Torthaí cuardaigh - Mehdi Zarrei

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  1. 1
    Variable phenotype expression in a family segregating microdeletions of the NRXN1 and MBD5 autism spectrum disorder susceptibility genes

    Variable phenotype expression in a family segregating microdeletions of the NRXN1 and MBD5 autism spectrum disorder susceptibility genes de réir 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

    Foilsithe / Cruthaithe 2017
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  2. 2
    Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly

    Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly de réir 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

    Foilsithe / Cruthaithe 2017
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  3. 3
    Clinically relevant copy number variations detected in cerebral palsy

    Clinically relevant copy number variations detected in cerebral palsy de réir Maryam Oskoui, Matthew J. Gazzellone, Bhooma Thiruvahindrapuram, Mehdi Zarrei, John Andersen, John Wei, Zhuozhi Wang, Richard F. Wintle, Christian R. Marshall, Ronald D. Cohn, Rosanna Weksberg, Dimitri J. Stavropoulos, Darcy Fehlings, Michael Shevell, Stephen W. Scherer

    Foilsithe / Cruthaithe 2015
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  4. 4
    Mutations in trpγ, the homologue of TRPC6 autism candidate gene, causes autism-like behavioral deficits in Drosophila

    Mutations in trpγ, the homologue of TRPC6 autism candidate gene, causes autism-like behavioral deficits in Drosophila de réir Angelina Palacios-Muñoz, Danielle de Paula Moreira, Valeria Silva, Isaac E. García, Francisco Aboitiz, Mehdi Zarrei, Gabriele da Silva Campos, Olivia Rennie, Jennifer Howe, Evdokia Anagnostou, Patricia Ambrozewic, Stephen W. Scherer, Maria Rita Passos‐Bueno, John Ewer

    Foilsithe / Cruthaithe 2022
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  5. 5
    Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome

    Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome de réir Daniele Merico, Mehdi Zarrei, Gregory Costain, Lucas Ogura, Babak Alipanahi, Matthew J. Gazzellone, Nancy J. Butcher, Bhooma Thiruvahindrapuram, Thomas Nalpathamkalam, Eva W.C. Chow, Danielle M. Andrade, Brendan J. Frey, Christian R. Marshall, Stephen W. Scherer, Anne S. Bassett

    Foilsithe / Cruthaithe 2015
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  6. 6
    Five vicarious genera from Gondwana: the Velloziaceae as shown by molecules and morphology

    Five vicarious genera from Gondwana: the Velloziaceae as shown by molecules and morphology de réir Renato de Mello‐Silva, Déborah Yara Alves Cursino dos Santos, Maria Luiza Faria Salatino, Lucimar B. Motta, Marina Blanco Cattai, Denise Sasaki, Juliana Lovo, Patrícia B. Pita, Cíntia Rocini, Cristiane Del Nero Rodrigues, Mehdi Zarrei, Mark W. Chase

    Foilsithe / Cruthaithe 2011
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  7. 7
    Five vicariant genera from Gondwana: the Velloziaceae as shown by molecules and morphology

    Five vicariant genera from Gondwana: the Velloziaceae as shown by molecules and morphology de réir Renato de Mello‐Silva, Déborah Yara Alves Cursino dos Santos, Maria Luiza Faria Salatino, Lícia Maria Henrique da Mota, Marina Blanco Cattai, Denise Sasaki, Juliana Lovo, Patrícia B. Pita, Cíntia Rocini, Cristiane Del Nero Rodrigues, Mehdi Zarrei, Mark W. Chase

    Foilsithe / Cruthaithe 2011
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  8. 8
    Rare CACNA1H and RELN variants interact through mTORC1 pathway in oligogenic autism spectrum disorder

    Rare CACNA1H and RELN variants interact through mTORC1 pathway in oligogenic autism spectrum disorder de réir André Luíz Teles e Silva, Talita Glaser, Karina Griesi‐Oliveira, Juliana Corrêa-Velloso, Jaqueline Yu Ting Wang, Gabriele da Silva Campos, Henning Ulrich, Andrea Balan, Mehdi Zarrei, Edward J. Higginbotham, Stephen W. Scherer, Maria Rita Passos‐Bueno, Andréa L. Sertié

