Genetics of austim: complex aetiology for a heterogeneous disorder

[1]  J. Gilbert,et al.  Genomic screen and follow-up analysis for autistic disorder. , 2002, American journal of medical genetics.

[2]  T. Bourgeron,et al.  Linkage and association of the glutamate receptor 6 gene with autism , 2002, Molecular Psychiatry.

[3]  A. Monaco,et al.  A forkhead-domain gene is mutated in a severe speech and language disorder , 2001, Nature.

[4]  Stephen J. Guter,et al.  A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p. , 2001, American journal of human genetics.

[5]  J. Sutcliffe,et al.  Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families. , 2001, Genomics.

[6]  D. Geschwind,et al.  A genomewide screen for autism susceptibility loci. , 2001, American journal of human genetics.

[7]  S. Folstein,et al.  Evidence supporting WNT2 as an autism susceptibility gene. , 2001, American journal of medical genetics.

[8]  D. Cohen,et al.  Role of the serotonin transporter gene in the behavioral expression of autism , 2001, Molecular Psychiatry.

[9]  K. Davis,et al.  Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity. , 2001, American journal of human genetics.

[10]  M. Lauritsen,et al.  The genetics of autism , 2001, Acta psychiatrica Scandinavica.

[11]  R. Ebstein,et al.  Evidence for an association with the serotonin transporter promoter region polymorphism and autism. , 2001, American journal of medical genetics.

[12]  S. Hyman,et al.  Measles-mumps-rubella vaccine and autistic spectrum disorder: report from the New Challenges in Childhood Immunizations Conference convened in Oak Brook, Illinois, June 12-13, 2000. , 2001, Pediatrics.

[13]  F. Macciardi,et al.  Genetically determined low maternal serum dopamine beta-hydroxylase levels and the etiology of autism spectrum disorders. , 2001, American journal of medical genetics.

[14]  J. Gilbert,et al.  De novo partial duplication of chromosome 7p in a male with autistic disorder. , 2001, American journal of medical genetics.

[15]  T. Wassink,et al.  Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder , 2001, Molecular Psychiatry.

[16]  H Jick,et al.  Mumps, measles, and rubella vaccine and the incidence of autism recorded by general practitioners: a time trend analysis , 2001, BMJ : British Medical Journal.

[17]  S. Folstein,et al.  An autosomal genomic screen for autism. , 1999, American journal of medical genetics.

[18]  C. Walsh,et al.  Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations , 2001, Nature Genetics.

[19]  J. Rapoport,et al.  Childhood-onset schizophrenia/autistic disorder and t(1;7) reciprocal translocation: identification of a BAC contig spanning the translocation breakpoint at 7q21. , 2000, American journal of medical genetics.

[20]  P. Rodier,et al.  Discovery of allelic variants of HOXA1 and HOXB1: genetic susceptibility to autism spectrum disorders. , 2000, Teratology.

[21]  D. Franz,et al.  Autism and the Cerebellum: Evidence from Tuberous Sclerosis , 2000, Journal of autism and developmental disorders.

[22]  H. Peltola,et al.  Serious adverse events after measles-mumps-rubella vaccination during a fourteen-year prospective follow-up. , 2000, The Pediatric infectious disease journal.

[23]  S. Scherer,et al.  Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual. , 2000, American journal of human genetics.

[24]  S. Folstein,et al.  Chromosome 7q: where autism meets language disorder? , 2000, American journal of human genetics.

[25]  A. Monaco,et al.  The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder. , 2000, American journal of human genetics.

[26]  J. Gilbert,et al.  Three probands with autistic disorder and isodicentric chromosome 15. , 2000, American journal of medical genetics.

[27]  P Bolton,et al.  Variable expression of the autism broader phenotype: findings from extended pedigrees. , 2000, Journal of child psychology and psychiatry, and allied disciplines.

[28]  J. Miles,et al.  Value of a clinical morphology examination in autism. , 2000, American journal of medical genetics.

[29]  G. Baird,et al.  Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31. , 2000, American journal of medical genetics.

[30]  Psychoeducational Outcome in Children With Early-Treated Congenital Hypothyroidism , 2000, Pediatrics.

[31]  J. Gilbert,et al.  Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder. , 2000, American journal of medical genetics.

[32]  A. Persico,et al.  Lack of association between serotonin transporter gene promoter variants and autistic disorder in two ethnically distinct samples. , 2000, American journal of medical genetics.

[33]  D. Skuse,et al.  Imprinting, the X-Chromosome, and the Male Brain: Explaining Sex Differences in the Liability to Autism , 2000, Pediatric Research.

[34]  J. Gilbert,et al.  Genetic studies in autistic disorder and chromosome 15 , 2000, Neurogenetics.

