Yah-Huei Wu-Chou
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Explore the profile of Yah-Huei Wu-Chou including associated specialties, affiliations and a list of published articles.
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Recent Articles
1.
Wu-Chou Y, Hsieh C, Liao C, Lin Y, Fan W, Yang C
Pathol Res Pract
. 2021 May;
223:153474.
PMID: 33993060
Oral squamous cell carcinoma (OSCC) is the most common malignancy of the oral cavity with poor prognosis. The dysregulation of Notch signaling pathway has been implicated in the OSCC tumorigenesis....
2.
Kuipers D, Mandemakers W, Lu C, Olgiati S, Breedveld G, Fevga C, et al.
Ann Neurol
. 2020 Nov;
89(3):485-497.
PMID: 33236446
Objective: The study was undertaken to identify a monogenic cause of early onset, generalized dystonia. Methods: Methods consisted of genome-wide linkage analysis, exome and Sanger sequencing, clinical neurological examination, brain...
3.
Wu-Chou Y, Chen K, Lu Y, Lin Y, Chang H, Lo L
Cleft Palate Craniofac J
. 2020 Jan;
57(6):671-677.
PMID: 31950859
Objective: Nonsyndromic oral clefts are common birth defect with complex etiology. In the present study, we attempt to further validate the possible role for ABCA4 and ARHGAP29 in the susceptibility...
4.
Yeh J, Liu W, Wang C, Lu J, Chen C, Wu-Chou Y, et al.
Acta Cardiol Sin
. 2019 Dec;
35(6):571-584.
PMID: 31879508
Background: Approximately one-third of cases of dilated cardiomyopathy (DCM) are caused by genetic mutations. With new sequencing technologies, numerous variants have been associated with this inherited cardiomyopathy, however the prevalence...
5.
Wu-Chou Y, Lu Y, Chen K, Chang H, Lin Y, Lo L
Cleft Palate Craniofac J
. 2018 Nov;
56(6):778-785.
PMID: 30419764
Objective: To evaluate genetic variants within the regulatory regions of interferon regulatory factor 6 () and for the etiology of nonsyndromic oral clefts risk factors. Design: We performed allelic transmission...
6.
Wu-Chou Y, Hung T, Lin Y, Cheng H, Lin J, Lin C, et al.
J Biomed Sci
. 2018 Oct;
25(1):72.
PMID: 30290804
Background: Neurofibromatosis type 1 (NF1) is a dominantly inherited tumor predisposition syndrome that targets the peripheral nervous system. It is caused by mutations of the NF1 gene which serve as...
7.
Quadri M, Mandemakers W, Grochowska M, Masius R, Geut H, Fabrizio E, et al.
Lancet Neurol
. 2018 Jun;
17(7):597-608.
PMID: 29887161
Background: Most patients with Parkinson's disease, Parkinson's disease dementia, and dementia with Lewy bodies do not carry mutations in known disease-causing genes. The aim of this study was to identify...
8.
Hu C, Hu C, Wu-Chou Y, Lo L
J Craniofac Surg
. 2018 May;
29(6):1601-1603.
PMID: 29750726
Background: Primary systemic carnitine deficiency (SCD) is an autosomal-recessive disorder caused by SLC22A5 gene mutation resulting in defective cellular carnitine transporter organic cation transporter 2. Defective carnitine transporter causes renal...
9.
Yu K, Chang P, Chang S, Wu-Chou Y, Wu L, Chen D, et al.
Sci Rep
. 2017 Sep;
7(1):9988.
PMID: 28855613
The objective of the present study was to determine whether there was an association between single nucleotide polymorphisms (SNPs) in ABCG2 and gout. We recruited 333 participants including 210 patients...
10.
Peng H, Chang N, Chen K, Lu J, Chang P, Chang S, et al.
BMC Med Genet
. 2016 Aug;
17(1):59.
PMID: 27527345
Background: Nonsyndromic orofacial cleft is a common birth defect with a complex etiology, including multiple genetic and environmental risk factors. Recent whole genome analyses suggested associations between nonsyndromic orofacial cleft...