Works by Sham, Pak


Results: 326
    1

    Genetically deprived vitamin D exposure predisposes to atrial fibrillation.

    Published in:
    2017
    By:
    • Yap-Hang Chan;
    • Kai-Hang Yiu;
    • Jo Jo Hai;
    • Pak-Hei Chan;
    • Tai-Hing Lam;
    • Ben J. Cowling;
    • Pak-Chung Sham;
    • Chu-Pak Lau;
    • Karen Siu-Ling Lam;
    • Chung-Wah Siu;
    • Hung-Fat Tse;
    • Chan, Yap-Hang;
    • Yiu, Kai-Hang;
    • Hai, Jo Jo;
    • Chan, Pak-Hei;
    • Lam, Tai-Hing;
    • Cowling, Ben J;
    • Sham, Pak-Chung;
    • Lau, Chu-Pak;
    • Lam, Karen Siu-Ling
    Publication type:
    journal article
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    Population differences in the International Multi-Centre ADHD Gene Project.

    Published in:
    Genetic Epidemiology, 2008, v. 32, n. 2, p. 98, doi. 10.1002/gepi.20265
    By:
    • Neale, Benjamin M.;
    • Sham, Pak C.;
    • Purcell, Shaun;
    • Banaschewski, Tobias;
    • Buitelaar, Jan;
    • Franke, Barbara;
    • Sonuga-Barke, Edmund;
    • Ebstein, Richard;
    • Eisenberg, Jacques;
    • Mulligan, Aisling;
    • Gill, Michael;
    • Manor, Iris;
    • Miranda, Ana;
    • Mulas, Fernando;
    • Oades, Robert D.;
    • Roeyers, Herbert;
    • Rothenberger, Aribert;
    • Sergeant, Joseph;
    • Steinhausen, Hans-Christoph;
    • Taylor, Eric
    Publication type:
    Article
    16

    Erratum.

    Published in:
    Genetic Epidemiology, 2008, v. 32, n. 2, p. 186, doi. 10.1002/gepi.20293
    By:
    • Neale, Benjamin M.;
    • Sham, Pak C.;
    • Purcell, Shaun;
    • Banaschewski, Tobias;
    • Buitelaar, Jan;
    • Franke, Barbara;
    • Sonuga-Barke, Edmund;
    • Ebstein, Richard;
    • Eisenberg, Jacques;
    • Mulligan, Aisling;
    • Gill, Michael;
    • Manor, Iris;
    • Miranda, Ana;
    • Mulas, Fernando;
    • Oades, Robert D.;
    • Roeyers, Herbert;
    • Rothenberger, Aribert;
    • Sergeant, Joseph;
    • Steinhausen, Hans-Christoph;
    • Taylor, Eric
    Publication type:
    Article
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    Rare coding variants in MAPK7 predispose to adolescent idiopathic scoliosis.

    Published in:
    Human Mutation, 2017, v. 38, n. 11, p. 1500, doi. 10.1002/humu.23296
    By:
    • Gao, Wenjie;
    • Chen, Chong;
    • Zhou, Taifeng;
    • Yang, Shulan;
    • Gao, Bo;
    • Zhou, Hang;
    • Lian, Chengjie;
    • Wu, Zizhao;
    • Qiu, Xianjian;
    • Yang, Xiaoming;
    • Alattar, Esam;
    • Liu, Wentao;
    • Su, Deying;
    • Sun, Silong;
    • Chen, Yulan;
    • Cheung, Kenneth M. C.;
    • Song, Youqiang;
    • Luk, Keith K. D.;
    • Chan, Danny;
    • Sham, Pak Chung
    Publication type:
    Article
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    Predicting regulatory variants with composite statistic.

    Published in:
    Bioinformatics, 2016, v. 32, n. 18, p. 2729, doi. 10.1093/bioinformatics/btw288
    By:
    • Jiexing Wu;
    • Mulin Jun Li;
    • Liu, Jun S.;
    • Panwen Wang;
    • Feng Xu;
    • Zhicheng Pan;
    • Pak Chung Sham;
    • Miaoxin Li;
    • Zipeng Liu;
    • Yun Zhu;
    • Junwen Wang;
    • Zhengyuan Xia;
    • Kocher, Jean-Pierre A.
    Publication type:
    Article
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    Mapping of a Hirschsprung's disease locus in 3p21.

    Published in:
    European Journal of Human Genetics, 2008, v. 16, n. 7, p. 833, doi. 10.1038/ejhg.2008.18
    By:
    • Garcia-Barceló, Maria-Mercè;
    • Pui-yee Fong;
    • Tang, Clara S.;
    • Xiao-ping Miao;
    • Man-ting So;
    • Zhen-wei Yuan;
    • Li, Long;
    • Wei-hong Guo;
    • Lei Liu;
    • Bin Wang;
    • Xiao-bing Sun;
    • Liu-ming Huang;
    • Jin-fa Tou;
    • Kak-yuen Wong, Kenneth;
    • Elly Sau-wai Ngan;
    • Vincent Chi-hang Lui;
    • Cherny, Stacey S.;
    • Pak-chung Sham;
    • Paul Kwong-hang Tam
    Publication type:
    Article
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    The support of human genetic evidence for approved drug indications.

    Published in:
    Nature Genetics, 2015, v. 47, n. 8, p. 856, doi. 10.1038/ng.3314
    By:
    • Nelson, Matthew R;
    • Painter, Jeffery L;
    • Shen, Judong;
    • Tipney, Hannah;
    • Whittaker, John C;
    • Sanseau, Philippe;
    • Nicoletti, Paola;
    • Shen, Yufeng;
    • Floratos, Aris;
    • Sham, Pak Chung;
    • Li, Mulin Jun;
    • Wang, Junwen;
    • Cardon, Lon R
    Publication type:
    Article
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    A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25.

    Published in:
    Nature Genetics, 2010, v. 42, n. 10, p. 902, doi. 10.1038/ng.664
    By:
    • Hysi, Pirro G.;
    • Young, Terri L.;
    • Mackey, David A.;
    • Andrew, Toby;
    • Fernández-Medarde, Alberto;
    • Solouki, Abbas M.;
    • Hewitt, Alex W.;
    • Macgregor, Stuart;
    • Vingerling, Johannes R.;
    • Yi-Ju Li;
    • Ikram, M. Kamran;
    • Lee Yiu Fai;
    • Sham, Pak C.;
    • Manyes, Lara;
    • Porteros, Angel;
    • Lopes, Margarida C.;
    • Carbonaro, Francis;
    • Fahy, Samantha J.;
    • Martin, Nicholas G.;
    • van Duijn, Cornelia M.
    Publication type:
    Article
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