Association of rare missense variants in the second intracellular loop of Na V 1.7 sodium channels with familial autism
Rubinstein, M, Patowary, A, Stanaway, I B, McCord, E, Nesbitt, R R, Archer, M, Scheuer, T, Nickerson, D, Raskind, W H, Wijsman, E M, Bernier, R, Catterall, W A, Brkanac, Z
Published in Molecular psychiatry (01.02.2018)
Published in Molecular psychiatry (01.02.2018)
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Association of rare missense variants in the second intracellular loop of NaV1.7 sodium channels with familial autism
Rubinstein, M, Patowary, A, Stanaway, I B, McCord, E, Nesbitt, R R, Archer, M, Scheuer, T, Nickerson, D, Raskind, W H, Wijsman, E M, Bernier, R, Catterall, W A, Brkanac, Z
Published in Molecular psychiatry (01.02.2018)
Published in Molecular psychiatry (01.02.2018)
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Meta-analysis of 32 genome-wide linkage studies of schizophrenia
Ng, M Y M, Levinson, D F, Faraone, S V, Suarez, B K, DeLisi, L E, Arinami, T, Riley, B, Paunio, T, Pulver, A E, Irmansyah, Holmans, P A, Escamilla, M, Wildenauer, D B, Williams, N M, Laurent, C, Mowry, B J, Brzustowicz, L M, Maziade, M, Sklar, P, Garver, D L, Abecasis, G R, Lerer, B, Fallin, M D, Gurling, H M D, Gejman, P V, Lindholm, E, Moises, H W, Byerley, W, Wijsman, E M, Forabosco, P, Tsuang, M T, Hwu, H-G, Okazaki, Y, Kendler, K S, Wormley, B, Fanous, A, Walsh, D, O'Neill, F A, Peltonen, L, Nestadt, G, Lasseter, V K, Liang, K Y, Papadimitriou, G M, Dikeos, D G, Schwab, S G, Owen, M J, O'Donovan, M C, Norton, N, Hare, E, Raventos, H, Nicolini, H, Albus, M, Maier, W, Nimgaonkar, V L, Terenius, L, Mallet, J, Jay, M, Godard, S, Nertney, D, Alexander, M, Crowe, R R, Silverman, J M, Bassett, A S, Roy, M-A, Mérette, C, Pato, C N, Pato, M T, Roos, J Louw, Kohn, Y, Amann-Zalcenstein, D, Kalsi, G, McQuillin, A, Curtis, D, Brynjolfson, J, Sigmundsson, T, Petursson, H, Sanders, A R, Duan, J, Jazin, E, Myles-Worsley, M, Karayiorgou, M, Lewis, C M
Published in Molecular psychiatry (01.08.2009)
Published in Molecular psychiatry (01.08.2009)
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The Alzheimer's Disease Sequencing Project: Study design and sample selection
Beecham, Gary W, Bis, J C, Martin, E R, Choi, S-H, DeStefano, A L, van Duijn, C M, Fornage, M, Gabriel, S B, Koboldt, D C, Larson, D E, Naj, A C, Psaty, B M, Salerno, W, Bush, W S, Foroud, T M, Wijsman, E, Farrer, L A, Goate, A, Haines, J L, Pericak-Vance, Margaret A, Boerwinkle, E, Mayeux, R, Seshadri, S, Schellenberg, G
Published in Neurology. Genetics (01.10.2017)
Published in Neurology. Genetics (01.10.2017)
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Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders
Truong, D. T., Shriberg, L. D., Smith, S. D., Chapman, K. L., Scheer-Cohen, A. R., DeMille, M. M. C., Adams, A. K., Nato, A. Q., Wijsman, E. M., Eicher, J. D., Gruen, J. R.
Published in Human genetics (01.12.2016)
Published in Human genetics (01.12.2016)
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Variants regulating ZBTB4 are associated with age‐at‐onset of Alzheimer's disease
Blue, E. E., Yu, C.‐E., Thornton, T. A., Chapman, N. H., Kernfeld, E., Jiang, N., Shively, K. M., Buckingham, K. J., Marvin, C. T., Bamshad, M. J., Bird, T. D., Wijsman, E. M.
Published in Genes, brain and behavior (01.07.2018)
Published in Genes, brain and behavior (01.07.2018)
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The Number of Trait Loci in Late-Onset Alzheimer Disease
Daw, E. Warwick, Payami, Haydeh, Nemens, Ellen J., Nochlin, David, Bird, Thomas D., Schellenberg, Gerard D., Wijsman, Ellen M.
