10.1016/j.spen.2004.07.003
Crossref journal-article
Elsevier BV
Seminars in Pediatric Neurology (78)
Bibliography

Spence, S. J. (2004). The genetics of autism. Seminars in Pediatric Neurology, 11(3), 196–204.

Authors 1
  1. Sarah J. Spence (first)
References 161 Referenced 48
  1. 10.1016/S1056-4993(18)30061-0 / Child Adolesc Psychiatr Clin N Am / Genetics of autism by Cook (2001)
  2. 10.1093/hmg/9.6.861 / Hum Mol Genet / Autism by Lamb (2000)
  3. 10.1038/sj.mp.4001505 / Mol Psychiatry / Molecular genetics of autism spectrum disorder by Veenstra-VanderWeele (2004)
  4. 10.1017/S0033291700028099 / Psychol Med / Autism as a strongly genetic disorder by Bailey (1995)
  5. 10.1111/j.1469-7610.1977.tb00443.x / J Child Psychol Psychiatry / Infantile autism by Folstein (1977)
  6. 10.1111/j.1469-7610.1996.tb01475.x / J Child Psychol Psychiatry / A broader phenotype of autism by Le Couteur (1996)
  7. 10.1176/ajp.142.1.74 / Am J Psychiatry / Concordance for the syndrome of autism in 40 pairs of afflicted twins by Ritvo (1985)
  8. 10.1111/j.1469-7610.1991.tb01928.x / J Child Psychol Psychiatry / Debate and argument. Concordance for the syndrome of autism by Ritvo (1991)
  9. 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. 10.1111/1469-7610.00423 / J Child Psychol Psychiatry / Genetics and child psychiatry, II by Rutter (1999)
  11. 10.1007/BF02211816 / J Autism Dev Disord / Stoppage rules and genetic studies of autism by Jones (1988)
  12. 10.1002/gepi.4.abs / Genet Epidemiol / Stoppage by Slager (2001)
  13. {'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)
  14. 10.1111/j.1469-7610.1994.tb02300.x / J Child Psychol Psychiatry / A case-control family history study of autism by Bolton (1994)
  15. 10.1002/ajmg.1320540107 / Am J Med Genet / Genetics of autism by Spiker (1994)
  16. 10.1023/A:1026048320785 / J Autism Dev Disord / Autism by Bailey (1998)
  17. {'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)
  18. 10.1044/jshr.3406.1339 / J Speech Hear Res / Spontaneous narrative-discourse performance of parents of autistic individuals by Landa (1991)
  19. 10.1017/S0033291700032918 / Psychol Med / Social language use in parents of autistic individuals by Landa (1992)
  20. 10.1097/00004583-199105000-00019 / J Am Acad Child Adolesc Psychiatry / Psychiatric disorders in the parents of autistic individuals by Piven (1991)
  21. 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)
  22. 10.1017/S0033291700027938 / Psychol Med / Personality characteristics of the parents of autistic individuals by Piven (1994)
  23. 10.1002/ajmg.1320600105 / Am J Med Genet / Autism, affective disorders, and social phobia by Smalley (1995)
  24. 10.1176/ajp.156.4.557 / Am J Psychiatry / Psychiatric disorder and the broad autism phenotype by Piven (1999)
  25. 10.1016/S0165-1781(02)00304-9 / Psychiatry Res / Obsessive-compulsive behaviors in parents of multiplex autism families by Hollander (2003)
  26. 10.1017/S0033291799002949 / Psychol Med / Personality traits of the relatives of autistic probands by Murphy (2000)
  27. 10.1111/1469-7610.00528 / J Child Psychol Psychiatry / Predictors of cognitive test patterns in autism families by Folstein (1999)
  28. 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)
  29. 10.1176/ajp.146.3.361 / Am J Psychiatry / Psychometric assessment of first-degree relatives of 62 autistic probands in Utah by Freeman (1989)
  30. 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)
  31. 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)
  32. 10.1176/ajp.154.2.185 / Am J Psychiatry / Broader autism phenotype by Piven (1997)
  33. {'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)
  34. 10.1002/ajmg.1320600110 / Am J Med Genet / Chromosomal abnormalities in a psychiatric population by Lewis (1995)
  35. 10.1097/00041444-200106000-00001 / Psychiatr Genet / Chromosomal abnormalities in a clinic sample of individuals with autistic disorder by Wassink (2001)
  36. 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)
  37. 10.1023/A:1022155201662 / J Autism Dev Disord / Chromosomal abnormalities in a series of children with autistic disorder by Konstantareas (1999)
  38. 10.1111/j.1469-8749.1985.tb04539.x / Dev Med Child Neurol / Chromosome abnormalities in infantile autism and other childhood psychoses by Gillberg (1985)
