Ying Zhu

Chinese University of Hong Kong — China

Biochemistry, Genetics and Molecular Biology · Life Sciences

22h-index2.1kcitations67works0.52yr avg
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Research Topics

Muscle Physiology and Disorders(11), Biofuel production and bioconversion(9), Photosynthetic Processes and Mechanisms(9), RNA Research and Splicing(9), Microbial Metabolic Engineering and Bioproduction(8)

Publications67 total

Ataxin-2 Coordinates Neuronal and Glial Pathways to Promote Neuroprotection
2025Open Access
Eucommia alleviates high fat diet-induced MASLD via the F. prausnitzii/butyrate/GPR43/GLP-1 signaling
Journal of Ethnopharmacology·2025
Decoding the Han paternal legacy: a Y chromosomal genealogy of Xuzhou as the cradle of the Han civilization
Anthropologischer Anzeiger·2025
Author Correction: A plant Bro1 domain protein BRAF regulates multivesicular body biogenesis and membrane protein homeostasis
Nature Communications·2025Open Access
Nationwide, Couple-Based Genetic Carrier Screening
Obstetric Anesthesia Digest·2025
Local Search-Based Attribute Reduction Approach for Neighborhood Rough Sets Using Hash Hypercube
SSRN Electronic Journal·2025Open Access
Structure-Enhanced Protein Instruction Tuning: Towards General-Purpose Protein Understanding with LLMs
arXiv (Cornell University)·2024Open Access
Reversal of injury-associated retinal ganglion cell gene expression by a phosphodiesterase anchoring disruptor peptide
Experimental Eye Research·2024Open Access
Table of Contents
Genetics in Medicine·2024
A DNA-Programmed Cargo Distributing System in Living Cells
CCS Chemistry·2024· 3 citedOpen Access
Clinical and genetic interpretation of uncertain DMD missense variants: evidence from mRNA and protein studies
Orphanet Journal of Rare Diseases·2024· 2 citedOpen Access
Clinical study and genetic analysis of Cornelia de Lange syndrome caused by a novel <scp>MAU2</scp> gene variant in a Chinese boy
Molecular Genetics & Genomic Medicine·2023· 3 citedOpen Access
Integration of <scp>EpiSign</scp>, facial phenotyping, and likelihood ratio interpretation of clinical abnormalities in the re‐classification of an <scp><i>ARID1B</i></scp> missense variant
American Journal of Medical Genetics Part C Seminars in Medical Genetics·2023· 7 citedOpen Access
A natural gene drive system confers reproductive isolation in rice
Cell·2023· 60 citedOpen Access
[Analysis of 4 children with DYNC1H1 gene related spinal muscular atrophy with lower extremity predominant 1].
PubMed·2023
Seizures and EEG characteristics in a cohort of pediatric patients with dystroglycanopathies
Seizure·2022· 12 cited
The plant ESCRT component FREE1 regulates peroxisome-mediated turnover of lipid droplets in germinating <i>Arabidopsis</i> seedlings
The Plant Cell·2022· 25 citedOpen Access
Thigh MRI in antisynthetase syndrome, and comparisons with dermatomyositis and immune-mediated necrotizing myopathy
Lara D. Veeken·2022· 19 cited
PIGV P.L472p mutation identified by exome sequencing in a neonate with a glycosylation disorder confirmed by flow cytometry
Pathology·2022
Correlation of vacuole morphology with stomatal lineage development by whole-cell electron tomography
PLANT PHYSIOLOGY·2022· 29 citedOpen Access
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Frequent Co-authors

Yun Yuan(8), Liwen Jiang(7), Wei Zhang(6), Jiangxi Xiao(6), Shang‐Tian Yang(5), Qiong Zhao(5), Binbin Wang(5), Yunxia Cao(5), Tony Roscioli(5), Zhaoxia Wang(5), Jinbo Shen(4), Beili Chen(4), Wenhan Cao(4), Shuxian Huang(4), Yong Cui(4), Meng Yu(4), Yonglun Zeng(3), Caiji Gao(3), Kerith‐Rae Dias(3), Edwin P. Kirk(3)