Found: 2

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  • Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15 q11.2, Specifically Breakpoints 1 to 2.

    Published in:
    Autism Research: Official Journal of the International Society for Autism Research, 2014, v. 7, n. 3, p. 355, doi. 10.1002/aur.1378
    By:
    • Chaste, Pauline;
    • Sanders, Stephan J.;
    • Mohan, Kommu N.;
    • Klei, Lambertus;
    • Song, Youeun;
    • Murtha, Michael T.;
    • Hus, Vanessa;
    • Lowe, Jennifer K.;
    • Willsey, A. Jeremy;
    • Moreno‐De‐Luca, Daniel;
    • Yu, Timothy W.;
    • Fombonne, Eric;
    • Geschwind, Daniel;
    • Grice, Dorothy E.;
    • Ledbetter, David H.;
    • Lord, Catherine;
    • Mane, Shrikant M.;
    • Martin, Donna M.;
    • Morrow, Eric M.;
    • Walsh, Christopher A.
    Publication type:
    Article

  • De novo mutations revealed by whole-exome sequencing are strongly associated with autism.

    Published in:
    Nature, 2012, v. 485, n. 7397, p. 237, doi. 10.1038/nature10945
    By:
    • Sanders, Stephan J.;
    • Murtha, Michael T.;
    • Gupta, Abha R.;
    • Murdoch, John D.;
    • Raubeson, Melanie J.;
    • Willsey, A. Jeremy;
    • Ercan-Sencicek, A. Gulhan;
    • DiLullo, Nicholas M.;
    • Parikshak, Neelroop N.;
    • Stein, Jason L.;
    • Walker, Michael F.;
    • Ober, Gordon T.;
    • Teran, Nicole A.;
    • Song, Youeun;
    • El-Fishawy, Paul;
    • Murtha, Ryan C.;
    • Choi, Murim;
    • Overton, John D.;
    • Bjornson, Robert D.;
    • Carriero, Nicholas J.
    Publication type:
    Article