Divergent patterns of cytosolic TDP-43 and neuronal progranulin expression following axotomy: Implications for TDP-43 in the physiological response to neuronal injury von Moisse, Katie, Volkening, Kathryn, Leystra-Lantz, Cheryl, Welch, Ian, Hill, Tracy, Strong, Michael J

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The complement factor C5a receptor is upregulated in NFL−/− mouse motor neurons von Humayun, Saima, Gohar, May, Volkening, Kathryn, Moisse, Katie, Leystra-Lantz, Cheryl, Mepham, Jennifer, McLean, Jesse, Strong, Michael J

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Cytosolic TDP-43 expression following axotomy is associated with caspase 3 activation in NFL super(-) super(/) super(-) mice: Support for a role for TDP-43 in the physiological res... von Moisse, K, Mepham, J, Volkening, K, Welch, I, Hill, T, Strong, MJ

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How can students-as-partners work inform assessment? von Cook-Sather, A, Slates, S, Acai, A, Aquilina, S, Ajani, K, Arm, K, Besson, M, Brennan, J, Brockbank, M, Carter, K, Cassum, S, Clampton, C, Crawford, R, Curtis, N, Dhanoa, J, Diez, PA, Evans, G, Fleisig, R, Ferguson, AK, Ghias, K, Gonsalves, C, Hassan, S, Hawes, M, Jabeen, K, Jankowski, N, Khan, S, Kim, J, Klaf, S, Lesnick, A, Mahmud, O, Matiullah, J, Medland, E, Merrony, I, Mohamed, S, Moisse, K, Noel, N, Paliktzoglou, V, Parkin, J, Perkins, J, Pryor, M, Sabzwari, S, Shamsheri, T, Siddiqui, A, Signorini, A, Streule, M, Turi, S, Wilkinson, W, Wilson, M, Wilson-Scott, J, Winstone, N

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Whole-genome sequencing reveals that variants in the Interleukin 18 Receptor Accessory Protein 3′UTR protect against ALS von Eitan, Chen, Siany, Aviad, Barkan, Elad, Olender, Tsviya, van Eijk, Kristel R., Moisse, Matthieu, Farhan, Sali M. K., Danino, Yehuda M., Yanowski, Eran, Marmor-Kollet, Hagai, Rivkin, Natalia, Yacovzada, Nancy Sarah, Hung, Shu-Ting, Cooper-Knock, Johnathan, Yu, Chien-Hsiung, Louis, Cynthia, Masters, Seth L., Kenna, Kevin P., van der Spek, Rick A. A., Sproviero, William, Al Khleifat, Ahmad, Iacoangeli, Alfredo, Shatunov, Aleksey, Jones, Ashley R., Elbaz-Alon, Yael, Cohen, Yahel, Chapnik, Elik, Rothschild, Daphna, Weissbrod, Omer, Beck, Gilad, Ainbinder, Elena, Ben-Dor, Shifra, Werneburg, Sebastian, Schafer, Dorothy P., Brown, Robert H., Shaw, Pamela J., Van Damme, Philip, van den Berg, Leonard H., Phatnani, Hemali, Segal, Eran, Ichida, Justin K., Al-Chalabi, Ammar, Veldink, Jan H., Hornstein, Eran

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Whole-genome sequencing reveals that variants in the Interleukin 18 Receptor Accessory Protein 3 ' UTR protect against ALS von Eitan, Chen, Siany, Aviad, Barkan, Elad, Olender, Tsviya, van Eijk, Kristel R, Moisse, Matthieu, Farhan, Sali M.K, Danino, Yehuda M, Yanowski, Eran, Marmor-Kollet, Hagai, Rivkin, Natalia, Yacovzada, Nancy Sarah, Hung, Shu-Ting, Cooper-Knock, Johnathan, Yu, Chien-Hsiung, Louis, Cynthia, Masters, Seth L, Kenna, Kevin P, van der Spek, Rick A.A, Sproviero, William, Al Khleifat, Ahmad, Iacoangeli, Alfredo, Shatunov, Aleksey, Jones, Ashley R, Elbaz-Alon, Yael, Cohen, Yahel, Chapnik, Elik, Rothschild, Daphna, Weissbrod, Omer, Beck, Gilad, Ainbinder, Elena, Ben-Dor, Shifra, Werneburg, Sebastian, Schafer, Dorothy P, Brown, Robert H, Shaw, Pamela J, Van Damme, Philip, van den Berg, Leonard H, Phatnani, Hemali, Segal, Eran, Ichida, Justin K, Al-Chalabi, Ammar, Veldink, Jan H, Hornstein, Eran

