Analysis of protein-coding genetic variation in 60,706 humans von Lek, Monkol, Karczewski, Konrad J., Minikel, Eric V., Samocha, Kaitlin E., Banks, Eric, Fennell, Timothy, O’Donnell-Luria, Anne H., Ware, James S., Hill, Andrew J., Cummings, Beryl B., Tukiainen, Taru, Birnbaum, Daniel P., Kosmicki, Jack A., Duncan, Laramie E., Estrada, Karol, Zhao, Fengmei, Zou, James, Pierce-Hoffman, Emma, Berghout, Joanne, Cooper, David N., Deflaux, Nicole, DePristo, Mark, Do, Ron, Flannick, Jason, Fromer, Menachem, Gauthier, Laura, Goldstein, Jackie, Gupta, Namrata, Howrigan, Daniel, Kiezun, Adam, Kurki, Mitja I., Moonshine, Ami Levy, Natarajan, Pradeep, Orozco, Lorena, Peloso, Gina M., Poplin, Ryan, Rivas, Manuel A., Ruano-Rubio, Valentin, Rose, Samuel A., Ruderfer, Douglas M., Shakir, Khalid, Stenson, Peter D., Stevens, Christine, Thomas, Brett P., Tiao, Grace, Tusie-Luna, Maria T., Weisburd, Ben, Won, Hong-Hee, Yu, Dongmei, Altshuler, David M., Ardissino, Diego, Boehnke, Michael, Danesh, John, Donnelly, Stacey, Elosua, Roberto, Florez, Jose C., Gabriel, Stacey B., Getz, Gad, Glatt, Stephen J., Hultman, Christina M., Kathiresan, Sekar, Laakso, Markku, McCarroll, Steven, McCarthy, Mark I., McGovern, Dermot, McPherson, Ruth, Neale, Benjamin M., Palotie, Aarno, Purcell, Shaun M., Saleheen, Danish, Scharf, Jeremiah M., Sklar, Pamela, Sullivan, Patrick F., Tuomilehto, Jaakko, Tsuang, Ming T., Watkins, Hugh C., Wilson, James G., Daly, Mark J., MacArthur, Daniel G.

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Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders von Singh, Tarjinder, Kurki, Mitja I, Curtis, David, Purcell, Shaun M, Crooks, Lucy, McRae, Jeremy, Suvisaari, Jaana, Chheda, Himanshu, Blackwood, Douglas, Breen, Gerome, Pietiläinen, Olli, Gerety, Sebastian S, Ayub, Muhammad, Blyth, Moira, Cole, Trevor, Collier, David, Coomber, Eve L, Craddock, Nick, Daly, Mark J, Danesh, John, DiForti, Marta, Foster, Alison, Freimer, Nelson B, Geschwind, Daniel, Johnstone, Mandy, Joss, Shelagh, Kirov, Georg, Körkkö, Jarmo, Kuismin, Outi, Holmans, Peter, Hultman, Christina M, Iyegbe, Conrad, Lönnqvist, Jouko, Männikkö, Minna, McCarroll, Steve A, McGuffin, Peter, McIntosh, Andrew M, McQuillin, Andrew, Moilanen, Jukka S, Moore, Carmel, Murray, Robin M, Newbury-Ecob, Ruth, Ouwehand, Willem, Paunio, Tiina, Prigmore, Elena, Rees, Elliott, Roberts, David, Sambrook, Jennifer, Sklar, Pamela, Clair, David St, Veijola, Juha, Walters, James T R, Williams, Hywel, Sullivan, Patrick F, Hurles, Matthew E, O'Donovan, Michael C, Palotie, Aarno, Owen, Michael J, Barrett, Jeffrey C

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Ultra-rare disruptive and damaging mutations influence educational attainment in the general population von Ganna, Andrea, Genovese, Giulio, Howrigan, Daniel P, Byrnes, Andrea, Kurki, Mitja I, Zekavat, Seyedeh M, Whelan, Christopher W, Kals, Mart, Nivard, Michel G, Bloemendal, Alex, Bloom, Jonathan M, Goldstein, Jacqueline I, Poterba, Timothy, Seed, Cotton, Handsaker, Robert E, Natarajan, Pradeep, Mägi, Reedik, Gage, Diane, Robinson, Elise B, Metspalu, Andres, Salomaa, Veikko, Suvisaari, Jaana, Purcell, Shaun M, Sklar, Pamela, Kathiresan, Sekar, Daly, Mark J, McCarroll, Steven A, Sullivan, Patrick F, Palotie, Aarno, Esko, Tõnu, Hultman, Christina M, Neale, Benjamin M

