Author
Sheppard Pratt Health SystemORCID 0000-0003-3800-2864Unclaimed ORCID profile · follow to get notified of new preprints
Mutual co-authors in cluster
5 papers
Recent·Most cited
Omar Shanta, Marieke Klein, Molly Sacks…·Annette M. Hartmann
The paper identifies novel CNV loci and dose-dependent gene effects across six psychiatric disorders using genome-wide analysis.
Worrawat Engchuan, Omar Shanta, Kuldeep Kumar…·Michael Foster Green
The paper identifies shared and divergent genetic mechanisms across psychiatric disorders using gene-set burden analysis of copy number variants.
Epi25 Collaborative, Siwei Chen, Bassel W Abou-Khalil…·Alica M. Goldman
This study identifies shared and distinct ultra-rare genetic risk factors for epilepsy subtypes using whole-exome sequencing of 20,979 patients and 33,444 controls.
Vassily Trubetskoy, Antonio F. Pardiñas, Ting Qi…·Elliot S. Gershon
A genome-wide association study of 69,369 schizophrenia cases and 236,642 controls identifies 270 risk loci, prioritizes 130 genes, and links common and rare risk variants to neuronal synaptic biology.
Duncan S. Palmer, Daniel P. Howrigan, Sinéad B. Chapman…·Benjamin M. Neale
The paper reports exome sequencing findings in bipolar disorder, identifying AKAP11 as a shared risk gene with schizophrenia through ultra-rare protein-truncating variants.