Works by Grice, Dorothy E.


Results: 19
    1
    2

    Investigation of gene–environment interactions in relation to tic severity.

    Published in:
    Journal of Neural Transmission, 2021, v. 128, n. 11, p. 1757, doi. 10.1007/s00702-021-02396-y
    By:
    • Abdulkadir, Mohamed;
    • Yu, Dongmei;
    • Osiecki, Lisa;
    • King, Robert A.;
    • Fernandez, Thomas V.;
    • Brown, Lawrence W.;
    • Cheon, Keun-Ah;
    • Coffey, Barbara J.;
    • Garcia-Delgar, Blanca;
    • Gilbert, Donald L.;
    • Grice, Dorothy E.;
    • Hagstrøm, Julie;
    • Hedderly, Tammy;
    • Heyman, Isobel;
    • Hong, Hyun Ju;
    • Huyser, Chaim;
    • Ibanez-Gomez, Laura;
    • Kim, Young Key;
    • Kim, Young-Shin;
    • Koh, Yun-Joo
    Publication type:
    Article
    3
    4

    Characterization of <i>SLITRK1</i> Variation in Obsessive-Compulsive Disorder.

    Published in:
    PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0070376
    By:
    • Ozomaro, Uzoezi;
    • Cai, Guiqing;
    • Kajiwara, Yuji;
    • Yoon, Seungtai;
    • Makarov, Vladimir;
    • Delorme, Richard;
    • Betancur, Catalina;
    • Ruhrmann, Stephan;
    • Falkai, Peter;
    • Grabe, Hans Jörgen;
    • Maier, Wolfgang;
    • Wagner, Michael;
    • Lennertz, Leonhard;
    • Moessner, Rainald;
    • Murphy, Dennis L.;
    • Buxbaum, Joseph D.;
    • Züchner, Stephan;
    • Grice, Dorothy E.
    Publication type:
    Article
    5

    Protein-truncating variants and deletions of SHANK2 are associated with autism spectrum disorder and other neurodevelopmental concerns.

    Published in:
    Journal of Neurodevelopmental Disorders, 2025, v. 17, n. 1, p. 1, doi. 10.1186/s11689-025-09600-0
    By:
    • Silver, Hailey;
    • Greenberg, Rori;
    • Siper, Paige M.;
    • Zweifach, Jessica;
    • Soufer, Renee;
    • Sahin, Mustafa;
    • Berry-Kravis, Elizabeth;
    • Soorya, Latha Valluripalli;
    • Thurm, Audrey;
    • Bernstein, Jonathan A.;
    • Kolevzon, Alexander;
    • Grice, Dorothy E.;
    • Buxbaum, Joseph D.;
    • Levy, Tess
    Publication type:
    Article
    6

    Identification of rare de novo epigenetic variations in congenital disorders.

    Published in:
    Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-04540-x
    By:
    • Joshi, Ricky S.;
    • Garg, Paras;
    • Martin-Trujillo, Alejandro;
    • Patel, Nihir;
    • Jadhav, Bharati;
    • Watson, Corey T.;
    • Gibson, William;
    • Tessereau, Chloe;
    • Gelb, Bruce D.;
    • Sharp, Andrew J.;
    • Barbosa, Mafalda;
    • Buxbaum, Joseph D.;
    • Grice, Dorothy E.;
    • Soares, Gabriela;
    • De Rubeis, Silvia;
    • Reichert, Jennifer;
    • Chetnik, Kelsey;
    • Edelmann, Lisa;
    • Hui Mei;
    • Lopes, Fatima
    Publication type:
    Article
    7
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    10

    Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder.

