Erik Boot

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 27

Top Topics

Systematic Review

Congenital Heart Disease

Top Venues

American journal of medical genetics. Part A

Movement disorders clinical practice

This page only lists publications with an associated author ORCID identifier.

Publications

Hadassa Kwetsie, Malu van Schaijk, Sven J Van der Lee, Dederieke Maes-Festen, Leontine W Ten Hoopen, Mieke M van Haelst, Michael Coesmans, Esther Van Den Berg, Marie Claire Y De Wit, Yolande Pijnenburg, Eleonora M A Aronica, Erik Boot, Agnies M Van Eeghen
Dementia in Rare Genetic Neurodevelopmental Disorders: A Systematic Literature Review. Neurology 102 (11) (2024)
Hadassa Kwetsie, Malu van Schaijk, Sven J Van der Lee, Dederieke Maes-Festen, Leontine W Ten Hoopen, Mieke M van Haelst, Michael Coesmans, Esther Van Den Berg, Marie Claire Y De Wit, Yolande Pijnenburg, Eleonora M A Aronica, Erik Boot, Agnies M Van Eeghen
Dementia in Rare Genetic Neurodevelopmental Disorders: A Systematic Literature Review. Neurology 102 (11) (2024)
Hadassa Kwetsie, Malu van Schaijk, Sven J Van der Lee, Dederieke Maes-Festen, Leontine W Ten Hoopen, Mieke M van Haelst, Michael Coesmans, Esther Van Den Berg, Marie Claire Y De Wit, Yolande Pijnenburg, Eleonora M A Aronica, Erik Boot, Agnies M Van Eeghen
Dementia in Rare Genetic Neurodevelopmental Disorders: A Systematic Literature Review. Neurology 102 (11) (2024)
Hadassa Kwetsie, Malu van Schaijk, Sven J Van der Lee, Dederieke Maes-Festen, Leontine W Ten Hoopen, Mieke M van Haelst, Michael Coesmans, Esther Van Den Berg, Marie Claire Y De Wit, Yolande Pijnenburg, Eleonora M A Aronica, Erik Boot, Agnies M Van Eeghen
Dementia in Rare Genetic Neurodevelopmental Disorders: A Systematic Literature Review. Neurology 102 (11) (2024)
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, Sólveig Óskarsdóttir, Erik Boot, Sixto Garcia-Minaur, Maria Cristina Digilio, Bruno Marino, Beverly Coleman, Julie S Moldenhauer, Anne Susan Bassett, Donna M McDonald-McGinn
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes 14 (1) (2023)
Cathelijne C Linders, Agnies M van Eeghen, Janneke R Zinkstok, Marie-José van den Boogaard, Erik Boot
Intellectual and Behavioral Phenotypes of Smith-Magenis Syndrome: Comparisons between Individuals with a 17p11.2 Deletion and Pathogenic RAI1 Variant. Genes 14 (8) (2023)
Dorinde Korteling, Jiska L I Musch, Janneke R Zinkstok, Erik Boot
Psychiatric and neurological manifestations in adults with Smith-Magenis syndrome: A scoping review. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics (2023)
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, Sólveig Óskarsdóttir, Erik Boot, Sixto Garcia-Minaur, Maria Cristina Digilio, Bruno Marino, Beverly Coleman, Julie S Moldenhauer, Anne Susan Bassett, Donna M McDonald-McGinn
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes 14 (1) (2023)
Emma N M M von Scheibler, Josine C C Widdershoven, Denise C P B M van Barneveld, Nina Schröder, Agnies M van Eeghen, Therese A M J van Amelsvoort, Erik Boot
Hearing loss and history of otolaryngological conditions in adults with microdeletion 22q11.2. American journal of medical genetics. Part A (2023)
