(Q38616673)

4 September 2017

title

Recurrent copy number variations as risk factors for neurodevelopmental disorders: critical overview and analysis of clinical implications (English)

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neurodevelopmental disorder

4 September 2017

main subject

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4 September 2017

Fátima Torres

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4 September 2017

Mafalda Barbosa

series ordinal

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4 September 2017

language of work or name

English

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publication date

26 October 2015

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Journal of Medical Genetics

4 September 2017

published in

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4 September 2017

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4 September 2017

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4 September 2017

page(s)

73-90

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

4 September 2017

1 reference

Schizophrenia as a disorder of neurodevelopment

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

The genetic variability and commonality of neurodevelopmental disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Finding the missing heritability of complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

CNVs: harbingers of a rare variant revolution in psychiatric genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Common and rare variants in multifactorial susceptibility to common diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Most genetic risk for autism resides with common variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Global variation in copy number in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Genetic association analysis of copy-number variation (CNV) in human disease pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

A copy number variation morbidity map of developmental delay

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Rare copy number variants are an important cause of epileptic encephalopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Copy number variants are frequent in genetic generalized epilepsy with intellectual disability

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Relative impact of nucleotide and copy number variation on gene expression phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Relating CNVs to transcriptome data at fine resolution: assessment of the effect of variant size, type, and overlap with functional regions

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Analysis of copy number variations in brain DNA from patients with schizophrenia and other psychiatric disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Comprehensive survey of CNVs influencing gene expression in the human brain and its implications for pathophysiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Large recurrent microdeletions associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Analysis of copy number variations at 15 schizophrenia-associated loci.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Microdeletions of 3q29 confer high risk for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Estimates of penetrance for recurrent pathogenic copy-number variations

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Genetic counseling for susceptibility loci and neurodevelopmental disorders: the del15q11.2 as an example.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Recurrent 16p11.2 microdeletions in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Implication of a rare deletion at distal 16p11.2 in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Disruption of neurexin 1 associated with autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Neurexin 1 (NRXN1) deletions in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Refining analyses of copy number variation identifies specific genes associated with developmental delay

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Disruption of contactin 4 in three subjects with autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Understanding the impact of 1q21.1 copy number variant

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

AMP-activated protein kinase phosphorylates retinoblastoma protein to control mammalian brain development

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Novel rare variants in F-box protein 45 (FBXO45) in schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Genetically complex epilepsies, copy number variants and syndrome constellations

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Iterative phenotyping of 15q11.2, 15q13.3 and 16p13.11 microdeletion carriers in pediatric epilepsies

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Functional characterization of NIPA2, a selective Mg2+ transporter

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

NIPA1 Gene Mutations Cause Autosomal Dominant Hereditary Spastic Paraplegia (SPG6)

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Regulation of molecular pathways in the Fragile X Syndrome: insights into Autism Spectrum Disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

GCP5 and GCP6: two new members of the human gamma-tubulin complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Delineation of 15q13.3 microdeletions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

The human clinical phenotypes of altered CHRNA7 copy number

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

The human CHRNA7 and CHRFAM7A genes: A review of the genetics, regulation, and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Analysis of CHRNA7 rare variants in autism spectrum disorder susceptibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

From toxins targeting ligand gated ion channels to therapeutic molecules

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Alpha7 nicotinic acetylcholine receptor is a target in pharmacology and toxicology

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Maximizing the effect of an α7 nicotinic receptor PAM in a mouse model of schizophrenia-like sensory inhibition deficits.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

The interaction between maternal immune activation and alpha 7 nicotinic acetylcholine receptor in regulating behaviors in the offspring

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Scan statistic-based analysis of exome sequencing data identifies FAN1 at 15q13.3 as a susceptibility gene for schizophrenia and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

On the role of FAN1 in Fanconi anemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Association between microdeletion and microduplication at 16p11.2 and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Microduplications of 16p11.2 are associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Regulation of synaptic functions in central nervous system by endocrine hormones and the maintenance of energy homoeostasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Large, rare chromosomal deletions associated with severe early-onset obesity

