Gene-wide tagging study of the association between KCNT1 polymorphisms and the susceptibility and efficacy of genetic generalized epilepsy in Chinese population. (Q35054372)

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English	Gene-wide tagging study of the association between KCNT1 polymorphisms and the susceptibility and efficacy of genetic generalized epilepsy in Chinese population.	scientific article

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scholarly article

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1 March 2020

Gene-wide tagging study of the association between KCNT1 polymorphisms and the susceptibility and efficacy of genetic generalized epilepsy in Chinese population (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24279416%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

generalized epilepsy

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based on heuristic

inferred from title

6

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1 March 2020

17

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1 March 2020

author name string

Jian Qu

1

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1 March 2020

Ying Zhang

2

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1 March 2020

Zhi-Quan Yang

3

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1 March 2020

Xiao-Yuan Mao

4

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1 March 2020

Bo-Ting Zhou

5

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1 March 2020

Hui He

7

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1 March 2020

Xiang-Ping Li

8

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1 March 2020

Hong-Yu Long

9

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1 March 2020

Nan Lv

10

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1 March 2020

Xiao-Jing Xu

11

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1 March 2020

Bo Xiao

12

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1 March 2020

Yu Zhang

13

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1 March 2020

Qiang Tang

14

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1 March 2020

Dong-Li Hu

15

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1 March 2020

Hong-Hao Zhou

16

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1 March 2020

publication date

27 November 2013

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1 March 2020

CNS Neuroscience & Therapeutics

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1 March 2020

20

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1 March 2020

2

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1 March 2020

140-146

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1 March 2020

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

1 reference

https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

Genetic mechanisms in idiopathic epilepsies

1 reference

https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

Epidemiology of idiopathic generalized epilepsies

1 reference

https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy

1 reference

https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

The clinical impact of pharmacogenetics on the treatment of epilepsy

1 reference

https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

For K+ channels, Na+ is the new Ca2+.

1 reference

https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.

1 reference

https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy

1 reference

https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

Blinders, phenotype, and fashionable genetic analysis: a critical examination of the current state of epilepsy genetic studies

1 reference

https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

A partition-ligation-combination-subdivision EM algorithm for haplotype inference with multiallelic markers: update of the SHEsis (http://analysis.bio-x.cn).

1 reference

https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

Mechanisms of human inherited epilepsies

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https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

Genetics of idiopathic generalized epilepsies

1 reference

https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

Exploration of the genetic architecture of idiopathic generalized epilepsies.

1 reference

https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study

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https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study

1 reference

https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

The Epilepsy Genetic Association Database (epiGAD): analysis of 165 genetic association studies, 1996-2008.

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https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

Epilepsy genetics—past, present, and future

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https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

KCNT1 mutations in ADNFLE and MMPSI: a new driver in the etiology and pathophysiology of early-onset epileptic syndromes.

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https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

ABCC2 polymorphisms and haplotype are associated with drug resistance in Chinese epileptic patients

1 reference

https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

Association of ABCB1 Gene Polymorphisms and Their Haplotypes with Response to Antiepileptic Drugs: a Systematic Review and Meta-Analysis

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https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

Association between SCN1A polymorphism and carbamazepine-resistant epilepsy

1 reference

https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

Non-response to antiepileptic pharmacotherapy is associated with the ABCC2 -24C>T polymorphism in young and adult patients with epilepsy.

1 reference

https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

Amino-termini isoforms of the Slack K+ channel, regulated by alternative promoters, differentially modulate rhythmic firing and adaptation

1 reference

https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy

1 reference

https://api.crossref.org/works/10.1111%2FCNS.12169

21 January 2018

SHEsis, a powerful software platform for analyses of linkage disequilibrium, haplotype construction, and genetic association at polymorphism loci

1 reference

https://pubmed.ncbi.nlm.nih.gov/24279416

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene-wide tagging study of the association betweenABCC2,ABCC5andABCG2genetic polymorphisms and multidrug resistance in epilepsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/24279416

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epilepsy as a spectrum disorder: Implications from novel clinical and basic neuroscience

1 reference

https://pubmed.ncbi.nlm.nih.gov/24279416

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1111/CNS.12169

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Europe PubMed Central

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1 March 2020

PMC publication ID

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1 March 2020

PubMed publication ID

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Europe PubMed Central

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1 March 2020

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