  39. 10.1111/j.1469-7610.1994.tb01164.x / J Child Psychol Psychiatry / Autism and known medical conditions by Rutter (1994)
  40. {'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)
  41. 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)
  42. 10.1023/A:1025857422026 / J Autism Dev Disord / Autistic behaviors among girls with fragile X syndrome by Mazzocco (1997)
  43. 10.1023/A:1026000404855 / J Autism Dev Disord / Autism by Feinstein (1998)
  44. 10.1023/A:1017956224167 / J Autism Dev Disord / Legitimacy of comparing fragile X with autism questioned by Rapin (2002)
  45. 10.1111/j.1469-8749.1994.tb11765.x / Dev Med Child Neurol / Autistic behaviour and attention deficits in tuberous sclerosis by Gillberg (1994)
  46. 10.1023/A:1026032413811 / J Autism Dev Disord / Autism in tuberous sclerosis complex by Gutierrez (1998)
  47. 10.1007/BF01046223 / J Autism Dev Disord / A prevalence study of autism in tuberous sclerosis by Hunt (1993)
  48. 10.1023/A:1026052421693 / J Autism Dev Disord / Autism and tuberous sclerosis by Smalley (1998)
  49. 10.1111/j.1469-8749.1987.tb02135.x / Dev Med Child Neurol / Psychiatric disorders among children with tuberous sclerosis by Hunt (1987)
  50. {'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)
  51. 10.1053/ejpn.2001.0538 / Eur J Paediatr Neurol / Tuberous sclerosis complex by Curatolo (2002)
  52. 10.1002/ajmg.a.10187 / Am J Med Genet / Association study of autistic disorder and chromosome 16p by Lucarelli (2003)
  53. 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)
  54. {'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)
  55. 10.1086/321980 / Am J Hum Genet / A genome-wide screen for autism susceptibility loci by Liu (2001)
  56. 10.1136/jmg.40.11.e119 / J Med Genet / Association of INPP1, PIK3CG, and TSC2 gene variants with autistic disorder by Serajee (2003)
  57. {'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)
  58. 10.1038/13810 / Nat Genet / Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 by Amir (1999)
  59. 10.1016/S0014-5793(00)01994-3 / FEBS Lett / MECP2 mutation in male patients with nonspecific X-linked mental retardation by Orrico (2000)
  60. 10.1016/S0887-8994(02)00624-0 / Pediatr Neurol / Identification of MeCP2 mutations in a series of females with autistic disorder by Carney (2003)
  61. 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)
  62. 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)
  63. 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)
  64. {'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)
  65. 10.1086/301832 / Am J Hum Genet / Linkage-disequilibrium mapping of autistic disorder, with 15q11–13 markers by Cook (1998)
  66. 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)
  67. 10.1046/j.1365-2788.1998.00091.x / J Intellect Disabil Res / Chromosomes in autism and related pervasive developmental disorders by Weidmer-Mikhail (1998)
  68. 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)
  69. 10.1023/A:1026004505764 / J Autism Dev Disord / Chromosomal disorders and autism by Gillberg (1998)
  70. 10.1111/1469-7610.00451 / J Child Psychol Psychiatry / Infantile autism and associated autosomal chromosome abnormalities by Lauritsen (1999)
  71. 10.1007/BF02408551 / J Autism Dev Disord / Childhood psychosis and neurofibromatosis by Gillberg (1984)
  72. 10.1023/A:1026012414193 / J Autism Dev Disord / Brief report by Williams (1998)
  73. 10.1111/j.1469-8749.1993.tb11734.x / Dev Med Child Neurol / Autism and hypomelanosis of Ito in twins by Zappella (1993)
  74. 10.1111/j.1651-2227.1989.tb11076.x / Acta Paediatr Scand / Autistic behaviour in Moebius syndrome by Gillberg (1989)
  75. 10.1016/0887-8994(96)00011-2 / Pediatr Neurol / Autism in Angelman syndrome by Steffenburg (1996)
  76. 10.1177/088307389901401003 / J Child Neurol / Autism and autistic behavior in Joubert syndrome by Ozonoff (1999)
  77. 10.1017/S001216229900033X / Dev Med Child Neurol / Comorbidity of autistic spectrum disorders in children with Down syndrome by Kent (1999)
  78. 10.1016/S0022-3476(85)80296-1 / J Pediatr / Autism associated with Williams syndrome by Reiss (1985)
  79. 10.1007/BF01957694 / Eur J Pediatr / Autistic disorder in Sotos syndrome by Morrow (1990)
