(Q28296551)

Kirsty Wing

5

0 references

Dalila Pinto

Dalila Pinto

11

0 references

Massimo Molteni

Massimo Molteni

10

0 references

James S. Sutcliffe

James S Sutcliffe

14

0 references

Maria Clara Bonaglia

Maria Clara Bonaglia

6

0 references

Andrew D. Paterson

Andrew D Paterson

16

0 references

Anthony Monaco

Anthony P Monaco

19

0 references

Peter Szatmari

15

Peter Szatmari

0 references

Stephen W. Scherer

17

Stephen W Scherer

0 references

Veronica J Vieland

18

Veronica J Vieland

0 references

Alistair T Pagnamenta

1

Alistair T Pagnamenta

0 references

Tom Berney

8

Tom Berney

0 references

Ann Le Couteur

12

Ann Le Couteur

0 references

Joachim Hallmayer

13

Joachim Hallmayer

0 references

Dianne Gerrelli

4

Dianne Gerrelli

0 references

author name string

Hameed Khan

2

0 references

Susan Walker

3

0 references

Elisa Mani

Journal of Medical Genetics

9

0 references

language of work or name

English

0 references

publication date

January 2011

0 references

published in

0 references

volume

48

0 references

page(s)

48-54

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issue

1

0 references

cites work

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1 reference

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

20 March 2017

1 reference

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Identifying autism loci and genes by tracing recent shared ancestry

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003876

Contribution of SHANK3 mutations to autism spectrum disorder

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003876

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

20 March 2017

1 reference

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

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003876

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

20 March 2017

1 reference

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dbSNP: the NCBI database of genetic variation

20 March 2017

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

20 March 2017

1 reference

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Cadherin-8 is required for the first relay synapses to receive functional inputs from primary sensory afferents for cold sensation

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003876

Origins and functional impact of copy number variation in the human genome

20 March 2017

1 reference

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

20 March 2017

1 reference

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PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping 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=3003876

A synaptic trek to 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=3003876

A double hit implicates DIAPH3 as an autism risk gene.

7 April 2017

1 reference

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A genome-wide association study of alcohol dependence

29 September 2017

1 reference

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Normal variation in fronto-occipital circuitry and cerebellar structure with an autism-associated polymorphism of CNTNAP2

29 September 2017

1 reference

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A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003876

Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003876

A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003876

A genome-wide linkage and association scan reveals novel loci for autism

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003876

High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003876

Forging links between human mental retardation-associated CNVs and mouse gene knockout models

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003876

Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003876

Alterations in CDH15 and KIRREL3 in patients with mild to severe intellectual disability

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003876

Genome-wide analyses of human perisylvian cerebral cortical patterning.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003876

Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003876

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003876

EEG features and epilepsy in patients with autism.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003876

Seizure disorders in autism

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003876

Replication of GWAS of bipolar disorder: association of SNPs near CDH7 with bipolar disorder and visual processing

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003876

Autism meets schizophrenia via cadherin pathway.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003876

Kinesin family member 6 variant Trp719Arg does not associate with angiographically defined coronary artery disease in the Ottawa Heart Genomics Study.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003876

Thermometers: something for statistical geneticists to think about

27 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20972252