Search Results - Erik Boot

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  1. 1
    Neurobiological perspective of 22q11.2 deletion syndrome

    Neurobiological perspective of 22q11.2 deletion syndrome by Janneke Zinkstok, Erik Boot, Anne S. Bassett, Noboru Hiroi, Nancy J. Butcher, Claudia Vingerhoets, Jacob Vorstman, Thérèse van Amelsvoort

    Published 2019
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  2. 2
    Obesity in adults with 22q11.2 deletion syndrome

    Obesity in adults with 22q11.2 deletion syndrome by Sarah L. Voll, Erik Boot, Nancy J. Butcher, Samantha Cooper, Tracy Heung, Eva W.C. Chow, Candice K. Silversides, Anne S. Bassett

    Published 2016
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  3. 3
    A mouse model of 22q11.2 deletions: Molecular and behavioral signatures of Parkinson’s disease and schizophrenia

    A mouse model of 22q11.2 deletions: Molecular and behavioral signatures of Parkinson’s disease and schizophrenia by Akiko Sumitomo, Kouta Horike, Kazuko Hirai, Nancy J. Butcher, Erik Boot, Takeshi Sakurai, Frederick C. Nucifora, Anne S. Bassett, Akira Sawa, Toshifumi Tomoda

    Published 2018
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  4. 4
    A genetic model for multimorbidity in young adults

    A genetic model for multimorbidity in young adults by Sarah Malecki, Spencer van Mil, Justin Graffi, Elemi Breetvelt, Maria Corral, Erik Boot, Eva W.C. Chow, Marcos Sanches, Amol A. Verma, Anne S. Bassett

    Published 2019
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  5. 5
    Movement disorders and other motor abnormalities in adults with 22q11.2 deletion syndrome

    Movement disorders and other motor abnormalities in adults with 22q11.2 deletion syndrome by Erik Boot, Nancy J. Butcher, Thérèse A. van Amelsvoort, Anthony E. Lang, Connie Marras, Margarita Pondal, Danielle M. Andrade, Wai Lun Alan Fung, Anne S. Bassett

    Published 2015
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  6. 6
    All-cause mortality and survival in adults with 22q11.2 deletion syndrome

    All-cause mortality and survival in adults with 22q11.2 deletion syndrome by Lily Van, Tracy Heung, Justin Graffi, Enoch Ng, Sarah Malecki, Spencer van Mil, Erik Boot, Maria Corral, Eva W.C. Chow, Kathleen Hodgkinson, Candice K. Silversides, Anne S. Bassett

    Published 2019
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  7. 7
    Lower striatal dopamine D2/3 receptor availability in obese compared with non-obese subjects

    Lower striatal dopamine D2/3 receptor availability in obese compared with non-obese subjects by Barbara A. de Weijer, Elsmarieke van de Giessen, Thérèse A. van Amelsvoort, Erik Boot, Breg Braak, Ignace M. C. Janssen, Arnold van de Laar, Eric Fliers, Mireille J. Serlie, Jan Booij

    Published 2011
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  8. 8
    Elucidating the diagnostic odyssey of 22q11.2 deletion syndrome

    Elucidating the diagnostic odyssey of 22q11.2 deletion syndrome by Lisa D. Palmer, Nancy J. Butcher, Erik Boot, Kathleen Hodgkinson, Tracy Heung, Eva W.C. Chow, Alina Guna, T. Blaine Crowley, Elaine H. Zackai, Donna M. McDonald‐McGinn, Anne S. Bassett

    Published 2018
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  9. 9
    Neuroimaging and clinical features in adults with a 22q11.2 deletion at risk of Parkinson’s disease

    Neuroimaging and clinical features in adults with a 22q11.2 deletion at risk of Parkinson’s disease by Nancy J. Butcher, Connie Marras, Margarita Pondal, Pablo Rusjan, Erik Boot, Leigh Christopher, Gabriela M. Repetto, Rosemarie Fritsch, Eva W.C. Chow, Mario Masellis, Antonio P. Strafella, Anthony E. Lang, Anne S. Bassett

    Published 2017
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  10. 10
    Systematic Review of N-of-1 Studies in Rare Genetic Neurodevelopmental Disorders

    Systematic Review of N-of-1 Studies in Rare Genetic Neurodevelopmental Disorders by Annelieke R. Müller, Marion M. Brands, Peter M. van de Ven, Kit C. B. Roes, Martina C. Cornel, Clara van Karnebeek, Frits A. Wijburg, Joost G. Daams, Erik Boot, Agnies M. van Eeghen

    Published 2021
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  11. 11
    Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions

    Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions by Natalie Blagowidow, Beata Nowakowska, Erica Schindewolf, Francesca Romana Grati, Carolina Putotto, Jeroen Breckpot, Ann Swillen, T. Blaine Crowley, Joanne C. Y. Loo, Lauren A. Lairson, Sólveig Óskarsdóttir, Erik Boot, Sixto García‐Miñaúr, M. Cristina Digilio, Bruno Marino, Beverly G. Coleman, Julie S. Moldenhauer, Anne S. Bassett, Donna M. McDonald‐McGinn

