Works matching AU Wu-Chou, Yah-Huei

Results: 22

The LRRK2 Arg1628Pro variant is a risk factor for Parkinson’s disease in the Chinese population.

Published in:

Neurogenetics, 2008, v. 9, n. 4, p. 271, doi. 10.1007/s10048-008-0140-6

By:

Lu, Chin-Song;
Wu-Chou, Yah-Huei;
Doeselaar, Marina;
Simons, Erik;
Chang, Hsiu-Chen;
Breedveld, Guido;
Fonzo, Alessio;
Chen, Rou-Shayn;
Weng, Yi-Hsin;
Lai, Szu-Chia;
Oostra, Ben;
Bonifati, Vincenzo

Publication type:

Article

Examining Markers in 8q24 to Explain Differences in Evidence for Association With Cleft Lip With/Without Cleft Palate Between Asians and Europeans.

Published in:

Genetic Epidemiology, 2012, v. 36, n. 4, p. 392, doi. 10.1002/gepi.21633

By:

Murray, Tanda;
Taub, Margaret A.;
Ruczinski, Ingo;
Scott, Alan F.;
Hetmanski, Jacqueline B.;
Schwender, Holger;
Patel, Poorav;
Zhang, Tian Xiao;
Munger, Ronald G.;
Wilcox, Allen J.;
Ye, Xiaoqian;
Wang, Hong;
Wu, Tao;
Wu-Chou, Yah Huei;
Shi, Bing;
Jee, Sun Ha;
Chong, Samuel;
Yeow, Vincent;
Murray, Jeffrey C.;
Marazita, Mary L.

Publication type:

Article

Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 6, p. 469, doi. 10.1002/gepi.20595

By:

Beaty, Terri H.;
Ruczinski, Ingo;
Murray, Jeffrey C.;
Marazita, Mary L.;
Munger, Ronald G.;
Hetmanski, Jacqueline B.;
Murray, Tanda;
Redett, Richard J.;
Fallin, M. Daniele;
Liang, Kung Yee;
Wu, Tao;
Patel, Poorav J.;
Jin, Sheng-Chih;
Zhang, Tian Xiao;
Schwender, Holger;
Wu-Chou, Yah Huei;
Chen, Philip K.;
Chong, Samuel S.;
Cheah, Felicia;
Yeow, Vincent

Publication type:

Article

Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations.

Published in:

Genetic Epidemiology, 2008, v. 32, n. 6, p. 505, doi. 10.1002/gepi.20323

By:

Sull, Jae Woong;
Liang, Kung-Yee;
Hetmanski, Jacqueline B.;
Fallin, Margaret Daniele;
Ingersoll, Roxann G.;
Park, Jiwan;
Wu-Chou, Yah-Huei;
Chen, Philip K.;
Chong, Samuel S.;
Cheah, Felicia;
Yeow, Vincent;
Park, Beyoung Yun;
Jee, Sun Ha;
Jabs, Ethylin Wang;
Redett, Richard;
Jung, Euiju;
Ruczinski, Ingo;
Scott, Alan F.;
Beaty, Terri H.

Publication type:

Article

Paroxysmal exercise-induced dystonia within the phenotypic spectrum of ECHS1 deficiency.

Published in:

2016

By:

Olgiati, Simone;
Skorvanek, Matej;
Quadri, Marialuisa;
Minneboo, Michelle;
Graafland, Josja;
Breedveld, Guido J.;
Bonte, Ramon;
Ozgur, Zeliha;
Hout, Mirjam C.G.N.;
Schoonderwoerd, Kees;
Verheijen, Frans W.;
IJcken, Wilfred F.J.;
Chien, Hsin Fen;
Barbosa, Egberto Reis;
Chang, Hsiu‐Chen;
Lai, Szu‐Chia;
Yeh, Tu‐Hsueh;
Lu, Chin‐Song;
Wu‐Chou, Yah‐Huei;
Kievit, Anneke J.A.

Publication type:

journal article

Neuronal intranuclear inclusion disease: Two cases of dopa-responsive juvenile parkinsonism with drug-induced dyskinesia.

Published in:

Movement Disorders, 2010, v. 25, n. 9, p. 1274, doi. 10.1002/mds.22876

By:

Lai, Szu-Chia;
Jung, Shih-Ming;
Grattan-Smith, Padraic;
Sugo, Ella;
Lin, Yen-Wen;
Chen, Rou-Shayn;
Chen, Chiung-Chu;
Wu-Chou, Yah-Huei;
Lang, Anthony E.;
Lu, Chin-Song

Publication type:

Article

Dopa-responsive parkinsonism phenotype of spinocerebellar ataxia type 2.

Published in:

Movement Disorders, 2002, v. 17, n. 5, p. 1046, doi. 10.1002/mds.10243

By:

Lu, Chin-Song;
Wu Chou, Yah-Huei;
Yen, Tzu-Chen;
Tsai, Chon-Haw;
Chen, Rou-Shayn;
Chang, Hsiu-Chen

Publication type:

Article

X-linked markers in the Duchenne muscular dystrophy gene associated with oral clefts.

