Evidence for the involvement of ZNF804A in cognitive processes of relevance to reading and spelling

Translational Psychiatry

Volumn 2, Issue , 2012, Pages

  Becker, J ^a   Czamara, D ^b   Hoffmann, P ^a   Landerl, K ^c   Blomert, L ^d   Brandeis, D ^e,f   Vaessen, A ^d   Maurer, U ^e   Moll, K ^g,i   Ludwig, K U ^a   Muller Myhsok B ^b   Nothen M M ^a   Schulte Korne G ^h   Schumacher, J ^a  

^a UNIVERSITY OF BONN   (Germany)

^b MAX PLANCK INSTITUTE OF PSYCHIATRY   (Germany)

^c UNIVERSITY OF GRAZ   (Austria)

^d MAASTRICHT UNIVERSITY   (Netherlands)

^e UNIVERSITY OF ZURICH   (Switzerland)

^f MEDICAL FACULTY MANNHEIM HEIDELBERG UNIVERSITY   (Germany)

^g UNIVERSITY OF SALZBURG   (Austria)

^h LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

ⁱ UNIVERSITY OF YORK   (United Kingdom)

Author keywords

cognitive processes; dyslexia; genetic association; reading and spelling; schizophrenia; ZNF804A

Indexed keywords

ACTIVATING TRANSCRIPTION FACTOR 4; NEUROGRANIN; UNCLASSIFIED DRUG; ZINC FINGER PROTEIN; ZINC FINGER PROTEIN 804A;

ALLELE; ARTICLE; COGNITION; CONTROLLED STUDY; DYSLEXIA; GENE; GENETIC ASSOCIATION; GENETIC RISK; GENETIC TRAIT; GENETIC VARIABILITY; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MEMORY; PHENOTYPE; PSYCHOMOTOR PERFORMANCE; READING; SCHIZOPHRENIA; SPELLING; ZNF804A GENE;

CASE-CONTROL STUDIES; DYSLEXIA; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; GENOTYPE; HUMANS; KRUPPEL-LIKE TRANSCRIPTION FACTORS; LANGUAGE; MALE; NEUROGRANIN; NEUROPSYCHOLOGICAL TESTS; READING; SCHIZOPHRENIA;

EID: 84863739396     PISSN: None     EISSN: 21583188     Source Type: Journal    
DOI: 10.1038/tp.2012.62     Document Type: Article

References (10)

1. O'Donovan MC, Craddock N, Norton N, Williams H, Peirce T, Moskvina V et al. Identification of loci associated with schizophrenia by genome-wide association and follow-up. Nat Genet 2008; 40: 1053-1055.
2. Stefansson H, Ophoff RA, Steinberg S, Andreassen OA, Cichon S, Rujescu D et al. Common variants conferring risk of schizophrenia. Nature 2009; 460: 744-747.
3. Gejman PV, Sanders AR, Kendler KS. Genetics of schizophrenia: new findings and challenges. Annu Rev Genomics Hum Genet 2011; 12: 121-144.
4. Leonard CM, Kuldau JM, Maron L, Ricciuti N, Mahoney B, Bengtson M et al. Identical neural risk factors predict cognitive deficit in dyslexia and schizophrenia. Neuropsychology 2008; 22: 147-158. (Pubitemid 351626503)
5. Bersani G, Maneschi ML, Tarolla E, Pancheri P. Dyslexia as a possible aspect of neurocognitive impairment in schizophrenia. Schizophr Res 2006; 82: 265-266. (Pubitemid 43290691)
6. Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 2007; 81: 559-575. (Pubitemid 47330214)
7. Cocchella A, Malacarne M, Forzano F, Marciano C, Pierluigi M, Perroni L et al. The refinement of the critical region for the 2q31.2q32.3 deletion syndrome indicates candidate genes for mental retardation and speech impairment. Am J Med Genet B Neuropsychiatr Genet 2010; 153B: 1342-1346.
8. Walters JT, Corvin A, Owen MJ, Williams H, Dragovic M, Quinn EM et al. Psychosis susceptibility gene ZNF804A and cognitive performance in schizophrenia. Arch Gen Psychiatry 2010; 67: 692-700.
9. Vellutino FR, Fletcher JM, Snowling MJ, Scanlon DM. Specific reading disability (dyslexia): what have we learned in the past four decades? J Child Psychol Psychiatry 2004; 45: 2-40. (Pubitemid 38196253)
10. Donohoe G, Morris DW, Corvin A. The psychosis susceptibility gene ZNF804A: associations, functions, and phenotypes. Schizophr Bull 2010; 36: 904-909.