Author

Yong Huang

University of VirginiaORCID 0009-0001-1989-8223Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Yong Huang6 papers · BioArctic Neuroscience (Sweden)

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Approach:Bayesian inference· 1 Research Focus:benchmarking· 1 Research Focus:differential expression· 1 Approach:machine learning (classical)· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Aitana Alonso-GonzáleziD· 2 shared Ayodeji AdegunsoyeiD· 2 shared Carlos FloresiD· 2 shared Christine Kim GarciaiD· 2 shared David JáspeziD· 2 shared David ZhangiD· 2 shared Emma StricklandiD· 2 shared Gisli R. JenkinsiD· 2 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Aitana Alonso-GonzálezORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintApr 18, 2026

Polygenic risk scores enhance the identification of carriers of monogenic forms of idiopathic pulmonary fibrosis

Aitana Alonso-González, David Jáspez, Jose Miguel Lorenzo-Salazar…·Carlos Flores

This study shows that polygenic risk scores improve the identification of IPF patients carrying rare variants associated with monogenic pulmonary fibrosis.

1 citation

humanwhole-genome sequencing

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Genetic & Genomic MedicinemedRxivPreprintOct 12, 2024

Rare variants and survival of patients with idiopathic pulmonary fibrosis

Aitana Alonso-González, David Jáspez, Jose Miguel Lorenzo-Salazar…·Carlos Flores

This study investigates the impact of rare variants and polygenic risk scores on survival in idiopathic pulmonary fibrosis patients, finding that rare variants are associated with worse outcomes.

2 citations

humanwhole-genome sequencing

𝕏 PostBluesky