    Foilsithe / Cruthaithe 2022
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  9. 9
    Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation

    Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation de réir Matthew J. Gazzellone, Mehdi Zarrei, Christie L. Burton, Susan Walker, Mohammed Uddin, S.‐M. Shaheen, Julie Coste, Rageen Rajendram, Reva Schachter, Marlena Colasanto, Gregory L. Hanna, David R. Rosenberg, Noam Soreni, Kate D. Fitzgerald, Christian R. Marshall, Janet A. Buchanan, Daniele Merico, Paul Arnold, Stephen W. Scherer

    Foilsithe / Cruthaithe 2016
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  10. 10
    De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy

    De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy de réir Mehdi Zarrei, Darcy Fehlings, Karizma Mawjee, Lauren Switzer, Bhooma Thiruvahindrapuram, Susan Walker, Daniele Merico, Guillermo Casallo, Mohammed Uddin, Jeffrey R. MacDonald, Matthew J. Gazzellone, Edward J. Higginbotham, Craig Campbell, Gabrielle deVeber, Pam Frid, Jan Willem Gorter, Carolyn Hunt, Anne Kawamura, Marie Kim, Anna McCormick, Ronit Mesterman, Dawa Samdup, Christian R. Marshall, Dimitri J. Stavropoulos, Richard F. Wintle, Stephen W. Scherer

    Foilsithe / Cruthaithe 2017
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  11. 11
    Gene copy number variation and pediatric mental health/neurodevelopment in a general population

    Gene copy number variation and pediatric mental health/neurodevelopment in a general population de réir 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

    Foilsithe / Cruthaithe 2023
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  12. 12
    Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay

    Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay de réir Mohammed Uddin, Giovanna Pellecchia, Bhooma Thiruvahindrapuram, Lia D’Abate, Daniele Merico, Ada J. S. Chan, Mehdi Zarrei, Kristiina Tammimies, Susan Walker, Matthew J. Gazzellone, Thomas Nalpathamkalam, Ryan K. C. Yuen, Koenraad Devriendt, Géraldine Mathonnet, Emmanuelle Lemyre, Sonia Nizard, Mary Shago, Ann M. Joseph‐George, Abdul Noor, Melissa T. Carter, Grace Yoon, Pekka Kannus, Frédérique Tihy, Erik C. Thorland, Christian R. Marshall, Janet A. Buchanan, Marsha Speevak, Dimitri J. Stavropoulos, Stephen W. Scherer

    Foilsithe / Cruthaithe 2016
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  13. 13
    Rearrangement bursts generate canonical gene fusions in bone and soft tissue tumors

    Rearrangement bursts generate canonical gene fusions in bone and soft tissue tumors de réir Nathaniel D. Anderson, Richard de Borja, Matthew D. Young, Fabio Fuligni, Andrej Rosic, Nicola D. Roberts, Simon Hajjar, Mehdi Layeghifard, Ana Novokmet, Paul E. Kowalski, Matthew Anaka, Scott Davidson, Mehdi Zarrei, Badr Id Said, Laura Schreiner, Remi Marchand, Joseph Sitter, Nalan Gökgöz, Ledia Brunga, Garrett T. Graham, Anthony Fullam, Nischalan Pillay, Jeffrey A. Toretsky, Akihiko Yoshida, Tatsuhiro Shibata, Markus Metzler, Gino R. Somers, Stephen W. Scherer, Adrienne M. Flanagan, Peter J. Campbell, Joshua D. Schiffman, Mary Shago, Ludmil B. Alexandrov, Jay S. Wunder, Irene L. Andrulis, David Malkin, Sam Behjati, Adam Shlien

    Foilsithe / Cruthaithe 2018
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  14. 14
    Genome-wide characteristics of de novo mutations in autism

