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ArticlesPeer ReviewedFull Text
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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ArticlesPeer ReviewedFull Text
A p53-Dependent Mouse Spindle Checkpoint
Author / Creator:Cross, Shawn M. ; Sanchez, Carissa A. ; Morgan, Catherine A. ; Schimke, Melana K. ; Ramel, Stig ; Idzerda, Rejean L. ; Raskind, Wendy H. ; Reid, Brian J.
Publisher:Washington, DC: American Society for the Advancement of Science
Journal title:Science (American Association for the Advancement of Science), 1995-03, Vol.267 (5202), p.1353-1356
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ArticlesPeer ReviewedFull Text
Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder
Author / Creator:Chapman, N. H. ; Bernier, R. A. ; Webb, S. J. ; Munson, J. ; Blue, E. M. ; Chen, D.-H. ; Heigham, E. ; Raskind, W. H. ; Wijsman, Ellen M.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Human genetics, 2018-10, Vol.137 (10), p.807-815
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ArticlesPeer ReviewedFull Text
Loss of Heterozygosity Involving the APC and MCC Genetic Loci Occurs in the Majority of Human Esophageal Cancers
Author / Creator:Boynton, Robert F. ; Blount, Patricia L. ; Yin, Jing ; Brown, Victoria L. ; Huang, Ying ; Tong, Yi ; McDaniel, Tim ; Newkirk, Carnell ; Resau, James H. ; Raskind, Wendy H. ; Haggitt, Rodger C. ; Reid, Brian J. ; Meltzer, Stephen J.
Publisher:Washington, DC: National Academy of Sciences of the United States of America
Journal title:Proceedings of the National Academy of Sciences - PNAS, 1992-04, Vol.89 (8), p.3385-3388
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ArticlesPeer ReviewedFull Text
Clonal Development, Stem-Cell Differentiation, and Clinical Remissions in Acute Nonlymphocytic Leukemia
Author / Creator:Fialkow, Philip J ; Singer, Jack W ; Raskind, Wendy H ; Adamson, John W ; Jacobson, Robert J ; Bernstein, Irwin D ; Dow, Lois W ; Najfeld, Vesna ; Veith, Robert
Publisher:Boston, MA: Massachusetts Medical Society
Journal title:The New England journal of medicine, 1987-08, Vol.317 (8), p.468-473
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ArticlesPeer ReviewedFull Text
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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ArticlesPeer ReviewedFull Text
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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ArticlesPeer ReviewedFull Text
Evaluation of locus heterogeneity and EXT1 mutations in 34 families with hereditary multiple exostoses
Author / Creator:Raskind, Wendy H. ; Conrad III, Ernest U. ; Matsushita, Mark ; Wijsman, Ellen M. ; Wells, Dan E. ; Chapman, Nicola ; Sandell, Linda J. ; Wagner, Michael ; Houck, John
Publisher:New York: Wiley Subscription Services, Inc., A Wiley Company
Journal title:Human mutation, 1998, Vol.11 (3), p.231-239
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ArticlesPeer ReviewedFull Text
Familial aggregation patterns in mathematical ability
Author / Creator:Wijsman, Ellen M ; Robinson, Nancy M ; Ainsworth, Kathryn H ; Rosenthal, Elisabeth A ; Holzman, Ted ; Raskind, Wendy H
Publisher:United States: Springer Nature B.V
Journal title:Behavior genetics, 2004-01, Vol.34 (1), p.51-62
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ArticlesPeer ReviewedFull Text
Expression of cartilage extracellular matrix and potential regulatory genes in a new human chondrosarcoma cell line
Author / Creator:Chansky, Howard ; Robbins, James R. ; Cha, Steven ; Raskind, Wendy H. ; Conrad, Ernest U. ; Sandell, Linda J.
Publisher:Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Journal title:Journal of orthopaedic research, 1998-09, Vol.16 (5), p.521-530
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ArticlesPeer ReviewedFull Text
Expression of the Gene Defect in X-Linked Agammaglobulinemia
Author / Creator:Conley, Mary Ellen ; Brown, Persymphonie ; Pickard, Allan R ; Buckley, Rebecca H ; Miller, Debra S ; Raskind, Wendy H ; Singer, Jack W ; Fialkow, Philip J
Publisher:Boston, MA: Massachusetts Medical Society
Journal title:The New England journal of medicine, 1986-08, Vol.315 (9), p.564-567
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ArticlesPeer ReviewedFull Text
Current Understanding of the Genetic Basis of Reading and Spelling Disability
Author / Creator:Raskind, Wendy H.
Publisher:Los Angeles, CA: Council for Learning Disabilities
Journal title:Learning disability quarterly, 2001-08, Vol.24 (3), p.141-157
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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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A p53-Dependent Mouse Spindle Checkpoint

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Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder

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Loss of Heterozygosity Involving the APC and MCC Genetic Loci Occurs in the Majority of Human Esophageal Cancers

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Clonal Development, Stem-Cell Differentiation, and Clinical Remissions in Acute Nonlymphocytic Leukemia

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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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Evaluation of locus heterogeneity and EXT1 mutations in 34 families with hereditary multiple exostoses

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Familial aggregation patterns in mathematical ability

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Expression of cartilage extracellular matrix and potential regulatory genes in a new human chondrosarcoma cell line

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Expression of the Gene Defect in X-Linked Agammaglobulinemia

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Current Understanding of the Genetic Basis of Reading and Spelling Disability

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