[35]  S. Waisbren,et al.  "Maternal Thyroid Deficiency During Pregnancy and Subsequent Neuropsychological Development of the Child" (1999), by James E. Haddow et al. , 2014 .

[36]  J. Gilbert,et al.  Genetic studies of autistic disorder and chromosome 7. , 1999, Genomics.

[37]  A. Bailey,et al.  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. , 1999, American journal of medical genetics.

[38]  Courtney A. Harper,et al.  A genomic screen of autism: evidence for a multilocus etiology. , 1999, American journal of human genetics.

[39]  M. Konstantareas,et al.  Chromosomal Abnormalities in a Series of Children with Autistic Disorder , 1999, Journal of autism and developmental disorders.

[40]  E. Fombonne,et al.  The epidemiology of autism: a review , 1999, Psychological Medicine.

[41]  Jun Li,et al.  Autism and measles, mumps, and rubella vaccine: no epidemiological evidence for a causal association , 1999, The Lancet.

[42]  C. Gillberg,et al.  Autism: not an extremely rare disorder , 1999, Acta psychiatrica Scandinavica.

[43]  Paul Law,et al.  Familial Clustering of Autoimmune Disorders and Evaluation of Medical Risk Factors in Autism , 1999, Journal of child neurology.

[44]  Christopher Gillberg,et al.  Genome-Wide Scan for Autism Susceptibility Genes , 1999 .

[45]  A. Pestronk,et al.  Serum autoantibodies to brain in Landau-Kleffner variant, autism, and other neurologic disorders. , 1999, The Journal of pediatrics.

[46]  W. Brown,et al.  5-HTTLPR variants not associated with autistic spectrum disorders , 1999, Neurogenetics.

[47]  R. Rothermel,et al.  Developmental changes in brain serotonin synthesis capacity in autistic and nonautistic children , 1999, Annals of neurology.

[48]  Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism. , 1999, American journal of medical genetics.

[49]  S. Folstein,et al.  Predictors of cognitive test patterns in autism families. , 1999, Journal of child psychology and psychiatry, and allied disciplines.

[50]  J. Fryns,et al.  The neurobiology of autism. , 1999, Genetic counseling.

[51]  E. Simonoff.  Genetic Counseling in Autism and Pervasive Developmental Disorders , 1998, Journal of autism and developmental disorders.

[52]  L. Jocelyn,et al.  Outcomes of Genetic Evaluation in Children with Pervasive Developmental Disorder , 1998, Journal of developmental and behavioral pediatrics : JDBP.

[53]  Christopher Gillberg,et al.  Chromosomal Disorders and Autism , 1998, Journal of autism and developmental disorders.

[54]  A. Sabrá,et al.  Ileal-lymphoid-nodular hyperplasia, non-specific colitis, and pervasive developmental disorder in children , 1998, The Lancet.

[55]  Stephen J. Guter,et al.  Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers. , 1998, American journal of human genetics.

[56]  M. Cuccaro,et al.  Autism and maternally derived aberrations of chromosome 15q. , 1998, American journal of medical genetics.

[57]  C. Francks,et al.  A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium. , 1998, Human molecular genetics.

[58]  P. Rodier,et al.  Early environmental factors in autism , 1998 .

[59]  R. Warren,et al.  Possible immunogenetic basis for autism , 1998 .

[60]  T. Insel,et al.  Voles and vasopressin: a review of molecular, cellular, and behavioral studies of pair bonding and paternal behaviors. , 1998, Progress in brain research.

[61]  R. Nusse,et al.  Wnt signaling: a common theme in animal development. , 1997, Genes & development.

[62]  A Benner,et al.  Serotonin transporter (5-HTT) gene variants associated with autism? , 1997, Human molecular genetics.

[63]  R. Rothermel,et al.  Altered serotonin synthesis in the dentatothalamocortical pathway in autistic boys , 1997, Annals of neurology.

[64]  Richard Paylor,et al.  Social Interaction and Sensorimotor Gating Abnormalities in Mice Lacking Dvl1 , 1997, Cell.

[65]  C. Gillberg,et al.  Attention deficits and autistic spectrum problems in children exposed to alcohol during gestation: a follow‐up study , 1997, Developmental medicine and child neurology.

[66]  P. Bolton,et al.  A family study of autism: cognitive patterns and levels in parents and siblings. , 1997, Journal of child psychology and psychiatry, and allied disciplines.

[67]  J. Hersh,et al.  A male with fetal valproate syndrome and autism , 1997, Developmental medicine and child neurology.

[68]  P. A. Jacobs,et al.  Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function , 1997, Nature.

[69]  T. Insel,et al.  A neurobiological basis of social attachment. , 1997, The American journal of psychiatry.

