Matsushita M - Search Results

1

Evidence for involvement of GNB1L in autism.

Chen YZ, Matsushita M, Girirajan S, Lisowski M, Sun E, Sul Y, Bernier R, Estes A, Dawson G, Minshew N, Shellenberg GD, Eichler EE, Rieder MJ, Nickerson DA, Tsuang DW, Tsuang MT, Wijsman EM, Raskind WH, Brkanac Z. Chen YZ, et al. Among authors: matsushita m. Am J Med Genet B Neuropsychiatr Genet. 2012 Jan;159B(1):61-71. doi: 10.1002/ajmg.b.32002. Epub 2011 Nov 16. Am J Med Genet B Neuropsychiatr Genet. 2012. PMID: 22095694 Free PMC article.

2

Motor sequencing deficit as an endophenotype of speech sound disorder: a genome-wide linkage analysis in a multigenerational family.

Peter B, Matsushita M, Raskind WH. Peter B, et al. Among authors: matsushita m. Psychiatr Genet. 2012 Oct;22(5):226-34. doi: 10.1097/YPG.0b013e328353ae92. Psychiatr Genet. 2012. PMID: 22517379 Free PMC article.

3

Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia.

Brkanac Z, Chapman NH, Matsushita MM, Chun L, Nielsen K, Cochrane E, Berninger VW, Wijsman EM, Raskind WH. Brkanac Z, et al. Among authors: matsushita mm. Am J Med Genet B Neuropsychiatr Genet. 2007 Jun 5;144B(4):556-60. doi: 10.1002/ajmg.b.30471. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17450541

4

Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple loci.

Brkanac Z, Chapman NH, Igo RP Jr, Matsushita MM, Nielsen K, Berninger VW, Wijsman EM, Raskind WH. Brkanac Z, et al. Among authors: matsushita mm. Behav Genet. 2008 Sep;38(5):462-75. doi: 10.1007/s10519-008-9215-2. Epub 2008 Jul 8. Behav Genet. 2008. PMID: 18607713 Free PMC article.

5

Autosomal dominant familial dyskinesia and facial myokymia: single exome sequencing identifies a mutation in adenylyl cyclase 5.

Chen YZ, Matsushita MM, Robertson P, Rieder M, Girirajan S, Antonacci F, Lipe H, Eichler EE, Nickerson DA, Bird TD, Raskind WH. Chen YZ, et al. Among authors: matsushita mm. Arch Neurol. 2012 May;69(5):630-5. doi: 10.1001/archneurol.2012.54. Arch Neurol. 2012. PMID: 22782511 Free PMC article.

6

Genome scan for cognitive trait loci of dyslexia: Rapid naming and rapid switching of letters, numbers, and colors.

Rubenstein KB, Raskind WH, Berninger VW, Matsushita MM, Wijsman EM. Rubenstein KB, et al. Among authors: matsushita mm. Am J Med Genet B Neuropsychiatr Genet. 2014 Jun;165B(4):345-56. doi: 10.1002/ajmg.b.32237. Epub 2014 May 8. Am J Med Genet B Neuropsychiatr Genet. 2014. PMID: 24807833 Free PMC article.

7

Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech.

Peter B, Wijsman EM, Nato AQ Jr; University of Washington Center for Mendelian Genomics; Matsushita MM, Chapman KL, Stanaway IB, Wolff J, Oda K, Gabo VB, Raskind WH. Peter B, et al. Among authors: matsushita mm. PLoS One. 2016 Apr 27;11(4):e0153864. doi: 10.1371/journal.pone.0153864. eCollection 2016. PLoS One. 2016. PMID: 27120335 Free PMC article.

8

Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32.

Brkanac Z, Fernandez M, Matsushita M, Lipe H, Wolff J, Bird TD, Raskind WH. Brkanac Z, et al. Among authors: matsushita m. Am J Med Genet. 2002 May 8;114(4):450-7. doi: 10.1002/ajmg.10361. Am J Med Genet. 2002. PMID: 11992570

9

Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxia.

Chen DH, Brkanac Z, Verlinde CL, Tan XJ, Bylenok L, Nochlin D, Matsushita M, Lipe H, Wolff J, Fernandez M, Cimino PJ, Bird TD, Raskind WH. Chen DH, et al. Among authors: matsushita m. Am J Hum Genet. 2003 Apr;72(4):839-49. doi: 10.1086/373883. Epub 2003 Mar 17. Am J Hum Genet. 2003. PMID: 12644968 Free PMC article.

10

Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q.

Chapman NH, Igo RP, Thomson JB, Matsushita M, Brkanac Z, Holzman T, Berninger VW, Wijsman EM, Raskind WH. Chapman NH, et al. Among authors: matsushita m. Am J Med Genet B Neuropsychiatr Genet. 2004 Nov 15;131B(1):67-75. doi: 10.1002/ajmg.b.30018. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15389770

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