W-P Liao
Overview
Explore the profile of W-P Liao including associated specialties, affiliations and a list of published articles.
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Articles
5
Citations
108
Followers
0
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Recent Articles
1.
Zhou P, He N, Zhang J, Lin Z, Wang J, Yan L, et al.
Genes Brain Behav
. 2018 Jan;
17(8):e12456.
PMID: 29314583
Epileptic encephalopathies are severe epilepsy disorders with strong genetic bases. We performed targeted next-generation sequencing (NGS) in 70 patients with epileptic encephalopathies. The likely pathogenicity of variants in candidate genes...
2.
Chen Y, Shi Y, Xu H, Chen M, Gao M, Sun W, et al.
Mol Neurobiol
. 2014 Jul;
51(3):1263-70.
PMID: 24990319
Mutations in the sodium channel gene, SCN1A (NaV1.1), have been linked to a spectrum of epilepsy syndromes, and many of these mutations occur in the pore region of the channel....
3.
Tian H, Cao Y, Zhang X, Liao W, Yi Y, Lian J, et al.
Cell Death Dis
. 2013 May;
4:e617.
PMID: 23640459
Our previous studies have shown that microRNA-383 (miR-383) expression is downregulated in the testes of infertile men with maturation arrest (MA). Abnormal testicular miR-383 expression may potentiate the connections between...
4.
Liu X, Wu M, He N, Meng H, Wen L, Wang J, et al.
Genes Brain Behav
. 2012 Nov;
12(2):234-40.
PMID: 23190448
Paroxysmal dyskinesias (PDs) are a group of episodic movement disorders with marked variability in clinical manifestation and potential association with epilepsy. PRRT2 has been identified as a causative gene for...
5.
Shi Y, Yu M, Long Y, Qin B, He N, Meng H, et al.
Genes Brain Behav
. 2011 Dec;
11(2):170-6.
PMID: 22151702
SCN1A is the most relevant epilepsy gene. Mutations of SCN1A generate phenotypes ranging from the extremely severe form of Dravet syndrome (DS) to a mild form of generalized epilepsy with...