檢索結果 - Anjené Addington

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  1. 1
    The genetics of childhood-onset schizophrenia: When madness strikes the prepubescent

    The genetics of childhood-onset schizophrenia: When madness strikes the prepubescent 由 Anjené Addington, Judith L. Rapoport

    出版 2009
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  2. 2
    Novel Autism Subtype-Dependent Genetic Variants Are Revealed by Quantitative Trait and Subphenotype Association Analyses of Published GWAS Data

    Novel Autism Subtype-Dependent Genetic Variants Are Revealed by Quantitative Trait and Subphenotype Association Analyses of Published GWAS Data 由 Valerie W. Hu, Anjené Addington, Alexander Hyman

    出版 2011
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  3. 3
    Autism Spectrum Disorders and Childhood-Onset Schizophrenia: Clinical and Biological Contributions to a Relation Revisited

    Autism Spectrum Disorders and Childhood-Onset Schizophrenia: Clinical and Biological Contributions to a Relation Revisited 由 Judith L. Rapoport, Alexis Chavez, Deanna Greenstein, Anjené Addington, Nitin Gogtay

    出版 2008
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  4. 4
    Microduplications disrupting the MYT1L gene (2p25.3) are associated with schizophrenia

    Microduplications disrupting the MYT1L gene (2p25.3) are associated with schizophrenia 由 Yohan Lee, Anand Mattai, Robert T. Long, Judith L. Rapoport, Nitin Gogtay, Anjené Addington

    出版 2012
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  5. 5
    Trajectories of Anatomic Brain Development as a Phenotype

    Trajectories of Anatomic Brain Development as a Phenotype 由 Jay N. Giedd, Rhoshel Lenroot, Philip Shaw, François Lalonde, Mark J. Celano, Samantha White, Julia W. Tossell, Anjené Addington, Nitin Gogtay

    出版 2008
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  6. 6
    Association of the dopamine receptor D4 (<i>DRD4</i>) gene 7‐repeat allele with children with attention‐deficit/hyperactivity disorder (ADHD): An update

    Association of the dopamine receptor D4 (<i>DRD4</i>) gene 7‐repeat allele with children with attention‐deficit/hyperactivity disorder (ADHD): An update 由 Michele C. Gornick, Anjené Addington, Philip Shaw, Andrew J. Bobb, Wendy Sharp, Deanna Greenstein, Sampath Arepalli, F. Xavier Castellanos, Judith L. Rapoport

    出版 2006
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  7. 7
    Longitudinally mapping the influence of sex and androgen signaling on the dynamics of human cortical maturation in adolescence

    Longitudinally mapping the influence of sex and androgen signaling on the dynamics of human cortical maturation in adolescence 由 Armin Raznahan, Yohan Lee, Reva Stidd, Robert T. Long, Dede Greenstein, Liv Clasen, Anjené Addington, Nitin Gogtay, Judith L. Rapoport, Jay N. Giedd

    出版 2010
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  8. 8
    22q11 deletion syndrome in childhood onset schizophrenia: an update

    22q11 deletion syndrome in childhood onset schizophrenia: an update 由 Alexandra Sporn, Anjené Addington, Allan L. Reiss, Michael Dean, Nitin Gogtay, Uroš Potočnik, Deanna Greenstein, Joachim Hallmayer, Peter Gochman, Marge Lenane, Natalie Baker, Julia W. Tossell, Judith L. Rapoport

    出版 2003
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  9. 9
    A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders

    A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders 由 Anjené Addington, J Gauthier, Amélie Piton, Fadi F. Hamdan, A Raymond, Nitin Gogtay, Rachel Miller, Julia W. Tossell, Jennifer L. Bakalar, G Germain, Peter Gochman, R Long, Judith L. Rapoport, Guy A. Rouleau

    出版 2010
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  10. 10
    Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability

    Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability 由 Lam Son Nguyen, Lachlan A. Jolly, Cheryl Shoubridge, Wai-Kin Chan, Lulu Huang, Frédéric Laumonnier, Martine Raynaud, Anna Hackett, Michael Field, Jayson Rodriguez, Anand Srivastava, Y Lee, R Long, Anjené Addington, Judith L. Rapoport, Suganthi Suren, Christopher N Hahn, Jennifer R. Gamble, Miles Wilkinson, Mark Corbett, Jozef Gécz

    出版 2011
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  11. 11
    Mutations in<i>SYNGAP1</i>in Autosomal Nonsyndromic Mental Retardation

