Berninger VW - Search Results

1

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: berninger vw. 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

2

Familial aggregation of dyslexia phenotypes. II: paired correlated measures.

Hsu L, Wijsman EM, Berninger VW, Thomson JB, Raskind WH. Hsu L, et al. Among authors: berninger vw. Am J Med Genet. 2002 May 8;114(4):471-8. doi: 10.1002/ajmg.10523. Am J Med Genet. 2002. PMID: 11992573

3

Segregation analysis of phenotypic components of learning disabilities. II. Phonological decoding.

Chapman NH, Raskind WH, Thomson JB, Berninger VW, Wijsman EM. Chapman NH, et al. Among authors: berninger vw. Am J Med Genet B Neuropsychiatr Genet. 2003 Aug 15;121B(1):60-70. doi: 10.1002/ajmg.b.20068. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12898577

4

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: berninger vw. 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

5

Genomewide scan for real-word reading subphenotypes of dyslexia: novel chromosome 13 locus and genetic complexity.

Igo RP Jr, Chapman NH, Berninger VW, Matsushita M, Brkanac Z, Rothstein JH, Holzman T, Nielsen K, Raskind WH, Wijsman EM. Igo RP Jr, et al. Among authors: berninger vw. Am J Med Genet B Neuropsychiatr Genet. 2006 Jan 5;141B(1):15-27. doi: 10.1002/ajmg.b.30245. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16331673 Free PMC article.

6

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: berninger vw. 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.

7

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: berninger vw. 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.

8

A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency.

Raskind WH, Igo RP, Chapman NH, Berninger VW, Thomson JB, Matsushita M, Brkanac Z, Holzman T, Brown M, Wijsman EM. Raskind WH, et al. Among authors: berninger vw. Mol Psychiatry. 2005 Jul;10(7):699-711. doi: 10.1038/sj.mp.4001657. Mol Psychiatry. 2005. PMID: 15753956 Clinical Trial.

9

Writing problems in developmental dyslexia: under-recognized and under-treated.

Berninger VW, Nielsen KH, Abbott RD, Wijsman E, Raskind W. Berninger VW, et al. J Sch Psychol. 2008 Feb;46(1):1-21. doi: 10.1016/j.jsp.2006.11.008. J Sch Psychol. 2008. PMID: 18438452 Free PMC article.

10

A multidisciplinary approach to understanding developmental dyslexia within working-memory architecture: genotypes, phenotypes, brain, and instruction.

Berninger VW, Raskind W, Richards T, Abbott R, Stock P. Berninger VW, et al. Dev Neuropsychol. 2008;33(6):707-44. doi: 10.1080/87565640802418662. Dev Neuropsychol. 2008. PMID: 19005912 Review.

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