Spectrum of movement disorders and motor abnormalities in adults with a 22q11.2 microdeletion: Comment on the literature and retrospective study of 92 adults
EUROPEAN JOURNAL OF HUMAN GENETICS (2022)
Journal
EUROPEAN JOURNAL OF HUMAN GENETICS
Volume 30, Issue 12, Pages 1314-1317Publisher
SPRINGERNATURE
Keywords
Ask authors/readers for more resources
Authors
I am an author on this paper
Reviews
Recommended
Clinical Course and Outcome of Prenatally Detected 22q11.2 Deletion Syndrome-A Retrospective Analysis
Chiara Paternostro, Stephanie Springer, Gregor Kasprian, Guelen Yerlikaya-Schatten, Theresa Reischer
DIAGNOSTICS (2023)
A systematic review of the prognostic value of motor abnormalities on clinical outcome in psychosis
Lydia E. Pieters, Niluja Nadesalingam, Sebastian Walther, Peter N. van Harten
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS (2022)
Using Technology to Identify Children With Autism Through Motor Abnormalities
Roberta Simeoli, Nicola Milano, Angelo Rega, Davide Marocco
FRONTIERS IN PSYCHOLOGY (2021)
A deep learning latent variable model to identify children with autism through motor abnormalities
Nicola Milano, Roberta Simeoli, Angelo Rega, Davide Marocco
FRONTIERS IN PSYCHOLOGY (2023)
The role of interpersonal synchrony in forming impressions of autistic and non-autistic adults
I. S. Plank, L. S. Traiger, A. M. Nelson, J. C. Koehler, S. F. Lang, R. Tepest, K. Vogeley, A. L. Georgescu, C. M. Falter-Wagner
SCIENTIFIC REPORTS (2023)
Post-traumatic stress in adults with 22q11.2 deletion syndrome
Emma N. M. M. von Scheibler, Therese A. M. J. van Amelsvoort, Claudia Vingerhoets, Agnies M. van Eeghen, Erik Boot
BJPSYCH OPEN (2022)
White matter abnormalities in adults with bipolar disorder type-II and unipolar depression
Anna Manelis, Adriane Soehner, Yaroslav O. Halchenko, Skye Satz, Rachel Ragozzino, Mora Lucero, Holly A. Swartz, Mary L. Phillips, Amelia Versace
SCIENTIFIC REPORTS (2021)
Characterising the Early Presentation of Motor Difficulties in Autistic Children
Jess E. Reynolds, Andrew J. O. Whitehouse, Gail A. Alvares, Hannah Waddington, Ella Macaskill, Melissa K. Licari
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS (2022)
Difference in the alveolar bone remodeling between the adolescents and adults during upper incisor retraction: a retrospective study
Ya Zheng, Chenjing Zhu, Meng Zhu, Lang Lei
SCIENTIFIC REPORTS (2022)
Hearing loss and history of otolaryngological conditions in adults with microdeletion 22q11.2
Emma N. M. M. von Scheibler, Josine C. C. Widdershoven, Denise C. P. B. M. van Barneveld, Nina Schroder, Agnies M. van Eeghen, Therese A. M. J. van Amelsvoort, Erik Boot
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2023)
Elderly may benefit more from motor imagery training in gaining muscle strength than young adults: A systematic review and meta-analysis
Xiao J. Liu, Sha Ge, Alberto Cordova, Zayd Yaghi, Bo Y. Jiang, Guang H. Yue, Wan X. Yao
FRONTIERS IN PSYCHOLOGY (2023)
Motor Abnormalities in Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder Are Associated With Regional Grey Matter Volumes
Ariadna Albajara Saenz, Thomas Villemonteix, Peter Van Schuerbeek, Simon Baijot, Mathilde Septier, Pierre Defresne, Veronique Delvenne, Gianfranco Passeri, Hubert Raeymaekers, Laurent Victoor, Eric Willaye, Philippe Peigneux, Nicolas Deconinck, Isabelle Massat
FRONTIERS IN NEUROLOGY (2021)
Motor skills predict adaptive behavior in autistic children and adolescents
Nicholas E. Fears, Stephanie A. Palmer, Haylie L. Miller
AUTISM RESEARCH (2022)
Association between weight change and risk of metabolic abnormalities in non-overweight/obese and overweight/obese population: A retrospective cohort study among Chinese adults
Yanyan Dai, Yujuan Li, Shu Yang, Weiwei Xu, Hong Jia, Chao Yang
FRONTIERS IN ENDOCRINOLOGY (2022)
The Mirroring Dance: Synchrony and Interaction Quality of Five Adolescents and Adults on the Autism Spectrum in Dance/Movement Therapy
Elizabeth Manders, Sharon Goodill, Sabine C. Koch, Ellen Giarelli, Marcia Polansky, Kathleen Fisher, Thomas Fuchs
FRONTIERS IN PSYCHOLOGY (2021)
Sexual knowledge and behaviour in 22q11.2 deletion syndrome, a complex care condition
Lisa D. Palmer, Tracy Heung, Maria Corral, Erik Boot, Stephanie G. Brooks, Anne S. Bassett
JOURNAL OF APPLIED RESEARCH IN INTELLECTUAL DISABILITIES (2022)
