Functional characterization of AC5 gain-of-function variants: Impact on the molecular basis of ADCY5-related dyskinesia von Doyle, T.B., Hayes, M.P., Chen, D.H., Raskind, W.H., Watts, V.J.

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A clinic-based study of the LRRK2 gene in parkinson disease yields new mutations von ZABETIAN, C. P, SAMII, A, MOSLEY, A. D, ROBERTS, J. W, LEIS, B. C, YEAROUT, D, RASKIND, W. H, GRIFFITH, A

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Mutation of a Putative Mitochondrial Iron Transporter Gene (ABC7) in X-Linked Sideroblastic Anemia and Ataxia (XLSA/A) von Allikmets, Rando, Raskind, Wendy H., Hutchinson, Amy, Schueck, Nichole D., Dean, Michael, Koeller, David M.

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The clinical and genetic spectrum of spinocerebellar ataxia 14 von CHEN, D.-H, CIMINO, P. J, WOLFF, J, MORGAN, C, LAU, D, FERNANDEZ, M, SASAKI, H, RASKIND, W. H, BIRD, T. D, RANUM, L. P. W, ZOGHBI, H. Y, YABE, I, SCHUT, L, MARGOLIS, R. L, LIPE, H. P, FELEKE, A, MATSUSHITA, M

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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 von 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

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Mutations in the TSGA14 gene in families with autism spectrum disorders von Korvatska, O., Estes, A., Munson, J., Dawson, G., Bekris, L.M., Kohen, R., Yu, C.-E., Schellenberg, G.D., Raskind, W.H.

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

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

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A p53-Dependent Mouse Spindle Checkpoint von Cross, Shawn M., Sanchez, Carissa A., Morgan, Catherine A., Schimke, Melana K., Ramel, Stig, Idzerda, Rejean L., Raskind, Wendy H., Reid, Brian J.

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

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Mutations in the EXT1 and EXT2 Genes in Hereditary Multiple Exostoses von Wuyts, Wim, Van Hul, Wim, De Boulle, Kristel, Hendrickx, Jan, Bakker, Egbert, Vanhoenacker, Filip, Mollica, Florindo, Lüdecke, Hermann-Josef, Sayli, Bekir Sitki, Pazzaglia, Ugo E., Mortier, Geert, Hamel, Ben, Conrad, Ernest U., Matsushita, Mark, Raskind, Wendy H., Willems, Patrick J.

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Clonal development of myeloproliferative disorders: clues to hematopoietic differentiation and multistep pathogenesis of cancer von Raskind, W H, Steinmann, L, Najfeld, V

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

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Segregation Analysis of Phenotypic Components of Learning Disabilities. I. Nonword Memory and Digit Span von Wijsman, Ellen M., Peterson, Do, Leutenegger, Anne-Louise, Thomson, Jennifer B., Goddard, Katrina A.B., Hsu, Li, Berninger, Virginia W., Raskind, Wendy H.

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Further localization of a gene for paroxysmal dystonic choreoathetosis to a 5-cM region on chromosome 2q34 von RASKIND, W. H, BOLIN, T, WOLFF, J, FINK, J, MATSUSHITA, M, LITT, M, LIPE, H, BIRD, T. D

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Complete deletion of the proteolipid protein gene (PLP) in a family with X-linked Pelizaeus-Merzbacher disease von RASKIND, W. H, WILLIAMS, C. A, HUDSON, L. D, BIRD, T. D

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CAG Repeat Expansion in Autosomal Dominant Familial Spastic Paraparesis: Novel Expansion in a Subset of Patients von Benson, Kathleen F., Horwitz, Marshall, Wolff, John, Friend, Kathy, Thompson, Elizabeth, White, Sue, Richards, Robert I., Raskind, Wendy H., Bird, Thomas D.

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DIFFERENT PATTERNS OF X-INACTIVATION IN MZ TWINS DISCORDANT FOR RED-GREEN COLOR-VISION DEFICIENCY von JORGENSEN, AL, PHILIP, J, RASKIND, WH, MATSUSHITA, M, CHRISTENSEN, B, DREYER, MOTULSKY, AG

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Evidence for a Multistep Pathogenesis of a Myelodysplastic Syndrome von Raskind, Wendy H., Tirumali, Nagendra, Jacobson, Robert, Singer, Jack, Fialkow, Philip J.

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Expression of cartilage extracellular matrix and potential regulatory genes in a new human chondrosarcoma cell line von Chansky, Howard, Robbins, James R., Cha, Steven, Raskind, Wendy H., Conrad, Ernest U., Sandell, Linda J.

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