313 related articles for article (PubMed ID: 20956978)
21. Association of a rare variant with mismatch negativity in a region between KIAA0319 and DCDC2 in dyslexia.
Czamara D; Bruder J; Becker J; Bartling J; Hoffmann P; Ludwig KU; Müller-Myhsok B; Schulte-Körne G
Behav Genet; 2011 Jan; 41(1):110-9. PubMed ID: 21104116
[TBL] [Abstract][Full Text] [Related]
22. Genetics of dyslexia: the evolving landscape.
Schumacher J; Hoffmann P; Schmäl C; Schulte-Körne G; Nöthen MM
J Med Genet; 2007 May; 44(5):289-97. PubMed ID: 17307837
[TBL] [Abstract][Full Text] [Related]
23. [Psychocognitive and psychiatric disorders associated with developmental dyslexia: A clinical and scientific issue].
Huc-Chabrolle M; Barthez MA; Tripi G; Barthélémy C; Bonnet-Brilhault F
Encephale; 2010 Apr; 36(2):172-9. PubMed ID: 20434636
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. 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]
26. 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]
27. 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]
28. Neocortical disruption and behavioral impairments in rats following in utero RNAi of candidate dyslexia risk gene Kiaa0319.
Szalkowski CE; Fiondella CG; Galaburda AM; Rosen GD; Loturco JJ; Fitch RH
Int J Dev Neurosci; 2012 Jun; 30(4):293-302. PubMed ID: 22326444
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Association between
Deng KG; Zhao H; Zuo PX
J Genet; 2019 Jun; 98(1):. PubMed ID: 31204720
[TBL] [Abstract][Full Text] [Related]
31. Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.
Becker J; Czamara D; Scerri TS; Ramus F; Csépe V; Talcott JB; Stein J; Morris A; Ludwig KU; Hoffmann P; Honbolygó F; Tóth D; Fauchereau F; Bogliotti C; Iannuzzi S; Chaix Y; Valdois S; Billard C; George F; Soares-Boucaud I; Gérard CL; van der Mark S; Schulz E; Vaessen A; Maurer U; Lohvansuu K; Lyytinen H; Zucchelli M; Brandeis D; Blomert L; Leppänen PH; Bruder J; Monaco AP; Müller-Myhsok B; Kere J; Landerl K; Nöthen MM; Schulte-Körne G; Paracchini S; Peyrard-Janvid M; Schumacher J
Eur J Hum Genet; 2014 May; 22(5):675-80. PubMed ID: 24022301
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Breakthroughs in the search for dyslexia candidate genes.
McGrath LM; Smith SD; Pennington BF
Trends Mol Med; 2006 Jul; 12(7):333-41. PubMed ID: 16781891
[TBL] [Abstract][Full Text] [Related]
34. Further evidence for a susceptibility locus contributing to reading disability on chromosome 15q15-q21.
Schumacher J; König IR; Schröder T; Duell M; Plume E; Propping P; Warnke A; Libertus C; Ziegler A; Müller-Myhsok B; Schulte-Körne G; Nöthen MM
Psychiatr Genet; 2008 Jun; 18(3):137-42. PubMed ID: 18496212
[TBL] [Abstract][Full Text] [Related]
35. Genetics of developmental dyslexia.
Scerri TS; Schulte-Körne G
Eur Child Adolesc Psychiatry; 2010 Mar; 19(3):179-97. PubMed ID: 20091194
[TBL] [Abstract][Full Text] [Related]
36. Position of neocortical neurons transfected at different gestational ages with shRNA targeted against candidate dyslexia susceptibility genes.
Adler WT; Platt MP; Mehlhorn AJ; Haight JL; Currier TA; Etchegaray MA; Galaburda AM; Rosen GD
PLoS One; 2013; 8(5):e65179. PubMed ID: 23724130
[TBL] [Abstract][Full Text] [Related]
37. [Sense and nonsense with respect to the gene for dyslexia].
Jennekens-Schinkel A
Ned Tijdschr Geneeskd; 1998 Nov; 142(45):2445-7. PubMed ID: 10028322
[TBL] [Abstract][Full Text] [Related]
38. The human lexinome: genes of language and reading.
Gibson CJ; Gruen JR
J Commun Disord; 2008; 41(5):409-20. PubMed ID: 18466916
[TBL] [Abstract][Full Text] [Related]
39. Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family.
Einarsdottir E; Svensson I; Darki F; Peyrard-Janvid M; Lindvall JM; Ameur A; Jacobsson C; Klingberg T; Kere J; Matsson H
Hum Genet; 2015 Nov; 134(11-12):1239-48. PubMed ID: 26400686
[TBL] [Abstract][Full Text] [Related]
40. The genetics of reading disability.
Petryshen TL; Pauls DL
Curr Psychiatry Rep; 2009 Apr; 11(2):149-55. PubMed ID: 19302769
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
