(Q33581309)

28 July 2017

title

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

1 reference

28 July 2017

author

Daniel Moreno-De-Luca

4

object named as

Daniel Moreno-De-Luca

0 references

Andres Moreno-De-Luca

1

object named as

Andres Moreno-De-Luca

0 references

David H. Ledbetter

6

object named as

David H Ledbetter

1 reference

28 July 2017

author name string

Andres Moreno-De-Luca

1

1 reference

28 July 2017

Scott M Myers

2

1 reference

28 July 2017

Thomas D Challman

3

1 reference

28 July 2017

Daniel Moreno-De-Luca

4

1 reference

28 July 2017

David W Evans

5

1 reference

28 July 2017

publication date

18 March 2013

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28 July 2017

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28 July 2017

volume

12

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28 July 2017

issue

4

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28 July 2017

page(s)

406-414

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

28 July 2017

cites work

1 reference

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14 July 2018

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14 July 2018

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14 July 2018

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14 July 2018

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14 July 2018

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14 July 2018

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14 July 2018

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14 July 2018

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14 July 2018

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14 July 2018

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14 July 2018

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14 July 2018

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

14 July 2018

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A copy number variation morbidity map of developmental delay

14 July 2018

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Understanding the impact of 1q21.1 copy number variant

14 July 2018

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Exome sequencing supports a de novo mutational paradigm for schizophrenia.

14 July 2018

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Comorbidity of intellectual disability and mental disorder in children and adolescents: a systematic review

14 July 2018

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Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

14 July 2018

1 reference

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Practical guidelines for managing patients with 22q11.2 deletion syndrome

14 July 2018

1 reference

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Developmental comorbidity in attention-deficit/hyperactivity disorder

14 July 2018

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Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia

14 July 2018

1 reference

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The quantitative nature of autistic social impairment

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

Understanding the Complex Etiologies of Developmental Disorders: Behavioral and Molecular Genetic Approaches

14 July 2018

1 reference

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Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders

14 July 2018

1 reference

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

14 July 2018

1 reference

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CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila

14 July 2018

1 reference

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Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12.

14 July 2018

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Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders.

14 July 2018

1 reference

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Childhood developmental disorders: an academic and clinical convergence point for psychiatry, neurology, psychology and pediatrics

14 July 2018

1 reference

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Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects females

14 July 2018

1 reference

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A 15q13.3 microdeletion segregating with autism

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

Large recurrent microdeletions associated with schizophrenia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

Rare chromosomal deletions and duplications increase risk of schizophrenia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

Relations among speech, language, and reading disorders

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

Recurrent 16p11.2 microdeletions in autism

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

The epidemiology of cerebral palsy: incidence, impairments and risk factors

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

Atypical brain development: a conceptual framework for understanding developmental learning disabilities

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

Ritual, habit, and perfectionism: the prevalence and development of compulsive-like behavior in normal young children

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

A pediatric overview of the spectrum of developmental disabilities

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

Syndromes of minimal brain dysfunction in children

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

Familial mental retardation: a continuing dilemma

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

Revised Neurological Examination for Subtle Signs (1985).

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

Cognitive development in retarded and nonretarded persons: Piagetian tests of the similar sequence hypothesis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

Infantile convulsions and paroxysmal kinesigenic dyskinesia with 16p11.2 microdeletion.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

Deep sequencing reveals 50 novel genes for recessive cognitive disorders.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

The ESSENCE in child psychiatry: Early Symptomatic Syndromes Eliciting Neurodevelopmental Clinical Examinations

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

Autism in three patients with cystic or hyperechogenic kidneys and chromosome 17q12 deletion.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

Identifying infants and young children with developmental disorders in the medical home: an algorithm for developmental surveillance and screening.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

Chromosome 1q21.1 contiguous gene deletion is associated with congenital heart disease

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

Validation of a brief quantitative measure of autistic traits: comparison of the social responsiveness scale with the autism diagnostic interview-revised.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

Motor coordination and kinaesthesis in boys with attention deficit-hyperactivity disorder.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

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

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4013791

10.1016/S1474-4422(13)70011-5

31 October 2018

Identifiers

DOI

1 reference

release_rtkftv7ebfbnholifysv272zji

28 July 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/rtkftv7ebfbnholifysv272zji

mapped directly with Wikidata item

24 November 2022

based on heuristic

PMC publication ID

4013791

1 reference

28 July 2017

1 reference