(Q24791718)

2 July 2017

title

A genetic study of autism in Costa Rica: multiple variables affecting IQ scores observed in a preliminary sample of autistic cases (English)

1 reference

2 July 2017

0 references

0 references

L Alison McInnes

1

1 reference

2 July 2017

Patricia Jiménez González

2

1 reference

2 July 2017

Elina R Manghi

3

1 reference

2 July 2017

Marcela Esquivel

4

1 reference

2 July 2017

Silvia Monge

5

1 reference

2 July 2017

Marietha Fallas Delgado

6

1 reference

2 July 2017

Eduardo Fournier

7

1 reference

2 July 2017

Pamela Bondy

8

1 reference

2 July 2017

Kathryn Castelle

9

1 reference

2 July 2017

language of work or name

English

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publication date

21 March 2005

1 reference

2 July 2017

1 reference

2 July 2017

volume

5

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2 July 2017

issue

1

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page(s)

15

1 reference

The Arg451Cys-neuroligin-3 mutation associated with autism reveals a defect in protein processing

2 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

Are rare variants responsible for susceptibility to complex diseases?

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

A genomic screen of autism: evidence for a multilocus etiology

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

Genetics of austim: complex aetiology for a heterogeneous disorder

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

The incidence of autism in Olmsted County, Minnesota, 1976-1997: results from a population-based study

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

Genome-wide scan for loci of Asperger syndrome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

Evidence for allelic association on chromosome 3q25-27 in families with autism spectrum disorders originating from a subisolate of Finland

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

A case-control family history study of autism

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

Meta-analysis of intellectual and neuropsychological test performance in attention-deficit/hyperactivity disorder

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

Autism spectrum disorders in children with normal intellectual levels: associated impairments and subgroups

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

Perinatal factors and the development of autism: a population study

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

Increased Prevalence of Familial Autoimmunity in Probands With Pervasive Developmental Disorders

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

Epidemiological surveys of autism and other pervasive developmental disorders: an update

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

Small intestinal enteropathy with epithelial IgG and complement deposition in children with regressive autism

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

An international perspective on Tourette syndrome: selected findings from 3,500 individuals in 22 countries

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

Practice parameter: screening and diagnosis of autism: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Child Neurology Society

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

Randomized trial of intensive early intervention for children with pervasive developmental disorder

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

Early Intervention Project: can its claims be substantiated and its effects replicated?

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

Familial heterogeneity in infantile autism.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

Correlation of family history with specific autistic subgroups: Asperger's syndrome and bipolar affective disease.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

Siblings and parents of children with autism: a controlled population-based study

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1084355

Familial aggregation of emotional and behavioral problems of childhood in the general population.

30 May 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-5-15

Genetics of autism: overview and new directions

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-5-15

Symptom domains in autism and related conditions: evidence for familiality

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-5-15

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.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-5-15

Incorporating language phenotypes strengthens evidence of linkage to autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-5-15

Genetic studies of neuropsychiatric disorders in Costa Rica: a model for the use of isolated populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-5-15

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-5-15

Analysis of prevalence trends of autism spectrum disorder in Minnesota

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-5-15

Autistic spectrum disorder: a child population profile.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-5-15

Best estimate of lifetime psychiatric diagnosis: a methodological study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-5-15

Age and IQ at intake as predictors of placement for young children with autism: a four- to six-year follow-up.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-5-15

Co-occurrence of ADHD and low IQ has genetic origins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-5-15

Epilepsy is not a prominent feature of primary autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-5-15

A family genetic study of autism associated with profound mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-5-15

Autism spectrum disorders in children with normal intellectual levels: associated impairments and subgroups

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-5-15

Genetic demography of Antioquia (Colombia) and the Central Valley of Costa Rica

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15780135

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

2-year-old boy who has been diagnosed with autism

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-5-15

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1186/1471-244X-5-15

1 reference

Dimensions Publication ID

2 July 2017

1043351412

0 references

PMC publication ID

1084355

0 references

1 reference