    Mutations in<i>SYNGAP1</i>in Autosomal Nonsyndromic Mental Retardation 由 Fadi F. Hamdan, Julie Gauthier, Dan Spiegelman, Anne Noreau, Yanlian Yang, Stéphanie Pellerin, Sylvia Dobrzeniecka, Mélanie Côté, Elizabeth Perreau-Linck, Lionel Carmant, Guy D’Anjou, Éric Fombonne, Anjené Addington, Judith L. Rapoport, Lynn E. DeLisi, Marie‐Odile Krebs, Fayçal Mouaffak, Ridha Joober, Laurent Mottron, Pierre Drapeau, Claude Marineau, Ronald G. Lafrenière, Jean Claude Lacaille, Guy A. Rouleau, Jacques L. Michaud

    出版 2009
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  12. 12
    Whole genome sequencing in psychiatric disorders: the WGSPD consortium

    Whole genome sequencing in psychiatric disorders: the WGSPD consortium 由 Stephan Sanders, Benjamin M. Neale, Hailiang Huang, Donna M. Werling, Joon‐Yong An, Shan Dong, Gonçalo R. Abecasis, P. Alexander Arguello, John Blangero, Michael Boehnke, Mark J. Daly, Kevin Eggan, Daniel H. Geschwind, David C. Glahn, David B. Goldstein, Raquel E. Gur, Robert E. Handsaker, Steven A. McCarroll, Roel A. Ophoff, Aarno Palotie, Carlos N. Pato, Chiara Sabatti, Matthew W. State, A. Jeremy Willsey, Steven E. Hyman, Anjené Addington, Thomas Lehner, Nelson B. Freimer

    出版 2017
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  13. 13
    Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia

    Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia 由 Amélie Piton, J Gauthier, Fadi F. Hamdan, Ronald G. Lafrenière, Yanlian Yang, Édouard Henrion, S. B. Laurent, Anne Noreau, Patrick H. Thibodeau, Liliane Karemera, Dan Spiegelman, Frédéric Kuku, J Duguay, Laurie Destroismaisons, Philippe Jolivet, M. Côté, Karine Lachapelle, Ousmane Diallo, A Raymond, Claude Marineau, Nathalie Champagne, Lan Xiong, Cláudia Gaspar, J-B Rivière, Julien Tarabeux, Patrick Cossette, Marie‐Odile Krebs, Judith L. Rapoport, Anjené Addington, Lynn E. DeLisi, Laurent Mottron, Ridha Joober, Éric Fombonne, Pierre Drapeau, Guy A. Rouleau

    出版 2010
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  14. 14
    Direct Measure of the De Novo Mutation Rate in Autism and Schizophrenia Cohorts

    Direct Measure of the De Novo Mutation Rate in Autism and Schizophrenia Cohorts 由 Philip Awadalla, Julie Gauthier, Rachel A. Myers, Ferrán Casals, Fadi F. Hamdan, Alexander R. Griffing, Mélanie Côté, Édouard Henrion, Dan Spiegelman, Julien Tarabeux, Amélie Piton, Yanlian Yang, Adam R. Boyko, Carlos D. Bustamante, Lan Xiong, Judith L. Rapoport, Anjené Addington, J. Lynn E. DeLisi, Marie‐Odile Krebs, Ridha Joober, Bruno Millet, Éric Fombonne, Laurent Mottron, Martine Zilversmit, Jon Keebler, Hussein Daoud, Claude Marineau, Marie‐Hélène Roy‐Gagnon, Marie‐Pierre Dubé, Adam Eyre‐Walker, Pierre Drapeau, Eric A. Stone, Ronald G. Lafrenière, Guy A. Rouleau

    出版 2010
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  15. 15
    De novo mutations in the gene encoding the synaptic scaffolding protein<i>SHANK3</i>in patients ascertained for schizophrenia

    De novo mutations in the gene encoding the synaptic scaffolding protein<i>SHANK3</i>in patients ascertained for schizophrenia 由 Julie Gauthier, Nathalie Champagne, Ronald G. Lafrenière, Lan Xiong, Dan Spiegelman, Edna Brustein, Mathieu Lapointe, Huashan Peng, Mélanie Côté, Anne Noreau, Fadi F. Hamdan, Anjené Addington, Judith L. Rapoport, Lynn E. DeLisi, Marie‐Odile Krebs, Ridha Joober, Ferid Fathalli, Fayçal Mouaffak, A. Pejmun Haghighi, Christian Néri, Marie‐Pierre Dubé, Mark Samuels, Claude Marineau, Eric A. Stone, Philip Awadalla, Philip Barker, Salvatore Carbonetto, Pierre Drapeau, Guy A. Rouleau, Kathleen Daignault, Ousmane Diallo, Joannie Duguay, Marina Drits, Édouard Henrion, Philippe Jolivet, Frédéric Kuku, Karine Lachapelle, Guy Laliberté, Sandra B. Laurent, Meijiang Liao, Carlos Marino, Amélie Piton, A Raymond, Annie Reynolds, Daniel Rochefort, Judith St‐Onge, Pascale Thibodeau, Kazuya Tsurudome, Yanlian Yang, Sophie Leroy, Katia Ossian, Mélanie Chayet, David Gourion

