Area of research
Genetics · Artificial Intelligence
Research interest
Research interests include Genetic Associations and Epidemiology, AI in cancer detection, Medical Image Segmentation Techniques, and Pituitary Gland Disorders and Treatments.
Multi-task learning-based histologic subtype classification of non-small cell lung cancer
Towards label-efficient automatic diagnosis and analysis: a comprehensive survey of advanced deep learning-based weakly-supervised, semi-supervised and self-supervised techniques in histopathological image analysis
DGMIL: Distribution Guided Multiple Instance Learning for Whole Slide Image Classification
Energy Transfer Mediated Enhancement of Room‐Temperature Phosphorescence of Carbon Dots Embedded in Matrixes
Multiemissive Room-Temperature Phosphorescent Carbon Dots@ZnAl<sub>2</sub>O<sub>4</sub> Composites by Inorganic Defect Triplet-State Energy Transfer
Recyclable and Fluorescent Epoxy Polymer Networks from Cardanol Via Solvent-Free Epoxy-Thiol Chemistry
Clinically significant genomic alterations in the Chinese and Western patients with intrahepatic cholangiocarcinoma
Clinically Significant Shared and Distinct Genomic Alterations in Chinese and Western Patients with Intrahepatic Cholangiocarcinoma
Integrated Proteogenomic Characterization of HBV-Related Hepatocellular Carcinoma
Identification of recurrent USP48 and BRAF mutations in Cushing’s disease
Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia
Germline Mutations in CDH23, Encoding Cadherin-Related 23, Are Associated with Both Familial and Sporadic Pituitary Adenomas
The genome-wide mutational landscape of pituitary adenomas
Genome-Wide Association Study of Bladder Cancer in a Chinese Cohort Reveals a New Susceptibility Locus at 5q12.3
Alteration of the Intra- and Cross- Hemisphere Posterior Default Mode Network in Frontal Lobe Glioma Patients
Recurrent gain-of-function USP8 mutations in Cushing's disease
Genome-wide Analysis of the Role of Copy Number Variation in Schizophrenia Risk in Chinese
Common variants at 10p12.31, 10q21.1 and 13q12.13 are associated with sporadic pituitary adenoma