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Results: 1 to 20 of 21

1.

A common haplotype of KIAA0319 contributes to the phonological awareness skill in Chinese children.

Lim CK, Wong AM, Ho CS, Waye MM.

Behav Brain Funct. 2014 Jul 11;10:23. doi: 10.1186/1744-9081-10-23.

PMID:
25015435
[PubMed - in process]
Free PMC Article
2.

Speech sound processing deficits and training-induced neural plasticity in rats with dyslexia gene knockdown.

Centanni TM, Chen F, Booker AM, Engineer CT, Sloan AM, Rennaker RL, LoTurco JJ, Kilgard MP.

PLoS One. 2014 May 28;9(5):e98439. doi: 10.1371/journal.pone.0098439. eCollection 2014.

PMID:
24871331
[PubMed - in process]
Free PMC Article
3.

Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ.

Eicher JD, Powers NR, Miller LL, Mueller KL, Mascheretti S, Marino C, Willcutt EG, DeFries JC, Olson RK, Smith SD, Pennington BF, Tomblin JB, Ring SM, Gruen JR.

Hum Genet. 2014 Jul;133(7):869-81. doi: 10.1007/s00439-014-1427-3. Epub 2014 Feb 9.

PMID:
24509779
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.

Worthey EA, Raca G, Laffin JJ, Wilk BM, Harris JM, Jakielski KJ, Dimmock DP, Strand EA, Shriberg LD.

J Neurodev Disord. 2013 Oct 2;5(1):29. doi: 10.1186/1866-1955-5-29.

PMID:
24083349
[PubMed]
Free PMC Article
5.

Genome-wide association study of shared components of reading disability and language impairment.

Eicher JD, Powers NR, Miller LL, Akshoomoff N, Amaral DG, Bloss CS, Libiger O, Schork NJ, Darst BF, Casey BJ, Chang L, Ernst T, Frazier J, Kaufmann WE, Keating B, Kenet T, Kennedy D, Mostofsky S, Murray SS, Sowell ER, Bartsch H, Kuperman JM, Brown TT, Hagler DJ Jr, Dale AM, Jernigan TL, St Pourcain B, Davey Smith G, Ring SM, Gruen JR; Pediatric Imaging, Neurocognition, and Genetics Study.

Genes Brain Behav. 2013 Nov;12(8):792-801. doi: 10.1111/gbb.12085. Epub 2013 Oct 9.

PMID:
24024963
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments.

Eicher JD, Gruen JR.

Mol Genet Metab. 2013 Nov;110(3):201-12. doi: 10.1016/j.ymgme.2013.07.001. Epub 2013 Jul 17. Review.

PMID:
23916419
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Chromatin and epigenetic features of long-range gene regulation.

Harmston N, Lenhard B.

Nucleic Acids Res. 2013 Aug;41(15):7185-99. doi: 10.1093/nar/gkt499. Epub 2013 Jun 13. Review.

PMID:
23766291
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment.

Powers NR, Eicher JD, Butter F, Kong Y, Miller LL, Ring SM, Mann M, Gruen JR.

Am J Hum Genet. 2013 Jul 11;93(1):19-28. doi: 10.1016/j.ajhg.2013.05.008. Epub 2013 Jun 6. Erratum in: Am J Hum Genet. 2014 May 1;94(5):798.

PMID:
23746548
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

The genetics of reading disabilities: from phenotypes to candidate genes.

Raskind WH, Peter B, Richards T, Eckert MM, Berninger VW.

Front Psychol. 2013 Jan 7;3:601. doi: 10.3389/fpsyg.2012.00601. eCollection 2012.

PMID:
23308072
[PubMed]
Free PMC Article
10.

Approach to epigenetic analysis in language disorders.

Smith SD.

J Neurodev Disord. 2011 Dec;3(4):356-64. doi: 10.1007/s11689-011-9099-y. Epub 2011 Nov 24.

PMID:
22113455
[PubMed]
Free PMC Article
11.

Dissection of genetic associations with language-related traits in population-based cohorts.

Paracchini S.

J Neurodev Disord. 2011 Dec;3(4):365-73. doi: 10.1007/s11689-011-9091-6. Epub 2011 Sep 6.

PMID:
21894572
[PubMed]
Free PMC Article
12.

Maps of open chromatin guide the functional follow-up of genome-wide association signals: application to hematological traits.

Paul DS, Nisbet JP, Yang TP, Meacham S, Rendon A, Hautaviita K, Tallila J, White J, Tijssen MR, Sivapalaratnam S, Basart H, Trip MD; Cardiogenics Consortium; MuTHER Consortium, Göttgens B, Soranzo N, Ouwehand WH, Deloukas P.

PLoS Genet. 2011 Jun;7(6):e1002139. doi: 10.1371/journal.pgen.1002139. Epub 2011 Jun 30. Erratum in: PLoS Genet. 2011 Jul;7(7). doi: 10.1371/annotation/5d0c3be4-6f34-420a-960f-0a880bbf6128.

PMID:
21738486
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

DCDC2, KIAA0319 and CMIP are associated with reading-related traits.

Scerri TS, Morris AP, Buckingham LL, Newbury DF, Miller LL, Monaco AP, Bishop DV, Paracchini S.

Biol Psychiatry. 2011 Aug 1;70(3):237-45. doi: 10.1016/j.biopsych.2011.02.005. Epub 2011 Mar 31.

PMID:
21457949
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Risk alleles for chronic hepatitis B are associated with decreased mRNA expression of HLA-DPA1 and HLA-DPB1 in normal human liver.

O'Brien TR, Kohaar I, Pfeiffer RM, Maeder D, Yeager M, Schadt EE, Prokunina-Olsson L.

Genes Immun. 2011 Sep;12(6):428-33. doi: 10.1038/gene.2011.11. Epub 2011 Feb 24.

PMID:
21346778
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

In search of the perfect phenotype: an analysis of linkage and association studies of reading and reading-related processes.

Skiba T, Landi N, Wagner R, Grigorenko EL.

Behav Genet. 2011 Jan;41(1):6-30. doi: 10.1007/s10519-011-9444-7. Epub 2011 Jan 19. Review.

PMID:
21243420
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.

Newbury DF, Paracchini S, Scerri TS, Winchester L, Addis L, Richardson AJ, Walter J, Stein JF, Talcott JB, Monaco AP.

Behav Genet. 2011 Jan;41(1):90-104. doi: 10.1007/s10519-010-9424-3. Epub 2010 Dec 17.

PMID:
21165691
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Identification of candidate genes for dyslexia susceptibility on chromosome 18.

Scerri TS, Paracchini S, Morris A, MacPhie IL, Talcott J, Stein J, Smith SD, Pennington BF, Olson RK, DeFries JC, Monaco AP, Richardson AJ.

PLoS One. 2010 Oct 28;5(10):e13712. doi: 10.1371/journal.pone.0013712. Erratum in: PLoS One. 2010;5(12). doi: 10.1371/annotation/2294a38b-878d-42f0-9faf-0822db4a0248. Richardson, Alex J [added].

PMID:
21060895
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Balancing selection maintains a form of ERAP2 that undergoes nonsense-mediated decay and affects antigen presentation.

Andrés AM, Dennis MY, Kretzschmar WW, Cannons JL, Lee-Lin SQ, Hurle B; NISC Comparative Sequencing Program, Schwartzberg PL, Williamson SH, Bustamante CD, Nielsen R, Clark AG, Green ED.

PLoS Genet. 2010 Oct 14;6(10):e1001157. doi: 10.1371/journal.pgen.1001157.

PMID:
20976248
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

The dyslexia-associated KIAA0319 protein undergoes proteolytic processing with {gamma}-secretase-independent intramembrane cleavage.

Velayos-Baeza A, Levecque C, Kobayashi K, Holloway ZG, Monaco AP.

J Biol Chem. 2010 Dec 17;285(51):40148-62. doi: 10.1074/jbc.M110.145961. Epub 2010 Oct 13.

PMID:
20943657
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population.

Paracchini S, Ang QW, Stanley FJ, Monaco AP, Pennell CE, Whitehouse AJ.

Genes Brain Behav. 2011 Mar;10(2):158-65. doi: 10.1111/j.1601-183X.2010.00651.x. Epub 2010 Oct 19.

PMID:
20846247
[PubMed - indexed for MEDLINE]
Free PMC Article
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