Ocular findings in 22q11.2 deletion syndrome: A systematic literature review and results of a Dutch multicenter study
Emma N. M. M. von Scheibler, Emy S. van der Valk Bouman, Myrthe A. Nuijts, Noel J. C. Bauer, Tos T. J. M. Berendschot, Pit Vermeltfoort, Levinus A. Bok, Agnies M. van Eeghen, Michiel L. Houben, Therese A. M. J. van Amelsvoort, Erik Boot, Michelle B. van Egmond-Ebbeling
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2022)
Elevated regional cerebral blood flow in adults with 22q11.2 deletion syndrome
Maurice Pasternak, Zahra Shirzadi, Henk J. M. M. Mutsaerts, Erik Boot, Nancy J. Butcher, Bradley J. MacIntosh, Tracy Heung, Anne S. Bassett, Mario Masellis
WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY (2023)
Post-traumatic stress in adults with 22q11.2 deletion syndrome
Emma N. M. M. von Scheibler, Therese A. M. J. van Amelsvoort, Claudia Vingerhoets, Agnies M. van Eeghen, Erik Boot
BJPSYCH OPEN (2022)
Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review
Emma N. M. M. von Scheibler, Agnies M. van Eeghen, Tom J. de Koning, Mark L. Kuijf, Janneke R. Zinkstok, Annelieke R. Muller, Therese A. M. J. van Amelsvoort, Erik Boot
MOVEMENT DISORDERS CLINICAL PRACTICE (2023)
Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome
Erik Boot, Solveig Oskarsdottir, Joanne C. Y. Loo, Terrence Blaine Crowley, Ani Orchanian-Cheff, Danielle M. Andrade, Jill M. Arganbright, Rene M. Castelein, Christine Cserti-Gazdewich, Steven de Reuver, Ania M. Fiksinski, Gunilla Klingberg, Anthony E. Lang, Maria R. Mascarenhas, Edward M. Moss, Beata Anna Nowakowska, Erwin Oechslin, Lisa Palmer, Gabriela M. Repetto, Nikolai Gil D. Reyes, Maude Schneider, Candice Silversides, Kathleen E. Sullivan, Ann Swillen, Therese A. M. J. van Amelsvoort, Jason P. Van Batavia, Claudia Vingerhoets, Donna M. McDonald-McGinn, Anne S. Bassett
GENETICS IN MEDICINE (2023)
Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome
Solveig Oskarsdottir, Erik Boot, Terrence Blaine Crowley, Joanne C. Y. Loo, Jill M. Arganbright, Marco Armando, Adriane L. Baylis, Elemi J. Breetvelt, Rene M. Castelein, Madeline Chadehumbe, Christopher M. Cielo, Steven de Reuver, Stephan Eliez, Ania M. Fiksinski, Brian J. Forbes, Emily Gallagher, Sarah E. Hopkins, Oksana A. Jackson, Lorraine Levitz-Katz, Gunilla Klingberg, Michele P. Lambert, Bruno Marino, Maria R. Mascarenhas, Julie Moldenhauer, Edward M. Moss, Beata Anna Nowakowska, Ani Orchanian-Cheff, Carolina Putotto, Gabriela M. Repetto, Erica Schindewolf, Maude Schneider, Cynthia B. Solot, Kathleen E. Sullivan, Ann Swillen, Marta Unolt, Jason P. Van Batavia, Claudia Vingerhoets, Jacob Vorstman, Anne S. Bassett, Donna M. McDonald-McGinn
GENETICS IN MEDICINE (2023)
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions
Natalie Blagowidow, Beata Nowakowska, Erica Schindewolf, Francesca Romana Grati, Carolina Putotto, Jeroen Breckpot, Ann Swillen, Terrence Blaine Crowley, Joanne C. Y. Loo, Lauren A. Lairson, Solveig Oskarsdottir, Erik Boot, Sixto Garcia-Minaur, Maria Cristina Digilio, Bruno Marino, Beverly Coleman, Julie S. Moldenhauer, Anne S. Bassett, Donna M. McDonald-McGinn
GENES (2023)
Gathering the Stakeholder's Perspective: Experiences and Opportunities in Rare Genetic Disease Research
Lauren K. White, T. Blaine Crowley, Brenda Finucane, Emily J. McClellan, Sarah Donoghue, Sixto Garcia-Minaur, Gabriela M. Repetto, Matthias Fischer, Sebastien Jacquemont, Raquel E. Gur, Anne M. Maillard, Kirsten A. Donald, Anne S. Bassett, Ann Swillen, Donna M. McDonald-McGinn
GENES (2023)
Hearing loss and history of otolaryngological conditions in adults with microdeletion 22q11.2
Emma N. M. M. von Scheibler, Josine C. C. Widdershoven, Denise C. P. B. M. van Barneveld, Nina Schroder, Agnies M. van Eeghen, Therese A. M. J. van Amelsvoort, Erik Boot
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2023)
Psychiatric and neurological manifestations in adults with Smith-Magenis syndrome: A scoping review
Dorinde Korteling, Jiska L. I. Musch, Janneke R. Zinkstok, Erik Boot
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2023)
Intellectual and Behavioral Phenotypes of Smith-Magenis Syndrome: Comparisons between Individuals with a 17p11.2 Deletion and Pathogenic RAI1 Variant
Cathelijne C. Linders, Agnies M. van Eeghen, Janneke R. Zinkstok, Marie-Jose van den Boogaard, Erik Boot, Xingguang Luo
GENES (2023)