Works by Fengxiang WANG

Results: 48
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    Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic Analysis.

    Published in:
    Arthritis & Rheumatology, 2022, v. 74, n. 8, p. 1420, doi. 10.1002/art.42129
    By:
    • Li, Jin;
    • Li, Yun R.;
    • Glessner, Joseph T.;
    • Yang, Jie;
    • March, Michael E.;
    • Kao, Charlly;
    • Vaccaro, Courtney N.;
    • Bradfield, Jonathan P.;
    • Li, Junyi;
    • Mentch, Frank D.;
    • Qu, Hui‐Qi;
    • Qi, Xiaohui;
    • Chang, Xiao;
    • Hou, Cuiping;
    • Abrams, Debra J.;
    • Qiu, Haijun;
    • Wei, Zhi;
    • Connolly, John J.;
    • Wang, Fengxiang;
    • Snyder, James
    Publication type:
    Article
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    Advantage of Whole Exome Sequencing over Allele-Specific and Targeted Segment Sequencing in Detection of Novel TULP1 Mutation in Leber Congenital Amaurosis.

    Published in:
    Ophthalmic Genetics, 2015, v. 36, n. 4, p. 333, doi. 10.3109/13816810.2014.886269
    By:
    • Guo, Yiran;
    • Prokudin, Ivan;
    • Yu, Cong;
    • Liang, Jinlong;
    • Xie, Yi;
    • Flaherty, Maree;
    • Tian, Lifeng;
    • Crofts, Stephanie;
    • Wang, Fengxiang;
    • Snyder, James;
    • Donaldson, Craig;
    • Abdel-Magid, Nada;
    • Vazquez, Lyam;
    • Keating, Brendan;
    • Hakonarson, Hakon;
    • Wang, Jun;
    • Jamieson, Robyn V.
    Publication type:
    Article
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    Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population.

    Published in:
    Molecular Autism, 2014, v. 5, n. 1, p. 3, doi. 10.1186/2040-2392-5-5
    By:
    • Matsunami, Nori;
    • Hensel, Charles H.;
    • Baird, Lisa;
    • Stevens, Jeff;
    • Otterud, Brith;
    • Leppert, Tami;
    • Varvil, Tena;
    • Hadley, Dexter;
    • Glessner, Joseph T.;
    • Pellegrino, Renata;
    • Kim, Cecilia;
    • Thomas, Kelly;
    • Wang, Fengxiang;
    • Otieno, Frederick G.;
    • Ho, Karen;
    • Christensen, Gerald B.;
    • Dongying Li;
    • Prekeris, Rytis;
    • Lambert, Christophe G.;
    • Hakonarson, Hakon
    Publication type:
    Article
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    Copy Number Variations in Alternative Splicing Gene Networks Impact Lifespan.

    Published in:
    PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0053846
    By:
    • Glessner, Joseph T.;
    • Smith, Albert Vernon;
    • Panossian, Saarene;
    • Kim, Cecilia E.;
    • Takahashi, Nagahide;
    • Thomas, Kelly A.;
    • Fengxiang Wang;
    • Seidler, Kallyn;
    • Harris, Tamara B.;
    • Launer, Lenore J.;
    • Keating, Brendan;
    • Connolly, John;
    • Sleiman, Patrick M. A.;
    • Buxbaum, Joseph D.;
    • Grant, Struan F. A.;
    • Gudnason, Vilmundur;
    • Hakonarson, Hakon
    Publication type:
    Article
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    Sensorless model-based PCC for induction machine.

    Published in:
    IET Electric Power Applications (Wiley-Blackwell), 2017, v. 11, n. 5, p. 885, doi. 10.1049/iet-epa.2016.0220
    By:
    • Fengxiang Wang;
    • Zhenbin Zhang;
    • Junxiao Wang;
    • José Rodríguez
    Publication type:
    Article
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    Sensorless model‐based PCC for induction machine.

    Published in:
    IET Electric Power Applications (Wiley-Blackwell), 2017, v. 11, n. 5, p. 885, doi. 10.1049/iet-epa.2016.0220
    By:
    • Wang, Fengxiang;
    • Zhang, Zhenbin;
    • Wang, Junxiao;
    • Rodríguez, José
    Publication type:
    Article
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    An atypical form of AOA2 with myoclonus associated with mutations in SETX and AFG3L2.

    Published in:
    BMC Medical Genetics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12881-015-0159-0
    By:
    • Cecilia Mancini;
    • Laura Orsi;
    • Yiran Guo;
    • Jiankang Li;
    • Yulan Chen;
    • Fengxiang Wang;
    • Lifeng Tian;
    • Xuanzhu Liu;
    • Jianguo Zhang;
    • Hui Jiang;
    • Bruce Shike Nmezi;
    • Takashi Tatsuta;
    • Giorgio, Elisa;
    • Di Gregorio, Eleonora;
    • Cavalieri, Simona;
    • Pozzi, Elisa;
    • Mortara, Paolo;
    • Caglio, Maria Marcella;
    • Balducci, Alessandro;
    • Pinessi, Lorenzo
    Publication type:
    Article