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2. The DCDC2 intron 2 deletion impairs illusory motion perception unveiling the selective role of magnocellular-dorsal stream in reading (dis)ability. Gori S; Mascheretti S; Giora E; Ronconi L; Ruffino M; Quadrelli E; Facoetti A; Marino C Cereb Cortex; 2015 Jun; 25(6):1685-95. PubMed ID: 25270309 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. Alterations in neural activation in the ventral frontoparietal network during complex magnocellular stimuli in developmental dyslexia associated with READ1 deletion. Mascheretti S; Arrigoni F; Toraldo A; Giubergia A; Andreola C; Villa M; Lampis V; Giorda R; Villa M; Peruzzo D Behav Brain Funct; 2024 Jun; 20(1):16. PubMed ID: 38926731 [TBL] [Abstract][Full Text] [Related]
5. White matter deficits correlate with visual motion perception impairments in dyslexic carriers of the DCDC2 genetic risk variant. Perani D; Scifo P; Cicchini GM; Rosa PD; Banfi C; Mascheretti S; Falini A; Marino C; Morrone MC Exp Brain Res; 2021 Sep; 239(9):2725-2740. PubMed ID: 34228165 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Dorsal stream deficits suggest hidden dyslexia among deaf poor readers: correlated evidence from reduced perceptual speed and elevated coherent motion detection thresholds. Samar VJ; Parasnis I Brain Cogn; 2005 Aug; 58(3):300-11. PubMed ID: 15963380 [TBL] [Abstract][Full Text] [Related]
8. Visual deficits in pre-readers at familial risk for dyslexia. Kevan A; Pammer K Vision Res; 2008 Dec; 48(28):2835-9. PubMed ID: 18929591 [TBL] [Abstract][Full Text] [Related]
9. Cortical locus of coherent motion deficits in deaf poor readers. Samar VJ; Parasnis I Brain Cogn; 2007 Apr; 63(3):226-39. PubMed ID: 17046130 [TBL] [Abstract][Full Text] [Related]
10. The role of gene DCDC2 in German dyslexics. Wilcke A; Weissfuss J; Kirsten H; Wolfram G; Boltze J; Ahnert P Ann Dyslexia; 2009 Jun; 59(1):1-11. PubMed ID: 19238550 [TBL] [Abstract][Full Text] [Related]
11. The influence of contrast on coherent motion processing in dyslexia. Conlon EG; Lilleskaret G; Wright CM; Power GF Neuropsychologia; 2012 Jun; 50(7):1672-81. PubMed ID: 22484519 [TBL] [Abstract][Full Text] [Related]
13. Deficits of motion transparency perception in adult developmental dyslexics with normal unidirectional motion sensitivity. Hill GT; Raymond JE Vision Res; 2002 Apr; 42(9):1195-203. PubMed ID: 11997057 [TBL] [Abstract][Full Text] [Related]
14. The magnocellular theory of developmental dyslexia. Stein J Dyslexia; 2001; 7(1):12-36. PubMed ID: 11305228 [TBL] [Abstract][Full Text] [Related]
15. Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample. Lind PA; Luciano M; Wright MJ; Montgomery GW; Martin NG; Bates TC Eur J Hum Genet; 2010 Jun; 18(6):668-73. PubMed ID: 20068590 [TBL] [Abstract][Full Text] [Related]
16. Study of candidate genes for dyslexia in Brazilian individuals. Svidnicki MC; Salgado CA; Lima RF; Ciasca SM; Secolin R; Pomilio MC; Junqueira PA; Pinto MS; Pereira MM; Sartorato EL Genet Mol Res; 2013 Nov; 12(4):5356-64. PubMed ID: 24301907 [TBL] [Abstract][Full Text] [Related]
17. Mutation of the dyslexia-associated gene Dcdc2 impairs LTM and visuo-spatial performance in mice. Gabel LA; Marin I; LoTurco JJ; Che A; Murphy C; Manglani M; Kass S Genes Brain Behav; 2011 Nov; 10(8):868-75. PubMed ID: 21883923 [TBL] [Abstract][Full Text] [Related]
18. Abnormal visual motion processing is not a cause of dyslexia. Olulade OA; Napoliello EM; Eden GF Neuron; 2013 Jul; 79(1):180-90. PubMed ID: 23746630 [TBL] [Abstract][Full Text] [Related]
19. Comparison of form and motion coherence processing in autistic spectrum disorders and dyslexia. Tsermentseli S; O'Brien JM; Spencer JV J Autism Dev Disord; 2008 Aug; 38(7):1201-10. PubMed ID: 18034294 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]