Association study of a functional genetic variant in KIAA0319 in German dyslexics

Psychiatric Genetics

Volumn 22, Issue 4, 2012, Pages 216-217

  Kirsten, Holger ^a,b   Wilcke, Arndt ^a,b   Ligges, Carolin ^c   Boltze, Johannes ^a,b   Ahnert, Peter ^a  

^a UNIVERSITY OF LEIPZIG   (Germany)

^b FRAUNHOFER INSTITUTE FOR CELL THERAPY AND IMMUNOLOGY   (Germany)

^c JENA UNIVERSITY HOSPITAL   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; COMPREHENSION; DISEASE SEVERITY; DYSLEXIA; EARLY INTERVENTION; GENE; GENE EXPRESSION; GENE INTERACTION; GENETIC ASSOCIATION; GENETIC VARIABILITY; GERMANY; HUMAN; INTELLIGENCE; KIAA0319 GENE; MASS SPECTROMETRY; PRIORITY JOURNAL; READING;

CASE-CONTROL STUDIES; DYSLEXIA; GENE FREQUENCY; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GERMANY; HUMANS; NERVE TISSUE PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84863500479     PISSN: 09558829     EISSN: 14735873     Source Type: Journal    
DOI: 10.1097/YPG.0b013e32834c0c97     Document Type: Article

References (5)

1. Dennis MY, Paracchini S, Scerri TS, Prokunina-Olsson L, Knight JC, Wade-Martins R, et al. (2009). A common variant associated with dyslexia reduces expression of the KIAA0319 gene. PLoS Genet 5:e1000436.
2. Elbert A, Lovett MW, Cate-Carter T, Pitch A, Kerr EN, Barr CL (2011). Genetic variation in the KIAA0319 50 region as a possible contributor to dyslexia. Behav Genet 41:77-89.
3. Ludwig KU, Roeske D, Schumacher J, Schulte-Korne G, Konig IR, Warnke A, et al. (2008). Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample. J Neural Transm 115:1587-1589.
4. Scerri TS, Schulte-Korne G (2010). Genetics of developmental dyslexia. Eur Child Adolesc Psychiatry 19:179-197.
5. Wilcke A,Weissfuss J, Kirsten H,Wolfram G, Boltze J, Ahnert P (2009). The role of gene DCDC2 in German dyslexics. Dyslexia 59:1-11.