    Published in:
    Molecular Autism, 2021, v. 12, n. 1, p. 1, doi. 10.1186/s13229-021-00465-3
    By:
    • Mahjani, Behrang;
    • De Rubeis, Silvia;
    • Gustavsson Mahjani, Christina;
    • Mulhern, Maureen;
    • Xu, Xinyi;
    • Klei, Lambertus;
    • Satterstrom, F. Kyle;
    • Fu, Jack;
    • Talkowski, Michael E.;
    • Reichenberg, Abraham;
    • Sandin, Sven;
    • Hultman, Christina M.;
    • Grice, Dorothy E.;
    • Roeder, Kathryn;
    • Devlin, Bernie;
    • Buxbaum, Joseph D.
    Publication type:
    Article
    11

    Prospective and detailed behavioral phenotyping in DDX3X syndrome.

    Published in:
    Molecular Autism, 2021, v. 12, n. 1, p. 1, doi. 10.1186/s13229-021-00431-z
    By:
    • Tang, Lara;
    • Levy, Tess;
    • Guillory, Sylvia;
    • Halpern, Danielle;
    • Zweifach, Jessica;
    • Giserman-Kiss, Ivy;
    • Foss-Feig, Jennifer H.;
    • Frank, Yitzchak;
    • Lozano, Reymundo;
    • Belani, Puneet;
    • Layton, Christina;
    • Lerman, Bonnie;
    • Frowner, Emanuel;
    • Breen, Michael S.;
    • De Rubeis, Silvia;
    • Kostic, Ana;
    • Kolevzon, Alexander;
    • Buxbaum, Joseph D.;
    • Siper, Paige M.;
    • Grice, Dorothy E.
    Publication type:
    Article
    12
    13
    14

    Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach.

    Published in:
    European Archives of Psychiatry & Clinical Neuroscience, 2018, v. 268, n. 3, p. 301, doi. 10.1007/s00406-017-0808-8
    By:
    • Abdulkadir, Mohamed;
    • Londono, Douglas;
    • Gordon, Derek;
    • Fernandez, Thomas V.;
    • Brown, Lawrence W.;
    • Cheon, Keun-Ah;
    • Coffey, Barbara J.;
    • Elzerman, Lonneke;
    • Fremer, Carolin;
    • Fründt, Odette;
    • Garcia-Delgar, Blanca;
    • Gilbert, Donald L.;
    • Grice, Dorothy E.;
    • Hedderly, Tammy;
    • Heyman, Isobel;
    • Hong, Hyun Ju;
    • Huyser, Chaim;
    • Ibanez-Gomez, Laura;
    • Jakubovski, Ewgeni;
    • Kim, Young Key
    Publication type:
    Article
    15

    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
    16

    Familial Clustering of Tic Disorders and Obsessive-Compulsive Disorder.

    Published in:
    JAMA Psychiatry, 2015, v. 72, n. 4, p. 359, doi. 10.1001/jamapsychiatry.2014.2656
    By:
    • Browne, Heidi A.;
    • Hansen, Stefan N.;
    • Buxbaum, Joseph D.;
    • Gair, Shannon L.;
    • Nissen, Judith B.;
    • Nikolajsen, Kathrine H.;
    • Schendel, Diana E.;
    • Reichenberg, Abraham;
    • Parner, Erik T.;
    • Grice, Dorothy E.
    Publication type:
    Article
    17
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    Common genetic variants, acting additively, are a major source of risk for autism.

    Published in:
    Molecular Autism, 2012, v. 3, n. 1, p. 1, doi. 10.1186/2040-2392-3-9
    By:
    • Klei, Lambertus;
    • Sanders, Stephan J.;
    • Murtha, Michael T.;
    • Hus, Vanessa;
    • Lowe, Jennifer K.;
    • Jeremy Willsey, A.;
    • Moreno-De-Luca, Daniel;
    • Yu, Timothy W.;
    • Fombonne, Eric;
    • Geschwind, Daniel;
    • Grice, Dorothy E.;
    • Ledbetter, David H.;
    • Lord, Catherine;
    • Mane, Shrikant M.;
    • Martin, Christa Lese;
    • Martin, Donna M.;
    • Morrow, Eric M.;
    • Walsh, Christopher A.;
    • Melhem, Nadine M.;
    • Chaste, Pauline
    Publication type:
    Article