    Genome-wide characteristics of de novo mutations in autism de réir Ryan K. C. Yuen, Daniele Merico, Hongzhi Cao, Giovanna Pellecchia, Babak Alipanahi, Bhooma Thiruvahindrapuram, Xin Tong, Yuhui Sun, Dandan Cao, Tao Zhang, Xueli Wu, Xin Jin, Ze Zhou, Xiaomin Liu, Thomas Nalpathamkalam, Susan Walker, Jennifer Howe, Zhuozhi Wang, Jeffrey R. MacDonald, Ada J. S. Chan, Lia D’Abate, Éric Deneault, Michelle T. Siu, Kristiina Tammimies, Mohammed Uddin, Mehdi Zarrei, Mingbang Wang, Yingrui Li, Jun Wang, Jian Wang, Huanming Yang, Matt Bookman, Jonathan Bingham, Samuel S. Gross, Dion Loy, Mathew T. Pletcher, Christian R. Marshall, Evdokia Anagnostou, Lonnie Zwaigenbaum, Rosanna Weksberg, Bridget A. Fernandez, Wendy Roberts, Peter Szatmari, David Glazer, Brendan J. Frey, Robert H. Ring, Xun Xu, Stephen W. Scherer

    Foilsithe / Cruthaithe 2016
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  15. 15
    A large data resource of genomic copy number variation across neurodevelopmental disorders

    A large data resource of genomic copy number variation across neurodevelopmental disorders de réir 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

    Foilsithe / Cruthaithe 2019
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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 de réir 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

    Foilsithe / Cruthaithe 2017
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  17. 17
    Genomic architecture of autism from comprehensive whole-genome sequence annotation

    Genomic architecture of autism from comprehensive whole-genome sequence annotation de réir Brett Trost, Bhooma Thiruvahindrapuram, Ada J. S. Chan, Worrawat Engchuan, Edward J. Higginbotham, Jennifer Howe, Lívia O. Loureiro, Miriam S. Reuter, Delnaz Roshandel, J. Andrew Whitney, Mehdi Zarrei, Matthew Bookman, Cherith Somerville, Rulan Shaath, Mona Abdi, Elbay Aliyev, Rohan Patel, Thomas Nalpathamkalam, Giovanna Pellecchia, Omar Hamdan, Gaganjot Kaur, Zhuozhi Wang, Jeffrey R. MacDonald, John Wei, Wilson W. L. Sung, Sylvia Lamoureux, Ny Hoang, Thanuja Selvanayagam, Nicole Deflaux, Melissa Geng, Siavash Ghaffari, John Bates, Edwin J. Young, Qiliang Ding, Carole Shum, Lia D’Abate, Clarrisa A. Bradley, Annabel Rutherford, Vernie Aguda, Beverly Apresto, Nan Chen, Sachin Desai, Xiaoyan Du, Matthew L.Y. Fong, Sanjeev Pullenayegum, Kozue Samler, Ting Wang, Karen Ho, Tara Paton, Sérgio L. Pereira, Jo-Anne Herbrick, Richard F. Wintle, Jonathan Fuerth, Juti Noppornpitak, Heather Ward, Patrick Magee, Ayman Al Baz, Usanthan Kajendirarajah, Sharvari Kapadia, Jim Vlasblom, Monica Valluri, Joseph Green, Vicki Seifer, Morgan Quirbach, Olivia Rennie, Elizabeth Kelley, Nina Masjedi, Catherine Lord, Michael J. Szego, Ma’n H. Zawati, Michael Lang, Lisa J. Strug, Christian R. Marshall, Gregory Costain, Kristina Calli, Alana Iaboni, Afiqah Yusuf, Patricia Ambrozewicz, Louise Gallagher, David G. Amaral, Jessica Brian, Mayada Elsabbagh, Stelios Georgiades, Daniel S. Messinger, Sally Ozonoff, Jonathan Sebat, Calvin Sjaarda, Isabel M. Smith, Peter Szatmari, Lonnie Zwaigenbaum, Azadeh Kushki, Thomas Frazier, Jacob Vorstman, Khalid A. Fakhro, Bridget A. Fernandez, M. E. Suzanne Lewis, Rosanna Weksberg, Marc Fiume, Ryan K. C. Yuen, Evdokia Anagnostou

    Foilsithe / Cruthaithe 2022
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