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, Sólveig Óskarsdóttir, Erik Boot, Sixto Garcia-Minaur, Maria Cristina Digilio, Bruno Marino, Beverly Coleman, Julie S Moldenhauer, Anne Susan Bassett, Donna M McDonald-McGinn
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes 14 (1) (2023)
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, Sólveig Óskarsdóttir, Erik Boot, Sixto Garcia-Minaur, Maria Cristina Digilio, Bruno Marino, Beverly Coleman, Julie S Moldenhauer, Anne Susan Bassett, Donna M McDonald-McGinn
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes 14 (1) (2023)
Maurice Pasternak, Zahra Shirzadi, Henk-Jan Mm Mutsaerts, Erik Boot, Nancy J Butcher, Bradley J MacIntosh, Tracy Heung, Anne Susan Bassett, Mario Masellis
Elevated regional cerebral blood flow in adults with 22q11.2 deletion syndrome. The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry (2022)
Erik Boot, Connie Marras, Anne Susan Bassett
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 : EJHG 30 (12) (2022)
Emma N M M von Scheibler, Thérèse A M J van Amelsvoort, Claudia Vingerhoets, Agnies M van Eeghen, Erik Boot
Post-traumatic stress in adults with 22q11.2 deletion syndrome. BJPsych open 8 (4) (2022)
Emma N M M von Scheibler, Agnies M van Eeghen, Tom J de Koning, Mark L Kuijf, Janneke R Zinkstok, Annelieke R Müller, Therese A M J van Amelsvoort, Erik Boot
Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review. Movement disorders clinical practice 10 (1) (2022)
Emma N M M von Scheibler, Agnies M van Eeghen, Tom J de Koning, Mark L Kuijf, Janneke R Zinkstok, Annelieke R Müller, Therese A M J van Amelsvoort, Erik Boot
Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review. Movement disorders clinical practice 10 (1) (2022)
Tracy Heung, Brigid Conroy, Sarah Malecki, Joanne Ha, Erik Boot, Maria Corral, Anne Susan Bassett
Adult Height, 22q11.2 Deletion Extent, and Short Stature in 22q11.2 Deletion Syndrome. Genes 13 (11) (2022)
Emma N M M von Scheibler, Emilie Sophie van der Valk Bouman, Myrthe A Nuijts, Noël 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
Ocular findings in 22q11.2 deletion syndrome: A systematic literature review and results of a Dutch multicenter study. American journal of medical genetics. Part A (2021)
Annelieke R Müller, Marion M M G Brands, Peter M van de Ven, Kit C B Roes, Martina Cornelia Cornel, Clara D M van Karnebeek, Frits A Wijburg, Joost G Daams, Erik Boot, Agnies M van Eeghen
Systematic Review of N-of-1 Studies in Rare Genetic Neurodevelopmental Disorders: The Power of 1. Neurology 96 (11) (2021)
Erik Boot, Cathelijne C Linders, Sterre H Tromp, Marie-José van den Boogaard, Agnies M van Eeghen
Possible underreporting of pathogenic variants in RAI1 causing Smith-Magenis syndrome. American journal of medical genetics. Part A 185 (10) (2021)
Erik Boot, Thierry Q Mentzel, Lisa D Palmer, Peter N van Harten, Connie Marras, Anthony E Lang, Anne Susan Bassett
Age-Related Parkinsonian Signs in Microdeletion 22q11.2. Movement disorders : official journal of the Movement Disorder Society 35 (7) (2020)
Isabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, Tracy Heung, Aaron M Holleman, H Richard Johnston, Thomas Monfeuga, Donna M McDonald-McGinn, Raquel E Gur, Bernice E Morrow, Ann Swillen, Jacob A S Vorstman, Carrie E Bearden, Eva W C Chow, Marianne van den Bree, Beverly S Emanuel, Joris R Vermeesch, Stephen T Warren, Michael J Owen, Pankaj Chopra, David J Cutler, Richard Duncan, Alex V Kotlar, Jennifer G Mulle, Anna J Voss, Michael E Zwick, Alexander Diacou, Aaron Golden, Tingwei Guo, Jhih-Rong Lin, Tao Wang, Zhengdong Zhang, Yingjie Zhao, Christian R Marshall, Daniele Merico, Andrea Jin, Brenna Lilley, Harold I Salmons, Oanh Tran, Peter Holmans, Antonio F Pardinas, James T R Walters, Wolfram Demaerel, Erik Boot, Nancy J Butcher, Gregory A Costain, Chelsea Lowther, Rens Evers, Therese A M J van Amelsvoort, Esther van Duin, Claudia Vingerhoets, Jeroen Breckpot, Koen Devriendt, Elfi Vergaelen, Annick Vogels, Terrence Blaine Crowley, Daniel E McGinn, Edward M Moss, Robert J Sharkus, Marta Unolt, Elaine H Zackai, Monica E Calkins, Robert S Gallagher, Ruben C Gur, Sunny X Tang, Rosemarie Fritsch, Claudia Ornstein, Gabriela M Repetto, Elemi Breetvelt, Sasja N Duijff, Ania M Fiksinski, Hayley Moss, Maria Niarchou, Kieran C Murphy, Sarah E Prasad, Eileen M Daly, Maria Gudbrandsen, Clodagh M Murphy, Declan G M Murphy, Antonio Buzzanca, Fabio Di Fabio, Maria C Digilio, Maria Pontillo, Bruno Marino, Stefano Vicari, Karlene Coleman, Joseph F Cubells, Opal Y Ousley, Miri Carmel, Doron Gothelf, Ehud Mekori-Domachevsky, Elena Michaelovsky, Ronnie Weinberger, Abraham Weizman, Leila Kushan, Maria Jalbrzikowski, Marco Armando, Stéphan Eliez, Corrado Sandini, Maude Schneider, Frédérique Sloan Béna, Kevin M Antshel, Wanda Fremont, Wendy R Kates, Raoul Belzeaux, Tiffany Busa, Nicole Philip, Linda E Campbell, Kathryn L McCabe, Stephen R Hooper, Kelly Schoch, Vandana Shashi, Tony J Simon, Flora Tassone, Celso Arango, David Fraguas, Sixto García-Miñaúr, Jaume Morey-Canyelles, Jordi Rosell, Damià H Suñer, Jasna Raventos-Simic, null null, Michael P Epstein, Nigel M Williams, Anne S Bassett
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. Molecular psychiatry 26 (8) (2020)
Joanne C Y Loo, Erik Boot, Maria Corral, Anne Susan Bassett
Personalized medical information card for adults with 22q11.2 deletion syndrome: An initiative to improve communication between patients and healthcare providers. Journal of applied research in intellectual disabilities : JARID 33 (6) (2020)
Sarah L Voll, Spencer Van Mil, Justin Graffi, Elemi Breetvelt, Maria Corral, Erik Boot, Eva W C Chow, Marcos Sanches, Amol A Verma, Anne Susan Bassett
A genetic model for multimorbidity in young adults. Genetics in medicine : official journal of the American College of Medical Genetics 22 (1) (2019)
Petra C M Buijs, Anne Susan Bassett, Erik Boot
Non-pharmacological treatment of psychiatric disorders in individuals with 22q11.2 deletion syndrome; a systematic review. American journal of medical genetics. Part A 176 (8) (2018)
Nancy J Butcher, Erik Boot, Anthony E Lang, Danielle Andrade, Jacob Vorstman, Donna McDonald-McGinn, Anne Susan Bassett
Neuropsychiatric expression and catatonia in 22q11.2 deletion syndrome: An overview and case series. American journal of medical genetics. Part A 176 (10) (2018)
Akiko Sumitomo, Kouta Horike, Kazuko Hirai, Nancy Butcher, Erik Boot, Takeshi Sakurai, Frederick C Nucifora, Anne S Bassett, Akira Sawa, Toshifumi Tomoda
A mouse model of 22q11.2 deletions: Molecular and behavioral signatures of Parkinson's disease and schizophrenia. Science advances 4 (8) (2018)