180 related articles for article (PubMed ID: 23229871)
21. The DCDC2 deletion is not a risk factor for dyslexia.
Scerri TS; Macpherson E; Martinelli A; Wa WC; Monaco AP; Stein J; Zheng M; Suk-Han Ho C; McBride C; Snowling M; Hulme C; Hayiou-Thomas ME; Waye MMY; Talcott JB; Paracchini S
Transl Psychiatry; 2017 Jul; 7(7):e1182. PubMed ID: 28742079
[TBL] [Abstract][Full Text] [Related]
22. Dcdc2 knockout mice display exacerbated developmental disruptions following knockdown of doublecortin.
Wang Y; Yin X; Rosen G; Gabel L; Guadiana SM; Sarkisian MR; Galaburda AM; Loturco JJ
Neuroscience; 2011 Sep; 190():398-408. PubMed ID: 21689730
[TBL] [Abstract][Full Text] [Related]
23. Genetic variant in DIP2A gene is associated with developmental dyslexia in Chinese population.
Kong R; Shao S; Wang J; Zhang X; Guo S; Zou L; Zhong R; Lou J; Zhou J; Zhang J; Song R
Am J Med Genet B Neuropsychiatr Genet; 2016 Mar; 171B(2):203-8. PubMed ID: 26452339
[TBL] [Abstract][Full Text] [Related]
24. Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.
Schumacher J; Anthoni H; Dahdouh F; König IR; Hillmer AM; Kluck N; Manthey M; Plume E; Warnke A; Remschmidt H; Hülsmann J; Cichon S; Lindgren CM; Propping P; Zucchelli M; Ziegler A; Peyrard-Janvid M; Schulte-Körne G; Nöthen MM; Kere J
Am J Hum Genet; 2006 Jan; 78(1):52-62. PubMed ID: 16385449
[TBL] [Abstract][Full Text] [Related]
25. 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. PubMed ID: 21165691
[TBL] [Abstract][Full Text] [Related]
26. Association, characterisation and meta-analysis of SNPs linked to general reading ability in a German dyslexia case-control cohort.
Müller B; Wilcke A; Czepezauer I; Ahnert P; Boltze J; Kirsten H;
Sci Rep; 2016 Jun; 6():27901. PubMed ID: 27312598
[TBL] [Abstract][Full Text] [Related]
27. Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia.
Harold D; Paracchini S; Scerri T; Dennis M; Cope N; Hill G; Moskvina V; Walter J; Richardson AJ; Owen MJ; Stein JF; Green ED; O'Donovan MC; Williams J; Monaco AP
Mol Psychiatry; 2006 Dec; 11(12):1085-91, 1061. PubMed ID: 17033633
[TBL] [Abstract][Full Text] [Related]
28. The Roles of Genes in the Neuronal Migration and Neurite Outgrowth Network in Developmental Dyslexia: Single- and Multiple-Risk Genetic Variants.
Shao S; Kong R; Zou L; Zhong R; Lou J; Zhou J; Guo S; Wang J; Zhang X; Zhang J; Song R
Mol Neurobiol; 2016 Aug; 53(6):3967-3975. PubMed ID: 26184631
[TBL] [Abstract][Full Text] [Related]
29. Evaluation of visual motion perception ability in mice with knockout of the dyslexia candidate susceptibility gene Dcdc2.
Rendall AR; Perrino PA; LoTurco JJ; Fitch RH
Genes Brain Behav; 2019 Jun; 18(5):e12450. PubMed ID: 29232042
[TBL] [Abstract][Full Text] [Related]
30. Association between
Deng KG; Zhao H; Zuo PX
J Genet; 2019 Jun; 98(1):. PubMed ID: 31204720
[TBL] [Abstract][Full Text] [Related]
31. A dyslexia-associated variant in DCDC2 changes gene expression.
Meng H; Powers NR; Tang L; Cope NA; Zhang PX; Fuleihan R; Gibson C; Page GP; Gruen JR
Behav Genet; 2011 Jan; 41(1):58-66. PubMed ID: 21042874
[TBL] [Abstract][Full Text] [Related]
32. Study of Genetic Association With
Waye MMY; Poo LK; Ho CS
Clin Pract Epidemiol Ment Health; 2017; 13():104-114. PubMed ID: 29081827
[TBL] [Abstract][Full Text] [Related]
33. 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
Am J Med Genet B Neuropsychiatr Genet; 2007 Jun; 144B(4):556-60. PubMed ID: 17450541
[TBL] [Abstract][Full Text] [Related]
34. Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample.
Ludwig KU; Schumacher J; Schulte-Körne G; König IR; Warnke A; Plume E; Anthoni H; Peyrard-Janvid M; Meng H; Ziegler A; Remschmidt H; Kere J; Gruen JR; Müller-Myhsok B; Nöthen MM; Hoffmann P
Psychiatr Genet; 2008 Dec; 18(6):310-2. PubMed ID: 19018237
[TBL] [Abstract][Full Text] [Related]
35. 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; 70(3):237-45. PubMed ID: 21457949
[TBL] [Abstract][Full Text] [Related]
36. Developmental dyslexia susceptibility genes DNAAF4, DCDC2, and NRSN1 are associated with brain function in fluently reading adolescents and young adults.
Rinne N; Wikman P; Sahari E; Salmi J; Einarsdóttir E; Kere J; Alho K
Cereb Cortex; 2024 Apr; 34(4):. PubMed ID: 38610086
[TBL] [Abstract][Full Text] [Related]
37. The dyslexia-associated gene DCDC2 is required for spike-timing precision in mouse neocortex.
Che A; Girgenti MJ; LoTurco J
Biol Psychiatry; 2014 Sep; 76(5):387-96. PubMed ID: 24094509
[TBL] [Abstract][Full Text] [Related]
38. Frontotemporal dementia and language networks: cortical thickness reduction is driven by dyslexia susceptibility genes.
Paternicó D; Manes M; Premi E; Cosseddu M; Gazzina S; Alberici A; Archetti S; Bonomi E; Cotelli MS; Cotelli M; Turla M; Micheli A; Gasparotti R; Padovani A; Borroni B
Sci Rep; 2016 Aug; 6():30848. PubMed ID: 27484312
[TBL] [Abstract][Full Text] [Related]
39. Strong motion deficits in dyslexia associated with DCDC2 gene alteration.
Cicchini GM; Marino C; Mascheretti S; Perani D; Morrone MC
J Neurosci; 2015 May; 35(21):8059-64. PubMed ID: 26019324
[TBL] [Abstract][Full Text] [Related]
40. Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample.
Ludwig KU; Roeske D; Schumacher J; Schulte-Körne G; König IR; Warnke A; Plume E; Ziegler A; Remschmidt H; Müller-Myhsok B; Nöthen MM; Hoffmann P
J Neural Transm (Vienna); 2008 Nov; 115(11):1587-9. PubMed ID: 18810304
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]