(Q28205412)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14515138%20AND%20SRC:MED&resulttype=core&format=json

19 December 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14515138%20AND%20SRC:MED&resulttype=core&format=json

19 December 2019

main subject

autism spectrum disorder

0 references

0 references

0 references

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14515138%20AND%20SRC:MED&resulttype=core&format=json

19 December 2019

Irma Järvelä

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14515138%20AND%20SRC:MED&resulttype=core&format=json

19 December 2019

author name string

Auranen M

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14515138%20AND%20SRC:MED&resulttype=core&format=json

19 December 2019

Alen R

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14515138%20AND%20SRC:MED&resulttype=core&format=json

19 December 2019

Vanhala R

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14515138%20AND%20SRC:MED&resulttype=core&format=json

19 December 2019

Ayers K

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14515138%20AND%20SRC:MED&resulttype=core&format=json

19 December 2019

Kempas E

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14515138%20AND%20SRC:MED&resulttype=core&format=json

19 December 2019

Ylisaukko-Oja T

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14515138%20AND%20SRC:MED&resulttype=core&format=json

19 December 2019

Peltonen L

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14515138%20AND%20SRC:MED&resulttype=core&format=json

19 December 2019

language of work or name

English

0 references

publication date

1 October 2003

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14515138%20AND%20SRC:MED&resulttype=core&format=json

19 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14515138%20AND%20SRC:MED&resulttype=core&format=json

19 December 2019

volume

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14515138%20AND%20SRC:MED&resulttype=core&format=json

19 December 2019

issue

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14515138%20AND%20SRC:MED&resulttype=core&format=json

19 December 2019

page(s)

879-884

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14515138%20AND%20SRC:MED&resulttype=core&format=json

A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27

19 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

Autism: towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

Infantile autism: a genetic study of 21 twin pairs

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

Autism: the phenotype in relatives.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

Genetics of austim: complex aetiology for a heterogeneous disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

A genomic screen of autism: evidence for a multilocus etiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

A genomewide screen for autism susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

Genomic screen and follow-up analysis for autistic disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

The Finnish population structure A genetic and genealogical study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

Close linkage to chromosome 3p and conservation of ancestral founding haplotype in hereditary nonpolyposis colorectal cancer families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

The Epidemiology of Asperger Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

A general method for isolation of high molecular weight DNA from eukaryotes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

Gamete-competition models

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

Linkage analysis in the presence of errors IV: joint pseudomarker analysis of linkage and/or linkage disequilibrium on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

Strategies for multilocus linkage analysis in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

Avoiding recomputation in linkage analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

7 January 2021

The interval of linkage disequilibrium (LD) detected with microsatellite and SNP markers in chromosomes of Finnish populations with different histories

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

7 January 2021

The epidemiology of Asperger syndrome. A total population study

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

7 January 2021

Programs for pedigree analysis: Mendel, Fisher, and dGene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001299

7 January 2021