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CRISPR/Cas9 screen in human iPSC-derived cortical neurons identifies NEK6 as a novel disease modifier of C9orf72 poly(PR) toxicity von Guo, W, Wang, H, Kumar Tharkeshwar, A, Couthouis, J, Braems, E, Masrori, P, Van Schoor, E, Fan, Y, Ahuja, K, Moisse, M, Jacquemyn, M, Furtado Madeiro da Costa, R, Gajjar, M, Balusu, S, Tricot, T, Fumagalli, L, Hersmus, N, Janky, R, Impens, Francis, Vanden Berghe, P, Ho, R, Thal, DR, Vandenberghe, R, Hegde, ML, Chandran, S, De Strooper, B, Daelemans, D, Van Damme, P, Van Den Bosch, L, Verfaillie, C

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Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS von Hop, Paul J, Zwamborn, Ramona A.J, Hannon, Eilis, Shireby, Gemma L, Nabais, Marta F, Walker, Emma M, van Rheenen, Wouter, van Vugt, Joke J.F.A, Dekker, Annelot M, Westeneng, Henk-Jan, Tazelaar, Gijs H.P, van Eijk, Kristel R, Moisse, Matthieu, Baird, Denis, Al Khleifat, Ahmad, Iacoangeli, Alfredo, Ticozzi, Nicola, Ratti, Antonia, Cooper-Knock, Jonathan, Morrison, Karen E, Shaw, Pamela J, Basak, A. Nazli, Chio, Adriano, Calvo, Andrea, Moglia, Cristina, Canosa, Antonio, Brunetti, Maura, Grassano, Maurizio, Gotkine, Marc, Lerner, Yossef, Zabari, Michal, Vourc'h, Patrick, Corcia, Philippe, Couratier, Philippe, Pardina, Jesus S. Mora, Salas, Teresa, Dion, Patrick, Ross, Jay P, Henderson, Robert D, Mathers, Susan, McCombe, Pamela A, Needham, Merrilee, Nicholson, Garth, Rowe, Dominic B, Pamphlett, Roger, Mather, Karen A, Sachdev, Perminder S, Furlong, Sarah, Garton, Fleur C, Henders, Anjali K, Lin, Tian, Ngo, Shyuan T, Steyn, Frederik J, Wallace, Leanne, Williams, Kelly L, Neto, Miguel Mitne, Cauchi, Ruben J, Blair, Ian P, Kiernan, Matthew C, Drory, Vivian, Povedano, Monica, de Carvalho, Mamede, Pinto, Susana, Weber, Markus, Rouleau, Guy A, Silani, Vincenzo, Landers, John E, Shaw, Christopher E, Andersen, Peter M, McRae, Allan F, van Es, Michael A, Pasterkamp, R. Jeroen, Wray, Naomi R, McLaughlin, Russell L, Hardiman, Orla, Kenna, Kevin P, Tsai, Ellen, Runz, Heiko, Al-Chalabi, Ammar, van den Berg, Leonard H, Van Damme, Philip, Mill, Jonathan, Veldink, Jan H

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Meta-analysis of epigenome-wide association studies in neonates reveals widespread differential DNA methylation associated with birthweight von Kupers, LK, Monnereau, C, Sharp, GC, Salas, LA, Page, CM, Reese, SE, Wilcox, AJ, Starling, AP, Novoloaca, A, Lent, S, Roy, R, Hoyo, C, Breton, C, Allard, C, Bakulski, KM, Holloway, JW, Everson, TM, Xu, C-J, Van der Plaat, DA, Wielscher, M, Rezwan, F, Van Dongen, J, Langie, SAS, Richardson, TG, Magnus, MC, Nohr, EA, Xu, Z, Duijts, L, Zhao, S, Plusquin, M, Solomon, O, Jima, DD, Gao, L, Bustamante, M, Perron, P, Wright, RO, Hertz-Picciotto, I, Zhang, H, Karagas, MR, Gehring, U, Marsit, CJ, Beilin, LJ, Jarvelin, M-R, Bergstrom, A, Ewart, S, Villa, PM, Moore, SE, Willemsen, G, Standaert, ARL, Haberg, SE, Sorensen, TIA, Taylor, JA, Raikkonen, K, Yang, I, Nawrot, TS, Silver, MJ, Richiardi, L, Litonjua, AA, Eskenazi, B, Huen, K, Mbarek, H, Maguire, RL, Vrijheid, M, Baccarelli, AA, Croen, LA, Karmaus, W, De Vries, M, Sebert, S, Kere, J, Karlsson, R, Arshad, SH, Hamalainen, E, Routledge, MN, Boomsma, D, Feinberg, AP, Newschaffer, CJ, Govarts, E, Moisse, M, Melen, E, Prentice, AM, Kajantie, E, Almqvist, C, Oken, E, Dabelea, D, Boezen, HM, Wright, RJ, Trevisi, L, Hivert, M-F, Sunyer, J, Munthe-Kaas, MC, Corpeleijn, E, Holland, N, Herceg, Z, Binder, EB, Jaddoe, VWV, Lie, RT, London, SJ, Lawlor, DA, Relton, CL, Snieder, H