    出版 2010
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  16. 16
    Microduplications of 16p11.2 are associated with schizophrenia

    Microduplications of 16p11.2 are associated with schizophrenia 由 Shane McCarthy, Vladimir Makarov, George Kirov, Anjené Addington, Jon McClellan, Seungtai Yoon, Diana O. Perkins, Diane E. Dickel, Mary Kusenda, Olga Krastoshevsky, Verena Krause, Ravinesh A. Kumar, Detelina Grozeva, Dheeraj Malhotra, Tom Walsh, Elaine H. Zackai, Paige Kaplan, Jaya Ganesh, Ian D. Krantz, Nancy B. Spinner, Patricia Roccanova, Abhishek Bhandari, Kevin Pavon, B. Lakshmi, Anthony Leotta, Jude Kendall, Yoon-ha Lee, Vladimir Vacic, Sydney Gary, Lilia M. Iakoucheva, Timothy J. Crow, Susan L. Christian, Jeffrey A. Lieberman, T. Scott Stroup, Terho Lehtimäki, Kaija Puura, Chad R. Haldeman‐Englert, Justin Pearl, Meredith Goodell, Virginia L. Willour, Pamela DeRosse, Jo Steele, Layla Kassem, Jessica Wolff, Nisha Chitkara, Francis J. McMahon, Anil K. Malhotra, James B. Potash, Thomas G. Schulze, Markus M. Nöthen, Sven Cichon, Marcella Rietschel, Ellen Leibenluft, Vlad Kustanovich, Clara Lajonchere, James S. Sutcliffe, David Skuse, Michael Gill, Louise Gallagher, Nancy R. Mendell, Nick Craddock, Michael J. Owen, Michael O’Donovan, Tamim H. Shaikh, Ezra Susser, Lynn E. DeLisi, Patrick F. Sullivan, Curtis K. Deutsch, Judith L. Rapoport, Deborah L. Levy, Mary‐Claire King, Jonathan Sebat

    出版 2009
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  17. 17
    The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing

    The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing 由 Rachel E. Rodin, Yanmei Dou, Minseok Kwon, Maxwell A. Sherman, Alissa M. D’Gama, Ryan N. Doan, Lariza M. Rento, Kelly M. Girskis, Craig L. Bohrson, Sonia N. Kim, Ajay Nadig, Lovelace J. Luquette, D. Gulhan, Christopher A. Walsh, Javier Ganz, Mollie B. Woodworth, Pengpeng Li, Rachel E. Rodin, Robert Hill, Sara Bizzotto, Zinan Zhou, Eunjung A. Lee, Alison R. Barton, Alissa M. D’Gama, Alon Galor, Craig L. Bohrson, Daniel H. Kwon, D. Gulhan, Elaine T. Lim, Isidro Cortes, Lovelace J. Luquette, Maxwell A. Sherman, Michael E. Coulter, Michael A. Lodato, Peter J. Park, Rebeca B. Monroy, Sonia N. Kim, Yanmei Dou, Andrew Chess, Attila Gulyás-Kovács, Chaggai Rosenbluh, Schahram Akbarian, Ben Langmead, Jeremy Thorpe, Jonathan Pevsner, Soonweng Cho, Andrew E. Jaffe, Apuã C.M. Paquola, Daniel R. Weinberger, Jennifer A. Erwin, Jooheon Shin, Richard E. Straub, Rujuta Narurkar, Alexej Abyzov, Taejeong Bae, Anjené Addington, David M. Panchision, Yanmei Dou, Geetha Senthil, Lora Bingaman, Tara Dutka, Thomas Lehner, Laura Saucedo-Cuevas, Tara Conniff, Kenneth Daily, Mette A. Peters, Fred H. Gage, Meiyan Wang, Patrick Reed, Sara B. Linker, Alex E. Urban, Bo Zhou, Xiaowei Zhu, Aitor Serres, David Juan, Inna Povolotskaya, Irene Lobón, Manuel Solís-Moruno, Raquel García-Pérez, Tomàs Marquès‐Bonet, Gary W. Mathern, Jing Gu, Joseph G. Gleeson, Laurel Ball, Renee D. George, Tiziano Pramparo, Diane A. Flasch, Trenton J. Frisbie, Jeffrey M. Kidd, John B. Moldovan, John V. Moran, Kenneth Y. Kwan, Ryan E. Mills, Sarah B. Emery, Weichen Zhou, Yifan Wang, Aakrosh Ratan, Michael J. McConnell, Flora M. Vaccarino, Gianfilippo Coppola

    出版 2021
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