Výsledky vyhledávání - Sarah Spence

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  1. 1
    The Role of Epilepsy and Epileptiform EEGs in Autism Spectrum Disorders

    The Role of Epilepsy and Epileptiform EEGs in Autism Spectrum Disorders Autor Sarah Spence, Mark T Schneider

    Vydáno 2009
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  2. 2
    Common neurological co-morbidities in autism spectrum disorders

    Common neurological co-morbidities in autism spectrum disorders Autor Kiran Maski, Shafali Jeste, Sarah Spence

    Vydáno 2011
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  3. 3
    The association between epilepsy and autism symptoms and maladaptive behaviors in children with autism spectrum disorder

    The association between epilepsy and autism symptoms and maladaptive behaviors in children with autism spectrum disorder Autor Emma Viscidi, Ashley Johnson, Sarah Spence, Stephen L. Buka, Eric M. Morrow, Elizabeth W. Triche

    Vydáno 2013
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  4. 4
    The Autism Genetic Resource Exchange: A Resource for the Study of Autism and Related Neuropsychiatric Conditions

    The Autism Genetic Resource Exchange: A Resource for the Study of Autism and Related Neuropsychiatric Conditions Autor Daniel H. Geschwind, Janice Sowinski, Catherine Lord, Portia Iversen, Jonathan Shestack, Patrick Jones, Lee Ducat, Sarah Spence

    Vydáno 2001
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  5. 5
    Mapping cortical anatomy in preschool aged children with autism using surface-based morphometry

    Mapping cortical anatomy in preschool aged children with autism using surface-based morphometry Autor Armin Raznahan, Rhoshel Lenroot, Audrey Thurm, Marta Gozzi, Allison Hanley, Sarah Spence, Susan E. Swedo, Jay N. Giedd

    Vydáno 2012
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  6. 6
    Clinical Characteristics of Children with Autism Spectrum Disorder and Co-Occurring Epilepsy

    Clinical Characteristics of Children with Autism Spectrum Disorder and Co-Occurring Epilepsy Autor Emma Viscidi, Elizabeth W. Triche, Matthew F. Pescosolido, Rebecca L. McLean, Robert M. Joseph, Sarah Spence, Eric M. Morrow

    Vydáno 2013
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  7. 7
    Compared to What? Early Brain Overgrowth in Autism and the Perils of Population Norms

    Compared to What? Early Brain Overgrowth in Autism and the Perils of Population Norms Autor Armin Raznahan, Gregory L. Wallace, Ligia Antezana, Dede Greenstein, Rhoshel Lenroot, Audrey Thurm, Marta Gozzi, Sarah Spence, Alex Martin, Susan E. Swedo, Jay N. Giedd

    Vydáno 2013
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  8. 8
    The Co-Morbidity Burden of Children and Young Adults with Autism Spectrum Disorders

    The Co-Morbidity Burden of Children and Young Adults with Autism Spectrum Disorders Autor Isaac S. Kohane, Andrew McMurry, Griffin M. Weber, Douglas MacFadden, Leonard Rappaport, Louis M. Kunkel, Jonathan Bickel, Nich Wattanasin, Sarah Spence, Shawn N. Murphy, Susanne Churchill

    Vydáno 2012
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  9. 9
    Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways †

    Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways † Autor Yuhei Nishimura, Alastair J. Martin, Araceli Vázquez-López, Sarah Spence, Ana Isabel Alvarez-Retuerto, Marian Sigman, Corinna Steindler, Sandra Pellegrini, N. Carolyn Schanen, Stephen T. Warren, Daniel H. Geschwind

    Vydáno 2007
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  10. 10
    A Genomewide Screen of 345 Families for Autism-Susceptibility Loci

    A Genomewide Screen of 345 Families for Autism-Susceptibility Loci Autor Amanda L. Yonan, Maricela Alarcón, Rong Cheng, Patrik K. E. Magnusson, Sarah Spence, Abraham A. Palmer, Adina Grunn, Suh‐Hang Hank Juo, Joseph D. Terwilliger, Jianjun Liu, Rita M. Cantor, Daniel H. Geschwind, T. Conrad Gilliam

    Vydáno 2003
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  11. 11
    Clinical phenotype of the recurrent 1q21.1 copy-number variant

