AutDB: a gene reference resource for autism research (Q41883950)

13 October 2017

AutDB: a gene reference resource for autism research (English)

1 reference

13 October 2017

0 references

Saumyendra N Basu

1

1 reference

13 October 2017

Ravi Kollu

series ordinal

2

1 reference

13 October 2017

Sharmila Banerjee-Basu

series ordinal

3

1 reference

13 October 2017

10 November 2008

1 reference

13 October 2017

Nucleic Acids Research

1 reference

13 October 2017

37

1 reference

13 October 2017

Database issue

1 reference

13 October 2017

D832-6

1 reference

Identifying autism loci and genes by tracing recent shared ancestry

13 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2686502

Advances in autism genetics: on the threshold of a new neurobiology

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2686502

Structural variation of chromosomes in autism spectrum disorder

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2686502

Strong association of de novo copy number mutations with autism

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2686502

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2686502

Evaluation of a methodology for a collaborative multiple source surveillance network for autism spectrum disorders--Autism and Developmental Disabilities Monitoring Network, 14 sites, United States, 2002.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2686502

A review of gene linkage, association and expression studies in autism and an assessment of convergent evidence

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2686502

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2686502

The genetics of autistic disorders and its clinical relevance: a review of the literature

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2686502

Searching for ways out of the autism maze: genetic, epigenetic and environmental clues

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2686502

Epidemiology of autistic disorder and other pervasive developmental disorders

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2686502

Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2686502

Specific Genetic Disorders and Autism: Clinical Contribution Towards their Identification

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2686502

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2686502

Genetics of austim: complex aetiology for a heterogeneous disorder

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2686502

Pervasive Developmental Disorders in Preschool Children

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2686502

Autism spectrum disorders

5 June 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2686502

5 June 2018

https://api.crossref.org/works/10.1093%2FNAR%2FGKN835

A broader phenotype of autism: the clinical spectrum in twins

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2686502

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

5 June 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2686502

5 June 2018

https://api.crossref.org/works/10.1093%2FNAR%2FGKN835

The behavioral phenotype in fragile X: symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2686502

18 August 2018

Identifiers

DOI

10.1093/NAR/GKN835

1 reference

13 October 2017

journals/nar/BasuKB09

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

13 October 2017

PubMed publication ID

19015121

1 reference