[70]  N J Cox,et al.  Evidence of linkage between the serotonin transporter and autistic disorder , 1997, Molecular Psychiatry.

[71]  B. Leventhal,et al.  Autism or atypical autism in maternally but not paternally derived proximal 15q duplication. , 1997, American journal of human genetics.

[72]  Paul D Griffiths,et al.  Association of tuberous sclerosis of temporal lobes with autism and atypical autism , 1997, The Lancet.

[73]  S. Folstein,et al.  Macrocephaly in children and adults with autism. , 1997, Journal of the American Academy of Child and Adolescent Psychiatry.

[74]  L. Lotspeich,et al.  Austism and the X Chromosome: Multipoint sib-Pair Analysis , 1996 .

[75]  B. Leventhal,et al.  The serotonin system in autism. , 1996, Current opinion in pediatrics.

[76]  N. Risch,et al.  Mapping quantitative trait loci with extreme discordant sib pairs: sampling considerations. , 1996, American journal of human genetics.

[77]  S Arndt,et al.  Course of behavioral change in autism: a retrospective study of high-IQ adolescents and adults. , 1996, Journal of the American Academy of Child and Adolescent Psychiatry.

[78]  Sally Ozonoff,et al.  An Exploration of Right-Hemisphere Contributions to the Pragmatic Impairments of Autism , 1996, Brain and Language.

[79]  M. McDonald,et al.  Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation. , 1996, American journal of medical genetics.

[80]  I. Rapin,et al.  Autistic regression and disintegrative disorder: how important the role of epilepsy? , 1995, Seminars in pediatric neurology.

[81]  P Bolton,et al.  Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism. , 1995, American journal of human genetics.

[82]  N Risch,et al.  Extreme discordant sib pairs for mapping quantitative trait loci in humans. , 1995, Science.

[83]  P. Bolton,et al.  A case of autism associated with partial tetrasomy 15 , 1995, Journal of autism and developmental disorders.

[84]  A. Bailey,et al.  Autism as a strongly genetic disorder: evidence from a British twin study , 1995, Psychological Medicine.

[85]  M. Denckla.  The Biology of the Autistic Syndromes , 1994 .

[86]  J. Corbett,et al.  Duplication of the 15q11‐13 Region in a Patient with Autism, Epilepsy and Ataxia , 1994, Developmental medicine and child neurology.

[87]  S. Schwartz,et al.  Brief report: Duplication of chromosome 15q11-13 in two individuals with autistic disorder , 1994, Journal of autism and developmental disorders.

[88]  J. Rapoport,et al.  Brief report: Translocation involving chromosomes 1 and 7 in a boy with childhood-onset schizophrenia , 1994, Journal of autism and developmental disorders.

[89]  J. Kromberg,et al.  Fetal Valproate Syndrome: Clinical and Neuro‐developmental Features in Two Sibling Pairs , 1994 .

[90]  C. Gillberg,et al.  AUTISM IN THALIDOMIDE EMBRYOPATHY: A POPULATION STUDY , 1994, Developmental medicine and child neurology.

[91]  S. Sorbi.  Molecular genetics of Alzheimer’s disease , 1993, Aging.

[92]  Infantile autism among children in the county of Nordland. Prevalence and etiology , 1993 .

[93]  Anthony Bailey,et al.  Autism and megalencephaly , 1993, The Lancet.

[94]  V. Singh,et al.  Antibodies to Myelin Basic Protein in Children with Autistic Behavior , 1993, Brain, Behavior, and Immunity.

[95]  [Infantile autism among children in the county of Nordland. Prevalence and etiology]. , 1993, Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke.

[96]  J. Nanson.  Autism in fetal alcohol syndrome: a report of six cases. , 1992, Alcoholism, clinical and experimental research.

[97]  C. Gillberg,et al.  Hypothyroidism and autism spectrum disorders. , 1992, Journal of child psychology and psychiatry, and allied disciplines.

[98]  L. B. Andersen,et al.  Neurofibromatosis in infantile autism and other types of childhood psychoses. , 1992, Acta paedopsychiatrica.

[99]  C. Gillberg,et al.  Case Study: Autism Associated with Marker Chromosome , 1991 .

[100]  S. Folstein,et al.  Psychiatric disorders in the parents of autistic individuals. , 1991, Journal of the American Academy of Child and Adolescent Psychiatry.

[101]  K. Nelson.  Prenatal and perinatal factors in the etiology of autism. , 1991, Pediatrics.

[102]  C. Gillberg,et al.  Autism associated with marker chromosome. , 1991, Journal of the American Academy of Child and Adolescent Psychiatry.

[103]  L. Burd,et al.  Autism, profound mental retardation and atypical bipolar disorder in a 33-year-old female with a deletion of 15q12. , 2008, Journal of mental deficiency research.

