A Genomewide Screen for Autism Susceptibility Loci
Tóm tắt
Từ khóa
Tài liệu tham khảo
Adams, 1994, LABMAN and LINKMAN: a data management system specifically designed for genome searches of complex diseases, Genet Epidemiol, 11, 87, 10.1002/gepi.1370110109
Aita, 1999, A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus, Am J Hum Genet, 64, 210, 10.1086/302185
Anderson, 1987, Whole blood serotonin in autistic and normal subjects, J Child Psychol Psychiatry, 28, 885, 10.1111/j.1469-7610.1987.tb00677.x
Anderson, 1984, Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines, In Vitro, 20, 856, 10.1007/BF02619631
Ashley-Koch, 1999, Genetic studies of autistic disorder and chromosome 7, Genomics, 61, 227, 10.1006/geno.1999.5968
Bailey, 1995, Autism as a strongly genetic disorder: evidence from a British twin study, Psychol Med, 25, 63, 10.1017/S0033291700028099
Bailey, 1996, Autism: towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives, J Child Psychol Psychiatry, 37, 89, 10.1111/j.1469-7610.1996.tb01381.x
Barrett, 1999, An autosomal genomic screen for autism: collaborative linkage study of autism, Am J Med Genet, 88, 609, 10.1002/(SICI)1096-8628(19991215)88:6<609::AID-AJMG7>3.0.CO;2-L
Bertram, 2000, Evidence for genetic linkage of Alzheimer's disease to chromosome 10q, Science, 290, 2302, 10.1126/science.290.5500.2302
Bolton, 1994, A case-control family history study of autism, J Child Psychol Psychiatry, 35, 877, 10.1111/j.1469-7610.1994.tb02300.x
Brodkin, 1997, Clomipramine in adults with pervasive developmental disorders: a prospective open-label investigation, J Child Adolesc Psychopharmacol, 7, 109, 10.1089/cap.1997.7.109
Broman, 1998, Comprehensive human genetic maps: individual and sex-specific variation in recombination, Am J Hum Genet, 63, 861, 10.1086/302011
Buxbaum, 1999, A genome-wide linkage study in autism, Mol Psychiatry Suppl, 4, S13
Christian, 1999, Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13), Hum Mol Genet, 8, 1025, 10.1093/hmg/8.6.1025
Cook, 1997, Evidence of linkage between the serotonin transporter and autistic disorder, Mol Psychiatry, 2, 247, 10.1038/sj.mp.4000266
Cordell, 1995, An extension of the maximum LOD score method to X-linked loci, Ann Hum Genet, 59, 435, 10.1111/j.1469-1809.1995.tb00761.x
Creswell, 1999, Autism in association with Turner syndrome: genetic implications for male vulnerability to pervasive developmental disorders, Neurocase, 5, 111, 10.1080/13554799908402746
Ertekin-Taner, 2000, Linkage of plasma Aβ42 to a quantitative locus on chromosome 10 in late-onset Alzheimer's disease pedigrees, Science, 290, 2303, 10.1126/science.290.5500.2303
Faraway, 1993, Improved sib-pair linkage test for disease susceptibility loci, Genet Epidemiol, 10, 225, 10.1002/gepi.1370100403
Fatemi, 1998, Fluoxetine in treatment of adolescent patients with autism: a longitudinal open trial, J Autism Dev Disord, 28, 303, 10.1023/A:1026008602540
Feinstein, 1998, Autism: the point of view from fragile X studies, J Autism Dev Disord, 28, 393, 10.1023/A:1026000404855
Folstein, 1977, Infantile autism: a genetic study of 21 twin pairs, J Child Psychol Psychiatry, 18, 297, 10.1111/j.1469-7610.1977.tb00443.x
Gillberg, 1989, Asperger syndrome in 23 Swedish children, Dev Med Child Neurol, 31, 520, 10.1111/j.1469-8749.1989.tb04031.x
Gillberg, 1999, Autism: not an extremely rare disorder, Acta Psychiatr Scand, 99, 399, 10.1111/j.1600-0447.1999.tb00984.x
