(Q24684315)

5

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Jonathan Sebat

object named as

Jonathan Sebat

10

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Catherine Lord

9

object named as

Catherine Lord

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author name string

Xiaoyue Zhao

1

0 references

Anthony Leotta

2

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Vlad Kustanovich

3

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Clara Lajonchere

4

0 references

Kiely Law

6

0 references

Paul Law

7

0 references

Shanping Qiu

8

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Kenny Ye

Proceedings of the National Academy of Sciences of the United States of America

11

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language of work or name

English

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publication date

31 July 2007

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published in

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volume

104

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issue

31

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page(s)

12831-6

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cites work

Strong association of de novo copy number mutations with autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1933261

A genomewide screen of 345 families for autism-susceptibility loci

7 April 2017

1 reference

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1933261

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

7 April 2017

1 reference

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A genomic screen of autism: evidence for a multilocus etiology

7 April 2017

1 reference

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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

7 April 2017

1 reference

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Mapping autism risk loci using genetic linkage and chromosomal rearrangements

7 April 2017

1 reference

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

7 April 2017

1 reference

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Genomic rearrangements and gene copy-number alterations as a cause of nervous system disorders

7 April 2017

1 reference

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Advancing paternal age 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=1933261

Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families

7 April 2017

1 reference

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Identification and characterization of the tuberous sclerosis gene on chromosome 16

7 April 2017

1 reference

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

7 April 2017

2 references

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7 April 2017

https://api.crossref.org/works/10.1073/PNAS.0705803104

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

22 April 2017

1 reference

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Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1933261

Prevalence of autism spectrum disorders--autism and developmental disabilities monitoring network, 14 sites, United States, 2002.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1933261

Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1933261

Sex differences in the brain: implications for explaining autism

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1933261

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1933261

X-linked genes and mental functioning

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1933261

Molecular genetics of autism spectrum disorder.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1933261

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1933261

A genomewide screen for autism susceptibility loci

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1933261

Genomic imprinting of the X chromosome: a novel mechanism for the evolution of sexual dimorphism

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1933261

Fragile X genotype characterized by an unstable region of DNA.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1933261

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1933261

Trend analysis of the sex ratio at birth in the United States.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1933261

28 November 2018

Identifiers

DOI

10.1073/PNAS.0705803104

1 reference

ADS bibcode

2007PNAS..10412831Z

0 references

1 reference

1 reference

PubMed publication ID

17652511

1 reference