Published in American journal of human genetics (01.01.2000)
Published in American journal of human genetics (01.01.2000)
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A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency
RASKIND, W. H, IGO, R. P, CHAPMAN, N. H, BERNINGER, V. W, THOMSON, J. B, MATSUSHITA, M, BRKANAC, Z, HOLZMAN, T, BROWN, M, WIJSMAN, E. M
Published in Molecular psychiatry (01.07.2005)
Published in Molecular psychiatry (01.07.2005)
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Evidence for multiple loci from a genome scan of autism kindreds
Schellenberg, G D, Dawson, G, Sung, Y J, Estes, A, Munson, J, Rosenthal, E, Rothstein, J, Flodman, P, Smith, M, Coon, H, Leong, L, Yu, C-E, Stodgell, C, Rodier, P M, Spence, M A, Minshew, N, McMahon, W M, Wijsman, E M
Published in Molecular psychiatry (01.11.2006)
Published in Molecular psychiatry (01.11.2006)
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A Missense Mutation in the Desmin Rod Domain Is Associated with Autosomal Dominant Distal Myopathy, and Exerts a Dominant Negative Effect on Filament Formation
Sjöberg, Gunnar, Saavedra-Matiz, Carlos A., Rosen, Daniel R., Wijsman, Ellen M., Borg, Kristian, Horowitz, Steven H., Sejersen, Thomas
Published in Human molecular genetics (01.11.1999)
Published in Human molecular genetics (01.11.1999)
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Positional Cloning of the Werner's Syndrome Gene
Yu, Chang-En, Oshima, Junko, Fu, Ying-Hui, Wijsman, Ellen M., Hisama, Fuki, Alisch, Reid, Matthews, Shellie, Nakura, Jun, Miki, Tetsuro, Ouais, Samir, Martin, George M., Mulligan, John, Schellenberg, Gerard D.
Published in Science (American Association for the Advancement of Science) (12.04.1996)
Published in Science (American Association for the Advancement of Science) (12.04.1996)
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Evidence for multiple loci from a genome scan of autism kindreds
SCHELLENBERG, G. D, DAWSON, G, LEONG, L, YU, C.-E, STODGELL, C, RODIER, P. M, SPENCE, M. A, MINSHEW, N, MCMAHON, W. M, WIJSMAN, E. M, SUNG, Y. J, ESTES, A, MUNSON, J, ROSENTHAL, E, ROTHSTEIN, J, FLODMAN, P, SMITH, M, COON, H
Published in Molecular psychiatry (01.11.2006)
Published in Molecular psychiatry (01.11.2006)
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Gender difference in apolipoprotein E-associated risk for familial Alzheimer disease : A possible clue to the higher incidence of Alzheimer disease in women
PAYAMI, H, ZAREPARSI, S, SCHELLENBERG, G. D, MONTEE, K. R, SEXTON, G. J, KAYE, J. A, BIRD, T. D, CHANG-EN YU, WIJSMAN, E. M, HESTON, L. L, LITT, M
Published in American journal of human genetics (01.04.1996)
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Published in American journal of human genetics (01.04.1996)
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A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis
Bowcock, Anne M, Helms, Cynthia, Cao, Li, Krueger, James G, Wijsman, Ellen M, Chamian, Francesca, Gordon, Derek, Heffernan, Michael, Daw, Jil A Wright, Robarge, Jason, Ott, Jurg, Kwok, Pui-Yan, Menter, Alan
Published in Nature genetics (01.12.2003)
Published in Nature genetics (01.12.2003)
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Genetic Linkage Evidence for a Familial Alzheimer's Disease Locus on Chromosome 14
Schellenberg, Gerard D., Bird, Thomas D., Wijsman, Ellen M., Orr, Harry T., Anderson, Leojean, Nemens, Ellen, White, June A., Bonnycastle, Lori, Weber, James L., Alonso, M. Elisa, Potter, Huntington, Heston, Leonard L., Martin, George M.
Published in Science (American Association for the Advancement of Science) (23.10.1992)
Published in Science (American Association for the Advancement of Science) (23.10.1992)
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Genome-wide scan in a large complex pedigree with predominantly male schizophrenics from the island of Kosrae: evidence for linkage to chromosome 2q
WIJSMAN, E. M, ROSENTHAL, E. A, HALL, D, BLUNDELL, M. L, SOBIN, C, HEATH, S. C, WILLIAMS, R, BROWNSTEIN, M. J, GOGOS, J. A, KARAYIORGOU, M
Published in Molecular psychiatry (01.01.2003)
Published in Molecular psychiatry (01.01.2003)
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Differences in Lp[a] concentrations and apo[a] polymorphs between black and white Americans
Marcovina, S M, Albers, J J, Wijsman, E, Zhang, Z, Chapman, N H, Kennedy, H
Published in Journal of lipid research (01.12.1996)
Published in Journal of lipid research (01.12.1996)
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Chromosome 17 and hereditary dementia: linkage studies in three non-Alzheimer families and kindreds with late-onset FAD
Bird, T D, Wijsman, E M, Nochlin, D, Leehey, M, Sumi, S M, Payami, H, Poorkaj, P, Nemens, E, Rafkind, M, Schellenberg, G D
Published in Neurology (01.04.1997)
Published in Neurology (01.04.1997)
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