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Whole-genome sequencing reveals that variants in the Interleukin 18 Receptor Accessory Protein 3'UTR protect against ALS von Eitan, Chen, Siany, Aviad, Barkan, Elad, Olender, Tsviya, van Eijk, Kristel R, Moisse, Matthieu, Farhan, Sali M K, Danino, Yehuda M, Yanowski, Eran, Marmor-Kollet, Hagai, Rivkin, Natalia, Yacovzada, Nancy Sarah, Hung, Shu-Ting, Cooper-Knock, Johnathan, Yu, Chien-Hsiung, Louis, Cynthia, Masters, Seth L, Kenna, Kevin P, van der Spek, Rick A A, Sproviero, William, Al Khleifat, Ahmad, Iacoangeli, Alfredo, Shatunov, Aleksey, Jones, Ashley R, Elbaz-Alon, Yael, Cohen, Yahel, Chapnik, Elik, Rothschild, Daphna, Weissbrod, Omer, Beck, Gilad, Ainbinder, Elena, Ben-Dor, Shifra, Werneburg, Sebastian, Schafer, Dorothy P, Brown, Jr, Robert H, Shaw, Pamela J, Van Damme, Philip, van den Berg, Leonard H, Phatnani, Hemali, Segal, Eran, Ichida, Justin K, Al-Chalabi, Ammar, Veldink, Jan H, Hornstein, Eran

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Genetic modifiers of CHEK21100delC-associated breast cancer risk von Muranen, Taru A, Greco, Dario, Blomqvist, Carl, Aittomäki, Kristiina, Khan, Sofia, Hogervorst, Frans, Verhoef, Senno, Pharoah, Paul D.P, Dunning, Alison M, Shah, Mitul, Luben, Robert, Bojesen, Stig E, Nordestgaard, Børge G, Schoemaker, Minouk, Swerdlow, Anthony, García-Closas, Montserrat, Figueroa, Jonine, Dörk, Thilo, Bogdanova, Natalia V, Hall, Per, Li, Jingmei, Khusnutdinova, Elza, Bermisheva, Marina, Kristensen, Vessela, Borresen-Dale, Anne-Lise, Investigators, Nbcs, Peto, Julian, Dos Santos Silva, Isabel, Couch, Fergus J, Olson, Janet E, Hillemans, Peter, Park-Simon, Tjoung-Won, Brauch, Hiltrud, Hamann, Ute, Burwinkel, Barbara, Marme, Frederik, Meindl, Alfons, Schmutzler, Rita K, Cox, Angela, Cross, Simon S, Sawyer, Elinor J, Tomlinson, Ian, Lambrechts, Diether, Moisse, Matthieu, Lindblom, Annika, Margolin, Sara, Hollestelle, Antoinette, Martens, John W.M, Fasching, Peter A, Beckmann, Matthias W, Andrulis, Irene L, Knight, Julia A, Investigators, kConFab Aocs, Anton-Culver, Hoda, Ziogas, Argyrios, Giles, Graham G, Milne, Roger L, Brenner, Hermann, Arndt, Volker, Mannermaa, Arto, Kosma, Veli-Matti, Chang-Claude, Jenny, Rudolph, Anja, Devilee, Peter, Seynaeve, Caroline, Hopper, John L, Southey, Melissa C, John, Esther M, Whittemore, Alice S, Bolla, Manjeet K, Wang, Qin, Michailidou, Kyriaki, Dennis, Joe, Easton, Douglas F, Schmidt, Marjanka K, Nevanlinna, Heli

