313 related articles for article (PubMed ID: 20956978)
1. A theoretical molecular network for dyslexia: integrating available genetic findings.
Poelmans G; Buitelaar JK; Pauls DL; Franke B
Mol Psychiatry; 2011 Apr; 16(4):365-82. PubMed ID: 20956978
[TBL] [Abstract][Full Text] [Related]
2. Genes, cognition and dyslexia: learning to read the genome.
Fisher SE; Francks C
Trends Cogn Sci; 2006 Jun; 10(6):250-7. PubMed ID: 16675285
[TBL] [Abstract][Full Text] [Related]
3. Analysis of genetic variants of dyslexia candidate genes KIAA0319 and DCDC2 in Indian population.
Venkatesh SK; Siddaiah A; Padakannaya P; Ramachandra NB
J Hum Genet; 2013 Aug; 58(8):531-8. PubMed ID: 23677054
[TBL] [Abstract][Full Text] [Related]
4. Familial dyslexia in a large Swedish family: a whole genome linkage scan.
Svensson I; Nilsson S; Wahlström J; Jernås M; Carlsson LM; Hjelmquist E
Behav Genet; 2011 Jan; 41(1):43-9. PubMed ID: 20862559
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Polymorphisms in DCDC2 and S100B associate with developmental dyslexia.
Matsson H; Huss M; Persson H; Einarsdottir E; Tiraboschi E; Nopola-Hemmi J; Schumacher J; Neuhoff N; Warnke A; Lyytinen H; Schulte-Körne G; Nöthen MM; Leppänen PH; Peyrard-Janvid M; Kere J
J Hum Genet; 2015 Jul; 60(7):399-401. PubMed ID: 25877001
[TBL] [Abstract][Full Text] [Related]
7. Association study of developmental dyslexia candidate genes DCDC2 and KIAA0319 in Chinese population.
Sun Y; Gao Y; Zhou Y; Chen H; Wang G; Xu J; Xia J; Huen MS; Siok WT; Jiang Y; Tan LH
Am J Med Genet B Neuropsychiatr Genet; 2014 Dec; 165B(8):627-34. PubMed ID: 25230923
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Genetic variant in KIAA0319, but not in DYX1C1, is associated with risk of dyslexia: an integrated meta-analysis.
Zou L; Chen W; Shao S; Sun Z; Zhong R; Shi J; Miao X; Song R
Am J Med Genet B Neuropsychiatr Genet; 2012 Dec; 159B(8):970-6. PubMed ID: 23065966
[TBL] [Abstract][Full Text] [Related]
10. Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion.
Poelmans G; Engelen JJ; Van Lent-Albrechts J; Smeets HJ; Schoenmakers E; Franke B; Buitelaar JK; Wuisman-Frerker M; Erens W; Steyaert J; Schrander-Stumpel C
Am J Med Genet B Neuropsychiatr Genet; 2009 Jan; 150B(1):140-7. PubMed ID: 18521840
[TBL] [Abstract][Full Text] [Related]
11. [Genetics of dyslexia].
Schulte-Körne G; Warnke A; Remschmidt H
Z Kinder Jugendpsychiatr Psychother; 2006 Nov; 34(6):435-44. PubMed ID: 17094062
[TBL] [Abstract][Full Text] [Related]
12. A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.
Anthoni H; Zucchelli M; Matsson H; Müller-Myhsok B; Fransson I; Schumacher J; Massinen S; Onkamo P; Warnke A; Griesemann H; Hoffmann P; Nopola-Hemmi J; Lyytinen H; Schulte-Körne G; Kere J; Nöthen MM; Peyrard-Janvid M
Hum Mol Genet; 2007 Mar; 16(6):667-77. PubMed ID: 17309879
[TBL] [Abstract][Full Text] [Related]
13. Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects.
Loo SK; Fisher SE; Francks C; Ogdie MN; MacPhie IL; Yang M; McCracken JT; McGough JJ; Nelson SF; Monaco AP; Smalley SL
Mol Psychiatry; 2004 May; 9(5):485-93. PubMed ID: 14625563
[TBL] [Abstract][Full Text] [Related]
14. The genetics of developmental dyslexia.
Williams J; O'Donovan MC
Eur J Hum Genet; 2006 Jun; 14(6):681-9. PubMed ID: 16721404
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations.
Matsson H; Tammimies K; Zucchelli M; Anthoni H; Onkamo P; Nopola-Hemmi J; Lyytinen H; Leppanen PH; Neuhoff N; Warnke A; Schulte-Körne G; Schumacher J; Nöthen MM; Kere J; Peyrard-Janvid M
Behav Genet; 2011 Jan; 41(1):134-40. PubMed ID: 21203819
[TBL] [Abstract][Full Text] [Related]
17. The genetic lexicon of dyslexia.
Paracchini S; Scerri T; Monaco AP
Annu Rev Genomics Hum Genet; 2007; 8():57-79. PubMed ID: 17444811
[TBL] [Abstract][Full Text] [Related]
18. Developmental dyslexia: an update on genes, brains, and environments.
Grigorenko EL
J Child Psychol Psychiatry; 2001 Jan; 42(1):91-125. PubMed ID: 11205626
[TBL] [Abstract][Full Text] [Related]
19. Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice.
Martinez-Garay I; Guidi LG; Holloway ZG; Bailey MA; Lyngholm D; Schneider T; Donnison T; Butt SJ; Monaco AP; Molnár Z; Velayos-Baeza A
Brain Struct Funct; 2017 Apr; 222(3):1367-1384. PubMed ID: 27510895
[TBL] [Abstract][Full Text] [Related]
20. The role of READ1 and KIAA0319 genetic variations in developmental dyslexia: testing main and interactive effects.
Trezzi V; Forni D; Giorda R; Villa M; Molteni M; Marino C; Mascheretti S
J Hum Genet; 2017 Nov; 62(11):949-955. PubMed ID: 29066855
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]