  80. 10.1007/BF02409661 / J Autism Dev Disord / Infantile autism and Duchenne muscular dystrophy by Komoto (1984)
  81. 10.1023/A:1022947728569 / J Autism Dev Disord / Two children with muscular dystrophies ascertained due to referral for diagnosis of autism by Zwaigenbaum (2003)
  82. 10.1002/ajmg.1477 / Am J Med Genet / PTEN mutation in a family with Cowden syndrome and autism by Goffin (2001)
  83. 10.1023/A:1022999712639 / J Autism Dev Disord / Autism and phenylketonuria by Baieli (2003)
  84. 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)
  85. 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)
  86. 10.1023/A:1022943627660 / J Autism Dev Disord / Partial tetrasomy of chromosome 3q and mosaicism in a child with autism by Oliveira (2003)
  87. 10.1097/00125817-200201000-00002 / Genet Med / Pilot assessment of the subtelomeric regions of children with autism by Wolff (2002)
  88. 10.1016/S0140-6736(99)03070-6 / Lancet / Subtle chromosomal rearrangements in children with unexplained mental retardation by Knight (1999)
  89. 10.1002/bdra.20036 / Birth Defects Res A / Clinical and cytogenetic manifestations of subtelomeric aberrations by Font-Montgomery (2004)
  90. 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)
  91. 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)
  92. {'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)
  93. 10.1086/302497 / Am J Hum Genet / A genomic screen of autism by Risch (1999)
  94. 10.1002/ajmg.10513 / Am J Med Genet / A risk-factor model of epistatic interaction, focusing on autism by Jones (2002)
  95. 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)
  96. 10.1086/342720 / Am J Hum Genet / A genome-wide screen for autism-spectrum disorders by Auranen (2002)
  97. 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)
  98. 10.1093/hmg/10.9.973 / Hum Mol Genet / Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q (2001)
  99. 10.1002/ajmg.10153 / Am J Med Genet / Genomic screen and follow-up analysis for autistic disorder by Shao (2002)
  100. 10.1086/378778 / Am J Hum Genet / A genome-wide screen of 345 families for autism-susceptibility loci by Yonan (2003)
  101. 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)
  102. 10.1038/sj.mp.4001011 / Mol Psychiatry / Association between a GABRB3 polymorphism and autism by Buxbaum (2002)
  103. 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)
  104. 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)
  105. 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)
  106. 10.1006/geno.2001.6617 / Genomics / Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families by Nurmi (2001)
  107. 10.1038/sj.mp.4001033 / Mol Psychiatry / Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder by Kim (2002)
  108. 10.1093/hmg/6.13.2233 / Hum Mol Genet / Serotonin transporter (5-HTT) gene variants associated with autism? by Klauck (1997)
  109. 10.1038/sj.mp.4000266 / Mol Psychiatry / Evidence of linkage between the serotonin transporter and autistic disorder by Cook (1997)
  110. 10.1002/ajmg.1365 / Am J Med Genet / Evidence for an association with the serotonin transporter promoter region polymorphism and autism by Yirmiya (2001)
  111. 10.1038/sj.mp.4000873 / Mol Psychiatry / Role of the serotonin transporter gene in the behavioral expression of autism by Tordjman (2001)
  112. 10.1038/sj.mp.4001459 / Mol Psychiatry / Serotonin transporter gene and autism by Conroy (2004)
  113. 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)
  114. 10.1007/s100480050064 / Neurogenetics / 5-HTTLPR variants not associated with autistic spectrum disorders by Zhong (1999)
  115. 10.1038/sj.mp.4000923 / Mol Psychiatry / Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder by Betancur (2002)
  116. 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)
  117. 10.1023/A:1024414803151 / J Autism Dev Disord / The HOXA1 A218G polymorphism and autism by Collins (2003)
  118. 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)
  119. 10.1038/sj.mp.4001285 / Mol Psychiatry / Lack of association of HOXA1 and HOXB1 mutations and autism in Sicilian (Italian) patients by Romano (2003)
  120. 10.1136/jmg.39.11.e70 / J Med Genet / No association between HOXA1 and HOXB1 genes and autism spectrum disorders (ASD) by Talebizadeh (2002)
  121. 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)