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Dysfunction of complement receptors CR3 (CD11b/18) and CR4 (CD11c/18) in pre‐eclampsia: a genetic and functional study von Lokki, AI, Teirilä, L, Triebwasser, M, Daly, E, Bhattacharjee, A, Uotila, L, Llort Asens, M, Kurki, MI, Perola, M, Auro, K, Salmon, JE, Daly, M, Atkinson, JP, Laivuori, H, Fagerholm, S, Meri, S, Laivuori, Hannele, Heinonen, Seppo, Kere, Juha, Kivinen, Katja, Pouta, Anneli, Kajantie, Eero

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Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland von Martin, Alicia R., Karczewski, Konrad J., Kerminen, Sini, Kurki, Mitja I., Sarin, Antti-Pekka, Artomov, Mykyta, Eriksson, Johan G., Esko, Tõnu, Genovese, Giulio, Havulinna, Aki S., Kaprio, Jaakko, Konradi, Alexandra, Korányi, László, Kostareva, Anna, Männikkö, Minna, Metspalu, Andres, Perola, Markus, Prasad, Rashmi B., Raitakari, Olli, Rotar, Oxana, Salomaa, Veikko, Groop, Leif, Palotie, Aarno, Neale, Benjamin M., Ripatti, Samuli, Pirinen, Matti, Daly, Mark J.

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FinnGen provides genetic insights from a well-phenotyped isolated population (vol 613, pg 508, 2023) von Kurki, MI, Karjalainen, J, Palta, P, Sipila, TP, Kristiansson, K, Donner, KM, Reeve, MP, Laivuori, H, Aavikko, M, Kaunisto, MA

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Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families von Gormley, Padhraig, Kurki, Mitja I., Hiekkala, Marjo Eveliina, Häppölä, Paavo, Mitchell, Adele A., Lal, Dennis, Palta, Priit, Surakka, Ida, Kaunisto, Mari Anneli, Hämäläinen, Eija, Vepsäläinen, Salli, Havanka, Hannele, Harno, Hanna, Ilmavirta, Matti, Sumelahti, Marja-Liisa, Sillanpää, Matti, Metsähonkala, Liisa, Koskinen, Seppo, Raitakari, Olli, Jousilahti, Pekka, Anttila, Verneri, Salomaa, Veikko, Artto, Ville, Agee, Michelle, Alipanahi, Babak, Auton, Adam, Bell, Robert K., Elson, Sarah L., Furlotte, Nicholas A., Huber, Karen E., Kleinman, Aaron, Litterman, Nadia K., McCreight, Jennifer C., McIntyre, Matthew H., Mountain, Joanna L., Pitts, Steven J., Sathirapongsasuti, J. Fah, Shelton, Janie F., Shringarpure, Suyash, Tian, Chao, Vacic, Vladimir, Wilson, Catherine H., Anttila, Verneri, Artto, Ville, Belin, Andrea Carmine, Børte, Sigrid, Cherkas, Lynn, Christensen, Anne Francke, Cuenca-Leon, Ester, Dichgans, Martin, van Duijn, Cornelia, Esko, Tonu, Esserlind, Ann-Louise, Frants, Rune R., Freilinger, Tobias, Furlotte, Nick, Gormley, Padhraig, Hansen, Thomas Folkmann, Hiekkala, Marjo, Ikram, M Arfan, Ingason, Andres, Kajanne, Risto, Kallela, Mikko, Kaprio, Jaakko, Kaunisto, Mari, Kubisch, Christian, Kurth, Tobias, Launer, Lenore, Lehtimaki, Terho, Lessel, Davor, Ligthart, Lannie, Litterman, Nadia, van den Maagdenberg, Arn, Macaya, Alfons, Malik, Rainer, Muller-Myhsok, Bertram, Neale, Benjamin M., Northover, Carrie, Palta, Priit, Pedersen, Nancy, Posthuma, Danielle, Pressman, Alice, Quaye, Lydia, Raitakari, Olli, Schürks, Markus, Sintas, Celia, Stefansson, Kari, Stefansson, Hreinn, Steinberg, Stacy, Strachan, David, Terwindt, Gisela, Vila-Pueyo, Marta, Winsvold, Bendik S., Wrenthal, William, Daly, Mark J., Neale, Benjamin M., Ripatti, Samuli, Kallela, Mikko, Wessman, Maija, Palotie, Aarno

