Crossref
journal-article
Elsevier BV
Seminars in Pediatric Neurology (78)
References
161
Referenced
48
10.1016/S1056-4993(18)30061-0
/ Child Adolesc Psychiatr Clin N Am / Genetics of autism by Cook (2001)10.1093/hmg/9.6.861
/ Hum Mol Genet / Autism by Lamb (2000)10.1038/sj.mp.4001505
/ Mol Psychiatry / Molecular genetics of autism spectrum disorder by Veenstra-VanderWeele (2004)10.1017/S0033291700028099
/ Psychol Med / Autism as a strongly genetic disorder by Bailey (1995)10.1111/j.1469-7610.1977.tb00443.x
/ J Child Psychol Psychiatry / Infantile autism by Folstein (1977)10.1111/j.1469-7610.1996.tb01475.x
/ J Child Psychol Psychiatry / A broader phenotype of autism by Le Couteur (1996)10.1176/ajp.142.1.74
/ Am J Psychiatry / Concordance for the syndrome of autism in 40 pairs of afflicted twins by Ritvo (1985)10.1111/j.1469-7610.1991.tb01928.x
/ J Child Psychol Psychiatry / Debate and argument. Concordance for the syndrome of autism by Ritvo (1991)10.1111/j.1469-7610.1989.tb00254.x
/ J Child Psychol Psychiatry / A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden by Steffenburg (1989)10.1111/1469-7610.00423
/ J Child Psychol Psychiatry / Genetics and child psychiatry, II by Rutter (1999)10.1007/BF02211816
/ J Autism Dev Disord / Stoppage rules and genetic studies of autism by Jones (1988)10.1002/gepi.4.abs
/ Genet Epidemiol / Stoppage by Slager (2001){'key': '10.1016/j.spen.2004.07.003_bib13', 'first-page': '159', 'article-title': 'Heterogeneity and the genetics of autism', 'volume': '24', 'author': 'Szatmari', 'year': '1999', 'journal-title': 'J Psychiatry Neurosci'}
/ J Psychiatry Neurosci / Heterogeneity and the genetics of autism by Szatmari (1999)10.1111/j.1469-7610.1994.tb02300.x
/ J Child Psychol Psychiatry / A case-control family history study of autism by Bolton (1994)10.1002/ajmg.1320540107
/ Am J Med Genet / Genetics of autism by Spiker (1994)10.1023/A:1026048320785
/ J Autism Dev Disord / Autism by Bailey (1998){'key': '10.1016/j.spen.2004.07.003_bib17', 'first-page': '217', 'article-title': 'Autistic disturbances of affective contact', 'volume': '10', 'author': 'Kanner', 'year': '1943', 'journal-title': 'Nervous Child'}
/ Nervous Child / Autistic disturbances of affective contact by Kanner (1943)10.1044/jshr.3406.1339
/ J Speech Hear Res / Spontaneous narrative-discourse performance of parents of autistic individuals by Landa (1991)10.1017/S0033291700032918
/ Psychol Med / Social language use in parents of autistic individuals by Landa (1992)10.1097/00004583-199105000-00019
/ J Am Acad Child Adolesc Psychiatry / Psychiatric disorders in the parents of autistic individuals by Piven (1991)10.1097/00004583-199003000-00004
/ J Am Acad Child Adolesc Psychiatry / A family history study of neuropsychiatric disorders in the adult siblings of autistic individuals by Piven (1990)10.1017/S0033291700027938
/ Psychol Med / Personality characteristics of the parents of autistic individuals by Piven (1994)10.1002/ajmg.1320600105
/ Am J Med Genet / Autism, affective disorders, and social phobia by Smalley (1995)10.1176/ajp.156.4.557
/ Am J Psychiatry / Psychiatric disorder and the broad autism phenotype by Piven (1999)10.1016/S0165-1781(02)00304-9
/ Psychiatry Res / Obsessive-compulsive behaviors in parents of multiplex autism families by Hollander (2003)10.1017/S0033291799002949
/ Psychol Med / Personality traits of the relatives of autistic probands by Murphy (2000)10.1111/1469-7610.00528
/ J Child Psychol Psychiatry / Predictors of cognitive test patterns in autism families by Folstein (1999)10.1192/bjp.126.2.127
/ Br J Psychiatry / A comparative study of infantile autism and specific development receptive language disorder, I by Bartak (1975)10.1176/ajp.146.3.361
/ Am J Psychiatry / Psychometric assessment of first-degree relatives of 62 autistic probands in Utah by Freeman (1989)10.1002/(SICI)1096-8628(19970725)74:4<398::AID-AJMG11>3.0.CO;2-D
