Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2011 Jan;129(1):59-70.
doi: 10.1007/s00439-010-0899-z. Epub 2010 Oct 21.

Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16

Nicola H Chapman  1 , Annette Estes, Jeff Munson, Raphael Bernier, Sara J Webb, Joseph H Rothstein, Nancy J Minshew, Geraldine Dawson, Gerard D Schellenberg, Ellen M Wijsman
Affiliations

Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16

Nicola H Chapman et al. Hum Genet. 2011 Jan.

Abstract

Performance IQ (PIQ) greater than verbal IQ (VIQ) is often observed in studies of the cognitive abilities of autistic individuals. This characteristic is correlated with social and communication impairments, key parts of the autism diagnosis. We present the first genetic analyses of IQ discrepancy (PIQ-VIQ) as an autism-related phenotype. We performed genome-wide joint linkage and segregation analyses on 287 multiplex families, using a Markov chain Monte Carlo approach. Genetic data included a genome-scan of 387 micro-satellite markers in 210 families augmented with additional markers added in a subset of families. Empirical P values were calculated for five interesting regions. Linkage analysis identified five chromosomal regions with substantial regional evidence of linkage; 10p12 [P = 0.001; genome-wide (gw) P = 0.05], 16q23 (P = .015; gw P = 0.53), 2p21 (P = 0.03, gw P = 0.78), 6q25 (P = 0.047, gw P = 0.91) and 15q23-25 (P = 0.053, gw P = 0.93). The location of the chromosome 10 linkage signal coincides with a region noted in a much earlier genome-scan for autism, and the chromosome 16 signal coincides exactly with a linkage signal for non-word repetition in specific language impairment. This study provides strong evidence for a QTL influencing IQ discrepancy in families with autistic individuals on chromosome 10, and suggestive evidence for a QTL on chromosome 16. The location of the chromosome 16 signal suggests a candidate gene, CDH13, a T-cadherin expressed in the brain, which has been implicated in previous SNP studies of autism and ADHD.

PubMed Disclaimer

Conflict of interest statement

Conflict of interest All authors report no conflicts of interest. Experiments conducted comply with the current laws of the country in which they were performed.

Figures

Fig. 1
Fig. 1
Empirical distributions of IQ discrepancy (PIQ–VIQ) in parents (solid line), unaffected siblings (dashed line) and affected individuals (dot-dash)
Fig. 2
Fig. 2
Genome-scan results using the ABI dataset. The base-10 logarithm of the Bayes Factor, calculated in 4 cM intervals, is plotted against the genetic location along each chromosome using the Haldane map. Chromosomes are labeled across the bottom of the figure
Fig. 3
Fig. 3
Whole-chromosome scan results for each of the five chromosomes of interest, using both the ABI dataset (solid line) and the combined ABI and AGP datasets (dot-dash line). The base-10 logarithm of the Bayes Factor is plotted against the genetic location (cM) along the chromosome
See this image and copyright information in PMC

Similar articles

See all similar articles

Cited by

See all "Cited by" articles

References

    1. Alarcon M, Cantor RM, Liu J, Gilliam TC, Geschwind DH Consortium AGRE. Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families. Am J Hum Genet. 2002;70:60–71. - PMC - PubMed
    1. Alarcon M, Yonan AL, Gilliam TC, Cantor RM, Geschwind DH. Quantitative genome scan and ordered-subsets analysis of autism endophenotypes support language QTLs. Mol Psychiatry. 2005;10:747–757. - PubMed
    1. Allen-Brady K, Robison R, Cannon D, Varvil T, Villalobos ME, Pingree C, Leppert M, Miller J, McMahon WM, Coon H. Genome-wide linkage in Utah autism pedigrees. Mol Psychiatry. 2009;15:1006–1015. - PMC - PubMed
    1. Alm J, Kaufman AS. The Swedish WAIS-R factor structure and cognitive profiles for adults with dyslexia. J Learn Disabil. 2002;35:321–333. - PubMed
    1. Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Sykes N, Pagnamenta AT, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bolte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Carson AR, Casallo G, Casey J, Chu SH, Cochrane L, Corsello C, Crawford EL, Crossett A, Dawson G, de Jonge M, Delorme R, Drmic I, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Fombonne E, Freitag CM, Gilbert J, Gillberg C, Glessner JT, Goldberg J, Green J, Guter SJ, Hakonarson H, Heron EA, Hill M, Holt R, Howe JL, Hughes G, Hus V, Igliozzi R, Kim C, Klauck SM, Kolevzon A, Korvatska O, Kustanovich V, Lajonchere CM, Lamb JA, Laskawiec M, Leboyer M, Le Couteur A, Leventhal BL, Lionel AC, Liu XQ, Lord C, Lotspeich L, Lund SC, Maestrini E, Mahoney W, Mantoulan C, Marshall CR, McConachie H, McDougle CJ, McGrath J, McMahon WM, Melhem NM, Merikangas A, Migita O, Minshew NJ, Mirza GK, Munson J, Nelson SF, Noakes C, Noor A, Nygren G, Oliveira G, Papanikolaou K, Parr JR, Parrini B, Paton T, Pickles A, Piven J, Posey DJ, Poustka A, Poustka F. A genome-wide scan for common alleles affecting risk for autism. Hum Mol Genet. 2010;19:4072–4082. - PMC - PubMed

Publication types

LinkOut - more resources