(Q38174214)

30 August 2017

Copy-number variation in the pathogenesis of autism spectrum disorder (English)

1 reference

30 August 2017

0 references

autism spectrum disorder

0 references

0 references

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24372918%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

Branko Aleksic

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24372918%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

Norio Ozaki

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24372918%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

2

Branko Aleksic

1 reference

30 August 2017

29 December 2013

1 reference

Psychiatry and Clinical Neurosciences

30 August 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24372918%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

volume

68

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24372918%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24372918%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

page(s)

85-95

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24372918%20AND%20SRC:MED&resulttype=core&format=json

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

12 June 2020

cites work

1 reference

Evolution in health and medicine Sackler colloquium: Comparative genomics of autism and schizophrenia

21 January 2018

1 reference

Prevalence of autism spectrum disorders in a total population sample

21 January 2018

1 reference

Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism

21 January 2018

1 reference

Finishing the euchromatic sequence of the human genome

21 January 2018

1 reference

Strong association of de novo copy number mutations with autism

21 January 2018

1 reference

Mapping and sequencing of structural variation from eight human genomes

21 January 2018

1 reference

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

21 January 2018

1 reference

Rare inherited variation in autism: beginning to see the forest and a few trees

21 January 2018

1 reference

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

21 January 2018

1 reference

Large-scale copy number polymorphism in the human genome

21 January 2018

1 reference

Copy number variation: new insights in genome diversity

21 January 2018

1 reference

CNVs: harbingers of a rare variant revolution in psychiatric genetics

21 January 2018

1 reference

Activity-dependent neuronal signalling and autism spectrum disorder

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Genetic architecture in autism spectrum disorder

21 January 2018

1 reference

A copy number variation morbidity map of developmental delay

21 January 2018

1 reference

Major changes in our DNA lead to major changes in our thinking

21 January 2018

1 reference

Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism

21 January 2018

1 reference

Abnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autism

21 January 2018

1 reference

Mechanisms for recurrent and complex human genomic rearrangements

21 January 2018

1 reference

Genomic rearrangements and sporadic disease

21 January 2018

1 reference

Copy number variation in human health, disease, and evolution

21 January 2018

1 reference

Population analysis of large copy number variants and hotspots of human genetic disease

21 January 2018

1 reference

Sensitive and accurate detection of copy number variants using read depth of coverage

21 January 2018

1 reference

Next-generation sequencing transforms today's biology

21 January 2018

1 reference

Limitations of next-generation genome sequence assembly

21 January 2018

1 reference

Five years of GWAS discovery

21 January 2018

1 reference

Completing the map of human genetic variation

21 January 2018

1 reference

Molecular genetics of the platelet serotonin system in first-degree relatives of patients with autism

21 January 2018

1 reference

Reciprocal crossovers and a positional preference for strand exchange in recombination events resulting in deletion or duplication of chromosome 17p11.2.

21 January 2018

1 reference

Retrotransposition and structural variation in the human genome

21 January 2018

1 reference

Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans

21 January 2018

1 reference

Genetics. Insights into the pathogenesis of autism.

21 January 2018

1 reference

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

21 January 2018

1 reference

A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice

21 January 2018

1 reference

Ube3a is required for experience-dependent maturation of the neocortex.

21 January 2018

1 reference

Maternal loss of Ube3a produces an excitatory/inhibitory imbalance through neuron type-specific synaptic defects.

21 January 2018

1 reference

Global increases in both common and rare copy number load associated with autism

21 January 2018

1 reference

Diverse types of genetic variation converge on functional gene networks involved in schizophrenia

21 January 2018

1 reference

Simons Variation in Individuals Project (Simons VIP): a genetics-first approach to studying autism spectrum and related neurodevelopmental disorders

21 January 2018

1 reference

A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders

21 January 2018

1 reference

Genotype-phenotype correlation in 22q11.2 deletion syndrome

21 January 2018

1 reference

Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease

21 January 2018

1 reference

The 22q11.2 deletion in children: high rate of autistic disorders and early onset of psychotic symptoms.

21 January 2018

1 reference

Neuropsychiatric disorders in the 22q11 deletion syndrome

21 January 2018

1 reference

Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome

21 January 2018

1 reference

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

21 January 2018

1 reference

The Notch signalling system: recent insights into the complexity of a conserved pathway

21 January 2018

1 reference

Notch signalling in vertebrate neural development

21 January 2018

1 reference

The little R cell that could

21 January 2018

1 reference

Ras1 and a putative guanine nucleotide exchange factor perform crucial steps in signaling by the sevenless protein tyrosine kinase.

21 January 2018

1 reference