity and implicates voltage-gated sodium channels in schizophrenia pathogenesis. Biological Psychiatry 85 (7) , pp. 554-562. 10.1016/j.biopsych.2018.08.022

Legge, Sophie E., Pardinas, Antonio F., Helthuis, Marinka, Jansen, John A., Jollie, Karel, Knapper, Steven, MacCabe, James H., Rujescu, Dan, Collier, David A., O'Donovan, Michael C., Owen, Michael J. and Walters, James T. R. 2019. A genome-wide association study in individuals of African ancestry reveals the importance of the Duffy-null genotype in the assessment of clozapine-related neutropenia. Molecular Psychiatry 24 , pp. 328-337. 10.1038/s41380-018-0335-7

Li, Mingfeng, Santpere, Gabriel, Imamura Kawasawa, Yuka, Evgrafov, Oleg V., Gulden, Forrest O., Pochareddy, Sirisha, Sunkin, Susan M., Li, Zhen, Shin, Yurae, Zhu, Ying, Sousa, André M. M., Werling, Donna M., Kitchen, Robert R., Kang, Hyo Jung, Pletikos, Mihovil, Choi, Jinmyung, Muchnik, Sydney, Xu, Xuming, Wang, Daifeng, Lorente-Galdos, Belen, Liu, Shuang, Giusti-Rodríguez, Paola, Won, Hyejung, de Leeuw, Christiaan A., Pardinas, Antonio F., Hu, Ming, Jin, Fulai, Li, Yun, Owen, Michael J., O'Donovan, Michael C., Walters, James T. R., Posthuma, Danielle, Reimers, Mark A., Levitt, Pat, Weinberger, Daniel R., Hyde, Thomas M., Kleinman, Joel E., Geschwind, Daniel H., Hawrylycz, Michael J., State, Matthew W., Sanders, Stephan J., Sullivan, Patrick F., Gerstein, Mark B., Lein, Ed S., Knowles, James A. and Sestan, Nenad 2018. Integrative functional genomic analysis of human brain development and neuropsychiatric risks. Science 362 (6420) , eaat7615. 10.1126/science.aat7615

O'Brien, Heath E., Hannon, Eilis, Hill, Matthew J., Toste, Carolina C., Robertson, Matthew J., Morgan, Joanne E., McLaughlin, Gemma, Lewis, Cathryn M., Schalkwyk, Leonard C., Hall, Lynsey S., Pardinas, Antonio F., Owen, Michael J., O'Donovan, Michael C., Mill, Jonathan and Bray, Nicholas J. 2018. Expression quantitative trait loci in the developing human brain and their enrichment in neuropsychiatric disorders. Genome Biology 19 , 194. 10.1186/s13059-018-1567-1

Dahoun, Tarik, Pardinas, Antonio F., Veronese, Mattia, Bloomfield, Michael A. P., Jauhar, Sameer, Bonoldi, Ilaria, Froudist-Walsh, Sean, Nosarti, Chiara, Korth, Carsten, Hennah, William, Walters, James, Prata, Diana and Howes, Oliver D. 2018. The effect of the DISC1 Ser704Cys polymorphism on striatal dopamine synthesis capacity: an [18F]-DOPA PET study. Human Molecular Genetics 27 (20) , pp. 3498-3506. 10.1093/hmg/ddy242

Alonso-Llamazares, Carmen, Gomez, Carlos, Garcia-Manrique, Pablo, Pardinas, Antonio F. and Lopez, Belen 2018. Medical diagnostic methods applied to a medieval female with vitamin D deficiency from the North of Spain. International Journal of Paleopathology 22 , pp. 109-120. 10.1016/j.ijpp.2018.07.007

Skene, Nathan G., Bryois, Julien, Bakken, Trygve E., Breen, Gerome, Crowley, James J., Gaspar, Héléna A., Giusti-Rodriguez, Paola, Hodge, Rebecca D., Jeremy A., Miller, Muñoz-Manchado, Ana, O'Donovan, Michael C., Owen, Michael J., Pardinas, Antonio, Ryge, Jesper, Walters, James T. R., Linnarsson, Sten, Lein, Ed S., Sullivan, Patrick F. and Hjerling-Leffler, Jens 2018. Genetic identification of brain cell types underlying schizophrenia. Nature Genetics 50 , pp. 825-833. 10.1038/s41588-018-0129-5

