(Q28275583)

1

0 references

T D Als

2

0 references

H A Dahl

3

0 references

T J Flint

4

0 references

A G Wang

5

0 references

M Vang

6

0 references

T A Kruse

7

0 references

H Ewald

A case-control family history study of autism

8

0 references

language of work or name

English

0 references

publication date

January 2006

0 references

published in

Molecular Psychiatry

0 references

volume

11

0 references

issue

1

0 references

page(s)

37-46

0 references

cites work

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

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.4001754

A genomic screen of autism: evidence for a multilocus etiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

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.4001754

Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Analysis of the RELN gene as a genetic risk factor for autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Autistic spectrum disorder associated with partial duplication of chromosome 15; three case reports.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

21 January 2018

The genetics of autism

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Molecular genetics of the Finnish disease heritage.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Identification of a novel gene and a common variant associated with uric acid nephrolithiasis in a Sardinian genetic isolate

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Genome-wide scan for loci of Asperger syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

The origin of the isolated population of the Faroe Islands investigated using Y chromosomal markers

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Loci for primary ciliary dyskinesia map to chromosome 16p12.1-12.2 and 15q13.1-15.1 in Faroe Islands and Israeli Druze genetic isolates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Possible evidence for a common risk locus for bipolar affective disorder and schizophrenia on chromosome 4p16 in patients from the Faroe Islands

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Genome screening for linkage disequilibrium in a Costa Rican sample of patients with bipolar-I disorder: a follow-up study on chromosome 18.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Novel case-control test in a founder population identifies P-selectin as an atopy-susceptibility locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Complex trait mapping in isolated populations: Are specific statistical methods required?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Genome scanning for segments shared identical by descent among distant relatives in isolated populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Genomic screen and follow-up analysis for autistic disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

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/10.1038%2FSJ.MP.4001754

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.4001754

Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Partial trisomy 16p in an adolescent with autistic disorder and Tourette's syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Psychopathology, GABA, and the Rubinstein-Taybi syndrome: a review and case study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

FISH characterisation of an identical (16)(p11.2p12.2) tandem duplication in two unrelated patients with autistic behaviour.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

21 January 2018

The genetics of autism.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Association of INPP1, PIK3CG, and TSC2 gene variants with autistic disorder: implications for phosphatidylinositol signalling in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Molecular genetics of autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Autistic traits in the general population: a twin study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Diagnosing autism: analyses of data from the Autism Diagnostic Interview.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Interrelationship between Autism Diagnostic Observation Schedule-Generic (ADOS-G), Autism Diagnostic Interview-Revised (ADI-R), and the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV-TR) classification in children and adolescents with

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

The genetically isolated populations of Finland and Sardinia may not be a panacea for linkage disequilibrium mapping of common disease genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Linkage disequilibrium in human populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Use of population isolates for mapping complex traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

Linkage disequilibrium and demographic history of the isolated population of the Faroe Islands

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

spagedi: a versatile computer program to analyse spatial genetic structure at the individual or population levels

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

High incidence of cystic fibrosis on the Faroe Islands: a molecular and genealogical study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

7 January 2021

Molecular genetic basis and prevalence of glycogen storage disease type IIIA in the Faroe Islands

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

7 January 2021

Further evidence for a bipolar risk gene on chromosome 12q24 suggested by investigation of haplotype sharing and allelic association in patients from the Faroe Islands

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

7 January 2021

Monte Carlo tests for associations between disease and alleles at highly polymorphic loci

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

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.4001754

7 January 2021

Identification and characterization of the tuberous sclerosis gene on chromosome 16

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

7 January 2021

Are common disease susceptibility alleles the same in outbred and founder populations?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

7 January 2021

The value of isolated populations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

7 January 2021

The genetics of asthma. Mapping genes for complex traits in founder populations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001754

7 January 2021