Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis von Kwiatkowski, T.J. Jr, Bosco, D.A, LeClerc, A.L, Tamrazian, E, Vanderburg, C.R, Russ, C, Davis, A, Gilchrist, J, Kasarskis, E.J, Munsat, T, Valdmanis, P, Rouleau, G.A, Hosler, B.A, Cortelli, P, de Jong, P.J, Yoshinaga, Y, Haines, J.L, Pericak-Vance, M.A, Yan, J, Ticozzi, N, Siddique, T, McKenna-Yasek, D, Sapp, P.C, Horvitz, H.R, Landers, J.E, Brown, R.H. Jr

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Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort von TICOZZI, N, SILANI, V, BROWN, R. H, LANDERS, J. E, LECLERC, A. L, KEAGLE, P, GELLERA, C, RATTI, A, TARONI, F, KWIATKOWSKI, T. J, MCKENNA-YASEK, D. M, SAPP, P. C

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Mutational analysis reveals the FUS homolog TAF15 as a candidate gene for familial amyotrophic lateral sclerosis von Ticozzi, N., Vance, C., LeClerc, A.L., Keagle, P., Glass, J.D., McKenna-Yasek, D., Sapp, P.C., Silani, V., Bosco, D.A., Shaw, C.E., Brown Jr, R.H., Landers, J.E.

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Using high-throughput SNP technologies to study cancer von Engle, L J, Simpson, C L, Landers, J E

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A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALS von WILLS, A.-M, CRONIN, S, ROULEAU, G. A, FISHER, E. M. C, SHAW, P. J, MORRISON, K. E, PAMPHLETT, R, VAN DEN BERG, L. H, FIGLEWICZ, D. A, ANDERSEN, P. M, AL-CHALABI, A, HARDIMAN, O, SLOWIK, A, PURCELL, S, LANDERS, J. E, BROWN, Rh, KASPERAVICIUTE, D, VAN ES, M. A, MORAHAN, J. M, VALDMANIS, P. N, MEININGER, V, MELKI, J, SHAW, C. E

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New VAPB deletion variant and exclusion of VAPB mutations in familial ALS von LANDERS, J. E, LECLERC, A. L, AL-CHALABI, A, SHAW, C. E, LEIGH, P. N, RODRIGUEZ-LEYZA, I, MCKENNA-YASEK, D, SAPP, P. C, BROWN, R. H, SHI, L, VIRKUD, A, CHO, T, MAXWELL, M. M, HENRY, A. F, POLAK, M, GLASS, J. D, KWIATKOWSKI, T. J

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Paraoxonase 1 (PON1) organophosphate hydrolysis is not reduced in ALS von WILLS, A.-M, LANDERS, J. E, ZHANG, H, RICHTER, R. J, CARAGANIS, A. J, CUDKOWICZ, M. E, FURLONG, C. E, BROWN, R. H

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Motoneuron-specific NR3B gene : No association with ALS and evidence for a common null allele von NIEMANN, S, LANDERS, J. E, CHURCHILL, M. J, HOSLER, B, SAPP, P, SPEED, W. C, LAHN, B. T, KIDD, K. K, BROWN, R. H, HAYASHI, Y

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Translational enhancement of mdm2 oncogene expression in human tumor cells containing a stabilized wild-type p53 protein von LANDERS, J. E, CASSEL, S. L, GEORGE, D. L

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A loss of FUS/TLS function leads to impaired cellular proliferation von Ward, C L, Boggio, K J, Johnson, B N, Boyd, J B, Douthwright, S, Shaffer, S A, Landers, J E, Glicksman, M A, Bosco, D A

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Physical and functional interaction between wild-type p53 and mdm2 proteins von HAINES, D. S, LANDERS, J. E, ENGLE, L. J, GEORGE, D. L

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Isolation of a Candidate Gene for Choroideremia von Merry, Diane E., Janne, Pasi A., Landers, John E., Lewis, Richard Alan, Nussbaum, Robert L.