/ Am J Med Genet / Personality and language characteristics in parents from multiple-incidence autism families by Piven (1997)10.1097/00004583-199311000-00022
/ J Am Acad Child Adolesc Psychiatry / Lack of cognitive impairment in first-degree relatives of children with pervasive developmental disorders by Szatmari (1993)10.1176/ajp.154.2.185
/ Am J Psychiatry / Broader autism phenotype by Piven (1997){'key': '10.1016/j.spen.2004.07.003_bib33', 'first-page': '1561', 'article-title': 'Autism and associated medical disorders in a French epidemiological survey', 'volume': '36', 'author': 'Fombonne', 'year': '1997', 'journal-title': 'J Am Acad Child Adolesc Psychiatry'}
/ J Am Acad Child Adolesc Psychiatry / Autism and associated medical disorders in a French epidemiological survey by Fombonne (1997)10.1002/ajmg.1320600110
/ Am J Med Genet / Chromosomal abnormalities in a psychiatric population by Lewis (1995)10.1097/00041444-200106000-00001
/ Psychiatr Genet / Chromosomal abnormalities in a clinic sample of individuals with autistic disorder by Wassink (2001)10.1002/(SICI)1096-8628(20000410)91:4<245::AID-AJMG1>3.0.CO;2-2
/ Am J Med Genet / Value of a clinical morphology examination in autism by Miles (2000)10.1023/A:1022155201662
/ J Autism Dev Disord / Chromosomal abnormalities in a series of children with autistic disorder by Konstantareas (1999)10.1111/j.1469-8749.1985.tb04539.x
/ Dev Med Child Neurol / Chromosome abnormalities in infantile autism and other childhood psychoses by Gillberg (1985)10.1111/j.1469-7610.1994.tb01164.x
/ J Child Psychol Psychiatry / Autism and known medical conditions by Rutter (1994){'key': '10.1016/j.spen.2004.07.003_bib40', 'first-page': '825', 'article-title': 'The prevalence of fragile X in a sample of autistic individuals diagnosed using a standardized interview', 'volume': '30', 'author': 'Piven', 'year': '1991', 'journal-title': 'J Am Acad Child Adolesc Psychiatry'}
/ J Am Acad Child Adolesc Psychiatry / The prevalence of fragile X in a sample of autistic individuals diagnosed using a standardized interview by Piven (1991)10.1111/j.1469-7610.1993.tb01064.x
/ J Child Psychol Psychiatry / Prevalence of the fragile X anomaly amongst autistic twins and singletons by Bailey (1993)10.1023/A:1025857422026
/ J Autism Dev Disord / Autistic behaviors among girls with fragile X syndrome by Mazzocco (1997)10.1023/A:1026000404855
/ J Autism Dev Disord / Autism by Feinstein (1998)10.1023/A:1017956224167
/ J Autism Dev Disord / Legitimacy of comparing fragile X with autism questioned by Rapin (2002)10.1111/j.1469-8749.1994.tb11765.x
/ Dev Med Child Neurol / Autistic behaviour and attention deficits in tuberous sclerosis by Gillberg (1994)10.1023/A:1026032413811
/ J Autism Dev Disord / Autism in tuberous sclerosis complex by Gutierrez (1998)10.1007/BF01046223
/ J Autism Dev Disord / A prevalence study of autism in tuberous sclerosis by Hunt (1993)10.1023/A:1026052421693
/ J Autism Dev Disord / Autism and tuberous sclerosis by Smalley (1998)10.1111/j.1469-8749.1987.tb02135.x
/ Dev Med Child Neurol / Psychiatric disorders among children with tuberous sclerosis by Hunt (1987){'key': '10.1016/j.spen.2004.07.003_bib50', 'series-title': 'The Biology of the Autistic Syndromes', 'year': '1992'}
/ The Biology of the Autistic Syndromes (1992)10.1053/ejpn.2001.0538
/ Eur J Paediatr Neurol / Tuberous sclerosis complex by Curatolo (2002)10.1002/ajmg.a.10187
/ Am J Med Genet / Association study of autistic disorder and chromosome 16p by Lucarelli (2003)10.1093/hmg/7.3.571
/ Hum Mol Genet / A full genome screen for autism with evidence for linkage to a region on chromosome 7q (1998){'key': '10.1016/j.spen.2004.07.003_bib54', 'first-page': '805', 'article-title': 'Genome-wide scan for autism susceptibility genes', 'volume': '8', 'author': 'Philippe', 'year': '1999', 'journal-title': 'Paris Autism Research International Sibpair Study. Hum Mol Genet'}
