135 related articles for article (PubMed ID: 23954868)
1. Lack of association between genetic polymorphisms in ROBO1, MRPL19/C2ORF3 and THEM2 with developmental dyslexia.
Venkatesh SK; Siddaiah A; Padakannaya P; Ramachandra NB
Gene; 2013 Oct; 529(2):215-9. PubMed ID: 23954868
[TBL] [Abstract][Full Text] [Related]
2. 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]
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. Association of SNPs of DYX1C1 with developmental dyslexia in an Indian population.
Venkatesh SK; Siddaiah A; Padakannaya P; Ramachandra NB
Psychiatr Genet; 2014 Feb; 24(1):10-20. PubMed ID: 24362368
[TBL] [Abstract][Full Text] [Related]
5. KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia.
Mascheretti S; Riva V; Giorda R; Beri S; Lanzoni LF; Cellino MR; Marino C
J Hum Genet; 2014 Apr; 59(4):189-97. PubMed ID: 24430574
[TBL] [Abstract][Full Text] [Related]
6. Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions.
Pinel P; Fauchereau F; Moreno A; Barbot A; Lathrop M; Zelenika D; Le Bihan D; Poline JB; Bourgeron T; Dehaene S
J Neurosci; 2012 Jan; 32(3):817-25. PubMed ID: 22262880
[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. Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.
Cope N; Harold D; Hill G; Moskvina V; Stevenson J; Holmans P; Owen MJ; O'Donovan MC; Williams J
Am J Hum Genet; 2005 Apr; 76(4):581-91. PubMed ID: 15717286
[TBL] [Abstract][Full Text] [Related]
9. Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits.
Bates TC; Luciano M; Medland SE; Montgomery GW; Wright MJ; Martin NG
Behav Genet; 2011 Jan; 41(1):50-7. PubMed ID: 20949370
[TBL] [Abstract][Full Text] [Related]
10. An examination of candidate gene SNPs for dyslexia in an Indian sample.
Venkatesh SK; Siddaiah A; Padakannaya P; Ramachandra NB
Behav Genet; 2011 Jan; 41(1):105-9. PubMed ID: 21203818
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Association of the ROBO1 gene with reading disabilities in a family-based analysis.
Tran C; Wigg KG; Zhang K; Cate-Carter TD; Kerr E; Field LL; Kaplan BJ; Lovett MW; Barr CL
Genes Brain Behav; 2014 Apr; 13(4):430-8. PubMed ID: 24612512
[TBL] [Abstract][Full Text] [Related]
14. High-throughput single-nucleotide polymorphism analysis of the IL1RN locus in patients with ankylosing spondylitis by matrix-assisted laser desorption ionization-time-of-flight mass spectrometry.
Maksymowych WP; Reeve JP; Reveille JD; Akey JM; Buenviaje H; O'Brien L; Peloso PM; Thomson GT; Jin L; Russell AS
Arthritis Rheum; 2003 Jul; 48(7):2011-8. PubMed ID: 12847695
[TBL] [Abstract][Full Text] [Related]
15. Association analysis of dyslexia candidate genes in a Dutch longitudinal sample.
Carrion-Castillo A; Maassen B; Franke B; Heister A; Naber M; van der Leij A; Francks C; Fisher SE
Eur J Hum Genet; 2017 Apr; 25(4):452-460. PubMed ID: 28074887
[TBL] [Abstract][Full Text] [Related]
16. Association between
Deng KG; Zhao H; Zuo PX
J Genet; 2019 Jun; 98(1):. PubMed ID: 31204720
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. The molecular genetics and neurobiology of developmental dyslexia as model of a complex phenotype.
Kere J
Biochem Biophys Res Commun; 2014 Sep; 452(2):236-43. PubMed ID: 25078623
[TBL] [Abstract][Full Text] [Related]
20. Association of short-term memory with a variant within DYX1C1 in developmental dyslexia.
Marino C; Citterio A; Giorda R; Facoetti A; Menozzi G; Vanzin L; Lorusso ML; Nobile M; Molteni M
Genes Brain Behav; 2007 Oct; 6(7):640-6. PubMed ID: 17309662
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
