Author

Chi‐Hsin Hsu

Tri-Service General HospitalORCID 0000-0003-4318-7007Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetics· 2 Cancer Biology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Approach:statistical model· 3 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Approach:machine learning (classical)· 1

Frequent Co-Authors

Chih-Fen HuiD· 2 shared Feng-Chin Lee· 2 shared Jau‐Shyong HongiD· 2 shared San‐Pin WuiD· 2 shared Shih‐Ming HuangiD· 2 shared Cheng‐Han TsaiiD· 1 shared G. W. Gant LuxtoniD· 1 shared Pei-Ching ChangiD· 1 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetics

Chih-Fen HuORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Cancer BiologybioRxivPreprintSep 28, 2024

Distinct neuroendocrine subtypes predict treatment-induced neuroendocrine prostate cancer prognosis and provide clues for personalized treatment

Yung-Chih Hong, Cheng‐Han Tsai, Tze-Yun Hu…·Pei-Ching Chang

The paper identifies distinct neuroendocrine subtypes in CRPC using single-cell RNA sequencing and links them to prognosis and treatment response.

DOI 10.1101/2024.09.28.615561

𝕏 PostBluesky

GeneticsbioRxivPreprintMar 15, 2020

Whole exome sequencing identifies novel DYT1 dystonia-associated genome variants as potential disease modifiers

Chih-Fen Hu, G. W. Gant Luxton, Feng-Chin Lee…·San‐Pin Wu

The paper identifies novel genome variants associated with DYT1 dystonia through whole exome sequencing and suggests they may modify disease penetrance.

1 citation

humanwhole-exome sequencing

𝕏 PostBluesky

GeneticsbioRxivPreprintOct 17, 2019

Association of SYNE2 variants in accelerating the progress of DYT1 early-onset isolated dystonia

Feng-Chin Lee, San‐Pin Wu, Chi‐Hsin Hsu…·Chih-Fen Hu

The paper identifies SYNE2 variants associated with earlier onset of DYT1 dystonia by affecting TOR1A-SYNE2 protein interactions in a family with TOR1A mutations.

3 citations

humanwhole-exome sequencing

𝕏 PostBluesky