A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p

S Palferman, N Matthews, M Turner, J Moore, A Hervas, A Aubin, S Wallace, J Michelotti, C Wainhouse, A Paul, E Thompson, R Gupta, C Garner, M Murin, C Freitag, N Ryder, E Cottington, J Parr, A Pickles, M RutterA Bailey, G Barnby, JA Lamb, A Marlow, P Scudder, AP Monaco*, G Baird, A Cox, Z Docherty, P Warburton, EP Green, SJ Abbs, A Le Couteur, HR McConachie, T Berney, TP Kelly, PJ De Vries, PF Bolton, J Green, A Gilchrist, J Whittacker, B Bolton, R Packer, E Maestrini, F Blasi, H Van Engeland, MV De Jonge, C Kemner, SM Klauck, KS Beyer,

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Autism is characterized by impairments in reciprocal communication and social interaction and by repetitive and stereotyped patterns of activities and interests. Evidence for a strong underlying genetic predisposition comes from twin and family studies, although susceptibility genes have not yet been identified. A whole-genome screen for linkage, using 83 sib pairs with autism, has been completed, and 119 markers have been genotyped in 13 candidate regions in a further 69 sib pairs. The addition of new families and markers provides further support for previous reports of linkages on chromosomes 7q and 16p. Two new regions of linkage have also been identified on chromosomes 2q and 17q. The most significant finding was a multipoint maximum LOD score (MLS) of 3.74 at marker D2S2188 on chromosome 2; this MLS increased to 4.80 when only sib pairs fulfilling strict diagnostic criteria were included. The susceptibility region on chromosome 7 was the next most significant, generating a multipoint MLS of 3.20 at marker D7S477. Chromosome 16 generated a multipoint MLS of 2.93 at D16S3102, whereas chromosome 17 generated a multipoint MLS of 2.34 at HTTINT2. With the addition of new families, there was no increased allele sharing at a number of other loci originally showing some evidence of linkage. These results support the continuing collection of multiplex sib-pair families to identify autism-susceptibility genes.

Original languageEnglish
Pages (from-to)570-581
Number of pages12
JournalAmerican Journal of Human Genetics
Volume69
Issue number3
Publication statusPublished - Sept 2001

Keywords

  • DIAGNOSTIC OBSERVATION SCHEDULE
  • TRANSMISSION-RATIO DISTORTION
  • SEROTONIN TRANSPORTER 5-HTT
  • SIB-PAIR LINKAGE
  • TUBEROUS SCLEROSIS
  • MULTIPLEX FAMILIES
  • INFANTILE-AUTISM
  • COMPLEX TRAITS
  • X-CHROMOSOME
  • DISORDER

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