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Neuronal SH2B1 is essential for controlling energy and glucose homeostasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Critical role of the Src homology 2 (SH2) domain of neuronal SH2B1 in the regulation of body weight and glucose homeostasis in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

NDE1 and NDEL1: multimerisation, alternate splicing and DISC1 interaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

The essential role of centrosomal NDE1 in human cerebral cortex neurogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected]

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Deletion 16p13.11 uncovers NDE1 mutations on the non-deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruption.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

A common molecular basis for rearrangement disorders on chromosome 22q11

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

The 22q11 deletion syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Genetic, developmental, and physical factors associated with attention deficit hyperactivity disorder in patients with velocardiofacial syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Cognitive, behavioural and psychiatric phenotype in 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

The 22q11.2 deletion syndrome as a window into complex neuropsychiatric disorders over the lifespan.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Microduplication 22q11.2: a benign polymorphism or a syndrome with a very large clinical variability and reduced penetrance?--Report of two families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Microduplication 22q11.2: a new chromosomal syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Evidence that duplications of 22q11.2 protect against schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Role of TBX1 in human del22q11.2 syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Site-specific role of catechol-O-methyltransferase in dopamine overflow within prefrontal cortex and dorsal striatum

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Dopamine in socioecological and evolutionary perspectives: implications for psychiatric disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Association between a functional catechol O-methyltransferase gene polymorphism and schizophrenia: meta-analysis of case-control and family-based studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

PRODH mutations and hyperprolinemia in a subset of schizophrenic patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Transcriptional and behavioral interaction between 22q11.2 orthologs modulates schizophrenia-related phenotypes in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Proline affects brain function in 22q11DS children with the low activity COMT 158 allele

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Penetrance for copy number variants associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

The penetrance of copy number variations for schizophrenia and developmental delay.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Animal models of psychiatric disorders that reflect human copy number variation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Mutant mouse models of autism spectrum disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Animal models of human disease: zebrafish swim into view

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Using C. elegans to decipher the cellular and molecular mechanisms underlying neurodevelopmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

iPSCs and small molecules: a reciprocal effort towards better approaches for drug discovery

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Haploinsufficiency of Cyfip1 produces fragile X-like phenotypes in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

A mouse model that recapitulates cardinal features of the 15q13.3 microdeletion syndrome including schizophrenia- and epilepsy-related alterations

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Neuropathologic features in adults with 22q11.2 deletion syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Cxcr4 regulation of interneuron migration is disrupted in 22q11.2 deletion syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2015-103366

Evidence for altered hippocampal function in a mouse model of the human 22q11.2 microdeletion

21 January 2018

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The pattern of cortical dysfunction in a mouse model of a schizophrenia-related microdeletion

21 January 2018

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Derepression of a neuronal inhibitor due to miRNA dysregulation in a schizophrenia-related microdeletion

21 January 2018

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Neuroanatomical phenotypes in a mouse model of the 22q11.2 microdeletion

21 January 2018

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The human brain in a dish: the promise of iPSC-derived neurons

21 January 2018

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Induction of pluripotent stem cells from adult human fibroblasts by defined factors

21 January 2018

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Optimizing neuronal differentiation from induced pluripotent stem cells to model ASD

21 January 2018

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Phenotypic differences in hiPSC NPCs derived from patients with schizophrenia

21 January 2018

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Modelling schizophrenia using human induced pluripotent stem cells

21 January 2018

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Modeling psychiatric disorders through reprogramming

21 January 2018

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Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

21 January 2018

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Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts

21 January 2018

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Understanding variable expressivity in microdeletion syndromes.

21 January 2018

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

21 January 2018

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Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.

21 January 2018

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

21 January 2018

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Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence

21 January 2018

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CNVs conferring risk of autism or schizophrenia affect cognition in controls

21 January 2018

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Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases

21 January 2018

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DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

21 January 2018

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10.1136/JMEDGENET-2015-103366

21 January 2018

Identifiers

DOI

1 reference

4 September 2017

1 reference