Works matching IS 15524841 AND DT 2019 AND VI 180 AND IP 1

Results: 10
    1

    Predictive modeling of schizophrenia from genomic data: Comparison of polygenic risk score with kernel support vector machines approach.

    Published in:
    American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2019, v. 180, n. 1, p. 80, doi. 10.1002/ajmg.b.32705
    By:
    • Vivian‐Griffiths, Timothy;
    • Baker, Emily;
    • Schmidt, Karl M.;
    • Bracher‐Smith, Matthew;
    • Walters, James;
    • Artemiou, Andreas;
    • Holmans, Peter;
    • O'Donovan, Michael C.;
    • Owen, Michael J.;
    • Pocklington, Andrew;
    • Escott‐Price, Valentina
    Publication type:
    Article
    2
    3

    A case–control genome wide association study of substance use disorder (SUD) identifies novel variants on chromosome 7p14.1 in patients from the United Arab Emirates (UAE).

    Published in:
    American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2019, v. 180, n. 1, p. 68, doi. 10.1002/ajmg.b.32708
    By:
    • Alblooshi, Hiba;
    • Al Safar, Habiba;
    • Fisher, Holly F.;
    • Cordell, Heather J.;
    • El Kashef, Ahmed;
    • Al Ghaferi, Hamad;
    • Shawky, Mansour;
    • Reece, Stuart;
    • Hulse, Gary K.;
    • Tay, Guan K.
    Publication type:
    Article
    4

    The array of clinical phenotypes of males with mutations in Methyl‐CpG binding protein 2.

    Published in:
    American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2019, v. 180, n. 1, p. 55, doi. 10.1002/ajmg.b.32707
    By:
    • Neul, Jeffrey L.;
    • Benke, Timothy A.;
    • Marsh, Eric D.;
    • Skinner, Steven A.;
    • Merritt, Jonathan;
    • Lieberman, David N.;
    • Standridge, Shannon;
    • Feyma, Timothy;
    • Heydemann, Peter;
    • Peters, Sarika;
    • Ryther, Robin;
    • Jones, Mary;
    • Suter, Bernhard;
    • Kaufmann, Walter E.;
    • Glaze, Daniel G.;
    • Percy, Alan K.
    Publication type:
    Article
    5
    6

    Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy.

    Published in:
    American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2019, v. 180, n. 1, p. 35, doi. 10.1002/ajmg.b.32700
    By:
    • Foo, Jerome C.;
    • Streit, Fabian;
    • Frank, Josef;
    • Witt, Stephanie H.;
    • Treutlein, Jens;
    • Baune, Bernhard T.;
    • Moebus, Susanne;
    • Jöckel, Karl‐Heinz;
    • Forstner, Andreas J.;
    • Nöthen, Markus M.;
    • Rietschel, Marcella;
    • Sartorius, Alexander;
    • Kranaster, Laura
    Publication type:
    Article
    7

    Italian validation of the functional difficulties questionnaire (FDQ‐9) and its correlation with major determinants of quality of life in adults with hypermobile Ehlers–Danlos syndrome/hypermobility spectrum disorder.

    Published in:
    American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2019, v. 180, n. 1, p. 25, doi. 10.1002/ajmg.b.32698
    By:
    • Morlino, Silvia;
    • Dordoni, Chiara;
    • Sperduti, Isabella;
    • Clark, Carol J.;
    • Piedimonte, Caterina;
    • Fontana, Andrea;
    • Colombi, Marina;
    • Grammatico, Paola;
    • Copetti, Massimiliano;
    • Castori, Marco
    Publication type:
    Article
    8
    9

    Issue Information ‐ TOC.

    Published in:
    American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2019, v. 180, n. 1, p. 1, doi. 10.1002/ajmg.b.32665
    Publication type:
    Article
    10