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Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types von Kote-Jarai, Z, Lawrenson, K, Ramus, S. J, Michael, A, Gentry-Maharaj, A, Wolk, A, Wu, A. H, Lindblom, A, Swerdlow, A, Ekici, A. B, Nordestgaard, B. G, Blomqvist, C, Phelan, C, McLean, C, Cybulski, C, Maier, C, Teerlink, C. C, Cramer, Daniel William, Neal, D. E, Wokozorczyk, D, Yannoukakos, D, Sawyer, E. J, Bandera, E. V, Goode, E. L, Khusnutdinova, E, Song, F, Hamdy, F. C, Giles, G. G, Wildiers, H, Ulmer, H.-U, Pandha, H, Nevanlinna, H, Brenner, H, Brauch, H, Anton-Culver, H, Song, H, Lim, H.-Y, Campbell, I, Vergote, I, Stanford, J. L, Benitez, J, Permuth, J. B, Chang-Claude, J, Dennis, J, Kupryjanczyk, J, Figueroa, J, Cunningham, J. M, Pow-Sang, J, Lu, K. H, Herkommer, K, Matsuo, K, Muir, K, Chen, K, Moysich, K. B, Kiemeney, L. A, Massuger, L. F. A. G, Teixeira, M. R, Goodman, M. T, Rossing, M. A, Southey, M. C, Lush, M, Rahman, N, Orr, N, Wentzensen, N, Pashayan, N, Peterlongo, P, Brennan, P, Broberg, P, Li, Q, Kopperud, R. K, Travis, R. C, Benlloch, S, Olson, S. H, Tworoger, Shelley Slate, Berndt, S, Thibodeau, S. N, Bojesen, S. E, Kjaer, S. K, Pejovic, T, Do rk, T, Wahlfors, T, Key, T. J, Edwards, T. L, Hamann, U, Kosma, V.-M, Setiawan, V. W, Kristensen, V, Arndt, V, Zheng, W, Kluzniak, W, Shu, X.-O, Freedman, M. L, Berchuck, A, Spurdle, A, Sellers, T. A, Hunter, David J, Kraft, Peter Elias, Hall, P, Eeles, R, Lambrechts, D

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Genetic modifiers of CHEK21100delC-associated breast cancer risk von Muranen, Taru A, Greco, Dario, Blomqvist, Carl, Aittomäki, Kristiina, Khan, Sofia, Hogervorst, Frans, Verhoef, Senno, Pharoah, Paul DP, Dunning, Alison M, Shah, Mitul, Luben, Robert, Bojesen, Stig E, Nordestgaard, Børge G, Schoemaker, Minouk, Swerdlow, Anthony, García-Closas, Montserrat, Figueroa, Jonine, Dörk, Thilo, Bogdanova, Natalia V, Hall, Per, Li, Jingmei, Khusnutdinova, Elza, Bermisheva, Marina, Kristensen, Vessela, Borresen-Dale, Anne-Lise, NBCS Investigators, Peto, Julian, Dos Santos Silva, Isabel, Couch, Fergus J, Olson, Janet E, Hillemans, Peter, Park-Simon, Tjoung-Won, Brauch, Hiltrud, Hamann, Ute, Burwinkel, Barbara, Marme, Frederik, Meindl, Alfons, Schmutzler, Rita K, Cox, Angela, Cross, Simon S, Sawyer, Elinor J, Tomlinson, Ian, Lambrechts, Diether, Moisse, Matthieu, Lindblom, Annika, Margolin, Sara, Hollestelle, Antoinette, Martens, John WM, Fasching, Peter A, Beckmann, Matthias W, Andrulis, Irene L, Knight, Julia A, kConFab/AOCS Investigators, Anton-Culver, Hoda, Ziogas, Argyrios, Giles, Graham G, Milne, Roger L, Brenner, Hermann, Arndt, Volker, Mannermaa, Arto, Kosma, Veli-Matti, Chang-Claude, Jenny, Rudolph, Anja, Devilee, Peter, Seynaeve, Caroline, Hopper, John L, Southey, Melissa C, John, Esther M, Whittemore, Alice S, Bolla, Manjeet K, Wang, Qin, Michailidou, Kyriaki, Dennis, Joe, Easton, Douglas F, Schmidt, Marjanka K, Nevanlinna, Heli

