Harnessing rare variants in neuropsychiatric and neurodevelopment disorders-a Keystone Symposia report

Cable, J., Purcell, R. H., Robinson, E., Vorstman, J. A. S., Chung, W. K., Constantino, J. N., Sanders, S. J., Sahin, M., Dolmetsch, R. E., Shah, B. M., Thurm, A., Martin, C. L., Bearden, C. E., & Mulle, J. G. (2021). Harnessing rare variants in neuropsychiatric and neurodevelopment disorders—a Keystone Symposia report. Annals of the New York Academy of Sciences, 1506(1), 5–17. Portico. https://doi.org/10.1111/nyas.14658
Authors:
Jennifer Cable
Ryan H Purcell
Elise Robinson
Jacob A S Vorstman
Wendy K Chung
John N Constantino
Stephan J Sanders
Mustafa Sahin
Ricardo E Dolmetsch
Bina Maniar Shah
Audrey Thurm
Christa L Martin
Carrie E Bearden
Jennifer G Mulle
Affiliated Authors:
Wendy K Chung
Author Keywords:
autism
autism heterogeneity
autism spectrum disorder
copy number variant
intellectual disability
neurodevelopmental disorders
neuropsychiatric disorders
polygenic risk score
rare variants
schizophrenia
3q29 deletion
tsc
16p11
2 deletion
22q11
16p11.2 deletion
22q11.2 deletion
Publication Type:
Article
Unique ID:
10.1111/nyas.14658
PMID:
Publication Date:
Data Source:
PubMed

Record Created: