A genomewide scan for intelligence identifies quantitative trait loci on 2q and 6p

Am J Hum Genet. 2005 Aug;77(2):318-26. doi: 10.1086/432647. Epub 2005 Jul 1.

Abstract

Between 40% and 80% of the variation in human intelligence (IQ) is attributable to genetic factors. Except for many rare mutations resulting in severe cognitive dysfunction, attempts to identify these factors have not been successful. We report a genomewide linkage scan involving 634 sibling pairs designed to identify chromosomal regions that explain variation in IQ. Model-free multipoint linkage analysis revealed evidence of a significant quantitative-trait locus for performance IQ at 2q24.1-31.1 (LOD score 4.42), which overlaps the 2q21-33 region that has repeatedly shown linkage to autism. A second region revealed suggestive linkage for both full-scale and verbal IQs on 6p25.3-22.3 (LOD score 3.20 for full-scale IQ and 2.33 for verbal IQ), overlapping marginally with the 6p22.3-21.31 region implicated in reading disability and dyslexia.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Autistic Disorder / genetics
  • Chromosome Mapping
  • Chromosomes, Human, Pair 2*
  • Chromosomes, Human, Pair 6*
  • Dyslexia / genetics
  • Female
  • Genetic Linkage
  • Genome
  • Genome, Human*
  • Humans
  • Intelligence*
  • Learning Disabilities / genetics
  • Lod Score
  • Male
  • Middle Aged
  • Mutation
  • Quantitative Trait Loci*