Works by Zuberi, Aamir


Results: 20
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    Gain-of-function mutations of TRPV4 acting in endothelial cells drive blood-CNS barrier breakdown and motor neuron degeneration in mice.

    Published in:
    Science Translational Medicine, 2024, v. 16, n. 748, p. 1, doi. 10.1126/scitranslmed.adk1358
    By:
    • Sullivan, Jeremy M.;
    • Bagnell, Anna M.;
    • Alevy, Jonathan;
    • Avila, Elvia Mena;
    • Mihaljević, Ljubica;
    • Saavedra-Rivera, Pamela C.;
    • Kong, Lingling;
    • Huh, Jennifer S.;
    • McCray, Brett A.;
    • Aisenberg, William H.;
    • Zuberi, Aamir R.;
    • Bogdanik, Laurent;
    • Lutz, Cathleen M.;
    • Qiu, Zhaozhu;
    • Quinlan, Katharina A.;
    • Searson, Peter C.;
    • Sumner, Charlotte J.
    Publication type:
    Article
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    The Human Obesity Gene Map: The 2005 Update.

    Published in:
    Obesity (19307381), 2006, v. 14, n. 4, p. 529, doi. 10.1038/oby.2006.71
    By:
    • Rankinen, Tuomo;
    • Zuberi, Aamir;
    • Chagnon, Yvon C.;
    • Weisnagel, S. John;
    • Argyropoulos, George;
    • Walts, Brandon;
    • Pérusse, Louis;
    • Bouchard, Claude
    Publication type:
    Article
    8

    The Human Obesity Gene Map: The 2004 Update.

    Published in:
    Obesity (19307381), 2005, v. 13, n. 3, p. 381, doi. 10.1038/oby.2005.50
    By:
    • Pérusse, Louis;
    • Rankinen, Tuomo;
    • Zuberi, Aamir;
    • Chagnon, Yvon C.;
    • Weisnagel, S. John;
    • Argyropoulos, George;
    • Walts, Brandon;
    • Snyder, Eric E.;
    • Bouchard, Claude
    Publication type:
    Article
    9

    Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy.

    Published in:
    eLife, 2025, p. 1, doi. 10.7554/eLife.91204
    By:
    • Abreo, Timothy J.;
    • Thompson, Emma C.;
    • Madabushi, Anuraag;
    • Park, Kristen L.;
    • Heun Soh;
    • Varghese, Nissi;
    • Vanoye, Carlos G.;
    • Springer, Kristen;
    • Johnson, Jim;
    • Sims, Scotty;
    • Zhigang Ji;
    • Chavez, Ana G.;
    • Jankovic, Miranda J.;
    • Habte, Bereket;
    • Zuberi, Aamir R.;
    • Lutz, Cathleen M.;
    • Zhao Wang;
    • Krishnan, Vaishnav;
    • Dudler, Lisa;
    • Einsele-Scholz, Stephanie
    Publication type:
    Article
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    A Drosophila screen identifies NKCC1 as a modifier of NGLY1 deficiency.

    Published in:
    eLife, 2020, p. 1, doi. 10.7554/eLife.57831
    By:
    • Talsness, Dana M.;
    • Owings, Katie G.;
    • Coelho, Emily;
    • Mercenne, Gaelle;
    • Pleinis, John M.;
    • Partha, Raghavendran;
    • Hope, Kevin A.;
    • Zuberi, Aamir R.;
    • Clark, Nathan L.;
    • Lutz, Cathleen M.;
    • Rodan, Aylin R.;
    • Chow, Clement Y.
    Publication type:
    Article
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    Dominant mutations of the Notch ligand Jagged1 cause peripheral neuropathy.

    Published in:
    2020
    By:
    • Sullivan, Jeremy M.;
    • Motley, William W.;
    • Johnson, Janel O.;
    • Aisenberg, William H.;
    • Marshall, Katherine L.;
    • Barwick, Katy E. S.;
    • Lingling Kong;
    • Huh, Jennifer S.;
    • Saavedra-Rivera, Pamela C.;
    • McEntagart, Meriel M.;
    • Marion, Marie-Helene;
    • Hicklin, Lucy A.;
    • Modarres, Hamid;
    • Baple, Emma L.;
    • Farah, Mohamed H.;
    • Zuberi, Aamir R.;
    • Lutz, Cathleen M.;
    • Gaudet, Rachelle;
    • Traynor, Bryan J.;
    • Crosby, Andrew H.
    Publication type:
    journal article