检索结果 - Marc Woodbury‐Smith
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Asperger syndrome and criminal behaviour 由 Kalpana Dein, Marc Woodbury‐Smith
出版 2010Artigo -
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Pathways toward Positive Psychosocial Outcomes and Mental Health for Youth with Disabilities: A Knowledge Synthesis of Developmental Trajectories 由 Jan Willem Gorter, Debra Stewart, Marc Woodbury‐Smith, Gillian King, Marilyn Wright, Tram Nguyen, Matt Freeman, Marilyn Swinton
出版 2014Artigo -
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A Systematic Review of What Barriers and Facilitators Prevent and Enable Physical Healthcare Services Access for Autistic Adults 由 David Mason, Barry Ingham, Anna Urbanowicz, Cos Michael, Heather Birtles, Marc Woodbury‐Smith, Toni Brown, Ian A. James, Clare Scarlett, Christina Nicolaidis, Jeremy Parr
出版 2019Revisão -
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Variable phenotype expression in a family segregating microdeletions of the NRXN1 and MBD5 autism spectrum disorder susceptibility genes 由 Marc Woodbury‐Smith, Rob Nicolson, Mehdi Zarrei, Ryan K. C. Yuen, Susan Walker, Jennifer Howe, Mohammed Uddin, Ny Hoang, Janet A. Buchanan, Christina Chrysler, Ann Thompson, Peter Szatmari, Stephen W. Scherer
出版 2017Artigo -
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Autism spectrum disorder: advances in evidence-based practice 由 Evdokia Anagnostou, Lonnie Zwaigenbaum, Peter Szatmari, Éric Fombonne, Bridget A. Fernandez, Marc Woodbury‐Smith, Jessica Brian, Susan E. Bryson, Isabel M. Smith, Irene Drmic, Janet A. Buchanan, Wendy Roberts, Stephen W. Scherer
出版 2014Revisão -
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Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly 由 Marc Woodbury‐Smith, Éric Deneault, Ryan K. C. Yuen, Susan Walker, Mehdi Zarrei, Giovanna Pellecchia, Jennifer Howe, Ny Hoang, Mohammed Uddin, Christian R. Marshall, Christina Chrysler, Ann Thompson, Péter Szatmári, Stephen W. Scherer
出版 2017Artigo -
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Germline and somatic mutations in <i>STXBP1</i> with diverse neurodevelopmental phenotypes 由 Mohammed Uddin, Marc Woodbury‐Smith, Ada J. S. Chan, Ledia Brunga, Sylvia Lamoureux, Giovanna Pellecchia, Ryan K. C. Yuen, Muhammad Faheem, Dimitri J. Stavropoulos, James M. Drake, Cecil D. Hahn, Cynthia Hawkins, Adam Shlien, Christian R. Marshall, Lesley Turner, Berge A. Minassian, Stephen W. Scherer, Cyrus Boelman
出版 2017Artigo -
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OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion Syndrome 由 Mohammed Uddin, Brianna K. Unda, Vickie Kwan, Nicholas Holzapfel, Sean H. White, Leon Chalil, Marc Woodbury‐Smith, Karen J. Ho, Erin Harward, Nadeem Murtaza, Biren M. Dave, Giovanna Pellecchia, Lia D’Abate, Thomas Nalpathamkalam, Sylvia Lamoureux, John Wei, Marsha Speevak, James Stavropoulos, Kristin J. Hope, Bradley W. Doble, Jacob Nielsen, E. Robert Wassman, Stephen W. Scherer, Karun K. Singh
出版 2018Artigo -
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Gene copy number variation and pediatric mental health/neurodevelopment in a general population 由 Mehdi Zarrei, Christie L. Burton, Worrawat Engchuan, Edward J. Higginbotham, John Wei, Sabah Shaikh, Nicole M. Roslin, Jeffrey R. MacDonald, Giovanna Pellecchia, Thomas Nalpathamkalam, Sylvia Lamoureux, Roozbeh Manshaei, Jennifer Howe, Brett Trost, Bhooma Thiruvahindrapuram, Christian R. Marshall, Ryan K. C. Yuen, Richard F. Wintle, Lisa J. Strug, Dimitri J. Stavropoulos, Jacob Vorstman, Paul Arnold, Daniele Merico, Marc Woodbury‐Smith, Jennifer Crosbie, Russell Schachar, Stephen W. Scherer
出版 2023Artigo -
