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Fengyu Che

Observed names: Che, Fengyu, F Y Che
ORCID: 0000-0002-5589-0755
Observed ORCID: 0000-0002-5589-0755
OpenAlex ID: A5049433205
A Newly Identified Missense Mutation inFARS2Causes Autosomal-Recessive Spastic Paraplegia
2015 · Ying Yang, Wei Liu, et al. · Human Mutation · 58
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Novel Aptamer-Functionalized Nanoparticles Enhances Bone Defect Repair By Improving Stem Cell Recruitment
2019 · Meng Wang, Haibin Wu, et al. · International Journal of Nanomedicine · 38
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A Novel pH-Sensitive Multifunctional DNA Nanomedicine: An Enhanced and Harmless GD2 Aptamer-Mediated Strategy for Guiding Neuroblastoma Antitumor Therapy
2021 · Liyu Zhang, Meng Wang, et al. · International Journal of Nanomedicine · 27
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mGluR5 mediates ketamine antidepressant response in susceptible rats exposed to prenatal stress
2020 · Yi Wang, Wei He, et al. · Journal of Affective Disorders · 20
A GD2-aptamer-mediated, self-assembling nanomedicine for targeted multiple treatments in neuroblastoma theranostics
2021 · Liyu Zhang, Meng Wang, et al. · Molecular Therapy — Nucleic Acids · 18
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Identification of two novel variants of the BCL11B gene in two Chinese pedigrees associated with neurodevelopmental disorders
2022 · Fengyu Che, Xiaoling Tie, et al. · Frontiers in Molecular Neuroscience · 15
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Mutational Analysis of TYR , OCA2, and SLC45A2 Genes in Chinese Families with Oculocutaneous Albinism
2019 · Ye Lin, Xihui Chen, et al. · Molecular Genetics & Genomic Medicine · 14
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First report of paternal uniparental disomy of chromosome 8 with SLC52A2 mutation in Brown-vialetto-van laere syndrome type 2 and an analysis of genotype-phenotype correlations
2022 · Siyu Zhao, Fengyu Che, et al. · Frontiers in Genetics · 13
RETRACTED: SS30, a novel thioaptamer targeting CD123, inhibits the growth of acute myeloid leukemia cells
2019 · Meng Wang, Haibin Wu, et al. · Life Sciences · 13
A Novel Heterozygous Pathogenic Variation in CYCS Gene Cause Autosomal Dominant Non-Syndromic Thrombocytopenia 4 in a Large Chinese Family
2022 · Fengyu Che, Jiangang Zhao, et al. · Frontiers in Genetics · 11
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Novel Compound Heterozygous Pathogenic Variants in SUOX Cause Isolated Sulfite Oxidase Deficiency in a Chinese Han Family
2021 · Jiangang Zhao, Yao An, et al. · Frontiers in Genetics · 9
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CD123 thioaptamer protects against sepsis via the blockade between IL-3/CD123 in a cecal ligation and puncture rat model
2020 · Jiangang Zhao, Meng Wang, et al. · Nucleosides Nucleotides & Nucleic Acids · 8
Lethal variant in the C2A domain may cause severe SYT1-associated neurodevelopmental disorder in the newborns
2023 · Wendi Huang, Ying Yang, et al. · Neurogenetics · 5
Novel maternal duplication of 6p22.3-p25.3 with subtelomeric 6p25.3 deletion: new clinical findings and genotype–phenotype correlations
2023 · Liyu Zhang, Xiaoling Tie, et al. · Molecular Cytogenetics · 5
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Insights From a Novel Splicing Variant and Recurrent Arginine Variants in the CHD3 Gene Causing Snijders Blok–Campeau Syndrome
2024 · Xiaoling Tie, Fengyu Che, et al. · American Journal of Medical Genetics Part A · 3
Novel FOXP2 variant associated with speech and language dysfunction in a Chinese family and literature review
2024 · Fengyu Che, Chenhao Li, et al. · Journal of Applied Genetics · 3
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A Novel Homozygous Deletion Including Exon 1 of FA2H Gene Causes Spastic Paraplegia-35: Genetic and Lipidomics Analysis of the Patients
2024 · Lidangzhi Mo, Xiaoling Tie, et al. · Pediatric Neurology · 3
Aptamer-targeted hybrid nanoparticles based on human exosomes and LXR agonist-loaded liposomes for enhanced anti-AML therapy
2026 · Liyu Zhang, Ying Yang, et al. · Nucleosides Nucleotides & Nucleic Acids · 2
[Identification of a novel variant of SRD5A2 gene in a child featuring steroid 5α-reductase type 2 deficiency].
2021 · Mali Li, Fengyu Che, et al. · PubMed · 2
[Clinical features and genetic testing of a Chinese pedigree affected with Smith-Lemli-Opitz syndrome].
2021 · Fengyu Che, Chunxia He, et al. · PubMed · 2
Correction to: Novel FOXP2 variant associated with speech and language dysfunction in a Chinese family and literature review
2024 · Fengyu Che, Chenhao Li, et al. · Journal of Applied Genetics · 1
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Establishment of a novel human induced pluripotent stem cell line (SIPDi001-A) with compound heterozygous mutations in the UBR7 gene from a Li-Campeau syndrome patient
2023 · Benchang Li, Yafei Zhou, et al. · Stem Cell Research · 1
[Analysis of a child with X-linked mental retardation due to a de novo variant of DDX3X gene].
2022 · Qiong Wang, Ying Yang, et al. · PubMed · 1
[Clinical features and genetic analysis of two Chinese patients with Coffin Siris syndrome-1].
2022 · Fengyu Che, Ying Yang, et al. · PubMed · 1
[Analysis of clinical feature and genetic variants in two Chinese pedigrees affected with Bainbridge-Ropers syndrome].
2022 · Xiaoling Tie, Ying Yang, et al. · PubMed · 1
Works count: 43
Citation count: 281
H-index: 10
I10-index: 10
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