(Q24634148)

21

0 references

Daria Salyakina

2

Daria Salyakina

1 reference

ORCID Public Data File 2021

Holly N Cukier

Holly N Cukier

10

0 references

Jonathan L Haines

20

Jonathan L Haines

0 references

Gary W Beecham

13

Gary W Beecham

0 references

Eden R Martin

16

Eden R Martin

0 references

Michael L Cuccaro

19

Michael L Cuccaro

0 references

Ioanna Konidari

4

Ioanna Konidari

0 references

author name string

Deqiong Ma

1

0 references

James M Jaworski

3

0 references

Patrice L Whitehead

5

0 references

Ashley N Andersen

6

0 references

Joshua D Hoffman

7

0 references

Susan H Slifer

8

0 references

Dale J Hedges

9

0 references

Anthony J Griswold

11

0 references

Jacob L McCauley

12

0 references

Harry H Wright

14

0 references

Ruth K Abramson

15

0 references

John P Hussman

17

0 references

John R Gilbert

describes a project that uses

18

0 references

language of work or name

English

0 references

publication date

May 2009

0 references

published in

Annals of Human Genetics

0 references

volume

73

0 references

issue

Pt 3

0 references

page(s)

263-73

0 references

genome-wide association study

1 reference

based on heuristic

inferred from title

cites work

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918410

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk 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=2918410

A second generation human haplotype map of over 3.1 million SNPs

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918410

PLINK: a tool set for whole-genome association and population-based linkage analyses

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918410

Strong association of de novo copy number mutations 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=2918410

Population structure and eigenanalysis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918410

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918410

The structure of haplotype blocks in the human genome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918410

Association between microdeletion and microduplication at 16p11.2 and 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=2918410

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=2918410

Autism as a strongly genetic disorder: evidence from a British twin 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=2918410

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918410

A new multipoint method for genome-wide association studies by imputation of genotypes

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918410

Risk alleles for multiple sclerosis identified by a genomewide 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=2918410

Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918410

Structure and mechanism of cadherins and catenins in cell-cell contacts

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918410

Pervasive developmental disorders in preschool children: confirmation of high prevalence

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918410

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=2918410

A test for linkage and association in general pedigrees: the pedigree 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=2918410

Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918410

Expression of cadherin10, a type II classic cadherin gene, in the nervous system of the embryonic zebrafish

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918410

Correcting for a potential bias in the pedigree disequilibrium test

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918410

Common genetic variants on 5p14.1 associate with autism spectrum disorders

30 May 2018

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2009.00523.X

An analysis of 4,514 cases of renal biopsy in Korea

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2009.00523.X

Refining genetic associations in multiple sclerosis

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918410

A high-density SNP genome-wide linkage scan in a large autism extended pedigree.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918410

Genomic screen and follow-up analysis for autistic disorder.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918410

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

28 November 2018

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2009.00523.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1111/J.1469-1809.2009.00523.X

1 reference

1 reference

1 reference

PubMed publication ID

19456320

1 reference