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Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2 von Maguire, S, Johnson, N, Hopper, J. L, Apicella, C, Stone, J, Broeks, A, Gibson, L, Warren, H, Sawyer, E, Tomlinson, I, Kerin, M. J, Marme, F, Truong, T, Bojesen, S. E, Nordestgaard, B. G, Anton-Culver, H, Brenner, H, Arndt, V, Brauch, H, Justenhoven, C, Bruning, T, Ko, Y.-D, Aittomaki, K, Khan, S, Lindblom, A, Margolin, S, Mannermaa, A, Hartikainen, J. M, Chenevix-Trench, G, Lambrechts, D, Flesch-Janys, D, Peterlongo, P, Couch, F. J, Vachon, C, McLean, C, Haiman, C. A, Henderson, B. E, Simard, J, Goldberg, M. S, Kristensen, V, Nord, S, Zheng, W, Shrubsole, M, Pylkas, K, Jukkola-Vuorinen, A, Knight, J. A, Glendon, G, Devilee, P, Tollenaar, R. A. E. M, Van Asperen, C. J, Figueroa, J, Chanock, S. J, Lissowska, J, Darabi, H, Klevebring, D, Hollestelle, A, van Deurzen, C. H. M, Hall, P, Cross, S. S, Dunning, A. M, Perkins, B. J, Jakubowska, A, Jaworska-Bieniek, K, Durda, K, Schmutzler, R. K, Olswold, C, Toland, A. E, Muir, K, Stewart-Brown, S, Siriwanarangsan, P, Matsuo, K, Ito, H, Iwata, H, Van Den Berg, D, Stram, D. O, Teo, S. H, Ikram, M. K, Shu, X.-O, Gao, Y.-T, Cai, H, Kang, D, Noh, D.-Y, Lee, S. C, Sangrajrang, S, Shen, C.-Y, Blot, W, Signorello, L. B, Bayes, C, Healey, C. S, Gonzalez-Neira, A, Pita, G, Alonso, M. R, Herrero, D, Vincent, D, Lindstrom, S, Dennis, J, Bolla, M. K, Easton, D. F, dos Santos Silva, I,

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Genetic variability in sporadic amyotrophic lateral sclerosis von Van Daele, S.H, Moisse, M, van Vugt, J.J.F.A, Zwamborn, R.A.J, van der Spek, R, van Rheenen, W, Van Eijk, K, Kenna, K, Corcia, P, Vourc'h, P, Couratier, P, Hardiman, O, McLaughin, R, Gotkine, M, Drory, V, Ticozzi, N, Silani, V, Ratti, A, de Carvalho, M, Mora Pardina, J.S, Povedano, M, Andersen, P.M, Weber, M, Başak, N.A, Shaw, C, Shaw, P.J, Morrison, K.E, Landers, J.E, Glass, J.D, van Es, M.A, van den Berg, L.H, Al-Chalabi, A, Veldink, J, Van Damme, P

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Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence data von Al Khleifat, A, Iacoangeli, A, Jones, A.R, van Vugt, J.J.F.A, Moisse, M, Shatunov, A, Zwamborn, R.A.J, van der Spek, R.A.A, Cooper-Knock, J, Topp, S, van Rheenen, W, Kenna, B, Van Eijk, K.R, Kenna, K, Byrne, R, López, V, Opie-Martin, S, Vural, A, Campos, Y, Weber, M, Smith, B, Fogh, I, Silani, V, Morrison, K.E, Dobson, R, van Es, M.A, McLaughlin, R.L, Vourc’h, P, Chio, A, Corcia, P, de Carvalho, M, Gotkine, M, Panades, M.P, Mora, J.S, Shaw, P.J, Landers, J.E, Glass, J.D, Shaw, C.E, Basak, N, Hardiman, O, Robberecht, W, Van Damme, P, van den Berg, L.H, Veldink, J.H, Al-Chalabi, A

