Siwei Chen

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 4

Top Topics

Mitochondrial Dna

Attention Deficit Hyperactivity Disorder

Top Venues

medRxiv : the preprint server for health sciences

Molecular autism

This page only lists publications with an associated author ORCID identifier.

Publications

null null, Siwei Chen, Benjamin M Neale, Samuel Frank Berkovic
Shared and distinct ultra-rare genetic risk for diverse epilepsies: A whole-exome sequencing study of 54,423 individuals across multiple genetic ancestries. medRxiv : the preprint server for health sciences (2023)
null null, Siwei Chen, Benjamin M Neale, Samuel Frank Berkovic
Shared and distinct ultra-rare genetic risk for diverse epilepsies: A whole-exome sequencing study of 54,423 individuals across multiple genetic ancestries. medRxiv : the preprint server for health sciences (2023)
null null, Siwei Chen, Benjamin M Neale, Samuel Frank Berkovic
Shared and distinct ultra-rare genetic risk for diverse epilepsies: A whole-exome sequencing study of 54,423 individuals across multiple genetic ancestries. medRxiv : the preprint server for health sciences (2023)
Siwei Chen, Jiebiao Wang, A Ercument Cicek, Kathryn Roeder, Haiyuan Yu, Bernie Devlin
De novo missense variants disrupting protein-protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types. Molecular autism 11 (1) (2020)