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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Genetic variation among 82 pharmacogenes: The PGRNseq data from the eMERGE network von Bush, WS, Crosslin, DR, Owusu-Obeng, A, Wallace, J, Almoguera, B, Basford, MA, Bielinski, SJ, Carrell, DS, Connolly, JJ, Crawford, D, Doheny, KF, Gallego, CJ, Gordon, AS, Keating, B, Kirby, J, Kitchner, T, Manzi, S, Mejia, AR, Pan, V, Perry, CL, Peterson, JF, Prows, CA, Ralston, J, Scott, SA, Scrol, A, Smith, M, Stallings, SC, Veldhuizen, T, Wolf, W, Volpi, S, Wiley, K, Li, R, Manolio, T, Bottinger, E, Brilliant, MH, Carey, D, Chisholm, RL, Chute, CG, Haines, JL, Hakonarson, H, Harley, JB, Holm, IA, Kullo, IJ, Jarvik, GP, Larson, EB, McCarty, CA, Williams, MS, Denny, JC, Rasmussen-Torvik, LJ, Roden, DM, Ritchie, MD

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Analysis of the RELN gene as a genetic risk factor for autism von Skaar, D A, Shao, Y, Haines, J L, Stenger, J E, Jaworski, J, Martin, E R, DeLong, G R, Moore, J H, McCauley, J L, Sutcliffe, J S, Ashley-Koch, A E, Cuccaro, M L, Folstein, S E, Gilbert, J R, Pericak-Vance, M A

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HLA-DR2 Dose Effect on Susceptibility to Multiple Sclerosis and Influence on Disease Course von Barcellos, L.F., Oksenberg, J.R., Begovich, A.B., Martin, E.R., Schmidt, S., Vittinghoff, E., Goodin, D.S., Pelletier, D., Lincoln, R.R., Bucher, P., Swerdlin, A., Pericak-Vance, M.A., Haines, J.L., Hauser, S.L.

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Clinical characteristics of African Americans vs Caucasian Americans with multiple sclerosis von CREE, B. A. C, KHAN, O, HAINES, J. L, PERICAK-VANCE, M, DELOA, C, OKSENBERG, J. R, HAUSER, S. L, BOURDETTE, D, GOODIN, D. S, COHEN, J. A, MARRIE, R. A, GLIDDEN, D, WEINSTOCK-GUTTMAN, B, REICH, D, PATTERSON, N

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Genetics and pathogenesis of multiple sclerosis von Zuvich, R.L, McCauley, J.L, Pericak-Vance, M.A, Haines, J.L

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Paraoxonase cluster polymorphisms are associated with sporadic ALS von SAEED, M, SIDDIQUE, N, HUNG, W.-Y, USACHEVA, E, LIU, E, SUFIT, R. L, HELLER, S. L, HAINES, J. L, PERICAK-VANCE, M, SIDDIQUE, T

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Partial and generalized epilepsy with febrile seizures plus and a novel SCN1A mutation von ABOU-KHALIL, B, GE, Q, DESAI, R, RYTHER, R, BAZYK, A, BAILEY, R, HAINES, J. L, SUTCLIFFE, J. S, GEORGE, A. L

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Drug Transporter and Metabolizing Enzyme Gene Variants and Nonnucleoside Reverse-Transcriptase Inhibitor Hepatotoxicity von Ritchie, Marylyn D., Haas, David W., Motsinger, Alison A., Donahue, John P., Erdem, Huso, Raffanti, Stephen, Rebeiro, Peter, George, Alfred L., Kim, Richard B., Haines, Jonathan L., Sterling, Timothy R.

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Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP) von Reitz, C, Tosto, G, Vardarajan, B, Rogaeva, E, Ghani, M, Rogers, R S, Conrad, C, Haines, J L, Pericak-Vance, M A, Fallin, M D, Foroud, T, Farrer, L A, Schellenberg, G D, George-Hyslop, P S, Mayeux, R

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Gene Dose of Apolipoprotein E Type 4 Allele and the Risk of Alzheimer's Disease in Late Onset Families von Corder, E. H., Saunders, A. M., Strittmatter, W. J., Schmechel, D. E., Gaskell, P. C., Small, G. W., Roses, A. D., Haines, J. L., Pericak-Vance, M. A.

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A Genomewide Scan Identifies Novel Early-Onset Primary Open-Angle Glaucoma Loci on 9q22 and 20p12 von Wiggs, J.L., Lynch, S., Ynagi, G., Maselli, M., Auguste, J., Del Bono, E.A., Olson, L.M., Haines, J.L.

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Apolipoprotein E controls the risk and age at onset of Parkinson disease von LI, Y. J, HAUSER, M. A, PAHWA, R, STERN, M. B, HINER, B. C, JANKOVIC, J, GOETZ, C. G, SMALL, G. W, MASTAGLIA, F, HAINES, J. L, PERICAK-VANCE, M. A, VANCE, J. M, SCOTT, W. K, MARTIN, E. R, BOOZE, M. W, QIN, X. J, WALTER, J. W, NANCE, M. A, HUBBLE, J. P, KOLLER, W. C

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Genetic basis for clinical expression in multiple sclerosis von BARCELLOS, L. F, OKSENBERG, J. R, HAUSER, S. L, GREEN, A. J, BUCHER, P, RIMMLER, J. B, SCHMIDT, S, GARCIA, M. E, LINCOLN, R. R, PERICAK-VANCE, M. A, HAINES, J. L

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Examination of association of genes in the serotonin system to autism von Anderson, B. M., Schnetz-Boutaud, N. C., Bartlett, J., Wotawa, A. M., Wright, H. H., Abramson, R. K., Cuccaro, M. L., Gilbert, J. R., Pericak-Vance, M. A., Haines, J. L.

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Head injury and the risk of AD in the MIRAGE study von GUO, Z, CUPPLES, L. A, JOHNSON, K, GO, R. C, GROWDON, J. H, HAINES, J. L, KUKULL, W. A, FARRER, L. A, KURZ, A, AUERBACH, S. H, VOLICER, L, CHUI, H, GREEN, R. C, SADOVNICK, A. D, DUARA, R, DECARLI, C

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ApoE-4 and age at onset of Alzheimer's disease : The NIMH genetics initiative von BLACKER, D, HAINES, J. L, ALBERT, M. S, TANZI, R, RODES, L, TERWEDOW, H, GO, R. C. P, HARRELL, L. E, PERRY, R. T, BASSETT, S. S, CHASE, G, MEYERS, D

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GWAS analysis implicates NF-κB-mediated induction of inflammatory T cells in multiple sclerosis von Hussman, J P, Beecham, A H, Schmidt, M, Martin, E R, McCauley, J L, Vance, J M, Haines, J L, Pericak-Vance, M A

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Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease von Corder, E. H, Saunders, A. M, Risch, N. J, Strittmatter, W. J, Schmechel, D. E, Gaskell, P. C, Rimmler, J. B, Locke, P. A, Conneally, P. M, Schmader, K. E, Small, G. W, Roses, A. D, Haines, J. L, Pericak-Vance, M. A

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Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism von McCauley, J.L., Olson, L.M., Dowd, M., Amin, T., Steele, A., Blakely, R.D., Folstein, S.E., Haines, J.L., Sutcliffe, J.S.

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