Proteome-wide identification of HSP70/HSC70 chaperone clients in human cellsSeung Woo Ryu, Tanya T. Paull|PLoS Biology|2020Cited by 78
Exome sequencing of 18,994 ethnically diverse patients with suspected rare Mendelian disordersHeonjong Han, Hane Lee, Seung Woo Ryu et al.|npj Genomic Medicine|2025Cited by 8
Identification of a complex intrachromosomal inverted insertion in the long arm of chromosome 9 as a cause of tuberous sclerosis complex in a Korean familySeung Woo Ryu, Beom Hee Lee, Hane Lee et al.|Molecular Genetics & Genomic Medicine|2024Cited by 2
Comprehensive identification of HSP70/HSC70 Chaperone Clients in Human CellsSeung Woo Ryu, Tanya T. Paull|bioRxiv (Cold Spring Harbor Laboratory)|2019Cited by 2
Clinical utility of genome sequencing in rare diseases: lessons from a single-center study of 1,452 Korean familiesSeungbok Lee, Jong‐Hee Chae, Jangsup Moon et al.|npj Genomic Medicine|2025Cited by 2