O25: Bridging the neurodevelopmental diagnostic gap: A comprehensive multi-omics approach for transcriptomics and proteomics outliers with exome reanalysis
Brian Hon‐Yin Chung(Long Island Jewish Medical Center), Vicente A. Yépez(Technical University of Munich), Ines F. Scheller(Technical University of Munich), Sheila Suet-Na Wong, Anna Ka Yee Kwong(University of Hong Kong), Cheuk‐Wing Fung(Queen Mary Hospital), Christopher CY Mak(University of Hong Kong), Martin Man Chun Chui(Chinese University of Hong Kong)
Cited by 0
Related Papers
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
|Nature Genetics|2022|613
Meta-analysis Followed by Replication Identifies Loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as Associated with Systemic Lupus Erythematosus in Asians
|The American Journal of Human Genetics|2012|232
Clinical implementation of RNA sequencing for Mendelian disease diagnostics
|Genome Medicine|2022|215
A dyadic approach to the delineation of diagnostic entities in clinical genomics
|The American Journal of Human Genetics|2021|116