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Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum von Ganna, Andrea, Satterstrom, F. Kyle, Zekavat, Seyedeh M., Das, Indraniel, Kurki, Mitja I., Churchhouse, Claire, Alfoldi, Jessica, Martin, Alicia R., Havulinna, Aki S., Byrnes, Andrea, Thompson, Wesley K., Nielsen, Philip R., Karczewski, Konrad J., Saarentaus, Elmo, Rivas, Manuel A., Gupta, Namrata, Pietiläinen, Olli, Emdin, Connor A., Lescai, Francesco, Bybjerg-Grauholm, Jonas, Flannick, Jason, Mercader, Josep M., Udler, Miriam, Laakso, Markku, Salomaa, Veikko, Hultman, Christina, Ripatti, Samuli, Hämäläinen, Eija, Moilanen, Jukka S., Körkkö, Jarmo, Kuismin, Outi, Nordentoft, Merete, Hougaard, David M., Mors, Ole, Werge, Thomas, Mortensen, Preben Bo, MacArthur, Daniel, Daly, Mark J., Sullivan, Patrick F., Locke, Adam E., Palotie, Aarno, Børglum, Anders D., Kathiresan, Sekar, Neale, Benjamin M.

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Protective Low-Frequency Variants for Preeclampsia in the Fms Related Tyrosine Kinase 1 Gene in the Finnish Population von Lokki, A Inkeri, Daly, Emma, Triebwasser, Michael, Kurki, Mitja I, Roberson, Elisha D.O, Häppölä, Paavo, Auro, Kirsi, Perola, Markus, Heinonen, Seppo, Kajantie, Eero, Kere, Juha, Kivinen, Katja, Pouta, Anneli, Salmon, Jane E, Meri, Seppo, Daly, Mark, Atkinson, John P, Laivuori, Hannele

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Dysfunction of complement receptors CR3 (CD11b/18) and CR4 (CD11c/18) in preeclampsia: a genetic and functional study von AI, Lokki, Teirilä, L, Triebwasser, M, Daly, E, Bhattacharjee, A, Uotila, L, Llort Asens, M, Kurki, MI, Perola, M, Auro, K, Salmon, JE, Daly, M, Atkinson, JP, Laivuori, H, Fagerholm, S, Meri, S

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A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis von Rivas, Manuel A., Graham, Daniel, Sulem, Patrick, Stevens, Christine, Desch, A. Nicole, Goyette, Philippe, Gudbjartsson, Daniel, Jonsdottir, Ingileif, Thorsteinsdottir, Unnur, Degenhardt, Frauke, Mucha, Sören, Kurki, Mitja I., Li, Dalin, D’Amato, Mauro, Annese, Vito, Vermeire, Severine, Weersma, Rinse K., Halfvarson, Jonas, Paavola-Sakki, Paulina, Lappalainen, Maarit, Lek, Monkol, Cummings, Beryl, Tukiainen, Taru, Haritunians, Talin, Halme, Leena, Koskinen, Lotta L. E., Ananthakrishnan, Ashwin N., Luo, Yang, Heap, Graham A., Visschedijk, Marijn C., MacArthur, Daniel G., Neale, Benjamin M., Ahmad, Tariq, Anderson, Carl A., Brant, Steven R., Duerr, Richard H., Silverberg, Mark S., Cho, Judy H, Palotie, Aarno, Saavalainen, Päivi, Kontula, Kimmo, Färkkilä, Martti, McGovern, Dermot P. B., Franke, Andre, Stefansson, Kari, Rioux, John D., Xavier, Ramnik J., Daly, Mark J.

