Zhaoqi B. Liu
Beijing, China
Last Updated: 09/26/2026
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Found 47 publications
Spliceosomal mutation drives melanoma tumorigenesis via lineage-specific RAS activation.
Journal: Science advances
Published: May 01, 2026
Genetic evidence supports the combined targeting of lipoprotein(a) and LDL cholesterol to reduce coronary artery disease risk.
Journal: Nature cardiovascular research
Published: March 01, 2026
Oncogenic DHX15 mutation enhances mitochondrial metabolism and sustains leukemia stemness.
Journal: Leukemia
Published: January 29, 2026
SAA1 Promotes Pro-inflammatory Macrophage-mediated Bone Invasion in Silent Corticotroph Adenomas.
Journal: Genomics, proteomics & bioinformatics
Published: December 02, 2025
Contributions of Common, Rare, and Somatic Genetic Variants to Incidence of Atrial Fibrillation.
Journal: JAMA cardiology
Published: October 08, 2025
Ultra-precision deconvolution of spatial transcriptomics decodes immune heterogeneity and fate-defining programs in tissues.
Journal: Nature communications
Published: September 25, 2025
HELIX: a scalable model for predicting context-dependent regulation of RNA splicing and isoform usage.
Journal: Nature computational science
Published: September 03, 2025
Sequence-dependent splicing dysregulation drives therapy resistance in pediatric AML.
Journal: Cell reports. Medicine
Published: May 21, 2025
SUGP1 loss is the sole driver of SF3B1 hotspot mutant missplicing in cancer.
Journal: bioRxiv : the preprint server for biology
Published: March 03, 2025
An integrated germline and somatic genomic model for coronary artery disease.
Journal: Nature communications
Published: February 21, 2025
SUGP1 loss drives SF3B1 hotspot mutant missplicing in cancer.
Journal: Cell reports
Published: February 18, 2025
Last Updated: 09/26/2026