Pardinas, Antonio F., Holmans, Peter, Pocklington, Andrew J., Escott-Price, Valentina, Ripke, Stephan, Carrera, Noa, Legge, Sophie E., Bishop, Sophie, Cameron, Darren, Hamshere, Marian L., Han, Jun, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, MacCabe, James H., McCarroll, Steven A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda, Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nichols G., McIntosh, Andrew M., Plomin, Robert P., Porteous, David J., Wray, Naomi R., Caballero, Armando, Geschwind, Daniel H., Huckins, Laura M., Ruderfer, Douglas M., Santiago, Enrique, Sklar, Pamela, Stahl, Eli A., Won, Hyejung, Agerbo, Eeben A., Als, Thomas P., Andreassen, Ole A., Bækvad-Hansen, Marie, Mortensen, Preben Bo, Pedersen, Carsten Bocker, Børglum, Anders D., Bybjerg-Grauholm, Jonas, Djurovic, Srdjan, Durmishi, Naser, Giørtz Pedersenu, Marianne, Golimbet, Vera, Grove, Jakob, Hougaard, David M., Mattheisen, Manuel, Molden, Espen, Mors, Ole, Nordentoft, Merete, Pejovic-Milovancevic, Milica, Sigurdsson, Engilbert, Silagadze, Teimuraz, Søholm Hansen, Christine, Stefansson, Kari, Stefansson, Hreinn, Steinberg, Stacy, Tosato, Sarah, Werge, Thomas, Consortium, GERAD, Collier, David A., Rujescu, Dan, Kirov, George, Owen, Michael J, O'Donovan, Michael C., Walters, James T. R. and Williams, Julie 2018. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature Genetics 50 , pp. 381-389. 10.1038/s41588-018-0059-2

Gomes, Cláudia, Fondevila, Manuel, Palomo-Díez, Sara, Pardinas, Antonio, López-Matayoshi, César, Baeza-Richer, Carlos, López-Parra, Ana María, Lareu, María Victoria, López, Belén and Arroyo-Pardo, Eduardo 2017. Phenotyping the ancient world: the physical appearance and ancestry of very degraded samples from a chalcolithic human remains. Forensic Science International: Genetics Supplement Series 6 , e484-e486. 10.1016/j.fsigss.2017.09.188

Legge, S. E., Hamshere, M. L., Ripke, S., Pardinas, A. F., Goldstein, J. I., Rees, E., Richards, A. L., Leonenko, G., Jorskog, L. F., Goldstein, J. I., Jarskog, L. F., Hilliard, C., Alfirevic, A., Duncan, L., Fourches, D., Huang, H., Lek, M., Neale, B. M., Ripke, S., Shianna, K., Szatkiewicz, J. P., Tropsha, A., van den Oord, E. J. C. G., Cascorbi, I., Dettling, M., Gazit, E., Goff, D. C., Holden, A. L., Kelly, D. L., Malhotra, A. K, Nielsen, J., Pirmohamed, M., Rujescu, D., Werge, T., Levy, D. L., Josiassen, R. C., Kennedy, J. L., Lieberman, J. A., Daly, M. J., Sullivan, P. F., Chambert, K. D., Collier, D. A., Genovese, G., Giegling, I., Holmans, P., Jonasdottir, A., Kirov, G., McCarroll, S. A., MacCabe, J. H., Mantripragada, K, Moran, J. L., Neale, B. M., Stefansson, H., Rujescu, D., Daly, M. J., Sullivan, P. F., Owen, M. J., O'Donovan, M. C. and Walters, J.T. R 2017. Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia. Molecular Psychiatry 22 , pp. 1502-1508. 10.1038/mp.2016.97