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Common variant burden contributes to the familial aggregation of migraine in 1,589 families von Gormley, P, Kurki, MI, Hiekkala, ME, Veerapen, K, Häppölä, P, Mitchell, AA, Lal, D, Palta, P, Surakka, I, Kaunisto, MA, Hämäläinen, E, Vepsäläinen, S, Havanka, H, Harno, H, Ilmavirta, M, Nissilä, M, Säkö, E, Sumelahti, M-L, Liukkonen, J, Sillanpää, M, Metsähonkala, L, Koskinen, S, Lehtimäki, T, Raitakari, O, Männikkö, M, Ran, C, Belin, AC, Jousilahti, P, Anttila, V, Salomaa, V, Artto, V, Färkkilä, M, 23andMe Research Team, International Headache Genetics Consortium (IHGC), Runz, H, Daly, MJ, Neale, BM, Ripatti, S, Kallela, M, Wessman, M, Palotie, A

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De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype von Shashi, V, Pena, LD, Kim, K, Burton, B, Hempel, M, Schoch, K, Walkiewicz, M, McLaughlin, HM, Cho, M, Stong, N, Hickey, SE, Shuss, CM, Undiagnosed Diseases Network, Freemark, MS, Bellet, JS, Keels, MA, Bonner, MJ, El-Dairi, M, Butler, M, Kranz, PG, Stumpel, CT, Klinkenberg, S, Oberndorff, K, Alawi, M, Santer, R, Petrovski, S, Kuismin, O, Korpi-Heikkilä, S, Pietilainen, O, Aarno, P, Kurki, MI, Hoischen, A, Need, AC, Goldstein, DB, Kortüm, F

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Analysis of protein-coding genetic variation in 60,706 humans von Lek, M, Karczewski, KJ, Minikel, EV, Samocha, KE, Banks, E, Fennell, T, O'Donnell-Luria, AH, Ware, JS, Hill, AJ, Cummings, BB, Tukiainen, T, Birnbaum, DP, Kosmicki, JA, Duncan, LE, Estrada, K, Zhao, F, Zou, J, Pierce-Hoffman, E, Berghout, J, Cooper, DN, Deflaux, N, DePristo, M, Do, R, Flannick, J, Fromer, M, Gauthier, L, Goldstein, J, Gupta, N, Howrigan, D, Kiezun, A, Kurki, MI, Moonshine, AL, Natarajan, P, Orozco, L, Peloso, GM, Poplin, R, Rivas, MA, Ruano-Rubio, V, Rose, SA, Ruderfer, DM, Shakir, K, Stenson, PD, Stevens, C, Thomas, BP, Tiao, G, Tusie-Luna, MT, Weisburd, B, Won, HH, Yu, D, Altshuler, DM, Ardissino, D, Boehnke, M, Danesh, J, Donnelly, S, Elosua, R, Florez, JC, Gabriel, SB, Getz, G, Glatt, SJ, Hultman, CM, Kathiresan, S, Laakso, M, McCarroll, S, McCarthy, MI, McGovern, D, McPherson, R, Neale, BM, Palotie, A, Purcell, SM, Saleheen, D, Scharf, JM, Sklar, P, Sullivan, PF, Tuomilehto, J, Tsuang, MT, Watkins, HC, Wilson, JG, Daly, MJ, MacArthur, DG, Exome Aggregation Consortium

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Correction: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine von Gormley, P, Anttila, V, Winsvold, BS, Palta, P, Esko, T, Pers, TH, Farh, KH, Cuenca-Leon, E, Muona, M, Furlotte, NA, Kurth, T, Ingason, A, McMahon, G, Ligthart, L, Terwindt, GM, Kallela, M, Freilinger, TM, Ran, C, Gordon, SG, Stam, AH, Steinberg, S, Borck, G, Koiranen, M, Quaye, L, Adams, HHH, Lehtimäki, T, Sarin, AP, Wedenoja, J, Hinds, DA, Buring, JE, Schürks, M, Ridker, PM, Gudlaug Hrafnsdottir, M, Stefansson, H, Ring, SM, Hottenga, JJ, Penninx, BWJH, Färkkilä, M, Artto, V, Kaunisto, M, Vepsäläinen, S, Malik, R, Heath, AC, Madden, PAF, Martin, NG, Montgomery, GW, Kurki, MI, Kals, M, Mägi, R, Pärn, K, Hämäläinen, E, Huang, H, Byrnes, AE, Franke, L, Huang, J, Stergiakouli, E, Lee, PH, Sandor, C, Webber, C, Cader, Z, Muller-Myhsok, B, Schreiber, S, Meitinger, T, Eriksson, JG, Salomaa, V, Heikkilä, K, Loehrer, E, Uitterlinden, AG, Hofman, A, Van Duijn, CM, Cherkas, L, Pedersen, LM, Stubhaug, A, Nielsen, CS, Männikkö, M, Mihailov, E, Milani, L, Göbel, H, Esserlind, AL, Francke Christensen, A, Folkmann Hansen, T, Werge, T, Kaprio, J, Aromaa, AJ, Raitakari, O, Arfan Ikram, M, Spector, T, Järvelin, MR, Metspalu, A, Kubisch, C, Strachan, DP, Ferrari, MD, Belin, AC, Dichgans, M, Wessman, M, Van den Maagdenberg, AMJM, Zwart, JA, Boomsma, DI, Davey Smith, G

