Replication of autism linkage: fine-mapping peak at 17q21. (Q24530782)

4 July 2017

0 references

Replication of autism linkage: fine-mapping peak at 17q21. (English)

1 reference

4 July 2017

0 references

8

Daniel H Geschwind

1 reference

4 July 2017

1

Rita M Cantor

1 reference

4 July 2017

7

Stanley F Nelson

1 reference

4 July 2017

Naoko Kono

2

1 reference

4 July 2017

Jackie A Duvall

3

1 reference

4 July 2017

Ana Alvarez-Retuerto

4

1 reference

4 July 2017

Jennifer L Stone

5

1 reference

4 July 2017

Maricela Alarcón

6

1 reference

4 July 2017

language of work or name

English

0 references

publication date

1 April 2005

1 reference

American Journal of Human Genetics

4 July 2017

published in

1 reference

4 July 2017

volume

76

1 reference

4 July 2017

issue

6

1 reference

4 July 2017

page(s)

1050-1056

1 reference

A genomewide screen of 345 families for autism-susceptibility loci

4 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=1196442

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196442

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196442

A genomic screen of autism: evidence for a multilocus etiology

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196442

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=1196442

An autosomal genomic screen for autism. Collaborative linkage 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=1196442

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair 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=1196442

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=1196442

Parametric and nonparametric linkage analysis: a unified multipoint approach

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196442

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=1196442

Effects of updating linkage evidence across subsets of data: reanalysis of the autism genetic resource exchange data set.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196442

Sex-specific genetic architecture of whole blood serotonin levels

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196442

Evidence for sex-specific risk alleles in autism spectrum disorder

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196442

Serotonin transporter: gene, genetic disorders, and pharmacogenetics

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196442

Prevalence of autism in a US metropolitan area

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196442

PlA polymorphism of integrin beta 3 differentially modulates cellular migration on extracellular matrix proteins

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196442

Regional meta-analysis of published data supports linkage of autism with markers on chromosome 7.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196442

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196442

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196442

Accurate inference of relationships in sib-pair linkage studies

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196442

Toward localizing genes underlying cerebral asymmetry and mental health

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196442

Genome-wide association study identifies ITGB3 as a QTL for whole blood serotonin

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196442

Sex stratification of an inflammatory bowel disease genome search shows male-specific linkage to the HLA region of chromosome 6

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196442

Genomic screen and follow-up analysis for autistic disorder

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196442

Estimation of pairwise relationships in the presence of genotyping errors

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196442

Evidence for association and genetic linkage of the angiotensin-converting enzyme locus with hypertension and blood pressure in men but not women in the Framingham Heart Study

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196442

Linkage analysis of chromosome 2q in osteoarthritis

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15877280

12 December 2020

inferred from PubMed ID database lookup

The replication requirement

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15877280

12 December 2020

inferred from PubMed ID database lookup

Male–female differences in fertility and blood pressure in ACE-deficient mice

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15877280

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1086/430278

1 reference

release_s5lu3472gfbb7jn7u6enhane6y

4 July 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/s5lu3472gfbb7jn7u6enhane6y

24 November 2022

mapped directly with Wikidata item

PMC publication ID

1196442

1 reference

4 July 2017

1 reference