  122. 10.1038/sj.mp.4001248 / Mol Psychiatry / The role of Reelin in pathology of autism by Fatemi (2002)
  123. 10.1038/sj.mp.4001310 / Mol Psychiatry / Analysis of reelin as a candidate gene for autism by Bonora (2003)
  124. 10.1038/sj.mp.4000850 / Mol Psychiatry / Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder by Persico (2001)
  125. 10.1038/sj.mp.4001124 / Mol Psychiatry / Reelin gene alleles and susceptibility to autism spectrum disorders by Zhang (2002)
  126. 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)
  127. 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)
  128. 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)
  129. 10.1006/excr.1999.4710 / Exp Cell Res / Molecular genetic studies of Wnt signaling in the mouse by Uusitalo (1999)
  130. 10.1016/S0092-8674(00)80354-2 / Cell / Social interaction and sensorimotor gating abnormalities in mice lacking Dvl1 by Lijam (1997)
  131. 10.1002/ajmg.1401 / Am J Med Genet / Evidence supporting WNT2 as an autism susceptibility gene by Wassink (2001)
  132. 10.1002/ajmg.10182 / Am J Med Genet / No association between the WNT2 gene and autistic disorder by McCoy (2002)
  133. 10.1038/35097076 / Nature / A forkhead-domain gene is mutated in a severe speech and language disorder by Lai (2001)
  134. 10.1002/ajmg.a.10105 / Am J Med Genet / Mutation screening of FOXP2 in individuals diagnosed with autistic disorder by Gauthier (2003)
  135. 10.1086/339931 / Am J Hum Genet / FOXP2 is not a major susceptibility gene for autism or specific language impairment by Newbury (2002)
  136. 10.1002/ajmg.10415 / Am J Med Genet / Evaluation of FOXP2 as an autism susceptibility gene by Wassink (2002)
  137. 10.1002/ajmg.b.20162 / Am J Med Genet / Association between the FOXP2 gene and autistic disorder in Chinese population by Gong (2004)
  138. {'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)
  139. 10.1136/jmg.32.4.269 / J Med Genet / Association study with two markers of a human homeogene in infantile autism by Petit (1995)
  140. 10.1136/jmg.40.1.e4 / J Med Genet / No association between the EN2 gene and autistic disorder by Zhong (2003)
  141. 10.1086/320588 / Am J Hum Genet / Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity by Buxbaum (2001)
  142. 10.1086/339765 / Am J Hum Genet / Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder by Shao (2002)
  143. 10.1086/338241 / Am J Hum Genet / Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families by Alarcon (2002)
  144. 10.1002/ajmg.1497 / Am J Med Genet / Incorporating language phenotypes strengthens evidence of linkage to autism by Bradford (2001)
  145. 10.1086/367846 / Am J Hum Genet / Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes by Shao (2003)
  146. 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)
  147. 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)
  148. 10.1038/sj.mp.4001465 / Mol Psychiatry / Linkage analysis for autism in a subset of families with obsessive-compulsive behaviors by Buxbaum (2004)
  149. 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)
  150. 10.1034/j.1399-0004.2003.00115.x / Clin Genet / Association of autism severity with a monoamine oxidase A functional polymorphism by Cohen (2003)
  151. 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)
  152. {'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)
  153. 10.1038/sj.mp.4001125 / Mol Psychiatry / Transmission disequilibrium testing of arginine vasopressin receptor 1A (AVPR1A) polymorphisms in autism by Kim (2002)
  154. 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)
  155. 10.1007/s100480000104 / Neurogenetics / Autism by Bottini (2001)
  156. 10.1002/ajmg.10272 / Am J Med Genet / Two-loci ADA haplotypes in autistic disorder by Lucarelli (2002)
  157. 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)
  158. 10.1002/ajmg.b.20147 / Am J Med Genet / Association of tryptophan 2,3 dioxygenase gene polymorphism with autism by Nabi (2004)
  159. 10.1038/sj.mp.4000979 / Mol Psychiatry / Linkage and association of the glutamate receptor 6 gene with autism by Jamain (2002)
  160. 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)
  161. 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)
Funders 0

None

@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} }