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A large data resource of genomic copy number variation across neurodevelopmental disorders 由 Mehdi Zarrei, Christie L. Burton, Worrawat Engchuan, Edwin J. Young, Edward J. Higginbotham, Jeffrey R. MacDonald, Brett Trost, Ada J. S. Chan, Susan Walker, Sylvia Lamoureux, Tracy Heung, Bahareh A. Mojarad, Barbara Kellam, Tara Paton, Muhammad Faheem, Karin Miron, Chao Lu, Ting Wang, Kozue Samler, Xiaolin Wang, Gregory Costain, Ny Hoang, Giovanna Pellecchia, John Wei, Rohan Patel, Bhooma Thiruvahindrapuram, Maian Roifman, Daniele Merico, Tara Goodale, Irene Drmic, Marsha Speevak, Jennifer Howe, Ryan K. C. Yuen, Janet A. Buchanan, Jacob Vorstman, Christian R. Marshall, Richard F. Wintle, David R. Rosenberg, Gregory L. Hanna, Marc Woodbury‐Smith, Cheryl Cytrynbaum, Lonnie Zwaigenbaum, Mayada Elsabbagh, Janine Flanagan, Bridget A. Fernandez, Melissa T. Carter, Peter Szatmari, Wendy Roberts, Jason P. Lerch, Xudong Liu, Rob Nicolson, Stelios Georgiades, Rosanna Weksberg, Paul Arnold, Anne S. Bassett, Jennifer Crosbie, Russell Schachar, Dimitri J. Stavropoulos, Evdokia Anagnostou, Stephen W. Scherer
出版 2019Artigo -
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Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes 由 A. C. Lionel, Kristiina Tammimies, Andrea K. Vaags, Jill A. Rosenfeld, Joo Wook Ahn, Daniele Merico, Abdul Noor, Cassandra Runke, Vamsee Pillalamarri, M. T. Carter, Matthew J. Gazzellone, Bhooma Thiruvahindrapuram, Christina Fagerberg, Lone Walentin Laulund, Giovanna Pellecchia, Sylvia Lamoureux, Charu Deshpande, Jill Clayton‐Smith, A. Clinton White, Susan Leather, J Q Trounce, H. Melanie Bedford, Eli Hatchwell, Peggy S. Eis, Ryan K. C. Yuen, Susan Walker, Mohammed Uddin, Michael T. Geraghty, Sarah M. Nikkel, Eva Tomiak, Bridget A. Fernandez, Noam Soreni, Jennifer Crosbie, Paul Arnold, Russell Schachar, Wendy Roberts, Andrew D. Paterson, Jonathan So, Péter Szatmári, Christina Chrysler, Marc Woodbury‐Smith, R. Brian Lowry, Lonnie Zwaigenbaum, D. Mandyam, John Wei, Jeffrey R. MacDonald, Jennifer Howe, Thomas Nalpathamkalam, Z. Wang, Debbie Tolson, Donna Cobb, Timothy Wilks, Merete Juul Sørensen, Patricia I. Bader, Yu An, Bai-Lin Wu, S Musumeci, Corrado Romano, Diana Postorivo, A. Nardone, Matteo Della Monica, Gioacchino Scarano, Leonardo Zoccante, Francesca Novara, Orsetta Zuffardi, Roberto Ciccone, Vincenzo Antona, Massimo Carella, Leopoldo Zelante, Pietro Cavalli, Carlo Poggiani, Ugo Cavallari, Bob Argiropoulos, Judy Chernos, Charlotte Brasch‐Andersen, Marsha Speevak, Marco Fichera, Caroline Mackie Ogilvie, Ya Shen, JM Hodge, Michael E. Talkowski, Dimitri J. Stavropoulos, Christian R. Marshall, Stephen W. Scherer
出版 2013Artigo -
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Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder 由 Ryan K. C. Yuen, Daniele Merico, Matt Bookman, Jennifer Howe, Bhooma Thiruvahindrapuram, Rohan Patel, J. Andrew Whitney, Nicole Deflaux, Jonathan Bingham, Zhuozhi Wang, Giovanna Pellecchia, Janet A. Buchanan, Susan Walker, Christian R. Marshall, Mohammed Uddin, Mehdi Zarrei, Éric Deneault, Lia D’Abate, Ada J. S. Chan, Stephanie Koyanagi, Tara Paton, Sérgio L. Pereira, Ny Hoang, Worrawat Engchuan, Edward J. Higginbotham, Karen Ho, Sylvia Lamoureux, Weili Li, Jeffrey R. MacDonald, Thomas Nalpathamkalam, Wilson W. L. Sung, Fiona J. Tsoi, John Wei, Lizhen Xu, Anne-Marie Tasse, Emily Kirby, William Van Etten, Simon Twigger, Wendy Roberts, Irene Drmic, Sanne Jilderda, Bonnie MacKinnon Modi, Barbara Kellam, Michael J. Szego, Cheryl Cytrynbaum, Rosanna Weksberg, Lonnie Zwaigenbaum, Marc Woodbury‐Smith, Jessica Brian, Lili Senman, Alana Iaboni, Krissy A.R. Doyle‐Thomas, Ann Thompson, Christina Chrysler, Jonathan Leef, Tal Savion‐Lemieux, Isabel M. Smith, Xudong Liu, Rob Nicolson, Vicki Seifer, Angie Fedele, Edwin H. Cook, Stephen R. Dager, Annette Estes, Louise Gallagher, Beth A. Malow, Jeremy Parr, Sarah Spence, Jacob Vorstman, Brendan J. Frey, James Robinson, Lisa J. Strug, Bridget A. Fernandez, Mayada Elsabbagh, Melissa T. Carter, Joachim Hallmayer, Bartha Maria Knoppers, Evdokia Anagnostou, Peter Szatmari, Robert H. Ring, David Glazer, Mathew T. Pletcher, Stephen W. Scherer
出版 2017Artigo
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Autism
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Asperger syndrome
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