(Q30439767)

7 September 2017

0 references

De novo SCN2A splice site mutation in a boy with Autism spectrum disorder (English)

1 reference

7 September 2017

autism spectrum disorder

0 references

0 references

11

1 reference

7 September 2017

Teresa Tavassoli

1

0 references

Guiqing Cai

10

object named as

Guiqing Cai

1 reference

7 September 2017

5

Danielle Halpern

1 reference

7 September 2017

9

David Grodberg

1 reference

7 September 2017

7

Sarah Soffes

1 reference

7 September 2017

Alexander Kolevzon

2

1 reference

7 September 2017

A Ting Wang

3

1 reference

7 September 2017

Jocelyn Curchack-Lichtin

4

1 reference

7 September 2017

Lily Schwartz

6

1 reference

7 September 2017

Lauren Bush

8

1 reference

7 September 2017

20 March 2014

1 reference

7 September 2017

1 reference

7 September 2017

15

1 reference

7 September 2017

35

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2350-15-35

7 September 2017

0 references

cites work

Major channels involved in neuropsychiatric disorders and therapeutic perspectives

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994485

Early sensory over-responsivity in toddlers with autism spectrum disorders as a predictor of family impairment and parenting stress.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994485

Duplication of the sodium channel gene cluster on 2q24 in children with early onset epilepsy

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994485

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994485

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994485

Sensory Over-Responsivity and ADHD: Differentiating Using Electrodermal Responses, Cortisol, and Anxiety

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994485

Advances in autism genetics: on the threshold of a new neurobiology

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994485

Sensory processing in children with and without autism: a comparative study using the short sensory profile

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994485

Sensory correlations in autism

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994485

Sodium channel mutations in epilepsy and other neurological disorders

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994485

Voltage-gated sodium channel blockers; target validation and therapeutic potential

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994485

Severe epilepsy, retardation, and dysmorphic features with a 2q deletion including SCN1A and SCN2A

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994485

A nonsense mutation of the sodium channel gene SCN2A in a patient with intractable epilepsy and mental decline

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994485

Sodium channels SCN1A, SCN2A and SCN3A in familial autism

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994485

Sensory processing issues associated with Asperger syndrome: a preliminary investigation

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994485

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994485

A comparison of the performance of children with and without autism on the Sensory Profile.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994485

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3994485

20 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-15-35

Mosaic SCN1A mutations in familial partial epilepsy with antecedent febrile seizures.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-15-35

Clinical spectrum of SCN2A mutations expanding to Ohtahara syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-15-35

Disruption of the SCN2A and SCN3A genes in a patient with mental retardation, neurobehavioral and psychiatric abnormalities, and a history of infantile seizures.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-15-35

Brief report: the Autism Mental Status Examination: development of a brief autism-focused exam.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-15-35

Comparison of Sensory Profile scores of young children with and without autism spectrum disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-15-35

Brief report: sensory abnormalities as distinguishing symptoms of autism spectrum disorders in young children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-15-35

Sensory processing in adults with autism spectrum disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-15-35

Describing the sensory abnormalities of children and adults with autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-15-35

Pilot study of the Sensory Over-Responsivity Scales: assessment and inventory

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-15-35

Sensory modulation and affective disorders in children and adolescents with Asperger's disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-15-35

SCN2A Mutations and Benign Familial Neonatal-Infantile Seizures: The Phenotypic Spectrum

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-15-35

An interstitial duplication at 2q24.3 involving the SCN1A, SCN2A, SCN3A genes associated with infantile epilepsy

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24650168

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2350-15-35

1 reference

7 September 2017

1 reference

7 September 2017

PubMed publication ID

24650168

1 reference