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Molecular Biology

D-Index
50
Citations
8588
World Ranking
2575
National Ranking
72

Overview

Xiangyin Kong is affiliated with the Chinese Academy of Sciences in China and has conducted extensive research in the fields of biochemistry, genetics, molecular biology, and medicine. Their work spans multiple subfields, including molecular biology, oncology, immunology, cancer research, and pulmonary and respiratory medicine.

The scientist has contributed to research focusing on topics such as immune cell function and interaction, cancer immunotherapy and biomarkers, pancreatic and hepatic oncology research, immunotherapy and immune responses, epigenetics and DNA methylation, cancer-related molecular mechanisms, and cancer-related molecular pathways.

Notable recent papers authored by Xiangyin Kong include:

  • "Tumor microbiome contributes to an aggressive phenotype in the basal-like subtype of pancreatic cancer" (2021) published in Communications Biology
  • "A novel long noncoding RNA SP100-AS1 induces radioresistance of colorectal cancer via sponging miR-622 and stabilizing ATG3" (2022) published in Cell Death and Differentiation
  • "PI3Kα inhibitor CYH33 triggers antitumor immunity in murine breast cancer by activating CD8+T cells and promoting fatty acid metabolism" (2021) published in Journal for ImmunoTherapy of Cancer
  • "Scd1 controls de novo beige fat biogenesis through succinate-dependent regulation of mitochondrial complex II" (2020) published in Proceedings of the National Academy of Sciences
  • "CST6 protein and peptides inhibit breast cancer bone metastasis by suppressing CTSB activity and osteoclastogenesis" (2021) published in Theranostics

Xiangyin Kong regularly publishes in several scientific venues, with multiple contributions in Cell Death and Disease, Advanced Science, and Frontiers in Genetics, as well as publications in Communications Biology and Cell Death and Differentiation.

Frequent collaborators include:

  • Landian Hu
  • Yuchao Zhang
  • Yufei Zhu
  • Jing-Yu Lang
  • Qingyang Ma

Best Publications

  • Molecular Evolution of the SARS Coronavirus, during the Course of the SARS Epidemic in China

    Jian Feng He;Guo Wen Peng;Jun Min;De Wen Yu

  • Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP

    Shangxi Xiao;Shangxi Xiao;Chuan Yu;Xueming Chou;Wenjuan Yuan

  • Predicting drug-target interaction networks based on functional groups and biological features.

    Zhisong He;Jian Zhang;Xiao-He Shi;Le-Le Hu

  • Embryonic stem cells generated by nuclear transfer of human somatic nuclei into rabbit oocytes

    Ying Chen;Zhi Xu He;Ailian Liu;Kai Wang

  • Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract.

    Lei Bu;Yiping Jin;Yuefeng Shi;Renyuan Chu

  • miR-124 is frequently down-regulated in medulloblastoma and is a negative regulator of SLC16A1.

    Kay Ka Wai Li;Jesse Chung sean Pang;Arthur Ka keung Ching;Chun Kwok Wong

  • Simple sequence repeat-based consensus linkage map of Bombyx mori

    Xue-Xia Miao;Shi-Jie Xub;Ming-Hui Li;Mu-Wang Li

  • Analysis and prediction of the metabolic stability of proteins based on their sequential features, subcellular locations and interaction networks.

    Tao Huang;Xiao-He Shi;Ping Wang;Zhisong He

  • Genes that Escape X-Inactivation in Humans Have High Intraspecific Variability in Expression, Are Associated with Mental Impairment but Are Not Slow Evolving

    Yuchao Zhang;Atahualpa Castillo-Morales;Min Jiang;Yufei Zhu

  • Triphalangeal thumb–polysyndactyly syndrome and syndactyly type IV are caused by genomic duplications involving the long range, limb-specific SHH enhancer

    M. Sun;X. Zeng;Q. Liu

  • Loss-of-Function Mutations in the PRPS1 Gene Cause a Type of Nonsyndromic X-linked Sensorineural Deafness, DFN2

    Xuezhong Liu;Xuezhong Liu;Dongyi Han;Jianzhong Li;Bing Han

  • Gene Ontology and KEGG Pathway Enrichment Analysis of a Drug Target-Based Classification System.

    Lei Chen;Chen Chu;Jing Lu;Xiangyin Kong

  • A 3-nucleotide deletion in the polypyrimidine tract of intron 7 of the DFNA5 gene causes nonsyndromic hearing impairment in a Chinese family.

    Chuan Yu;Xiangming Meng;Shanfang Zhang;Guoping Zhao

  • Prediction and analysis of cell‑penetrating peptides using pseudo‑amino acid composition and random forest models

    Lei Chen;Lei Chen;Chen Chu;Tao Huang;Xiangyin Kong

  • A New Locus for Hereditary Gingival Fibromatosis (GINGF2) Maps to 5q13–q22

    Shangxi Xiao;Shangxi Xiao;Lei Bu;Lei Bu;Liqin Zhu;Guangyong Zheng

  • Genome-Wide Interaction-Based Association Analysis Identified Multiple New Susceptibility Loci for Common Diseases

    Yang Liu;Haiming Xu;Suchao Chen;Xianfeng Chen

  • Alternative promoters influence alternative splicing at the genomic level.

    Dedong Xin;Landian Hu;Landian Hu;Xiangyin Kong;Xiangyin Kong

  • Tumor microbiome contributes to an aggressive phenotype in the basal-like subtype of pancreatic cancer

    Wei Guo;Wei Guo;Yuchao Zhang;Yuchao Zhang;Shiwei Guo;Zi Mei

  • Prediction of deleterious non-synonymous SNPs based on protein interaction network and hybrid properties

    Tao Huang;Ping Wang;Zhiqiang Ye;Heng Xu

  • Noisy splicing, more than expression regulation, explains why some exons are subject to nonsense-mediated mRNA decay

    Zhenguo Zhang;Zhenguo Zhang;Dedong Xin;Ping Wang;Ping Wang;Li Zhou;Li Zhou

Frequent Co-Authors

Yu-Dong Cai
Yu-Dong Cai Shanghai University
Tao Huang
Tao Huang Chinese Academy of Sciences
Lei Chen
Lei Chen Shanghai Maritime University
Guoping Zhao
Guoping Zhao Chinese Academy of Sciences
Heng Xu
Heng Xu University of Florida
Laurence D. Hurst
Laurence D. Hurst University of Bath
Ning Zhang
Ning Zhang Tsinghua University
Kuo-Chen Chou
Kuo-Chen Chou The Gordon Life Science Institute
Wei Huang
Wei Huang Shanghai Jiao Tong University
Mingyue Zheng
Mingyue Zheng Chinese Academy of Sciences

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