Published in:

European Journal of Oral Sciences, 2013, v. 121, n. 2, p. 63, doi. 10.1111/eos.12025

By:

Patel, Poorav J.;
Beaty, Terri H.;
Ruczinski, Ingo;
Murray, Jeffrey C.;
Marazita, Mary L.;
Munger, Ronald G.;
Hetmanski, Jacqueline B.;
Wu, Tao;
Murray, Tanda;
Rose, Margaret;
Redett, Richard J.;
Jin, Sheng C.;
Lie, Rolv T.;
Wu ‐ Chou, Yah ‐ Huei;
Wang, Hong;
Ye, Xiaoqian;
Yeow, Vincent;
Chong, Samuel;
Jee, Sun H.;
Shi, Bing

Publication type:

Article

Evidence of Gene−Environment Interaction for Two Genes on Chromosome 4 and Environmental Tobacco Smoke in Controlling the Risk of Nonsyndromic Cleft Palate.

Published in:

PLoS ONE, 2014, v. 9, n. 2, p. 1, doi. 10.1371/journal.pone.0088088

By:

Wu, Tao;
Schwender, Holger;
Ruczinski, Ingo;
Murray, Jeffrey C.;
Marazita, Mary L.;
Munger, Ronald G.;
Hetmanski, Jacqueline B.;
Parker, Margaret M.;
Wang, Ping;
Murray, Tanda;
Taub, Margaret;
Li, Shuai;
Redett, Richard J.;
Fallin, M. Daniele;
Liang, Kung Yee;
Wu-Chou, Yah Huei;
Chong, Samuel S.;
Yeow, Vincent;
Ye, Xiaoqian;
Wang, Hong

Publication type:

Article

Neurofibromatosis 2 with peripheral neuropathies: Electrophysiological, pathological and genetic studies of a Taiwanese family.

Published in:

Neuropathology, 2010, v. 30, n. 5, p. 515, doi. 10.1111/j.1440-1789.2009.01099.x

By:

Kuo, Hung-Chou;
Chen, Shyue-Ru;
Jung, Shih-Ming;
Wu Chou, Yah-Huei;
Huang, Chin-Chang;
Chuang, Wen-Li;
Wei, Kuo-Chen;
Ro, Long-Sun

Publication type:

Article

Novel PKD1 and PKD2 mutations in Taiwanese patients with autosomal dominant polycystic kidney disease.

Published in:

Journal of Human Genetics, 2013, v. 58, n. 11, p. 720, doi. 10.1038/jhg.2013.91

By:

Chang, Ming-Yang;
Chen, Hsiao-Mang;
Jenq, Chang-Chyi;
Lee, Shen-Yang;
Chen, Yu-Ming;
Tian, Ya-Chung;
Chen, Yung-Chang;
Hung, Cheng-Chieh;
Fang, Ji-Tseng;
Yang, Chih-Wei;
Wu-Chou, Yah-Huei

Publication type:

Article

The SNP rs560426 Within ABCA4-ARHGAP29 Locus and the Risk of Nonsyndromic Oral Clefts.

Published in:

Cleft Palate Craniofacial Journal, 2020, v. 57, n. 6, p. 671, doi. 10.1177/1055665619899764

By:

Wu-Chou, Yah-Huei;
Chen, Kuo-Ting Philip;
Lu, Yi-Chieh;
Lin, Yin-Ting;
Chang, Hsien-Fang;
Lo, Lun-Jou

Publication type:

Article

Association Studies Between Regulatory Regions of IRF6 / TP63 Genes and Nonsyndromic Oral Clefts.

Published in:

Cleft Palate Craniofacial Journal, 2019, v. 56, n. 6, p. 778, doi. 10.1177/1055665618809244

By:

Wu-Chou, Yah-Huei;
Lu, Yi-Chieh;
Chen, Kuo-Ting Philip;
Chang, Hsien-Fang;
Lin, Yin-Ting;
Lo, Lun-Jou

Publication type:

Article

The FGF and FGFR Gene Family and Risk of Cleft Lip With or Without Cleft Palate.

Published in:

Cleft Palate Craniofacial Journal, 2013, v. 50, n. 1, p. 96, doi. 10.1597/11-132

By:

Hong Wang;
Tianxiao Zhang;
Tao Wu;
Hetmanski, Jacqueline B.;
Ruczinski, Ingo;
Schwender, Holger;
Kung Vee Liang;
Murray, Tanda;
Fallin, M. Daniele;
Redett, Richard J.;
Raymond, Gerald V.;
Sheng-Chih Jin;
Wu Chou, Yah-Huei;
Chen, Philip Kuo-Ting;
Yeow, Vincent;
Chong, Samuel S.;
Cheah, Felicia S. H.;
Sun Ha Jee;
Jabs, Ethylin W.;
Scott, Alan F.

Publication type:

Article

Gene-gene interaction of single nucleotide polymorphisms in 16p13.3 may contribute to the risk of non-syndromic cleft lip with or without cleft palate in Chinese case-parent trios.