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A novel phosphorylation site mutation in profilin 1 revealed in a large screen of US, Nordic, and German amyotrophic lateral sclerosis/frontotemporal dementia cohorts von Ingre, Caroline, Landers, John E, Rizik, Naji, Volk, Alexander E, Akimoto, Chizuru, Birve, Anna, Hübers, Annemarie, Keagle, Pamela J, Piotrowska, Katarzyna, Press, Rayomand, Andersen, Peter Munch, Ludolph, Albert C, Weishaupt, Jochen H

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The role of de novo mutations in the development of amyotrophic lateral sclerosis von Doormaal, Perry T.C., Ticozzi, Nicola, Weishaupt, Jochen H., Kenna, Kevin, Diekstra, Frank P., Verde, Federico, Andersen, Peter M., Dekker, Annelot M., Tiloca, Cinzia, Marroquin, Nicolai, Overste, Daniel J., Pensato, Viviana, Nürnberg, Peter, Pulit, Sara L., Schellevis, Raymond D., Calini, Daniela, Altmüller, Janine, Francioli, Laurent C., Muller, Bernard, Castellotti, Barbara, Motameny, Susanne, Ratti, Antonia, Wolf, Joachim, Gellera, Cinzia, Ludolph, Albert C., den Berg, Leonard H., Kubisch, Christian, Landers, John E., Veldink, Jan H., Silani, Vincenzo, Volk, Alexander E.

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A loss of FUS/TLS function leads to impaired cellular proliferation von Ward, C L, Boggio, K J, Johnson, B N, Boyd, J B, Douthwright, S, Shaffer, S A, Landers, J E, Glicksman, M A, Bosco, D A

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ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function von De Majo, M, Topp, SD, Smith, BN, Nishimura, AL, Chen, HJ, Soragia Gkazi, A, Wong, CH, Vance, C, Bass, F, Ten Ashbroek, ALMA, Kenna, KP, Ticozzi, N, Garcia Redondo, A, Esteban-Perez, J, Tiloca, C, Verde, F, Duga, S, Morrison, KE, Shaw, PJ, Kirby, J, Turner, MR, Talbot, K, Hardiman, O, Glass, JD, De Belleroche, JS, Gellera, C, Ratti, A, Al-Chalabi, A, Silani, V, Landers, JE, Shaw, C

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Social Support in Marriage von Dehle, Crystal, Larsen, Debra, Landers, John E.

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Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis von Smith, BN, Topp, SD, Fallini, C, Shibata, H, Chen, H-J, Troakes, C, King, A, Ticozzi, N, Kenna, KP, Soragia-Gkazi, A, Miller, JW, Sato, A, Dias, DM, Jeon, M, Vance, C, Wong, CH, De Majo, M, Kattuah, W, Mitchell, JC, Scotter, EL, Parkin, NW, Sapp, PC, Nolan, M, Nestor, PJ, Simpson, M, Weale, M, Lek, M, Baas, F, De Jong, JMV, Ten Asbroek, ALMA, Garcia Redondo, A, Esteban-Perez, J, Tiloca, C, Verde, F, Duga, S, Leigh, N, Pall, H, Morrison, KE, Al-Chalabi, A, Shaw, PJ, Kirby, J, Turner, MR, Talbot, K, Hardiman, O, Glass, JD, De Belleroche, J, Maki, M, Moss, SE, Miller, C, Gellera, C, Ratti, A, Al-Sarraj, S, Brown, RH, Silani, V, Landers, JE, Shaw, CE

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Genome-wide structural variant analysis identifies risk loci for non-Alzheimer's dementias von Kaivola, K, Chia, R, Ding, J, Rasheed, M, Fujita, M, Menon, V, Walton, RL, Collins, RL, Billingsley, K, Brand, H, Talkowski, M, Zhao, X, Dewan, R, Stark, A, Ray, A, Solaiman, S, Alvarez Jerez, P, Malik, L, Dawson, TM, Rosenthal, LS, Albert, MS, Pletnikova, O, Troncoso, JC, Masellis, M, Keith, J, Black, SE, Ferrucci, L, Resnick, SM, Tanaka, T, American Genome Center, International LBD Genomics Consortium, International ALS/FTD Consortium, PROSPECT Consortium, Topol, E, Torkamani, A, Tienari, P, Foroud, TM, Ghetti, B, Landers, JE, Ryten, M, Morris, HR, Hardy, JA, Mazzini, L, D'Alfonso, S, Moglia, C, Calvo, A, Serrano, GE, Beach, TG, Ferman, T, Graff-Radford, NR, Boeve, BF, Wszolek, ZK, Dickson, DW, Chiò, A, Bennett, DA, De Jager, PL, Ross, OA, Dalgard, CL, Gibbs, JR, Traynor, BJ, Scholz, SW

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Using high-throughput SNP technologies to study cancer: Polymorphisms and cancer von ENGLE, L. J, SIMPSON, C. L, LANDERS, J. E

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