An autosomal genomic screen for autism

Autism Diagnostic Interview-Revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

1994 • 8,662 citations

Fast and sensitive silver staining of DNA in polyacrylamide gels

1991 • 2,914 citations

Parametric and nonparametric linkage analysis: a unified multipoint approach.

1996 • 2,905 citations

Autism as a strongly genetic disorder: evidence from a British twin study

1995 • 2,442 citations

Handbook of Autism and Pervasive Developmental Disorders

2005 • 2,272 citations

Austism diagnostic observation schedule: A standardized observation of communicative and social behavior

1989 • 1,944 citations

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination.

1985 • 1,207 citations

A full genome search in multiple sclerosis

1996 • 666 citations

A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex

1996 • 650 citations

A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22

1996 • 638 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

Localisation of a gene implicated in a severe speech and language disorder

1998 • 476 citations

Evidence of linkage between the serotonin transporter and autistic disorder

1997 • 435 citations

A comparison of sib‐pair linkage tests for disease susceptibility loci

1985 • 407 citations

Autism and maternally derived aberrations of chromosome 15q

1998 • 369 citations

Linkage-Disequilibrium Mapping of Autistic Disorder, with 15q11-13 Markers

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Use of cyclosporin a in establishing epstein-barr virus-transformed human lymphoblastoid cell lines

1984 • 355 citations

Genomic Variation and Gene Conversion in Spinal Muscular Atrophy: Implications for Disease Process and Clinical Phenotype

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Genomewide Scan of Multiple Sclerosis in Finnish Multiplex Families

1997 • 308 citations

Testing for heterogeneity of recombination fraction values in Human Genetics

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

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The UCLA-University of Utah epidemiologic survey of autism: recurrence risk estimates and genetic counseling

1989 • 255 citations

Diagnostic Uses of the Vineland Adaptive Behavior Scales

1985 • 243 citations

Affected-sib-pair interval mapping and exclusion for complex genetic traits: Sampling considerations

1996 • 225 citations

Genetic approaches to mental disorders

1994 • 196 citations

A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps

1995 • 182 citations

Genetic Approaches to Mental Disorders

1995 • 173 citations

Lods, wrods, and mods: The interpretation of lod scores calculated under different models

1994 • 138 citations

Magnitude of type I error when single-locus linkage analysis is maximized over models: a simulation study.

1997 • 127 citations

Linkage Analysis in Nuclear Families

1994 • 117 citations

Brief report: Duplication of chromosome 15q11-13 in two individuals with autistic disorder

1994 • 108 citations

Adequacy of single‐locus approximations for linkage analyses of oligogenic traits

1992 • 107 citations

Inferring mode of inheritance by comparison of lod scores

1989 • 104 citations

Linkage Analysis in Nuclear Families

1994 • 100 citations

Further Evidence for the Increased Power of LOD Scores Compared with Nonparametric Methods

1999 • 88 citations

The problem of ascertainment for linkage analysis.

1996 • 48 citations

Using lod-score differences to determine mode of inheritance: a simple, robust method even in the presence of heterogeneity and reduced penetrance.

1994 • 29 citations

GenoMap: A distributed system for unifying genotyping and genetic linkage analysis

1998 • 3 citations

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