Brkanac Z - Search Results

1

Family-based genome scan for age at onset of late-onset Alzheimer's disease in whole exome sequencing data.

Saad M, Brkanac Z, Wijsman EM. Saad M, et al. Among authors: brkanac z. Genes Brain Behav. 2015 Nov;14(8):607-17. doi: 10.1111/gbb.12250. Epub 2015 Sep 23. Genes Brain Behav. 2015. PMID: 26394601 Free PMC article.

2

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

3

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.

4

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.

5

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

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. 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

Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample.

Peter B, Raskind WH, Matsushita M, Lisowski M, Vu T, Berninger VW, Wijsman EM, Brkanac Z. Peter B, et al. Among authors: brkanac z. J Neurodev Disord. 2011 Mar;3(1):39-49. doi: 10.1007/s11689-010-9065-0. Epub 2010 Nov 9. J Neurodev Disord. 2011. PMID: 21484596 Free PMC article.

8

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: brkanac z. 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.

9

Identification of rare variants from exome sequence in a large pedigree with autism.

Marchani EE, Chapman NH, Cheung CY, Ankenman K, Stanaway IB, Coon HH, Nickerson D, Bernier R, Brkanac Z, Wijsman EM. Marchani EE, et al. Among authors: brkanac z. Hum Hered. 2012;74(3-4):153-64. doi: 10.1159/000346560. Epub 2013 Apr 11. Hum Hered. 2012. PMID: 23594493 Free PMC article.

10

R47H Variant of TREM2 Associated With Alzheimer Disease in a Large Late-Onset Family: Clinical, Genetic, and Neuropathological Study.

Korvatska O, Leverenz JB, Jayadev S, McMillan P, Kurtz I, Guo X, Rumbaugh M, Matsushita M, Girirajan S, Dorschner MO, Kiianitsa K, Yu CE, Brkanac Z, Garden GA, Raskind WH, Bird TD. Korvatska O, et al. Among authors: brkanac z. JAMA Neurol. 2015 Aug;72(8):920-7. doi: 10.1001/jamaneurol.2015.0979. JAMA Neurol. 2015. PMID: 26076170 Free PMC article.

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