/ Paris Autism Research International Sibpair Study. Hum Mol Genet / Genome-wide scan for autism susceptibility genes by Philippe (1999)10.1086/321980
/ Am J Hum Genet / A genome-wide screen for autism susceptibility loci by Liu (2001)10.1136/jmg.40.11.e119
/ J Med Genet / Association of INPP1, PIK3CG, and TSC2 gene variants with autistic disorder by Serajee (2003){'key': '10.1016/j.spen.2004.07.003_bib57', 'series-title': 'Diagnostic and Statistical Manual of Mental Disorders (4th ed text rev)', 'year': '2000'}
/ Diagnostic and Statistical Manual of Mental Disorders (4th ed text rev) (2000)10.1038/13810
/ Nat Genet / Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 by Amir (1999)10.1016/S0014-5793(00)01994-3
/ FEBS Lett / MECP2 mutation in male patients with nonspecific X-linked mental retardation by Orrico (2000)10.1016/S0887-8994(02)00624-0
/ Pediatr Neurol / Identification of MeCP2 mutations in a series of females with autistic disorder by Carney (2003)10.1136/jmg.37.12.e41
/ J Med Genet / Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome by Lam (2000)10.1002/ajmg.b.10016
/ Am J Med Genet / Absence of MeCP2 mutations in patients from the South Carolina autism project by Lobo-Menendez (2003)10.1038/sj.ejhg.5200660
/ Eur J Hum Genet / No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients by Vourc’h (2001){'key': '10.1016/j.spen.2004.07.003_bib64', 'first-page': '928', 'article-title': 'Autism or atypical autism in maternally but not paternally derived proximal 15q duplication', 'volume': '60', 'author': 'Cook', 'year': '1997', 'journal-title': 'Am J Hum Genet'}
/ Am J Hum Genet / Autism or atypical autism in maternally but not paternally derived proximal 15q duplication by Cook (1997)10.1086/301832
/ Am J Hum Genet / Linkage-disequilibrium mapping of autistic disorder, with 15q11–13 markers by Cook (1998)10.1002/(SICI)1096-8628(19980401)76:4<327::AID-AJMG8>3.0.CO;2-M
/ Am J Med Genet / Autism and maternally derived aberrations of chromosome 15q by Schroer (1998)10.1046/j.1365-2788.1998.00091.x
/ J Intellect Disabil Res / Chromosomes in autism and related pervasive developmental disorders by Weidmer-Mikhail (1998)10.1002/1096-8628(20000612)96:3<365::AID-AJMG25>3.0.CO;2-X
/ Am J Med Genet / Three probands with autistic disorder and isodicentric chromosome 15 by Wolpert (2000)10.1023/A:1026004505764
/ J Autism Dev Disord / Chromosomal disorders and autism by Gillberg (1998)10.1111/1469-7610.00451
/ J Child Psychol Psychiatry / Infantile autism and associated autosomal chromosome abnormalities by Lauritsen (1999)10.1007/BF02408551
/ J Autism Dev Disord / Childhood psychosis and neurofibromatosis by Gillberg (1984)10.1023/A:1026012414193
/ J Autism Dev Disord / Brief report by Williams (1998)10.1111/j.1469-8749.1993.tb11734.x
/ Dev Med Child Neurol / Autism and hypomelanosis of Ito in twins by Zappella (1993)10.1111/j.1651-2227.1989.tb11076.x
/ Acta Paediatr Scand / Autistic behaviour in Moebius syndrome by Gillberg (1989)10.1016/0887-8994(96)00011-2
/ Pediatr Neurol / Autism in Angelman syndrome by Steffenburg (1996)10.1177/088307389901401003
/ J Child Neurol / Autism and autistic behavior in Joubert syndrome by Ozonoff (1999)10.1017/S001216229900033X
/ Dev Med Child Neurol / Comorbidity of autistic spectrum disorders in children with Down syndrome by Kent (1999)10.1016/S0022-3476(85)80296-1
/ J Pediatr / Autism associated with Williams syndrome by Reiss (1985)10.1007/BF01957694
/ Eur J Pediatr / Autistic disorder in Sotos syndrome by Morrow (1990)10.1007/BF02409661
/ J Autism Dev Disord / Infantile autism and Duchenne muscular dystrophy by Komoto (1984)10.1023/A:1022947728569
/ J Autism Dev Disord / Two children with muscular dystrophies ascertained due to referral for diagnosis of autism by Zwaigenbaum (2003)10.1002/ajmg.1477