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Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis von Al Khleifat, A, Iacoangeli, A, van Vugt, J.J.F.A, Bowles, H, Moisse, M, Zwamborn, R.A.J, van der Spek, R.A.A, Shatunov, A, Cooper-Knock, J, Topp, S, Byrne, R, Gellera, C, López, V, Jones, A.R, Opie-Martin, S, Vural, A, Campos, Y, van Rheenen, W, Kenna, B, Van Eijk, K.R, Kenna, K, Weber, M, Smith, B, Fogh, I, Silani, V, Morrison, K.E, Dobson, R, van Es, M.A, McLaughlin, R.L, Vourc’h, P, Chio, A, Corcia, P, de Carvalho, M, Gotkine, M, Panades, M.P, Mora, J.S, Shaw, P.J, Landers, J.E, Glass, J.D, Shaw, C.E, Basak, N, Hardiman, O, Robberecht, W, Van Damme, P, van den Berg, L.H, Veldink, J.H, Al-Chalabi, A

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Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence data von Al Khleifat, A, Iacoangeli, A, Jones, AR, van Vugt, JJFA, Moisse, M, Shatunov, A, Zwamborn, RAJ, van der Spek, RAA, Cooper-Knock, J, Topp, S, van Rheenen, W, Kenna, B, Van Eijk, KR, Kenna, K, Byrne, R, López, V, Opie-Martin, S, Vural, A, Campos, Y, Weber, M, Smith, B, Fogh, I, Silani, V, Morrison, KE, Dobson, R, van Es, MA, McLaughlin, RL, Vourc’h, P, Chio, A, Corcia, P, de Carvalho, M, Gotkine, M, Panades, MP, Mora, JS, Shaw, PJ, Landers, JE, Glass, JD, Shaw, CE, Basak, N, Hardiman, O, Robberecht, W, Van Damme, P, van den Berg, LH, Veldink, JH, Al-Chalabi, A

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The effect of SMN gene dosage on ALS risk and disease severity von Moisse, M, Zwamborn, R.A.J, Vugt, J, Spek, R, Rheenen, W, Kenna, B, Van Eijk, K, Kenna, K, Corcia, P, Couratier, P, Vourc'h, P, Hardiman, O, McLaughin, R, Gotkine, M, Drory, V, Ticozzi, N, Silani, V, Carvalho, M, Mora Pardina, J.S, Povedano, M, Andersen, P.M, Weber, M, Başak, N.A, Chen, X, Eberle, M.A, Al‐Chalabi, A, Shaw, C, Shaw, P.J, Morrison, K.E, Landers, J.E, Glass, J.D, Robberecht, W, Es, M, Berg, L, Veldink, J, Van Damme, P

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Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology von Bakker, MK, Westra, H-J, Deelen, P, Dolzhenko, E, Gawor, K, Tazelaar, GHP, Doherty, M, Al Khleifat, A, Shatunov, A, Smith, BN, Shaw, PJ, Sendtner, M, Fogh, I, Lauria, G, Sproviero, D, D’Alfonso, S, Sorarù, G, Siciliano, G, Padovani, A, Moglia, C, Brunetti, M, Lerner, Y, Zabari, M, Gotkine, M, Millecamps, S, Meininger, V, Rojas-García, R, Dion, PA, Ross, JP, Durr, A, Payan, CAM, Wood, NW, Franke, A, Ripke, S, Whiteman, DC, Gerardi, F, Cotelli, MS, Rinaldi, F, Guaita, MC, Ceroni, M, Ferrarese, C, Delodovici, ML, Vasta, R, Bombaci, A, Casale, F, Fuda, G, Salamone, P, Iazzolino, B, Peotta, L, Palumbo, F, Gallone, S, Sbaiz, L, Mauro, A, De Marchi, F, Gionco, M, Pignatta, P, De Mattei, M, Papurello, DM, Gusmaroli, G, Comi, C, Ruiz, L, Di Vito, N, Meineri, P, Ghiglione, P, Dotta, M, Di Sapio, A, Tiloca, C, Gagliardi, S, Ferlini, A, Mundi, C, Zarrelli, M, Cauchi, RJ, Wiedau-Pazos, M, Lomen-Hoerth, C, van Deerlin, VM, Jörk, A, Graff, C, Fominykh, V, Ataulina, A, Koritnik, B, Zidar, J, Glavač, D, Drory, V, McCombe, PA, Ngo, ST, Pamphlett, R, Williams, KL, Wallace, L, Brown, RH, Andersen, PM, van Es, MA, Fan, D, Garton, FC, Davey Smith, G, Mill, J, Hardiman, O, Wray, NR, Franke, L, van den Berg, LH, Veldink, JH

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