Works by Sanghun Lee

Results: 183
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    A PKCη missense mutation enhances Golgi-localized signaling and is associated with recessively inherited familial Alzheimer's disease.

    Published in:
    Science Signaling, 2025, v. 18, n. 893, p. 1, doi. 10.1126/scisignal.adv0970
    By:
    • Gauron, Maria Celeste;
    • Prokopenko, Dmitry;
    • Lee, Sanghun;
    • Wolfe, Sarah A.;
    • Hecker, Julian;
    • Willett, Julian;
    • Waqas, Mohammad;
    • Lordén, Gema;
    • Yang, Yimin;
    • Mayfield, Joshua E.;
    • Castanho, Isabel;
    • Mullin, Kristina;
    • Morgan, Sarah;
    • Hahn, Georg;
    • Demeo, Dawn L.;
    • Hide, Winston;
    • Bertram, Lars;
    • Lange, Christoph;
    • Newton, Alexandra C.;
    • Tanzi, Rudolph E.
    Publication type:
    Article
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    Genome‐wide association analysis of COVID‐19 mortality risk in SARS‐CoV‐2 genomes identifies mutation in the SARS‐CoV‐2 spike protein that colocalizes with P.1 of the Brazilian strain.

    Published in:
    Genetic Epidemiology, 2021, v. 45, n. 7, p. 685, doi. 10.1002/gepi.22421
    By:
    • Hahn, Georg;
    • Wu, Chloe M.;
    • Lee, Sanghun;
    • Lutz, Sharon M.;
    • Khurana, Surender;
    • Baden, Lindsey R.;
    • Haneuse, Sebastien;
    • Qiao, Dandi;
    • Hecker, Julian;
    • DeMeo, Dawn L.;
    • Tanzi, Rudolph E.;
    • Choudhary, Manish C.;
    • Etemad, Behzad;
    • Mohammadi, Abbas;
    • Esmaeilzadeh, Elmira;
    • Cho, Michael H.;
    • Li, Jonathan Z.;
    • Randolph, Adrienne G.;
    • Laird, Nan M.;
    • Weiss, Scott T.
    Publication type:
    Article
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    Light Weight and Flexible High-Performance Diagnostic Platform.

    Published in:
    Advanced Healthcare Materials, 2015, v. 4, n. 10, p. 1517, doi. 10.1002/adhm.201500128
    By:
    • Karnaushenko, Daniil;
    • Ibarlucea, Bergoi;
    • Lee, Sanghun;
    • Lin, Gungun;
    • Baraban, Larysa;
    • Pregl, Sebastian;
    • Melzer, Michael;
    • Makarov, Denys;
    • Weber, Walter M.;
    • Mikolajick, Thomas;
    • Schmidt, Oliver G.;
    • Cuniberti, Gianaurelio
    Publication type:
    Article
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    FGF20 and PGM2 variants are associated with childhood asthma in family-based whole-genome sequencing studies.

    Published in:
    Human Molecular Genetics, 2023, v. 32, n. 4, p. 696, doi. 10.1093/hmg/ddac258
    By:
    • Hecker, Julian;
    • Chun, Sung;
    • Samiei, Ahmad;
    • Liu, Cuining;
    • Laurie, Cecelia;
    • Kachroo, Priyadarshini;
    • Lutz, Sharon M;
    • Lee, Sanghun;
    • Smith, Albert V;
    • Lasky-Su, Jessica;
    • Cho, Michael H;
    • Sharma, Sunita;
    • Quirós, Manuel Enrique Soto;
    • Avila, Lydiana;
    • Celedón, Juan C;
    • Raby, Benjamin;
    • Zhou, Xiaobo;
    • Silverman, Edwin K;
    • DeMeo, Dawn L;
    • Consortium, NHLBI Trans-Omics for Precision Medicine (TOPMed)
    Publication type:
    Article
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