/ Am J Med Genet / PTEN mutation in a family with Cowden syndrome and autism by Goffin (2001)10.1023/A:1022999712639
/ J Autism Dev Disord / Autism and phenylketonuria by Baieli (2003)10.1002/1096-8628(20010115)98:2<191::AID-AJMG1030>3.0.CO;2-M
/ Am J Med Genet / Behavior phenotype in the RSH/Smith-Lemli-Opitz syndrome by Tierney (2001)10.1136/jmg.39.6.391
/ J Med Genet / A cryptic deletion of 2q35 including part of the PAX3 gene detected by breakpoint mapping in a child with autism and a de novo 2;8 translocation by Borg (2002)10.1023/A:1022943627660
/ J Autism Dev Disord / Partial tetrasomy of chromosome 3q and mosaicism in a child with autism by Oliveira (2003)10.1097/00125817-200201000-00002
/ Genet Med / Pilot assessment of the subtelomeric regions of children with autism by Wolff (2002)10.1016/S0140-6736(99)03070-6
/ Lancet / Subtle chromosomal rearrangements in children with unexplained mental retardation by Knight (1999)10.1002/bdra.20036
/ Birth Defects Res A / Clinical and cytogenetic manifestations of subtelomeric aberrations by Font-Montgomery (2004)10.1002/humu.10300
/ Hum Mutat / Subtelomeric deletions detected in patients with idiopathic mental retardation using multiplex ligation-dependent probe amplification (MLPA) by Rooms (2004)10.1002/ajmg.a.10042
/ Am J Med Genet / Routine cytogenetic and FISH studies for 17p11/15q11 duplications and subtelomeric rearrangement studies in children with autism spectrum disorders by Keller (2003){'key': '10.1016/j.spen.2004.07.003_bib92', 'first-page': '717', 'article-title': 'Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error', 'volume': '57', 'author': 'Pickles', 'year': '1995', 'journal-title': 'Am J Hum Genet'}
/ Am J Hum Genet / Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error by Pickles (1995)10.1086/302497
/ Am J Hum Genet / A genomic screen of autism by Risch (1999)10.1002/ajmg.10513
/ Am J Med Genet / A risk-factor model of epistatic interaction, focusing on autism by Jones (2002)10.1097/00004583-200301000-00018
/ J Am Acad Child Adolesc Psychiatry / Genetics of childhood disorders: XLVI. Autism, Part 5: Genetics of autism. by Veenstra-Vanderweele (2003)10.1086/342720
/ Am J Hum Genet / A genome-wide screen for autism-spectrum disorders by Auranen (2002)10.1002/(SICI)1096-8628(19991215)88:6<609::AID-AJMG7>3.0.CO;2-L
/ Am J Med Genet / An autosomal genomic screen for autism. Collaborative linkage study of autism by Barrett (1999)10.1093/hmg/10.9.973
/ Hum Mol Genet / Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q (2001)10.1002/ajmg.10153
/ Am J Med Genet / Genomic screen and follow-up analysis for autistic disorder by Shao (2002)10.1086/378778
/ Am J Hum Genet / A genome-wide screen of 345 families for autism-susceptibility loci by Yonan (2003)10.1038/sj.mp.4000922
/ Mol Psychiatry / Regional meta-analysis of published data supports linkage of autism with markers on chromosome 7 by Badner (2002)10.1038/sj.mp.4001011
/ Mol Psychiatry / Association between a GABRB3 polymorphism and autism by Buxbaum (2002)10.1002/(SICI)1096-8628(19991015)88:5<492::AID-AJMG11>3.0.CO;2-X
/ Am J Med Genet / Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium by Maestrini (1999)10.1002/(SICI)1096-8628(19991015)88:5<551::AID-AJMG21>3.0.CO;2-#
/ Am J Med Genet / Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism by Salmon (1999)10.1002/(SICI)1096-8628(20000207)96:1<43::AID-AJMG9>3.0.CO;2-3
/ Am J Med Genet / Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder by Martin (2000)10.1006/geno.2001.6617
/ Genomics / Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families by Nurmi (2001)10.1038/sj.mp.4001033
/ Mol Psychiatry / Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder by Kim (2002)10.1093/hmg/6.13.2233
/ Hum Mol Genet / Serotonin transporter (5-HTT) gene variants associated with autism? by Klauck (1997)10.1038/sj.mp.4000266
/ Mol Psychiatry / Evidence of linkage between the serotonin transporter and autistic disorder by Cook (1997)10.1002/ajmg.1365