Gudbjartsson, 2000, Allegro, a new computer program for multipoint linkage analysis, Nat Genet, 25, 12, 10.1038/75514
Hauser, 1996, Affected-sib-pair interval mapping and exclusion for complex genetic traits: sampling considerations, Genet Epidemiol, 13, 117, 10.1002/(SICI)1098-2272(1996)13:2<117::AID-GEPI1>3.0.CO;2-5
Hoh, 2000, Scan statistics to scan markers for susceptibility genes, Proc Natl Acad Sci USA, 97, 9615, 10.1073/pnas.170179197
Holmans, 1993, Asymptotic properties of affected-sib-pair linkage analysis, Am J Hum Genet, 52, 362
Holmans, 1995, Efficiency of typing unaffected relatives in an affected-sib-pair linkage study with single-locus and multiple tightly linked markers, Am J Hum Genet, 57, 1221
International Molecular Genetic Study of Autism Consortium, 1998, A full genome screen for autism with evidence for linkage to a region on chromosome 7q, Hum Mol Genet, 7, 571, 10.1093/hmg/7.3.571
Jorde, 1991, Complex segregation analysis of autism, Am J Hum Genet, 49, 932
Knapp, 1997, The affected sib pair method for linkage analysis, 150
Kruglyak, 1995, Complete multipoint sib-pair analysis of qualitative and quantitative traits, Am J Hum Genet, 57, 439
Lander, 1995, Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results, Nat Genet, 11, 241, 10.1038/ng1195-241
Lord, 1994, Autism Diagnostic Interview—Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders, J Autism Dev Disord, 24, 659, 10.1007/BF02172145
Maestrini, 1999, Search for autism susceptibility loci: genome screen follow-up and fine mapping of a candidate region on 7q, Am J Hum Genet Suppl, 65, A106
Maestrini, 1999, Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit β3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium, Am J Med Genet, 88, 492, 10.1002/(SICI)1096-8628(19991015)88:5<492::AID-AJMG11>3.0.CO;2-X
Magnuson, 1996, Substrate nucleotide-determined non-templated addition of adenine by Taq DNA polymerase: implications for PCR-based genotyping and cloning, Biotechniques, 21, 700, 10.2144/96214rr03
Myers, 2000, Susceptibility locus for Alzheimer's disease on chromosome 10, Science, 290, 2304, 10.1126/science.290.5500.2304
Philippe, 1999, Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study, Hum Mol Genet, 8, 805, 10.1093/hmg/8.5.805
Reik, 1998, Imprinting mechanisms in mammals, Curr Opin Genet Dev, 8, 154, 10.1016/S0959-437X(98)80136-6
Risch, 1990, Linkage strategies for genetically complex traits. II. The power of affected relative pairs, Am J Hum Genet, 46, 229
Risch, 1990, Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs, Am J Hum Genet, 46, 242
Risch, 1999, A genomic screen of autism: evidence for a multilocus etiology, Am J Hum Genet, 65, 493, 10.1086/302497
Sham, 1998, 110
Skuse, 2000, Imprinting, the X-chromosome, and the male brain: explaining sex differences in the liability to autism, Pediatr Res, 47, 9, 10.1203/00006450-200001000-00006
Skuse, 1997, Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function, Nature, 387, 705, 10.1038/42706
Szatmari, 1998, Genetics of autism: overview and new directions, J Autism Dev Disord, 28, 351, 10.1023/A:1026096203946
Terwilliger, 1994, 245
Terwilliger, 1997, True and false positive peaks in genomewide scans: applications of length-biased sampling to linkage mapping, Am J Hum Genet, 61, 430, 10.1086/514855
Wing, 1979, Severe impairments of social interaction and associated abnormalities in children: epidemiology and classification, J Autism Dev Disord, 9, 11, 10.1007/BF01531288