Author
University of California San DiegoORCID 0000-0003-4196-4749Unclaimed ORCID profile · follow to get notified of new preprints
7 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.
Danny Antaki, James Guevara, Adam X. Maihofer…·Jonathan L. Sebat
This study shows that autism spectrum disorder risk is influenced by rare variants, polygenic risk, and sex, with sex-specific effects on genetic liability and behavioral traits.
Martin W. Breuss, Danny Antaki, Renee D. George…·Joseph G. Gleeson
The paper quantifies autism recurrence risk by detecting paternal sperm mosaicism through single molecule genotyping and whole genome sequencing.
Yuqi Qiu, Thomas Arbogast, Sandra Martín Lorenzo…·Jonathan L. Sebat
The paper investigates the oligogenic effects of 16p11.2 copy number variation on craniofacial development across species, showing that individual genes and their combinations influence facial structure.
William M. Brandler, Danny Antaki, Madhusudan Gujral…·Jonathan L. Sebat
This study identifies rare paternally-inherited structural variants contributing to autism by disrupting noncoding regions and coding genes, with differential parental contributions.
William M Brandler, Danny Antaki, Madhusudan Gujral…·Jonathan Sebat
The paper identifies 1.2 million structural variants in 235 individuals, showing high de novo mutation diversity and complex mutation clusters, but finds no increased genome rearrangement rate for ASD.