IRCN will hold two-day joint workshop with our collaboration partner, NCCR synapsy.
Copy number variations in chromosome 22q underlie several forms of cognitive impairment, including schizophrenia (22q11) and autism spectrum disorder (22q13). Distinct mutations of even the same Shank3 gene can contribute to different disorders of psychosis and autism. This workshop will feature overlapping expertise in the dissection and understanding of 22q syndromes across Centers. By sharing insights, IRCN will seek to identify mutual areas of investigation for future collaboration across cultures and animal models.
Date: July 6-7, 2019
Venue: IRCN Seminar Room@13F, Faculty of Medicine Experimental Research Building, School of Medicine, Hongo Campus
9:00 Alexandre Dayer (NCCR Synapsy)
9:35 Takao Hensch (IRCN)
Session 1: Schizophrenia
10:30 Stefan Eliez (22q11DS cohort)
11:15 Kiyoto Kasai (AMED / ACMP cohort)
13:30 Alan Carleton (2211DS mouse model)
14:15 Kazuyuki Aihara (computational DNB)
15:30 Schizophrenia Breakout Session
Session 2: Autism
9:00 Marie Schaer (ASD cohort)
9:45 Camilla Bellone (Shank3 physiology)
11:00 Guoping Feng (Shank3 models)
11:45 Yukiko Gotoh (new ASD model)
14:00 ASD Breakout session
16:00 Integration & Closing
Registration: IRCN Members: Please register online. Other participants: Please register on site.
For more information: IRCN Administrative office email@example.com
Details are below or click here(PDF).