(Q24540104)

6 July 2017

title

A genomic screen of autism: evidence for a multilocus etiology (English)

1 reference

Luigi Luca Cavalli-Sforza

6 July 2017

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object named as

L L Cavalli-Sforza

1 reference

6 July 2017

N Risch

1 reference

6 July 2017

D Spiker

1 reference

6 July 2017

L Lotspeich

1 reference

6 July 2017

N Nouri

1 reference

6 July 2017

D Hinds

1 reference

6 July 2017

J Hallmayer

1 reference

6 July 2017

L Kalaydjieva

1 reference

6 July 2017

P McCague

1 reference

6 July 2017

S Dimiceli

1 reference

6 July 2017

T Pitts

1 reference

6 July 2017

L Nguyen

1 reference

6 July 2017

J Yang

1 reference

6 July 2017

C Harper

1 reference

6 July 2017

D Thorpe

1 reference

6 July 2017

S Vermeer

1 reference

6 July 2017

H Young

1 reference

6 July 2017

J Hebert

1 reference

6 July 2017

A Lin

1 reference

6 July 2017

J Ferguson

1 reference

6 July 2017

C Chiotti

1 reference

6 July 2017

S Wiese-Slater

1 reference

6 July 2017

T Rogers

1 reference

6 July 2017

B Salmon

1 reference

6 July 2017

P Nicholas

1 reference

6 July 2017

P B Petersen

1 reference

6 July 2017

C Pingree

1 reference

6 July 2017

W McMahon

1 reference

6 July 2017

D L Wong

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6 July 2017

H C Kraemer

1 reference

6 July 2017

R M Myers

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6 July 2017

language of work or name

English

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publication date

1 August 1999

1 reference

American Journal of Human Genetics

6 July 2017

published in

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6 July 2017

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6 July 2017

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6 July 2017

page(s)

493-507

1 reference

Autism or atypical autism in maternally but not paternally derived proximal 15q duplication

6 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=1377948

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

A case-control family history study of autism

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

Autism diagnostic observation schedule: a standardized observation of communicative and social behavior

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

Infantile autism: a genetic study of 21 twin pairs

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

Autism: the point of view from fragile X studies

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

Autism and genetics. A decade of research

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

Linkage strategies for genetically complex traits. I. Multilocus models

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

Complex segregation analysis of autism

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

The genetics, if any, of infantile autism and childhood schizophrenia

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

A conditional inference framework for extending the transmission/disequilibrium test.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

Tests for linkage and association in nuclear families

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

Autism and the X chromosome. Multipoint sib-pair analysis

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

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

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

Gene mapping studies with the syndrome of autism

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

Autism diagnostic interview: a standardized investigator-based instrument

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

The UCLA-University of Utah epidemiologic survey of autism: genealogical analysis of familial aggregation

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

Autism associated with marker chromosome

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

Chromosomal disorders and autism

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

Autism: the phenotype in relatives

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

Genetics of autism: overview and new directions

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377948

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

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10417292

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Autism and tuberous sclerosis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10417292

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

Crossref

https://api.crossref.org/works/10.1086%2F302497

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1086/302497

1 reference

6 July 2017

1 reference

6 July 2017

1 reference