/ Am J Med Genet / Evidence for an association with the serotonin transporter promoter region polymorphism and autism by Yirmiya (2001)10.1038/sj.mp.4000873
/ Mol Psychiatry / Role of the serotonin transporter gene in the behavioral expression of autism by Tordjman (2001)10.1038/sj.mp.4001459
/ Mol Psychiatry / Serotonin transporter gene and autism by Conroy (2004)10.1002/(SICI)1096-8628(20000207)96:1<123::AID-AJMG24>3.0.CO;2-N
/ Am J Med Genet / Lack of association between serotonin transporter gene promoter variants and autistic disorder in two ethnically distinct samples by Persico (2000)10.1007/s100480050064
/ Neurogenetics / 5-HTTLPR variants not associated with autistic spectrum disorders by Zhong (1999)10.1038/sj.mp.4000923
/ Mol Psychiatry / Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder by Betancur (2002)10.1002/1096-9926(200012)62:6<393::AID-TERA6>3.0.CO;2-V
/ Teratology / Discovery of allelic variants of HOXA1 and HOXB1 by Ingram (2000)10.1023/A:1024414803151
/ J Autism Dev Disord / The HOXA1 A218G polymorphism and autism by Collins (2003)10.1002/ajmg.10603
/ Am J Med Genet / No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network by Devlin (2002)10.1038/sj.mp.4001285
/ Mol Psychiatry / Lack of association of HOXA1 and HOXB1 mutations and autism in Sicilian (Italian) patients by Romano (2003)10.1136/jmg.39.11.e70
/ J Med Genet / No association between HOXA1 and HOXB1 genes and autism spectrum disorders (ASD) by Talebizadeh (2002)10.1002/ajmg.1618
/ Am J Med Genet / Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families by Li (2002)10.1038/sj.mp.4001248
/ Mol Psychiatry / The role of Reelin in pathology of autism by Fatemi (2002)10.1038/sj.mp.4001310
/ Mol Psychiatry / Analysis of reelin as a candidate gene for autism by Bonora (2003)10.1038/sj.mp.4000850
/ Mol Psychiatry / Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder by Persico (2001)10.1038/sj.mp.4001124
/ Mol Psychiatry / Reelin gene alleles and susceptibility to autism spectrum disorders by Zhang (2002)10.1002/ajmg.b.20125
/ Am J Med Genet / Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network by Devlin (2004)10.1038/sj.mp.4001071
/ Mol Psychiatry / Absence of association between a polymorphic GGC repeat in the 5′ untranslated region of the reelin gene and autism by Krebs (2002)10.1002/ajmg.b.20122
/ Am J Med Genet / Lack of evidence for an association between WNT2 and RELN polymorphisms and autism by Li (2004)10.1006/excr.1999.4710
/ Exp Cell Res / Molecular genetic studies of Wnt signaling in the mouse by Uusitalo (1999)10.1016/S0092-8674(00)80354-2
/ Cell / Social interaction and sensorimotor gating abnormalities in mice lacking Dvl1 by Lijam (1997)10.1002/ajmg.1401
/ Am J Med Genet / Evidence supporting WNT2 as an autism susceptibility gene by Wassink (2001)10.1002/ajmg.10182
/ Am J Med Genet / No association between the WNT2 gene and autistic disorder by McCoy (2002)10.1038/35097076
/ Nature / A forkhead-domain gene is mutated in a severe speech and language disorder by Lai (2001)10.1002/ajmg.a.10105
/ Am J Med Genet / Mutation screening of FOXP2 in individuals diagnosed with autistic disorder by Gauthier (2003)10.1086/339931
/ Am J Hum Genet / FOXP2 is not a major susceptibility gene for autism or specific language impairment by Newbury (2002)10.1002/ajmg.10415
/ Am J Med Genet / Evaluation of FOXP2 as an autism susceptibility gene by Wassink (2002)10.1002/ajmg.b.20162
/ Am J Med Genet / Association between the FOXP2 gene and autistic disorder in Chinese population by Gong (2004){'key': '10.1016/j.spen.2004.07.003_bib138', 'series-title': 'Mol Psychiatry 9540', 'article-title': 'Association of the homeobox transcription factor, ENGRAILED2, with autism spectrum disorder', 'author': 'Gharani', 'year': '2004'}
