Brkanac Z - Search Results

1

IFRD1 is a candidate gene for SMNA on chromosome 7q22-q23.

Brkanac Z, Spencer D, Shendure J, Robertson PD, Matsushita M, Vu T, Bird TD, Olson MV, Raskind WH. Brkanac Z, et al. Am J Hum Genet. 2009 May;84(5):692-7. doi: 10.1016/j.ajhg.2009.04.008. Epub 2009 Apr 30. Am J Hum Genet. 2009. PMID: 19409521 Free PMC article.

2

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. Am J Med Genet. 2002 May 8;114(4):450-7. doi: 10.1002/ajmg.10361. Am J Med Genet. 2002. PMID: 11992570

3

A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qter.

Brkanac Z, Bylenok L, Fernandez M, Matsushita M, Lipe H, Wolff J, Nochlin D, Raskind WH, Bird TD. Brkanac Z, et al. Arch Neurol. 2002 Aug;59(8):1291-5. doi: 10.1001/archneur.59.8.1291. Arch Neurol. 2002. PMID: 12164726

4

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: brkanac z. 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.

5

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: brkanac z. 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

6

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: brkanac z. Mol Psychiatry. 2005 Jul;10(7):699-711. doi: 10.1038/sj.mp.4001657. Mol Psychiatry. 2005. PMID: 15753956 Clinical Trial.

7

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: brkanac z. 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.

8

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. 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

9

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. 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.

10

Pharmacology and genetics of autism: implications for diagnosis and treatment.

Brkanac Z, Raskind WH, King BH. Brkanac Z, et al. Per Med. 2008 Nov;5(6):599-607. doi: 10.2217/17410541.5.6.599. Per Med. 2008. PMID: 19727434 Free PMC article.

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