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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
Author / Creator: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.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Human genetics, 2016-12, Vol.135 (12), p.1329-1341
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Evidence for multiple loci from a genome scan of autism kindreds
Author / Creator: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
Publisher:London: Nature Publishing Group UK
Journal title:Molecular psychiatry, 2006-11, Vol.11 (11), p.1049-1060
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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
Author / Creator: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
Publisher:London: Nature Publishing Group UK
Journal title:Molecular psychiatry, 2005-07, Vol.10 (7), p.699-711
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Association of rare missense variants in the second intracellular loop of NaV1.7 sodium channels with familial autism
Author / Creator: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
Publisher:London: Nature Publishing Group UK
Journal title:Molecular psychiatry, 2018-02, Vol.23 (2), p.231-239
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Genetic Linkage Evidence for a Familial Alzheimer's Disease Locus on Chromosome 14
Author / Creator: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.
Publisher:Washington, DC: American Society for the Advancement of Science
Journal title:Science (American Association for the Advancement of Science), 1992-10, Vol.258 (5082), p.668-671
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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
Author / Creator: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
Publisher:London: Nature Publishing Group UK
Journal title:Molecular psychiatry, 2003-07, Vol.8 (7), p.695-705
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Positional Cloning of the Werner's Syndrome Gene
Author / Creator: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.
Publisher:Washington, DC: American Society for the Advancement of Science
Journal title:Science (American Association for the Advancement of Science), 1996-04, Vol.272 (5259), p.258-262
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A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis
Author / Creator: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 ; Bowcock, Anne M
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2003-12, Vol.35 (4), p.349-356
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Genetic Variation at the 22q11 PRODH2/DGCR6 Locus Presents an Unusual Pattern and Increases Susceptibility to Schizophrenia
Author / Creator:Liu, Hui ; Heath, Simon C. ; Sobin, Christina ; Roos, J. Louw ; Galke, Brandi L. ; Blundell, Maude L. ; Lenane, Marge ; Robertson, Brian ; Wijsman, Ellen M. ; Rapoport, Judith L. ; Gogos, Joseph A. ; Karayiorgou, Maria
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2002-03, Vol.99 (6), p.3717-3722
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Identification of Rare Variants from Exome Sequence in a Large Pedigree with Autism
Author / Creator:Marchani, E.E. ; Chapman, N.H. ; Cheung, C.Y.K. ; Ankenman, K. ; Stanaway, I.B. ; Coon, H.H. ; Nickerson, D. ; Bernier, R. ; Brkanac, Z. ; Wijsman, E.M.
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Human heredity, 2012-01, Vol.74 (3/4), p.153-164
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Absence of Linkage of Chromosome 21q21 Markers to Familial Alzheimer's Disease
Author / Creator:Schellenberg, Gerard D. ; Bird, Thomas D. ; Wijsman, Ellen M. ; Moore, Deborah K. ; Boehnke, Michael ; Bryant, Eileen M. ; Lampe, Thomas H. ; Nochlin, David ; Sumi, Shuzo M. ; Deeb, Samir S. ; Beyreuther, Konrad ; Martin, George M.
Publisher:Washington, DC: The American Association for the Advancement of Science
Journal title:Science (American Association for the Advancement of Science), 1988-09, Vol.241 (4872), p.1507-1510
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Candidate Gene for the Chromosome 1 Familial Alzheimer's Disease Locus
Author / Creator:Levy-Lahad, Ephrat ; Wasco, Wilma ; Poorkaj, Parvoneh ; Romano, Donna M. ; Oshima, Junko ; Pettingell, Warren H. ; Yu, Chang-en ; Jondro, Paul D. ; Schmidt, Stephen D. ; Wang, Kai ; Crowley, Annette C. ; Fu, Ying-Hui ; Guenette, Suzanne Y. ; Galas, David ; Nemens, Ellen ; Wijsman, Ellen M. ; Bird, Thomas D. ; Schellenberg, Gerard D. ; Tanzi, Rudolph E.
Publisher:Washington, DC: American Society for the Advancement of Science
Journal title:Science (American Association for the Advancement of Science), 1995-08, Vol.269 (5226), p.973-977
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A familial Alzheimer's disease locus on chromosome 1
Author / Creator:Levy-Lahad, E ; Wijsman, E M ; Nemens, E ; Anderson, L ; Goddard, K A ; Weber, J L ; Bird, T D ; Schellenberg, G D
Publisher:United States
Journal title:Science (American Association for the Advancement of Science), 1995-08, Vol.269 (5226), p.970-973
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Homozygosity mapping and Werner's syndrome
Author / Creator:Schellenberg, G.D. ; Martin, G.M. ; Wijsman, E.M. ; Nakura, J. ; Miki, T. ; Ogihara, T.
Publisher:London: Elsevier Ltd
Journal title:The Lancet (British edition), 1992-04, Vol.339 (8799), p.1002-1002
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Genome scan for quantitative trait loci influencing HDL levels : evidence for multilocus inheritance in familial combined hyperlipidemia
Author / Creator:GAGNON, France ; JARVIK, Gail P ; BADZIOCH, Michael D ; MOTULSKY, Arno G ; BRUNZELL, John D ; WIJSMAN, Ellen M
Publisher:Heidelberg: Springer
Journal title:Human genetics, 2005-09, Vol.117 (5), p.494-505
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Joint oligogenic segregation and linkage analysis using bayesian Markov chain Monte Carlo methods
Author / Creator:WIJSMAN, Ellen M ; DONGMEI YU
Publisher:Totowa, NJ: Humana Press
Journal title:Molecular biotechnology, 2004-11, Vol.28 (3), p.205-226
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Association of rare missense variants in the second intracellular loop of Na V 1.7 sodium channels with familial autism
Author / Creator: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
Publisher:England
Journal title:Molecular psychiatry, 2018-02, Vol.23 (2), p.231
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Familial aggregation of dyslexia phenotypes
Author / Creator:Raskind, W H ; Hsu, L ; Berninger, V W ; Thomson, J B ; Wijsman, E M
Publisher:United States: Springer Nature B.V
Journal title:Behavior genetics, 2000-09, Vol.30 (5), p.385-396
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Evidence of linkage of HDL level variation to APOC3 in two samples with different ascertainment
Author / Creator:GAGNON, France ; JARVIK, Gail P ; MOTULSKY, Arno G ; DEEB, Samir S ; BRUNZELL, John D ; WIJSMAN, Ellen M
Publisher:Heidelberg: Springer
Journal title:Human genetics, 2003-11, Vol.113 (6), p.522-533
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Meta-analysis of 32 genome-wide linkage studies of schizophrenia
Author / Creator: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
Publisher:London: Nature Publishing Group UK
Journal title:Molecular psychiatry, 2009-08, Vol.14 (8), p.774-785
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Showing 1 to 20 of 38 results

