World's Best Scientists 2026 revealed!

D-Index & Metrics

Biology and Biochemistry

D-Index
57
Citations
12425
World Ranking
13785
National Ranking
5835

Overview

Hui Wang is affiliated with the Salk Institute for Biological Studies in the United States. Their research primarily spans the field of Medicine, with substantial contributions across key subfields including Pediatrics, Perinatology and Child Health, Molecular Biology, Surgery, Immunology, and Endocrinology, Diabetes and Metabolism.

The scientist's work covers a range of main topics, such as Birth, Development, and Health; Reproductive System and Pregnancy; Pregnancy and Preeclampsia Studies; Osteoarthritis Treatment and Mechanisms; Neonatal Respiratory Health Research; Pregnancy and Medication Impact; and Stress Responses and Cortisol.

Hui Wang's recent published papers reflect a focus on osteoarthritis, neurological conditions, and cancer progression. Notable publications include:

  • "Hyperglycemia-induced accumulation of advanced glycosylation end products in fibroblast-like synoviocytes promotes knee osteoarthritis" (2021), published in Experimental & Molecular Medicine
  • "Identification of the skeletal progenitor cells forming osteophytes in osteoarthritis" (2020), published in Annals of the Rheumatic Diseases
  • "Predictive role of heterozygous p.R4810K of RNF213 in the phenotype of Chinese moyamoya disease" (2020), published in Neurology
  • "Agrin induces long-term osteochondral regeneration by supporting repair morphogenesis" (2020), published in Science Translational Medicine
  • "MiR-210-3p-EphrinA3-PI3K/AKT axis regulates the progression of oral cancer" (2020), published in Journal of Cellular and Molecular Medicine

Collaborations with frequent co-authors show a network of ongoing research partnerships. Regular collaborators include Liaobin Chen, Dan Xu, Yinxian Wen, Yu Guo, and Wen Hu, indicating a cooperative approach in their scientific contributions.

The distribution of their published work includes numerous articles in journals such as:

  • SSRN Electronic Journal
  • Biochemical Pharmacology
  • Toxicology Letters
  • Research Square (Research Square)
  • Food and Chemical Toxicology

Best Publications

  • Evolutionary and biomedical insights from the rhesus macaque genome

    Richard A. Gibbs;Jeffrey Rogers

  • Epigenomic Profiling of Young and Aged HSCs Reveals Concerted Changes during Aging that Reinforce Self-Renewal

    Deqiang Sun;Min Luo;Mira Jeong;Benjamin Rodriguez

  • TET2 mutations predict response to hypomethylating agents in myelodysplastic syndrome patients.

    Rafael Bejar;Allegra Lord;Kristen Stevenson;Michal Bar-Natan

  • Nova regulates brain-specific splicing to shape the synapse

    Jernej Ule;Aljaž Ule;Joanna Spencer;Alan Williams

  • Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling

    Moumita Chaki;Rannar Airik;Amiya K. Ghosh;Rachel H. Giles

  • Discovery of tissue-specific exons using comprehensive human exon microarrays

    Tyson A Clark;Anthony C Schweitzer;Tina X Chen;Michelle K Staples

  • SVA elements : A hominid-specific retroposon family

    Hui Wang;Jinchuan Xing;Deepak Grover;Dale J. Hedges

  • Human genomic deletions mediated by recombination between Alu elements.

    Shurjo K. Sen;Kyudong Han;Jianxin Wang;Jungnam Lee

  • Role for CD47-SIRPα signaling in xenograft rejection by macrophages

    Kentaro Ide;Hui Wang;Hiroyuki Tahara;Jianxiang Liu

  • Large conserved domains of low DNA methylation maintained by Dnmt3a.

    Mira Jeong;Deqiang Sun;Min Luo;Yun Huang

  • Genome-wide RNAi screen reveals a specific sensitivity of IRES-containing RNA viruses to host translation inhibition

    Sara Cherry;Tammy Doukas;Susan Armknecht;Sean Whelan

  • Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements

    Feng Wang;Hui Wang;Han Fang Tuan;Duy H. Nguyen

  • Unusual intron conservation near tissue-regulated exons found by splicing microarrays.

    Charles W Sugnet;Karpagam Srinivasan;Tyson A Clark;Georgeann O'Brien

  • Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration

    Robert K Koenekoop;Hui Wang;Jacek Majewski;Xia Wang

  • Emergence of primate genes by retrotransposon-mediated sequence transduction.

    Jinchuan Xing;Hui Wang;Victoria P. Belancio;Richard Cordaux

  • Toll-like receptor alterations in myelodysplastic syndrome

    Yue Wei;Sophie Dimicoli;Carlos Bueso-Ramos;Rui Chen

  • HSP90-buffered genetic variation is common in Arabidopsis thaliana

    Todd A. Sangster;Neeraj Salathia;Hana N. Lee;Etsuko Watanabe

  • The Drosophila melanogaster transcriptome by paired-end RNA sequencing

    Bryce Daines;Hui Wang;Liguo Wang;Yumei Li

  • Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencing

    Xia Wang;Hui Wang;Hui Wang;Vincent Sun;Han Fang Tuan

  • 5'-transducing SVA retrotransposon groups spread efficiently throughout the human genome

    Annette Damert;Julija Raiz;Axel V. Horn;Johannes Löwer

Frequent Co-Authors

Rui Chen
Rui Chen Capital Medical University
Yong-Guang Yang
Yong-Guang Yang Jilin University
Robert K. Koenekoop
Robert K. Koenekoop McGill University Health Centre
Megan Sykes
Megan Sykes Columbia University
Jinchuan Xing
Jinchuan Xing Rutgers, The State University of New Jersey
Mark A. Batzer
Mark A. Batzer Louisiana State University
Richard A. Gibbs
Richard A. Gibbs Baylor College of Medicine
Wei Li
Wei Li Harvard University
Kang Zhang
Kang Zhang Macau University of Science and Technology
Tyson A. Clark
Tyson A. Clark Pacific Biosciences (United States)

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