ICPS
2019 International Convention of Psychological Science
Structural and Functional Brain Abnormalities in 16p11.2, 22q11.2, 1q21.1, and Other High-Risk Copy Number Variants
16p11.2, 22q11.2, and 1q21.1 are rare high-risk copy number variants (CNVs) associated with various neurodevelopmental disorders including intellectual disability, autism, and schizophrenia. Using different imaging techniques (e.g., EEG, MEG-MRS, MRI), paradigms, and animal models, we examine the impact of these and other rare high-risk CNVs on brain structure and function.
Chairs & Discussants
- Reem Al-JawahiriChair
University of Sheffield - Ana SilvaDiscussant
Cardiff University
Presentations
- Complexity and Power Spectral Density in 16p11.2 Deletion Human and MouseReem Al-Jawahiri, Myles Jones, Alessandro Gozzi, Marco Pagani, Cornelius Gross, Maria Esteban Masferrer, et al.
- The Neurodevelopmental 16p11.2 CNVs Have, As Yet Overlooked, Mirror Effect on Sexual Development in Humans and Animal ModelsKatrin Mannik, Maarja Lepamets, Anna Mikhaleva, Kaido Lepik, Zachary Kupchinsky, H. Ademi, et al.
- Enigma-CNV: Unraveling the Effects of Rare CNVs on Brain StructureIda Elken Sønderby, Bragi Walters, Dennis van der Meer, Srdjan Djurovic, Ingrid Melle, Lars Tjelta Westlye, et al.
- Excitatory-Inhibitory Balance in 22q11.2 Deletion Syndrome: A Magnetoencephalography Study and Pilot Magnetic Resonance Spectroscopy StudyJoanne Doherty, Michael Owen, David Linden, Krish Singh, Marianne van den Bree