[104]  J. Hurst,et al.  An extended Family with a Dominantly Inherited Speech Disorder , 1990, Developmental medicine and child neurology.

[105]  G A Chase,et al.  A family history study of neuropsychiatric disorders in the adult siblings of autistic individuals. , 1990, Journal of the American Academy of Child and Adolescent Psychiatry.

[106]  C. Williams,et al.  Cytogenetic survey for autistic fragile X carriers in a mental retardation center. , 1990, American journal of mental retardation : AJMR.

[107]  A. Freeman.  Biological and Psychological Factors in Cardiovascular Disease , 1989 .

[108]  C. Gillberg,et al.  A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden. , 1989, Journal of child psychology and psychiatry, and allied disciplines.

[109]  W. McMahon,et al.  Psychometric assessment of first-degree relatives of 62 autistic probands in Utah. , 1989, The American journal of psychiatry.

[110]  W. McMahon,et al.  The UCLA-University of Utah epidemiologic survey of autism: prevalence. , 1989, The American journal of psychiatry.

[111]  M. Wiznitzer,et al.  AIDS and the Nervous System , 1988, Neurology.

[112]  S. Folstein,et al.  Autism: Familial aggregation and genetic implications , 1988, Journal of autism and developmental disorders.

[113]  P. Szatmari,et al.  Stoppage rules and genetic studies of autism , 1988, Journal of autism and developmental disorders.

[114]  L. Tsai,et al.  Brief report: Magnetic resonance imaging of high level autism , 1987 .

[115]  F. Volkmar,et al.  Handbook of Autism and Pervasive Developmental Disorders , 1987 .

[116]  Magnetic resonance imaging of high level autism. , 1987, Journal of autism and developmental disorders.

[117]  C. Gillberg,et al.  Biology of the Autistic Syndromes , 1994 .

[118]  G. Groden,et al.  Brief report: Screening children with autism for fragile-X syndrome and phenylketonuria , 1985, Journal of autism and developmental disorders.

[119]  E. G. Stubbs,et al.  Autism and congenital cytomegalovirus , 1984, Journal of autism and developmental disorders.

[120]  C. Gillberg,et al.  Childhood psychosis and neurofibromatosis—more than a coincidence? , 1984, Journal of autism and developmental disorders.

[121]  G. Fischer,et al.  [Psychiatry in the press]. , 1983, Das Offentliche Gesundheitswesen.

[122]  Abraham Weizman,et al.  Abnormal immune response to brain tissue antigen in the syndrome of autism. , 1982, The American journal of psychiatry.

[123]  M. Seashore,et al.  Detection of phenylketonuria in autistic and psychotic children. , 1980, JAMA.

[124]  M. Rutter,et al.  Families of autistic and dysphasic children. I. Family life and interaction patterns. , 1979, Archives of general psychiatry.

[125]  E. G. Stubbs.  Autistic symptoms in a child with congenital cytomegaloviras infection , 1978, Journal of autism and childhood schizophrenia.

[126]  M. Rutter,et al.  Families of autistic and dysphasic children II. Mothers' speech to the children , 1977, Journal of autism and childhood schizophrenia.

[127]  S. Folstein,et al.  Infantile autism: a genetic study of 21 twin pairs. , 1977, Journal of child psychology and psychiatry, and allied disciplines.

[128]  S. Chess.  Follow-up report on autism in congenital rubella , 1977, Journal of autism and childhood schizophrenia.

[129]  S. Chess,et al.  Autism in children with congenital rubella , 1971, Journal of autism and childhood schizophrenia.

[130]  M. Rutter,et al.  A Five- to Fifteen-Year Follow-up Study of Infantile Psychosis , 1969, British Journal of Psychiatry.

[131]  E. Friedman.  The "autistic syndrome" and phenylketonuria. , 1969 .

[132]  M. Rutter,et al.  Concepts of autism: a review of research. , 1968, Journal of child psychology and psychiatry, and allied disciplines.

[133]  S. M. Finch,et al.  The Empty Fortress , 1968 .

[134]  L. Kanner.  Autistic disturbances of affective contact. , 1968, Acta paedopsychiatrica.

[135]  J. Melnick,et al.  Congenital rubella encephalitis. Course and early sequelae. , 1967, The Journal of pediatrics.

[136]  James N. Sussex,et al.  The Empty Fortress: Infantile Autism and the Birth of the Self , 1967, Pediatrics.

[137]  Bernard Rimland,et al.  Infantile Autism , 2014, Companion Encyclopedia of Psychology.

[138]  L. Eisenberg,et al.  The fathers of autistic children. , 1957, The American journal of orthopsychiatry.