Works matching IS 18661947 AND DT 2020 AND VI 12 AND IP 1

Results: 45
    1
    2
    3
    4
    5
    6
    7
    8
    9
    10
    11
    12
    13
    14
    15
    16
    17
    18
    19
    20

    Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophrenia.

    Published in:
    Journal of Neurodevelopmental Disorders, 2020, v. 12, n. 1, p. N.PAG, doi. 10.1186/s11689-020-09325-2
    By:
    • Ishizuka, Kanako;
    • Yoshida, Tomoyuki;
    • Kawabata, Takeshi;
    • Imai, Ayako;
    • Mori, Hisashi;
    • Kimura, Hiroki;
    • Inada, Toshiya;
    • Okahisa, Yuko;
    • Egawa, Jun;
    • Usami, Masahide;
    • Kushima, Itaru;
    • Morikawa, Mako;
    • Okada, Takashi;
    • Ikeda, Masashi;
    • Branko, Aleksic;
    • Mori, Daisuke;
    • Someya, Toshiyuki;
    • Iwata, Nakao;
    • Ozaki, Norio
    Publication type:
    Article
    21

    Natural clusters of tuberous sclerosis complex (TSC)-associated neuropsychiatric disorders (TAND): new findings from the TOSCA TAND research project.

    Published in:
    Journal of Neurodevelopmental Disorders, 2020, v. 12, n. 1, p. N.PAG, doi. 10.1186/s11689-020-09327-0
    By:
    • de Vries, Petrus J.;
    • Belousova, Elena;
    • Benedik, Mirjana P.;
    • Carter, Tom;
    • Cottin, Vincent;
    • Curatolo, Paolo;
    • D'Amato, Lisa;
    • Beure d'Augères, Guillaume;
    • Ferreira, José C.;
    • Feucht, Martha;
    • Fladrowski, Carla;
    • Hertzberg, Christoph;
    • Jozwiak, Sergiusz;
    • Lawson, John A.;
    • Macaya, Alfons;
    • Marques, Ruben;
    • Nabbout, Rima;
    • O'Callaghan, Finbar;
    • Qin, Jiong;
    • Sander, Valentin
    Publication type:
    Article
    22

    Obsessive-compulsive disorder and attention-deficit/hyperactivity disorder: distinct associations with DNA methylation and genetic variation.

    Published in:
    Journal of Neurodevelopmental Disorders, 2020, v. 12, n. 1, p. N.PAG, doi. 10.1186/s11689-020-09324-3
    By:
    • Goodman, Sarah J.;
    • Burton, Christie L.;
    • Butcher, Darci T.;
    • Siu, Michelle T.;
    • Lemire, Mathieu;
    • Chater-Diehl, Eric;
    • Turinsky, Andrei L.;
    • Brudno, Michael;
    • Soreni, Noam;
    • Rosenberg, David;
    • Fitzgerald, Kate D.;
    • Hanna, Gregory L.;
    • Anagnostou, Evdokia;
    • Arnold, Paul D.;
    • Crosbie, Jennifer;
    • Schachar, Russell;
    • Weksberg, Rosanna
    Publication type:
    Article
    23

    Properties of beta oscillations in Dup15q syndrome.

    Published in:
    Journal of Neurodevelopmental Disorders, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s11689-020-09326-1
    By:
    • Saravanapandian, Vidya;
    • Frohlich, Joel;
    • Hipp, Joerg F.;
    • Hyde, Carly;
    • Scheffler, Aaron W.;
    • Golshani, Peyman;
    • Cook, Edwin H.;
    • Reiter, Lawrence T.;
    • Senturk, Damla;
    • Jeste, Shafali S.
    Publication type:
    Article
    24
    25
    26
    27
    28
    29
    30
    31
    32

    Developmental studies in fragile X syndrome.

    Published in:
    Journal of Neurodevelopmental Disorders, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s11689-020-09310-9
    By:
    • Razak, Khaleel A.;
    • Dominick, Kelli C.;
    • Erickson, Craig A.
    Publication type:
    Article
    33
    34
    35

    Expressive language sampling as a source of outcome measures for treatment studies in fragile X syndrome: feasibility, practice effects, test-retest reliability, and construct validity.

    Published in:
    Journal of Neurodevelopmental Disorders, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s11689-020-09313-6
    By:
    • Abbeduto, Leonard;
    • Berry-Kravis, Elizabeth;
    • Sterling, Audra;
    • Sherman, Stephanie;
    • Edgin, Jamie O.;
    • McDuffie, Andrea;
    • Hoffmann, Anne;
    • Hamilton, Debra;
    • Nelson, Michael;
    • Aschkenasy, Jeannie;
    • Thurman, Angela John
    Publication type:
    Article
    36

    Expressive language sampling as a source of outcome measures for treatment studies in fragile X syndrome: feasibility, practice effects, test-retest reliability, and construct validity.

    Published in:
    Journal of Neurodevelopmental Disorders, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s11689-020-09313-6
    By:
    • Abbeduto, Leonardkk;
    • Berry-Kravis, Elizabeth;
    • Sterling, Audra;
    • Sherman, Stephanie;
    • Edgin, Jamie O.;
    • McDuffie, Andrea;
    • Hoffmann, Anne;
    • Hamilton, Debra;
    • Nelson, Michael;
    • Aschkenasy, Jeannie;
    • Thurman, Angela John
    Publication type:
    Article
    37
    38
    39
    40
    41

    Quantitative trait variation in ASD probands and toddler sibling outcomes at 24 months.

    Published in:
    Journal of Neurodevelopmental Disorders, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s11689-020-9308-7
    By:
    • Girault, Jessica B.;
    • Swanson, Meghan R.;
    • Meera, Shoba S.;
    • Grzadzinski, Rebecca L.;
    • Shen, Mark D.;
    • Burrows, Catherine A.;
    • Wolff, Jason J.;
    • Pandey, Juhi;
    • John, Tanya St;
    • Estes, Annette;
    • Zwaigenbaum, Lonnie;
    • Botteron, Kelly N.;
    • Hazlett, Heather C.;
    • Dager, Stephen R.;
    • Schultz, Robert T.;
    • Constantino, John N.;
    • Piven, Joseph;
    • for the IBIS Network;
    • Chappell, C.;
    • Shaw, D.
    Publication type:
    Article
    42

    Health comorbidities and cognitive abilities across the lifespan in Down syndrome.

    Published in:
    Journal of Neurodevelopmental Disorders, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s11689-019-9306-9
    By:
    • Startin, Carla M.;
    • D'Souza, Hana;
    • Ball, George;
    • Hamburg, Sarah;
    • Hithersay, Rosalyn;
    • Hughes, Kate M. O.;
    • Massand, Esha;
    • Karmiloff-Smith, Annette;
    • Thomas, Michael S. C.;
    • LonDownS Consortium;
    • Strydom, André;
    • Fisher, Elizabeth;
    • Nizetic, Dean;
    • Hardy, John;
    • Tybulewicz, Victor;
    • Thomas, Michael;
    • Mareschal, Denis;
    • Al-Janabi, Tamara;
    • Aggarwal, Nidhi;
    • Coyle, Tommy
    Publication type:
    Article
    43
    44
    45