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In pioneering work, the Bassett group is identifying and characterizing genetic subtypes of schizophrenia. It is now apparent that a substantial proportion of patients with schizophrenia may have a new or inherited genetic change involving one of several major copy number variants. These structural genetic changes represent an important genetic mechanism in schizophrenia that may also have congenital and later onset medical conditions as part of their expression. The associated genomic disorders present opportunities for research findings to be directly translated into clinical practice. 22q11.2 Deletion Syndrome (22q11.2DS) is the prototype of these multisystem disorders. The associated 22q11.2 deletion is the first and most powerful molecular risk factor identified for schizophrenia. Animal (e.g., mouse) models are available and can confirm and extend human research discoveries, including those related to physical illness, cognitive functioning, brain imaging, neuropathology and treatment response.
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Lisanne Vervoort,Nicolas Dierckxsens, Marta Sousa Santos, Senne Meynants,Erika Souche, Ruben Cools,Tracy Heung,Koen Devriendt,Hilde Peeters,Donna M. McDonald-McGinn,Ann Swillen,Jeroen Breckpot,
bioRxiv the preprint server for biology (2024)
Alexandra Finless,Andrea L. Rideout,Ting Xiong, Holly Carbyn,Patricia Lingley-Pottie,Lisa D. Palmer,Andrea Shugar,Donna M. McDonald-McGinn,Patrick J. McGrath,Anne S. Bassett,Cheryl Cytrynbaum,Matt Orr,
EUROPEAN JOURNAL OF PSYCHOTRAUMATOLOGYno. 1 (2024): 2353532-2353532
Neurological Sciencespp.1-6, (2024)
Kaitlin J. Stanley,Kelsey J. Kalbfleisch, Olivia M. Moran,Rajiv R. Chaturvedi,Maian Roifman, Xin Chen,Roozbeh Manshaei,Nicole Martin, Simina McDermott,Vanda McNiven,Diane Myles-Reid,Lynne E. Nield,
EUROPEAN JOURNAL OF HUMAN GENETICSno. 7 (2024): 795-803
npj Genomic Medicineno. 1 (2023): 17-17
Neurology. Geneticsno. 6 (2023): e200105-e200105
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#Papers: 410
#Citation: 18822
H-Index: 67
G-Index: 130
Sociability: 8
Diversity: 4
Activity: 50
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