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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

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Evidence for multiple loci from a genome scan of autism kindreds

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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

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Association of rare missense variants in the second intracellular loop of NaV1.7 sodium channels with familial autism

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Genetic Linkage Evidence for a Familial Alzheimer's Disease Locus on Chromosome 14

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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

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Positional Cloning of the Werner's Syndrome Gene

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A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis

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Genetic Variation at the 22q11 PRODH2/DGCR6 Locus Presents an Unusual Pattern and Increases Susceptibility to Schizophrenia

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Identification of Rare Variants from Exome Sequence in a Large Pedigree with Autism

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Absence of Linkage of Chromosome 21q21 Markers to Familial Alzheimer's Disease

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Candidate Gene for the Chromosome 1 Familial Alzheimer's Disease Locus

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A familial Alzheimer's disease locus on chromosome 1

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Homozygosity mapping and Werner's syndrome

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Genome scan for quantitative trait loci influencing HDL levels : evidence for multilocus inheritance in familial combined hyperlipidemia

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Joint oligogenic segregation and linkage analysis using bayesian Markov chain Monte Carlo methods

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Association of rare missense variants in the second intracellular loop of Na V 1.7 sodium channels with familial autism

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Familial aggregation of dyslexia phenotypes

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Evidence of linkage of HDL level variation to APOC3 in two samples with different ascertainment

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Meta-analysis of 32 genome-wide linkage studies of schizophrenia

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