Published in:

American Journal of Medical Genetics. Part A, 2017, v. 173, n. 6, p. 1489, doi. 10.1002/ajmg.a.38190

By:

Liu, Dongjing;
Wang, Hong;
Schwender, Holger;
Marazita, Mary L.;
Wang, Zhuqing;
Yuan, Yuan;
Wang, Ping;
Liang, Kung Yee;
Wu‐Chou, Yah Huei;
Wang, Mengying;
Shi, Bing;
Zhu, Hongping;
Wu, Tao;
Beaty, Terri H.

Publication type:

Article

Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts.

Published in:

American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 4, p. 784, doi. 10.1002/ajmg.a.35257

By:

Shi, Min;
Murray, Jeffrey C.;
Marazita, Mary L.;
Munger, Ronald G.;
Ruczinski, Ingo;
Hetmanski, Jacqueline B.;
Wu, Tao;
Murray, Tanda;
Redett, Richard J.;
Wilcox, Allen J.;
Lie, Rolv T.;
Jabs, Ethylin Wang;
Wu-Chou, Yah Huei;
Chen, Philip K.;
Wang, Hong;
Ye, Xiaoqian;
Yeow, Vincent;
Chong, Samuel S.;
Shi, Bing;
Christensen, Kaare

Publication type:

Article

EIF2AK2 Missense Variants Associated with Early Onset Generalized Dystonia.

Published in:

Annals of Neurology, 2021, v. 89, n. 3, p. 485, doi. 10.1002/ana.25973

By:

Kuipers, Demy J. S.;
Mandemakers, Wim;
Lu, Chin‐Song;
Olgiati, Simone;
Breedveld, Guido J.;
Fevga, Christina;
Tadic, Vera;
Carecchio, Miryam;
Osterman, Bradley;
Sagi‐Dain, Lena;
Wu‐Chou, Yah‐Huei;
Chen, Chiung C.;
Chang, Hsiu‐Chen;
Wu, Shey‐Lin;
Yeh, Tu‐Hsueh;
Weng, Yi‐Hsin;
Elia, Antonio E.;
Panteghini, Celeste;
Marotta, Nicolas;
Pauly, Martje G.

Publication type:

Article

Association ssudy between candidate genes on transforming growth factor-β signaling pathway and the risk: of non-syndromic cleft lip with or without cleft palate in Chinese populations.

Published in:

Journal of Health Sciences of Peking University / Beijing Daxue Xuebao (Yixue Ban), 2015, v. 47, n. 3, p. 384, doi. 10.3969/j.issn.1671-167X.2015.03.004

By:

WANG Zhu-qing;
WANG Ping;
WU-CHOU Yah-huei;
YE Xiao-qian;
HUANG Shang-zhi;
SHI Bing;
WANG Ke;
YUAN Yuan;
LIU Dong-jing;
WU Tao;
WANG Hong;
BEATY, Terri H.

Publication type:

Article

Association study for gene polymorphism of folic acid/homocysteine metabolic pathway and nonsyndromic cleft lip with or without cleft palate in Chinese populations.

Published in:

Journal of Health Sciences of Peking University / Beijing Daxue Xuebao (Yixue Ban), 2013, v. 45, n. 3, p. 352, doi. 10.3969/j.issn.1671-167X.2013.03.004

By:

WANG Ping;
WANG Hong;
WU-CHOU Yah-huei;
YE Xiao-qian;
HUANG Shang-zhi;
SHI Bing;
LIANG Kung-yee;
CAO Wei-hua;
WU Tao;
BEATY, Terri H.

Publication type:

Article

Fetal polymorphisms at the ABCB1-transporter gene locus are associated with susceptibility to non-syndromic oral cleft malformations.

Published in:

European Journal of Human Genetics, 2013, v. 21, n. 12, p. 1436, doi. 10.1038/ejhg.2013.25

By:

Omoumi, Ardeshir;
Wang, Zihua;
Yeow, Vincent;
Wu-Chou, Yah-Huei;
Chen, Philip K;
Ruczinski, Ingo;
Cheng, Joanne;
Cheah, Felicia S H;
Lee, Caroline G;
Beaty, Terri H;
Chong, Samuel S

Publication type:

Article

Genetic diagnosis of neurofibromatosis type 1: targeted next- generation sequencing with Multiple Ligation-Dependent Probe Amplification analysis.

Published in:

Journal of Biomedical Science, 2018, v. 25, n. 1, p. N.PAG, doi. 10.1186/s12929-018-0474-9

By:

Wu-Chou, Yah-Huei;
Hung, Tzu-Chao;
Lin, Yin-Ting;
Cheng, Hsing-Wen;
Lin, Ju-Li;
Lin, Chih-Hung;
Yu, Chung-Chih;
Chen, Kuo-Ting;
Yeh, Tu-Hsueh;
Chen, Yu-Ray

Publication type:

Article

A combined targeted mutation analysis of IRF6 gene would be useful in the first screening of oral facial clefts.

Published in:

BMC Medical Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2350-14-37

By:

Wu-Chou, Yah-Huei;
Lo, Lun-Jou;
Philip Chen, Kuo-Ting;
Frank Chang, Chun-Shin;
Chen, Yu-Ray

Publication type:

Article