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Quantifying the impact of rare coding variation across the phenotypic spectrum von Ganna, A, Satterstrom, FK, Zekavat, S, Das, I, Alfoldi, J, Kurki, MI, Thompson, WK, Byrnes, A, Karczewski, KJ, Rivas, MA, Churchhouse, C, Flannick, J, MacArthur, D, Daly, MJ, Sullivan, PF, Florez, JC, Palotie, A, Locke, AE, Borglum, A, Kathiresan, S, Neale, BM

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Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms von Van 't Hof, FNG, Ruigrok, YM, Lee, CH, Ripke, S, Anderson, G, De Andrade, M, Baas, AF, Blankensteijn, JD, Böttinger, EP, Bown, MJ, Broderick, J, Bijlenga, P, Carrell, DS, Crawford, DC, Crosslin, DR, Ebeling, C, Eriksson, JG, Fornage, M, Foroud, T, Von Und Zu Fraunberg, M, Friedrich, CM, Gaál, EI, Gottesman, O, Guo, D-C, Harrison, SC, Hernesniemi, J, Hofman, A, Inoue, I, Jääskeläinen, JE, Jones, GT, Kiemeney, LALM, Kivisaari, R, Ko, N, Koskinen, S, Kubo, M, Kullo, IJ, Kuivaniemi, H, Kurki, MI, Laakso, A, Lai, D, Leal, SM, Lehto, H, LeMaire, SA, Low, S-K, Malinowski, J, McCarty, CA, Milewicz, DM, Mosley, TH, Nakamura, Y, Nakaoka, H, Niemelä, M, Pacheco, J, Peissig, PL, Pera, J, Rasmussen-Torvik, L, Ritchie, MD, Rivadeneira, F, Van Rij, AM, Santos-Cortez, RLP, Saratzis, A, Slowik, A, Takahashi, A, Tromp, G, Uitterlinden, AG, Verma, SS, Vermeulen, SH, Wang, GT, Aneurysm Consortium, Vascular Research Consortium of New Zealand, Han, B, Rinkel, GJE, De Bakker, PIW

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Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine von Gormley, P, Anttila, V, Winsvold, BS, Palta, P, Esko, T, Pers, TH, Farh, K-H, Cuenca-Leon, E, Muona, M, Furlotte, NA, Kurth, T, McMahon, G, Ligthart, L, Terwindt, GM, Freilinger, TM, Ran, C, Gordon, SG, Stam, AH, Steinberg, S, Koiranen, M, Quaye, L, Lehtimaki, T, Sarin, A-P, Wedenoja, J, Hinds, DA, Buring, JE, Schurks, M, Hrafnsdottir, MG, Stefansson, H, Ring, SM, Hottenga, J-J, Penninx, BWJH, Farkkila, M, Artto, V, Kaunisto, M, Vepsalainen, S, Malik, R, Heath, AC, Madden, PAF, Martin, NG, Montgomery, GW, Kurki, MI, Kals, M, Magi, R, Parn, K, Hamalainen, E, Huang, H, Byrnes, AE, Franke, L, Huang, J, Stergiakouli, E, Lee, PH, Sandor, C, Webber, C, Cader, Z, Muller-Myhsok, B, Schreiber, S, Eriksson, JG, Salomaa, V, Heikkila, K, Loehrer, E, Uitterlinden, AG, Hofman, A, Van Duijn, CM, Cherkas, L, Pedersen, LM, Stubhaug, A, Nielsen, CS, Mannikko, M, Mihailov, E, Milani, L, Gobel, H, Esserlind, A-L, Christensen, AF, Hansen, TF, Werge, T, Kaprio, J, Aromaa, AJ, Raitakari, O, Ikram, MA, Spector, T, Jarvelin, M-R, Metspalu, A, Kubisch, C, Strachan, DP, Ferrari, MD, Belin, AC, Dichgans, M, Wessman, M, Van den Maagdenberg, AMJM, Zwart, J-A, Smith, GD, Stefansson, K, Eriksson, N, Daly, MJ, Neale, BM, Olesen, J, Chasman, DI, Nyholt, DR, Palotie, A

