A risk‐factor model of epistatic interaction, focusing on autism

The Future of Genetic Studies of Complex Human Diseases

1996 • 5,355 citations

Mindblindness: an essay on autism and theory of mind

1995 • 3,750 citations

Mindblindness

1995 • 3,081 citations

Searching for genetic determinants in the new millennium

2000 • 1,878 citations

Linkage strategies for genetically complex traits. I. Multilocus models.

1990 • 1,335 citations

INFANTILE AUTISM: A GENETIC STUDY OF 21 TWIN PAIRS

1977 • 1,333 citations

Are Rare Variants Responsible for Susceptibility to Complex Diseases?

2001 • 1,224 citations

Pervasive Developmental Disorders in Preschool Children

2001 • 1,151 citations

The Genetic Basis of Complex Human Behaviors

1994 • 1,028 citations

Genetics of austim: complex aetiology for a heterogeneous disorder

2001 • 769 citations

Broader autism phenotype: evidence from a family history study of multiple-incidence autism families

1997 • 757 citations

A Genomic Screen of Autism: Evidence for a Multilocus Etiology

1999 • 695 citations

APOLIPOPROTEIN E ALLELES AS RISK FACTORS IN ALZHEIMER'S DISEASE

1996 • 677 citations

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function

1997 • 670 citations

Autism or atypical autism in maternally but not paternally derived proximal 15q duplication.

1997 • 639 citations

A clinical study of 57 children with fetal anticonvulsant syndromes

2000 • 539 citations

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

1998 • 535 citations

Autism and tuberous sclerosis

1992 • 528 citations

Genome-Wide Scan for Autism Susceptibility Genes

1999 • 479 citations

AUTISM IN THALIDOMIDE EMBRYOPATHY: A POPULATION STUDY

1994 • 451 citations

A Genomewide Screen for Autism: Strong Evidence for Linkage to Chromosomes 2q, 7q, and 16p

2001 • 446 citations

Autism in children with congenital rubella

1971 • 435 citations

Evidence of linkage between the serotonin transporter and autistic disorder

1997 • 435 citations

Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism.

1995 • 391 citations

Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans

1999 • 386 citations

Prenatal exposure of rats to valproic acid reproduces the cerebellar anomalies associated with autism

2000 • 364 citations

An autosomal genomic screen for autism

1999 • 361 citations

A Genomewide Screen for Autism Susceptibility Loci

2001 • 314 citations

An autosomal genomic screen for autism

1999 • 302 citations

Autism and Known Medical Conditions: Myth and Substance

1994 • 296 citations

Imprinting, the X-Chromosome, and the Male Brain: Explaining Sex Differences in the Liability to Autism

2000 • 291 citations

Genetic linkage and complex diseases, with special reference to psychiatric disorders

1990 • 283 citations

Variable Expression of the Autism Broader Phenotype: Findings from Extended Pedigrees

2000 • 275 citations

Evidence for a Language Quantitative Trait Locus on Chromosome 7q in Multiplex Autism Families

2002 • 274 citations

Serotonin transporter (5-HTT) gene variants associated with autism?

1997 • 260 citations

Genomic screen and follow‐up analysis for autistic disorder

2001 • 254 citations

Genetics of autism: overview and new directions.

1998 • 245 citations

Prevalence of Pervasive Developmental Disorders in the British Nationwide Survey of Child Mental Health

2001 • 226 citations

A Family History Study of Neuropsychiatric Disorders in the Adult Siblings of Autistic Individuals

1990 • 205 citations

Genetic Influences in Childhood-Onset Psychiatric Disorders: Autism and Attention-Deficit/Hyperactivity Disorder

1997 • 204 citations

Autism, affective disorders, and social phobia

1995 • 197 citations

Genetics of Type 1A Diabetes

2001 • 179 citations

Analysis of linkage disequilibrium in ?-aminobutyric acid receptor subunit genes in autistic disorder

2000 • 161 citations

The Familial Aggregation of the Lesser Variant in Biological and Nonbiological Relatives of PDD Probands: a Family History Study

2000 • 137 citations

The Early Origins of Autism

2000 • 136 citations

The frequency of the fragile X chromosome among schoolchildren in Coventry.

1986 • 130 citations

Symptom domains in autism and related conditions: Evidence for familiality

2001 • 123 citations

Domains of Social Communication Handicap in Autism Spectrum Disorder

1999 • 117 citations

The biology of the autistic syndromes

2001 • 105 citations

Familial Factors Influence Level of Functioning in Pervasive Developmental Disorder

1999 • 103 citations

The Biology of the Autistic Syndromes, 3rd Edition

2001 • 91 citations

Increased Frequency of the Extended or Ancestral Haplotype B44-SC3O-DR4 in Autism

1995 • 84 citations

Searching for genes underlying normal variation in human adiposity

2001 • 83 citations

Clinical Misconceptions Dispelled by Epidemiological Research

1995 • 81 citations

Autism and Genetic Disorders

1986 • 75 citations

Thalidomide embryopathy: Revisited 27 years later

1993 • 65 citations

Chromosomes in autism and related pervasive developmental disorders: a cytogenetic study

1998 • 62 citations

Molecular analysis and test of linkage between the FMR-1 gene and infantile autism in multiplex families.

1994 • 58 citations

Possible association of c-harvey-ras-1 (HRAS-1) marker with autism

1993 • 57 citations

Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q, 13q, 15q, 16p, 17q, 19q and 22q in Finnish multiplex families

2000 • 55 citations

Textbook of pediatric neuropsychiatry

1999 • 54 citations

Current concepts on the genetics of asthma

2001 • 52 citations

Autism and the pervasive developmental disorders

1997 • 51 citations

Studies of the c-Harvey-Ras gene in psychiatric disorders

1996 • 43 citations

The prevalence of fragile X in a sample of autistic individuals diagnosed using a standardized interview

1991 • 42 citations

47,XYY Karyotypes and Pervasive Developmental Disorders

1998 • 40 citations

Childhood of males with the XYY syndrome

1973 • 35 citations

The Prevalence of Fragile X in a Sample of Autistic Individuals Diagnosed Using a Standardized Interview

1991 • 12 citations

Deleted Work

1955 • 0 citations