    Published 2023
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  12. 12
    Cannabidiol (Epidyolex®) for severe behavioral manifestations in patients with tuberous sclerosis complex, mucopolysaccharidosis type III and fragile X syndrome: protocol for a series of randomized, placebo-controlled N-of-1 trials

    Cannabidiol (Epidyolex®) for severe behavioral manifestations in patients with tuberous sclerosis complex, mucopolysaccharidosis type III and fragile X syndrome: protocol for a ser... by Annelieke R. Müller, Bibiche den Hollander, Peter M. van de Ven, Kit C. B. Roes, Lisa Geertjens, Hilgo Bruining, Clara van Karnebeek, Floor E. Jansen, Marie‐Claire Y. de Wit, Leontine W. ten Hoopen, André B. Rietman, Bram Dierckx, Frits A. Wijburg, Erik Boot, Marion M. Brands, Agnies M. van Eeghen

    Published 2024
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  13. 13
    Practical guidelines for managing adults with 22q11.2 deletion syndrome

    Practical guidelines for managing adults with 22q11.2 deletion syndrome by Wai Lun Alan Fung, Nancy J. Butcher, Gregory Costain, Danielle M. Andrade, Erik Boot, Eva W.C. Chow, Brian Hon‐Yin Chung, Cheryl Cytrynbaum, Hanna Faghfoury, Leona Fishman, Sixto García‐Miñaúr, Susan R. George, Anthony E. Lang, Gabriela M. Repetto, Andrea Shugar, Candice Silversides, Ann Swillen, Thérèse van Amelsvoort, Donna M. McDonald‐McGinn, Anne S. Bassett

    Published 2015
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  14. 14
    Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome

    Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome by Erik Boot, Sólveig Óskarsdóttir, Joanne C. Y. Loo, T. Blaine Crowley, Ani Orchanian‐Cheff, Danielle M. Andrade, Jill M. Arganbright, René M. Castelein, Christine Cserti‐Gazdewich, Steven de Reuver, Ania Fiksinski, Gunilla Klingberg, Anthony E. Lang, Maria R. Mascarenhas, Edward Moss, Beata Nowakowska, Erwin Oechslin, Lisa D. Palmer, Gabriela M. Repetto, Nikolai Gil D. Reyes, Maude Schneider, Candice Silversides, Kathleen E. Sullivan, Ann Swillen, Thérèse van Amelsvoort, Jason Van Batavia, Claudia Vingerhoets, Donna M. McDonald‐McGinn, Anne S. Bassett

    Published 2023
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  15. 15
    Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome

    Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome by Maude Schneider, Martin Debbané, Anne S. Bassett, Eva W.C. Chow, Wai Lun Alan Fung, Marianne B. M. van den Bree, Michael J. Owen, Kieran C. Murphy, Maria Niarchou, Wendy R. Kates, Kevin M. Antshel, Wanda Fremont, Donna M. McDonald‐McGinn, Raquel E. Gur, Elaine H. Zackai, Jacob Vorstman, Sasja N. Duijff, Petra Klaassen, Ann Swillen, Doron Gothelf, Tamar Green, Abraham Weizman, Thérèse van Amelsvoort, L. J. M. Evers, Erik Boot, Vandana Shashi, Stephen R. Hooper, Carrie E. Bearden, Maria Jalbrzikowski, Marco Armando, Stefano Vicari, Declan Murphy, Opal Ousley, Linda Campbell, Tony J. Simon, Stéphan Eliez

    Published 2014
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  16. 16
    Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2

    Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2 by Erik Boot, Nancy J. Butcher, Sean Udow, Connie Marras, Kin Y. Mok, Satoshi Kaneko, Matthew J. Barrett, Paolo Prontera, Brian D. Berman, Mario Masellis, Boris Dufournet, Karine Nguyen, Perrine Charles, Eugénie Mutez, Téodor Danaila, Aurélia Jacquette, Olivier Colin, Sophie Drapier, Michel Borg, Ania Fiksinski, Elfi Vergaelen, Ann Swillen, Annick Vogels, Annika Plate, Claudia Perandones, Thomas Gasser, Kristien Clerinx, Frédéric Bourdain, K.R. Mills, Nigel Williams, Nicholas Wood, Jan Booij, Anthony E. Lang, Anne S. Bassett, Nicola Tambasco, Gabriela M. Repetto, Rosemarie Fritsch, Barber M Tinselboer, Jacob Vorstman, Luis A. Pellene, Stephen G. Reich, Claudia Schulte, A. Dekker

    Published 2018
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  17. 17
    Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome

    Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome by Sólveig Óskarsdóttir, Erik Boot, T. Blaine Crowley, Joanne C. Y. Loo, Jill M. Arganbright, Marco Armando, Adriane L. Baylis, Elemi Breetvelt, René M. Castelein, Madeline Chadehumbe, Christopher M. Cielo︎, Steven de Reuver, Stéphan Eliez, Ania Fiksinski, Brian J. Forbes, Emily R. Gallagher, Sarah Hopkins, Oksana A. Jackson, Lorraine Levitz-Katz, Gunilla Klingberg, Michele P. Lambert, Bruno Marino, Maria R. Mascarenhas, Julie S. Moldenhauer, Edward Moss, Beata Nowakowska, Ani Orchanian‐Cheff, Carolina Putotto, Gabriela M. Repetto, Erica Schindewolf, Maude Schneider, Cynthia Solot, Kathleen E. Sullivan, Ann Swillen, Marta Unolt, Jason Van Batavia, Claudia Vingerhoets, Jacob Vorstman, Anne S. Bassett, Donna M. McDonald‐McGinn

    Published 2023
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  18. 18
    Rapporteur summaries of plenary, symposia, and oral sessions from the XXIIIrd World Congress of Psychiatric Genetics Meeting in Toronto, Canada, 16–20 October 2015

    Rapporteur summaries of plenary, symposia, and oral sessions from the XXIIIrd World Congress of Psychiatric Genetics Meeting in Toronto, Canada, 16–20 October 2015 by Gwyneth Zai, Bonnie Alberry, Janine Arloth, Zsófia Bánlaki, Cristina B. Bares, Erik Boot, Caroline Camilo, Kartikay Chadha, Qi Chen, C. B. Cole, Katherine Tombeau Cost, Megan Crow, Ibene Ekpor, Sascha B. Fischer, Laura Flatau, Sarah A. Gagliano Taliun, Umut Kırlı, Prachi Kukshal, Viviane Labrie, Maren Lang, Tristram A. Lett, Elisabetta Maffioletti, Robert Maier, Marina Mihaljević, Kirti Mittal, Eric T. Monson, Niamh L. O’Brien, Søren Dinesen Østergaard, Ellen S. Ovenden, Sejal Patel, Roseann E. Peterson, Jennie G. Pouget, Diego Luiz Rovaris, Lauren C. Seaman, Bhagya Shankarappa, Fotis Tsetsos, Andrea Vereczkei, Chenyao Wang, Khethelo Richman Xulu, Ryan K. C. Yuen, Jingjing Zhao, Clement C. Zai, James L. Kennedy

    Published 2016
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  19. 19
    Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome

    Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome by Anne S. Bassett, Chelsea Lowther, Daniele Merico, Gregory Costain, Eva W.C. Chow, Thérèse van Amelsvoort, Donna M. McDonald‐McGinn, Raquel E. Gur, Ann Swillen, Marianne B. M. van den Bree, Kieran C. Murphy, Doron Gothelf, Carrie E. Bearden, Stéphan Eliez, Wendy R. Kates, Nicole Philip, Vandana Sashi, Linda Campbell, Jacob Vorstman, Joseph F. Cubells, Gabriela M. Repetto, Tabassome Simon, Erik Boot, Tracy Heung, Rens Evers, Claudia Vingerhoets, Esther van Duin, Elaine H. Zackai, Elfi Vergaelen, Koenraad Devriendt, Joris Vermeesch, Michael J. Owen, Clodagh M. Murphy, Elena Michaelovosky, Leila Kushan, Maude Schneider, Wanda Fremont, Tiffany Busa, Stephen R. Hooper, Kathryn McCabe, Sasja N. Duijff, Keren Isaev, Giovanna Pellecchia, John Wei, Matthew J. Gazzellone, Stephen W. Scherer, Beverly S. Emanuel, Tingwei Guo, Bernice E. Morrow, Christian R. Marshall

    Published 2017
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  20. 20
    Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes

    Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes by Maria Delio, Tingwei Guo, Donna M. McDonald‐McGinn, Elaine H. Zackai, Sean Herman, Mark Kaminetzky, Anne Marie Higgins, Karlene Coleman, Carolyn Chow, Maria Jarlbrzkowski, Carrie E. Bearden, Alice Bailey, Anders Vangkilde, Line Olsen, Charlotte Olesen, Flemming Skovby, Thomas Werge, Ludivine Templin, Tiffany Busa, Nicole Philip, Ann Swillen, Joris Vermeesch, Koenraad Devriendt, Maude Schneider, Sophie Dahoun, Stéphan Eliez, Kelly Schoch, Stephen R. Hooper, Vandana Shashi, Joy Samanich, Robert Marion, Thérèse van Amelsvoort, Erik Boot, Petra Klaassen, Sasja N. Duijff, Jacob Vorstman, Tracy Yuen, Candice K. Silversides, Eva W.C. Chow, Anne S. Bassett, Amos Frisch, Abraham Weizman, Doron Gothelf, Maria Niarchou, Marianne B. M. van den Bree, Michael J. Owen, Damián Heine‐Suñer, Jordi Rosell Andreo, Marco Armando, Stefano Vicari, Maria Cristina Digilio, Adam Auton, Wendy R. Kates, Tao Wang, Robert J. Shprintzen, Beverly S. Emanuel, Bernice E. Morrow

    Published 2013
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