Recent advances in the genetics of autism spectrum disorder (Q38462559)

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scientific article published on June 2015

Language	Label	Description	Also known as
English	Recent advances in the genetics of autism spectrum disorder	scientific article published on June 2015

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

1 reference

Europe PubMed Central

Recent advances in the genetics of autism spectrum disorder (English)

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Europe PubMed Central

PubMed publication ID

3 September 2017

autism spectrum disorder

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2

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Silvia De Rubeis

object named as

Silvia De Rubeis

1

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language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 June 2015

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Europe PubMed Central

PubMed publication ID

3 September 2017

Current Neurology and Neuroscience Reports

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Europe PubMed Central

PubMed publication ID

3 September 2017

15

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Europe PubMed Central

PubMed publication ID

3 September 2017

6

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Europe PubMed Central

PubMed publication ID

3 September 2017

36

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Europe PubMed Central

PubMed publication ID

3 September 2017

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

The co-morbidity burden of children and young adults with autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Etiological heterogeneity in autism spectrum disorders: More than 100 genetic and genomic disorders and still counting

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Heritability in the genomics era — concepts and misconceptions

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Classical twin studies and beyond

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Concordance for the syndrome of autism in 40 pairs of afflicted twins

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Infantile autism: a genetic study of 21 twin pairs

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Most genetic risk for autism resides with common variation

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Common genetic variants, acting additively, are a major source of risk for autism

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Recurrence of autism spectrum disorders in full- and half-siblings and trends over time: a population-based cohort study

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Human genetic variation and its contribution to complex traits

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

A genome-wide scan for common alleles affecting risk for autism

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Do common variants play a role in risk for autism? Evidence and theoretical musings

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Individual common variants exert weak effects on the risk for autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Genetic architecture in autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Strong association of de novo copy number mutations with autism

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Structural variation of chromosomes in autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Functional impact of global rare copy number variation in autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

The story of Rett syndrome: from clinic to neurobiology

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Patterns and rates of exonic de novo mutations in autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

De Novo Gene Disruptions in Children on the Autistic Spectrum

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Using whole-exome sequencing to identify inherited causes of autism

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

A systematic survey of loss-of-function variants in human protein-coding genes

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

De novo mutations in human genetic disease

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Variation in genome-wide mutation rates within and between human families

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Analysis of genetic inheritance in a family quartet by whole-genome sequencing

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Rate of de novo mutations and the importance of father's age to disease risk

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Whole-genome sequencing in autism identifies hot spots for de novo germline mutation.

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

De novo copy number variants associated with intellectual disability have a paternal origin and age bias.

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

A comprehensive assessment of parental age and psychiatric disorders

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Autism risk across generations: a population-based study of advancing grandpaternal and paternal age.

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Advancing paternal age and risk of autism: new evidence from a population-based study and a meta-analysis of epidemiological studies

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Why are autism spectrum conditions more prevalent in males?

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Fragile X syndrome: causes, diagnosis, mechanisms, and therapeutics.

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders.

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

SHANK1 Deletions in Males with Autism Spectrum Disorder

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Phenotypic heterogeneity of genomic disorders and rare copy-number variants

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Examining and interpreting the female protective effect against autistic behavior

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

The Simons Simplex Collection: A Resource for Identification of Autism Genetic Risk Factors

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Postnatal Neurodevelopmental Disorders: Meeting at the Synapse?

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

De novo mutations in schizophrenia implicate synaptic networks

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Molecular and synaptic defects in intellectual disability syndromes

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Progress toward treatments for synaptic defects in autism

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Spatio-temporal transcriptome of the human brain

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Transcriptional landscape of the prenatal human brain

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Cell type-specific expression analysis to identify putative cellular mechanisms for neurogenetic disorders

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

De novo TBR1 mutations in sporadic autism disrupt protein functions

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Glial ankyrins facilitate paranodal axoglial junction assembly

1 reference

https://api.crossref.org/works/10.1007%2FS11910-015-0553-1

21 January 2018

Tbr1 haploinsufficiency impairs amygdalar axonal projections and results in cognitive abnormality

1 reference

https://pubmed.ncbi.nlm.nih.gov/25946996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/25946996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epidemiology of autistic disorder and other pervasive developmental disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/25946996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disruptive CHD8 mutations define a subtype of autism early in development

1 reference

https://pubmed.ncbi.nlm.nih.gov/25946996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A higher mutational burden in females supports a "female protective model" in neurodevelopmental disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/25946996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S11910-015-0553-1

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

ResearchGate publication ID

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