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Planck 2015 results. VII. HFI TOI and beam processing von Collaboration, Planck, Adam, R., Ade, P., Aghanim, N., Arnaud, M., Ashdown, M., Aumont, J., Baccigalupi, C., Banday, A., Barreiro, R., Bartolo, N., Battaner, E., Benabed, K., Benoît, A., Benoit-Levy, A., Bernard, J.-P., Bersanelli, M., Bertincourt, B., Bielewicz, P., Bock, J., Bonavera, L., Bond, J., Borrill, J., Bouchet, F., Boulanger, F., Bucher, M., Burigana, C., Calabrese, E., Cardoso, J.-F., Catalano, A., Challinor, A., Chamballu, A., Chary, R.-R., Chiang, H., Christensen, P., Clements, D., Colombi, S., Colombo, L., Combet, C., Couchot, F., Coulais, A., Crill, B., Curto, A., Cuttaia, F., Danese, L., Davies, R., Davis, R., de Bernardis, P., de Rosa, A., de Zotti, G., Delabrouille, J., Delouis, J.-M., Désert, F.-X., Diego, J., Dole, H., Donzelli, S., Doré, O., Douspis, M., Ducout, A., Dupac, X., Efstathiou, G., Elsner, F., Ensslin, T., Eriksen, H., Falgarone, E., Fergusson, J., Finelli, F., Forni, O., Frailis, M., Fraisse, A., Franceschi, E., Frejsel, A., Galeotta, S., Galli, S., Ganga, K., Ghosh, T., Giard, M., Giraud-Héraud, Y., Gjerløw, E., González-Nuevo, J., Górski, K., Gratton, Serge, Gruppuso, A., Gudmundsson, J., Hansen, F., Hanson, D., Harrison, D., Henrot-Versillé, S., Herranz, D., Hildebrandt, S., Hivon, E., Hobson, M. J, Holmes, W., Hornstrup, A., Hovest, W., Huffenberger, K., Hurier, G., Jaffe, A., Jaffe, T., Jones, W.

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Cherenkov probes and runaway electrons diagnostics von Kwiatkowski, R, Agostini, M, Alberti, S, Alessi, E, Allan, S, Anand, H, Auriemma, F, Bagnato, F, Boedo, J. A, Bolzonella, T, Bonanomi, N, Brida, D, Bucalossi, J, Buermans, Johan, Buratti, P, Calabró, G, Calacci, L, Carnevale, D, Carraro, L, Causa, F, Chellaï, O, Choi, D, Czarnecka, A, Molin, A. Dal, Decker, J, De Oliveira, H, Douai, D, Eich, T, Elmore, S, Faitsch, M, Fasoli, A, Feng, S, Feng, X, Fontana, M, Furno, I, Gahle, D. S, Gallo, A, Galperti, C, Gobbin, M, Goodman, T. P, Gospodarczyk, M, Gruca, M, Gyergyek, T, Harrer, G. F, Harrison, J, Havlíčková, E, Hawke, J, Hogge, J.-Ph, Hopf, C, Hubbard, A, Igochine, V, Kazantzidis, P.- V, Keeling, D, Komm, M, Kovacic, J, Kurki-Suonio, T, Lazzaro, E, Llobet, X, Macusova, E, Mantica, P, Marchetto, C, Marini, C, Matos, F, Meyer, H, Micheletti, D, Morales, J, Nespoli, F, Nocente, M, Offeddu, N, Paccagnella, R, Papp, G, Perek, A, Piovesan, P, Porte, L, Pucella, G, Puiatti, M. E, Pütterich, T, Ravensbergen, T, Reich, M, Ricci, D, Scheffer, M, Schlatter, Ch, Schneider, B. S, Schrittwieser, R, Shousha, R, Spolaore, M, Stipani, L, Biwole, A. S. Tema, Tomaž, G, Tsironis, C, Vallar, M, Verhaegh, K, Vermare, L, Villone, F, Voitsekhovitch, I, Vu, N. M. T, Weisen, H, Wilkie, G, Zisis, A, Team, EUROfusion MST

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