(Q37405551)

20 August 2017

GRIN2A mutations cause epilepsy-aphasia spectrum disorders (English)

1 reference

20 August 2017

0 references

18

1 reference

20 August 2017

Michael S. Hildebrand

19

1 reference

20 August 2017

Brigid M Regan

2

0 references

Brian J O'Roak

Brian J O'Roak

4

0 references

Ingrid Scheffer

Ingrid E Scheffer

21

0 references

Samuel Berkovic

Samuel F Berkovic

17

0 references

Lynette Sadleir

11

Lynette G Sadleir

1 reference

20 August 2017

22

Heather C Mefford

1 reference

20 August 2017

1

Gemma L Carvill

1 reference

20 August 2017

3

Simone C Yendle

1 reference

20 August 2017

8

Adiba Khan

1 reference

20 August 2017

10

Eileen Geraghty

1 reference

20 August 2017

Natalia Lozovaya

5

1 reference

20 August 2017

Nadine Bruneau

6

1 reference

20 August 2017

Nail Burnashev

7

1 reference

20 August 2017

Joseph Cook

9

1 reference

20 August 2017

Samantha J Turner

12

1 reference

20 August 2017

Meng-Han Tsai

13

1 reference

20 August 2017

Richard Webster

14

1 reference

20 August 2017

Robert Ouvrier

15

1 reference

20 August 2017

John A Damiano

16

1 reference

20 August 2017

Pierre Szepetowski

20

1 reference

20 August 2017

language of work or name

English

0 references

publication date

11 August 2013

1 reference

20 August 2017

1 reference

20 August 2017

45

1 reference

20 August 2017

9

1 reference

20 August 2017

1073-1076

1 reference

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.

20 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868952

Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868952

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868952

Specific sites within the ligand-binding domain and ion channel linkers modulate NMDA receptor gating

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868952

Glutamate receptor ion channels: structure, regulation, and function

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868952

Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868952

An autosomal dominant genetically heterogeneous variant of rolandic epilepsy and speech disorder

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868952

SRPX2 mutations in disorders of language cortex and cognition

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868952

Encephalopathy with electrical status epilepticus during slow sleep or ESES syndrome including the acquired aphasia

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868952

Speech and oromotor deficits of epileptic origin in benign partial epilepsy of childhood with rolandic spikes (BPERS). Relationship to the acquired aphasia-epilepsy syndrome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868952

Epileptic encephalopathies of the Landau-Kleffner and continuous spike and waves during slow-wave sleep types: genomic dissection makes the link with autism

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868952

Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868952

Clinical genetic study of the epilepsy-aphasia spectrum

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868952

Diagnostic exome sequencing in persons with severe intellectual disability

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868952

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

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868952

Familial epilepsy and developmental dysphasia: description of an Italian pedigree with autosomal dominant inheritance and screening of candidate loci.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868952

Clinical genetic studies in benign childhood epilepsy with centrotemporal spikes

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868952

Autosomal dominant rolandic epilepsy and speech dyspraxia: A new syndrome with anticipation

3 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868952

Somatic mutations in angiopoietin receptor gene TEK cause solitary and multiple sporadic venous malformations

3 December 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.2727

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NG.2727

1 reference

Dimensions Publication ID

20 August 2017

0 references

1 reference

20 August 2017

PubMed publication ID

23933818

1 reference