Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19. (Q47292278)

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English	Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19.	scientific article

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17 November 2019

Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19 (English)

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17 November 2019

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17 November 2019

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17 November 2019

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Silverman J

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17 November 2019

Keddache M

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17 November 2019

Smith CJ

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17 November 2019

Hollander E

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17 November 2019

Reichert JG

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17 November 2019

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1 February 2004

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17 November 2019

Molecular Psychiatry

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17 November 2019

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17 November 2019

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17 November 2019

144-150

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17 November 2019

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

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21 January 2018

Neurobiology of autism

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

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Infantile autism: a genetic study of 21 twin pairs

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Concordance for the syndrome of autism in 40 pairs of afflicted twins

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A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden

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A case-control family history study of autism

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Genetics of autism: overview and new directions

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A genomic screen of autism: evidence for a multilocus etiology

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Are rare variants responsible for susceptibility to complex diseases?

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Full-genome scans with autistic disorder: a review

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Autism: recent molecular genetic advances

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Symptom domains in autism and related conditions: evidence for familiality

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Genetics of autism: characteristics of affected and unaffected children from 37 multiplex families

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Overweight, weight concerns, and bulimic behaviors among girls and boys

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21 January 2018

Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity

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Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder

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A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

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Obsessive-compulsive behaviors in parents of multiplex autism families

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The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions

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A genomewide screen for autism susceptibility loci

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

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21 January 2018

Further evidence for the increased power of LOD scores compared with nonparametric methods

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The power to detect linkage in complex disease by means of simple LOD-score analyses

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21 January 2018

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

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A broader phenotype of autism: the clinical spectrum in twins

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

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21 January 2018

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

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21 January 2018

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

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21 January 2018

Disruption of two novel genes by a translocation co-segregating with schizophrenia

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Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family.

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21 January 2018

Disrupted-in-Schizophrenia-1 (DISC-1): mutant truncation prevents binding to NudE-like (NUDEL) and inhibits neurite outgrowth

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21 January 2018

Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes

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Association between the dopamine receptor D4 (DRD4) gene and obsessive-compulsive disorder

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Genomewide scan of hoarding in sib pairs in which both sibs have Gilles de la Tourette syndrome

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The genetics of autism

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TESTING FOR HETEROGENEITY OF RECOMBINATION FRACTION VALUES IN HUMAN GENETICS

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Effect of heterogeneity and assumed mode of inheritance on lod scores

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Adequacy of single-locus approximations for linkage analyses of oligogenic traits: extension to multigenerational pedigree structures

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7 January 2021

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Linkage analysis of two-locus diseases under single-locus and two-locus analysis models

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7 January 2021

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Genome-wide linkage analysis of families with obsessive-compulsive disorder ascertained through pediatric probands

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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