    Clinical phenotype of the recurrent 1q21.1 copy-number variant Autor Raphael Bernier, Kyle J. Steinman, Beau Reilly, Arianne S. Wallace, Elliott H. Sherr, Nicholas J. Pojman, Heather C. Mefford, Jennifer Gerdts, Rachel K. Earl, Ellen Hanson, Robin P. Goin‐Kochel, Leandra N. Berry, Stephen M. Kanne, LeeAnne Green Snyder, Sarah Spence, Melissa B. Ramocki, David W. Evans, John E. Spiro, Alastair J. Martin, David H. Ledbetter, Wendy K. Chung

    Vydáno 2015
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  12. 12
    Strong Association of De Novo Copy Number Mutations with Autism

    Strong Association of De Novo Copy Number Mutations with Autism Autor Jonathan Sebat, B. Lakshmi, Dheeraj Malhotra, Jennifer Troge, Christa Lese‐Martin, Tom Walsh, Boris Yamrom, Seungtai Yoon, A. Krasnitz, Jude Kendall, Anthony Leotta, Deepa Pai, Ray Zhang, Yoonha Lee, James Hicks, Sarah Spence, Annette T. Lee, Kaija Puura, Terho Lehtimäki, David H. Ledbetter, Peter K. Gregersen, Joel D. Bregman, James S. Sutcliffe, Vaidehi Jobanputra, Wendy K. Chung, Dorothy Warburton, Mary‐Claire King, David Skuse, Daniel H. Geschwind, T. Conrad Gilliam, Kenny Ye, Michael Wigler

    Vydáno 2007
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  13. 13
    A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders

    A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders Autor Flore Zufferey, Elliott H. Sherr, Noam D. Beckmann, Ellen Hanson, Anne Maillard, Loyse Hippolyte, Aurélien Mace, Carina Ferrari, Zoltán Kutalik, Joris Andrieux, Elizabeth Aylward, Mandy Barker, Raphael Bernier, Sonia Bouquillon, Philippe Conus, Bruno Delobel, W. Andrew Faucett, Robin P. Goin‐Kochel, P. Ellen Grant, Louise Harewood, Jill V. Hunter, Sébastien Lebon, David H. Ledbetter, Alastair J. Martin, Katrin Männik, Danielle Martinet, Pratik Mukherjee, Melissa B. Ramocki, Sarah Spence, Kyle J. Steinman, Jennifer Tjernagel, John E. Spiro, Alexandre Reymond, J. Beckmann, Wendy K. Chung, Sébastien Jacquemont

    Vydáno 2012
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  14. 14
    Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities

    Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities Autor Debra D’Angelo, Sébastien Lebon, Qixuan Chen, Sandra Martin-Brevet, LeeAnne Green Snyder, Loyse Hippolyte, Ellen Hanson, Anne Maillard, W. Andrew Faucett, Aurélien Mace, Aurélie Pain, Raphael Bernier, Samuel J. R. A. Chawner, Albert David, Joris Andrieux, Elizabeth Aylward, Geneviève Baujat, Inês Caldeira, Philippe Conus, Carrina Ferrari, Francesca Forzano, Marion Gérard, Robin P. Goin‐Kochel, P. Ellen Grant, Jill V. Hunter, Bertrand Isidor, Aurélia Jacquette, Aia Elise Jønch, Boris Keren, Didier Lacombe, Cédric Le Caignec, Alastair J. Martin, Katrin Männik, Andres Metspalu, Cyril Mignot, Pratik Mukherjee, Michael J. Owen, Marzia Passeggeri, Caroline Rooryck, Jill A. Rosenfeld, Sarah Spence, Kyle J. Steinman, Jennifer Tjernagel, Mieke M. van Haelst, Yiping Shen, Bogdan Draganski, Elliott H. Sherr, David H. Ledbetter, Marianne B. M. van den Bree, J. Beckmann, John E. Spiro, Alexandre Reymond, Sébastien Jacquemont, Wendy K. Chung

    Vydáno 2015
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  15. 15
    Utility of Exome Sequencing for Diagnosis in Unexplained Pediatric-Onset Epilepsy