/ Mol Psychiatry 9540 / Association of the homeobox transcription factor, ENGRAILED2, with autism spectrum disorder by Gharani (2004)10.1136/jmg.32.4.269
/ J Med Genet / Association study with two markers of a human homeogene in infantile autism by Petit (1995)10.1136/jmg.40.1.e4
/ J Med Genet / No association between the EN2 gene and autistic disorder by Zhong (2003)10.1086/320588
/ Am J Hum Genet / Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity by Buxbaum (2001)10.1086/339765
/ Am J Hum Genet / Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder by Shao (2002)10.1086/338241
/ Am J Hum Genet / Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families by Alarcon (2002)10.1002/ajmg.1497
/ Am J Med Genet / Incorporating language phenotypes strengthens evidence of linkage to autism by Bradford (2001)10.1086/367846
/ Am J Hum Genet / Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes by Shao (2003)10.1097/01.CHI.0000046868.56865.0F
/ J Am Acad Child Adolesc Psychiatry / Exploratory subsetting of autism families based on savant skills improves evidence of genetic linkage to 15q11-q13 by Nurmi (2003)10.1002/ajmg.b.20151
/ Am J Med Genet / Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism by McCauley (2004)10.1038/sj.mp.4001465
/ Mol Psychiatry / Linkage analysis for autism in a subset of families with obsessive-compulsive behaviors by Buxbaum (2004)10.1002/ajmg.10189
/ Am J Med Genet / Family-based and population study of a functional promoter-region monoamine oxidase A polymorphism in autism by Yirmiya (2002)10.1034/j.1399-0004.2003.00115.x
/ Clin Genet / Association of autism severity with a monoamine oxidase A functional polymorphism by Cohen (2003)10.1177/088307380101600509
/ J Child Neurol / A study of novel polymorphisms in the upstream region of vasoactive intestinal peptide receptor type 2 gene in autism by Asano (2001){'key': '10.1016/j.spen.2004.07.003_bib152', 'series-title': 'Mol Psychiatry', 'article-title': 'Examination of AVPR1a as an autism susceptibility gene', 'author': 'Wassink', 'year': '2004'}
/ Mol Psychiatry / Examination of AVPR1a as an autism susceptibility gene by Wassink (2004)10.1038/sj.mp.4001125
/ Mol Psychiatry / Transmission disequilibrium testing of arginine vasopressin receptor 1A (AVPR1A) polymorphisms in autism by Kim (2002)10.1002/1096-8628(20001204)96:6<784::AID-AJMG18>3.3.CO;2-Z
/ Am J Med Genet / Adenosine deaminase alleles and autistic disorder by Persico (2000)10.1007/s100480000104
/ Neurogenetics / Autism by Bottini (2001)10.1002/ajmg.10272
/ Am J Med Genet / Two-loci ADA haplotypes in autistic disorder by Lucarelli (2002)10.1176/appi.ajp.161.4.662
/ Am J Psychiatry / Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism by Ramoz (2004)10.1002/ajmg.b.20147
/ Am J Med Genet / Association of tryptophan 2,3 dioxygenase gene polymorphism with autism by Nabi (2004)10.1038/sj.mp.4000979
/ Mol Psychiatry / Linkage and association of the glutamate receptor 6 gene with autism by Jamain (2002)10.1097/00041444-200312000-00005
/ Psychiatr Genet / Mutation screening and association study of the UBE2H gene on chromosome 7q32 in autistic disorder by Vourc’h (2003)10.1016/j.biopsych.2003.10.005
/ Biol Psychiatry / Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism by Conciatori (2004)
Dates
Type | When |
---|---|
Created | 20 years, 8 months ago (Dec. 6, 2004, 2:55 p.m.) |
Deposited | 2 years, 4 months ago (April 30, 2023, 2:26 p.m.) |
Indexed | 1 month, 3 weeks ago (July 11, 2025, 6:24 a.m.) |
Issued | 21 years ago (Sept. 1, 2004) |
Published | 21 years ago (Sept. 1, 2004) |
Published Print | 21 years ago (Sept. 1, 2004) |
@article{Spence_2004, title={The genetics of autism}, volume={11}, ISSN={1071-9091}, url={http://dx.doi.org/10.1016/j.spen.2004.07.003}, DOI={10.1016/j.spen.2004.07.003}, number={3}, journal={Seminars in Pediatric Neurology}, publisher={Elsevier BV}, author={Spence, Sarah J.}, year={2004}, month=sep, pages={196–204} }