Hensman Moss, Davina J., Pardinas, Antonio F., Langbehn, Douglas, Lo, Kitty, Leavitt, Blair R., Roos, Raymund, Durr, Alexandra, Mead, Simon, Holmans, Peter, Jones, Lesley, Tabrizi, Sarah J., Coleman, A., Santos, R. Dar, Decolongon, J., Sturrock, A., Bardinet, E., Ret, C. Jauff, Justo, D., Lehericy, S., Marelli, C., Nigaud, K., Valabrègue, R., van den Bogaard, S. J. A., Dumas, E. M., van der Grond, J., t'Hart, E. P., Jurgens, C., Witjes-Ane, M.-N., Arran, N., Callaghan, J., Stopford, C., Frost, C., Jones, R., Hobbs, N., Lahiri, N., Ordidge, R., Owen, G., Pepple, T., Read, J., Say, M., Wild, E., Patel, A., Fox, N. C., Gibbard, C., Malone, I., Crawford, H., Whitehead, D., Keenan, S., Cash, D. M., Berna, C., Bechtel, N., Bohlen, S., Man, A . Hoff, Kraus, P., Axelson, E., Wang, C., Acharya, T., Lee, S., Monaco, W., Campbell, C., Queller, S., Whitlock, K., Campbell, C., Campbell, M., Frajman, E., Milchman, C., O'Regan, A., Labuschagne, I., Stout, J., Landwehrmeyer, B., Craufurd, D., Scahill, R., Hicks, S., Kennard, C., Johnson, H., Tobin, A., Rosas, H. D., Reilmann, R., Borowsky, B., Pourchot, C., Andrews, S. C., Bachoud-Lévi, Anne-Catherine, Bentivoglio, Anna Rita, Biunno, Ida, Bonelli, Raphael, Burgunder, Jean-Marc, Dunnett, Stephen, Ferreira, Joaquim, Handley, Olivia, Heiberg, Arvid, Illmann, Torsten, Landwehrmeyer, G. Bernhard, Levey, Jamie, Ramos-Arroyo, Maria A., Nielsen, Jørgen, Koivisto, Susana Pro, Päivärinta, Markku, Roos, Raymund A.C., Sebastián, A. Rojo, Tabrizi, Sarah, Vandenberghe, Wim, Verellen-Dumoulin, Christine, Uhrova, Tereza, Wahlström, Jan, Zaremba, Jacek, Baake, Verena, Barth, Katrin, Garde, Monica Bascuñana, Betz, Sabrina, Bos, Reineke, Callaghan, Jenny, Come, Adrien, Guedes, Leonor Correia, Ecker, Daniel, Finisterra, Ana Maria, Fullam, Ruth, Gilling, Mette, Gustafsson, Lena, Handley, Olivia J., Hvalstedt, Carina, Held, Christine, Koppers, Kerstin, Lamanna, Claudia, Laurà, Matilde, Descals, Asunción Martínez, Martinez-Horta, Saül, Mestre, Tiago, Minster, Sara, Monza, Daniela, Mütze, Lisanne, Oehmen, Martin, Orth, Michael, Padieu, Hélène, Paterski, Laurent, Peppa, Nadia, Koivisto, Susana Pro, Di Renzo, Martina, Rialland, Amandine, Røren, Niini, ?a?inková, Pavla, Timewell, Erika, Townhill, Jenny, Cubillo, Patricia Trigo, da Silva, Wildson Vieira, van Walsem, Marleen R, Whalstedt, Carina, Witjes-Ané, Marie-Noelle, Witkowski, Grzegorz, Wright, Abigail, Zielonka, Daniel, Zielonka, Eugeniusz, Zinzi, Paola, Bonelli, Raphael M., Lilek, Sabine, Hecht, Karen, Herranhof, Brigitte, Holl, Anna, Kapfhammer, Hans-Peter, Koppitz, Michael, Magnet, Markus, Müller, Nicole, Otti, Daniela, Painold, Annamaria, Reisinger, Karin, Scheibl, Monika, Schöggl, Helmut, Ullah, Jasmin, Braunwarth, Eva-Maria, Brugger, Florian, Buratti, Lisa, Hametner, Eva-Maria, Hepperger, Caroline, Holas, Christiane, Hotter, Anna, Hussl, Anna, Müller, Christoph, Poewe, Werner, Seppi, Klaus, Sprenger, Fabienne, Wenning, Gregor, Boogaerts, Andrea, Calmeyn, Godelinde, Delvaux, Isabelle, Liessens, Dirk, Somers, Nele, Dupuit, Michel, Minet, Cécile, van Paemel, Dominique, Ribaï, Pascale, Verellen-Dumoulin, Christine, Boogaerts, Andrea, Vandenberghe, Wim, van Reijen, Dimphna, Klempír, Jirí, Majerová, Veronika, Roth, Jan, Stárková, Irena, Hjermind, Lena E., Jacobsen, Oda, Nielsen, Jørgen E., Larsen, Ida Unmack, Vinther-Jensen, Tua, Hiivola, Heli, Hyppönen, Hannele, Martikainen, Kirsti, Tuuha, Katri, Allain, Philippe, Bonneau, Dominique, Bost, Marie, Gohier, Bénédicte, Guérid, Marie-Anne, Olivier, Audrey, Prundean, Adriana, Scherer-Gagou, Clarisse, Verny, Christophe, Babiloni, Blandine, Debruxelles, Sabrina, Duché, Charlotte, Goizet, Cyril, Jameau, Laetitia, Lafoucrière, Danielle, Spampinato, Umberto, Barthélémy, Rekha, De Bruycker, Christelle, Carette, Maryline Cabaret Anne-Sophie, Defebvre, Eric Decorte Luc, Delliaux, Marie, Delval, Arnaud, Destee, Alain, Dujardin, Kathy, Lemaire, Marie-Hélène, Manouvrier, Sylvie, Peter, Mireille, Plomhouse, Lucie, Sablonnière, Bernard, Simonin, Clémence, Thibault-Tanchou, Stéphanie, Vuillaume, Isabelle, Bellonet, Marcellin, Berrissoul, Hassan, Blin, Stéphanie, Courtin, Françoise, Duru, Cécile, Fasquel, Véronique, Godefroy, Olivier, Krystkowiak, Pierre, Mantaux, Béatrice, Roussel, Martine, Wannepain, Sandrine, Azulay, Jean-Philippe, Delfini, Marie, Eusebio, Alexandre, Fluchere, Frédérique, Mundler, Laura, Anheim, Mathieu, Julié, Celine, Boukbiza, Ouhaid Lagha, Longato, Nadine, Rudolf, Gabrielle, 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