    Utility of Exome Sequencing for Diagnosis in Unexplained Pediatric-Onset Epilepsy Autor Hyun Yong Koh, Lacey Smith, Kimberly Wiltrout, Archana Podury, Nitish Chourasia, Alissa M. D’Gama, Meredith Park, Devon Knight, Emma Sexton, Julia Koh, Brandon T. Oby, Rebecca Pinsky, Diane D. Shao, Courtney E. French, Wanqing Shao, Shira Rockowitz, Piotr Sliz, Bo Zhang, Sonal Mahida, Christelle Moufawad El Achkar, Christopher J. Yuskaitis, Heather E. Olson, Beth Rosen Sheidley, Annapurna Poduri, Elizabeth Barkoudah, Ann M. Bergin, Miya E. Bernson‐Leung, Elizabeth Binney, Jeffrey Bolton, Stephanie Donatelli, Darius Ebrahimi‐Fakhari, Mark Gorman, Chellamani Harini, Divya Jayaraman, Agnieszka Kielian, Lauren LaFortune, Kerri L. LaRovere, Mark H. Libenson, David N. Lieberman, Tobias Loddenkemper, Candice Marti, Anna Minster, Kate Mysak, Ann Paris, Archana A. Patel, Phillip L. Pearl, Jurriaan M. Peters, A Gomes Pinto, Peter Raffalli, Alexander Rotenberg, Catherine L. Salussolia, Rebecca Sarvendram, Hannah Shapiro, Janet S. Soul, Sarah Spence, Karen Spencer, Robert C. Stowe, Coral M. Stredny, Masanori Takeoka, Molly Tracy, Sara Trowbridge, Melissa Tsuboyama, David K. Urion

    Vydáno 2023
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  16. 16
    Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder

    Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder Autor 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

    Vydáno 2017
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  17. 17
    Mapping autism risk loci using genetic linkage and chromosomal rearrangements

    Mapping autism risk loci using genetic linkage and chromosomal rearrangements Autor Peter Szatmari, Andrew D. Paterson, Lonnie Zwaigenbaum, Wendy Roberts, Jessica Brian, Xiaoqing Liu, John B. Vincent, Jennifer Skaug, Ann Thompson, Lili Senman, Lars Feuk, Qian Cheng, Susan E. Bryson, Marshall B. Jones, Christian R. Marshall, Stephen W. Scherer, Veronica J. Vieland, Christopher W. Bartlett, La Vonne Mangin, Rhinda Goedken, Alberto M. Segre, Margaret A. Pericak‐Vance, Michael L. Cuccaro, John R. Gilbert, Harry H. Wright, Ruth K. Abramson, Catalina Betancur, Thomas Bourgeron, Christopher Gillberg, Marion Leboyer, Joseph D. Buxbaum, Kenneth L. Davis, Eric Hollander, Jeremy M. Silverman, Joachim Hallmayer, Linda Lotspeich, James S. Sutcliffe, Jonathan L. Haines, Susan E. Folstein, Joseph Piven, Thomas H. Wassink, Val C. Sheffield, Daniel H. Geschwind, Maja Bućan, W. Ted Brown, Rita M. Cantor, John N. Constantino, T. Conrad Gilliam, Martha R. Herbert, Clara Lajonchere, David H. Ledbetter, Christa Lese‐Martin, Janet Miller, Stan F. Nelson, Carol A Samango-Sprouse, Sarah Spence, Matthew W. State, Rudolph E. Tanzi, Hilary Coon, Géraldine Dawson, Bernie Devlin, Annette Estes, Pamela Flodman, Lambertus Klei, William M. McMahon, Nancy J. Minshew, Jeff Munson, Elena Korvatska, Patricia M. Rodier, Gerard D. Schellenberg, Moyra Smith, M. Anne Spence, Chris Stodgell, Ping G. Tepper, Ellen M. Wijsman, Chang-En Yu, Bernadette Rogé, Carine Mantoulan, Kerstin Wittemeyer, Annemarie Poustka, Bärbel Felder, Sabine M. Klauck, Claudia Schuster, Fritz Poustka, Sven Bölte, Sabine Feineis-Matthews, Evelyn Herbrecht, Gabi Schmötzer, John Tsiantis, Κaterina Papanikolaou, Elena Maestrini, Elena Bacchelli, Francesca Blasi, Simona Carone, Claudio Toma, Hermán van Engeland, Maretha Jonge, Chantal Kemner, Frederieke Koop, Frederike Koop

    Vydáno 2007
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