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M

Mingyu Han

modular b stanford

H指数:17

被引数:887

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Genetically informed causal links between gut microbiota and bone mass: pleiotropy and metabolic mediation

基因信息支持的肠道菌群与骨量之间的因果关系：多效性与代谢介导

Nature Communications

IF15.7

2025-11-280

OA

SMYD3–CDCP1 Axis Drives EMT and CAF Activation in Colorectal Cancer and Is Targetable for Oxaliplatin Sensitization

SMYD3–CDCP1轴驱动结直肠癌中的EMT和CAF活化，并可靶向用于奥沙利铂增敏。

Biomedicines 2025, Vol. 13, Page 2737

IF3.9

2025-11-090

OAAI

Recessive variants in TWNK cause syndromic and non-syndromic post-synaptic auditory neuropathy through MtDNA replication defects

隐性变异体通过线粒体DNA复制缺陷，导致TWNK基因相关的综合征性和非综合征性突触后听觉神经病变。

IF3.6

2025-09-080

PRE

lncSLERT Promotes Liver Metastasis in Colorectal Cancer by Down-Regulating HUNK Expression via RBM15-Mediated m6A Modification

lncSLERT 通过 RBM15 介导的 m6A 修饰下调 HUNK 表达，促进结直肠癌肝转移。

OncoTargets and Therapy

IF2.8

2025-05-090

OA

HIV-1 cell-to-cell infection of macrophages escapes type I interferon and host restriction factors, and is resistant to antiretroviral drugs

IF4.9

2025-04-010

OAAI

Targeted Linked-Read Sequencing for Direct Haplotype Phasing of Parental GJB2/SLC26A4 / SLC26A4 Alleles

JOURNAL OF MOLECULAR DIAGNOSTICS

IF3.4

2024-07-012

OAAI

Characterization of SH3GLB1 in the auditory system and its potential role in mitophagy

GENES & DISEASES

IF9.4

2024-07-010

OAAI

Multi-omics-based investigation of Bifidobacterium's inhibitory effect on glioma: regulation of tumor and gut microbiota, and MEK/ERK cascade

FRONTIERS IN MICROBIOLOGY

IF4.5

2024-04-188

OAAI

RDmaster: A novel phenotype-oriented dialogue system supporting differential diagnosis of rare disease

COMPUTERS IN BIOLOGY AND MEDICINE

IF6.3

2024-02-010

OAAI

Regulated cell death in glioma: promising targets for natural small-molecule compounds

FRONTIERS IN ONCOLOGY

IF3.3

2024-01-188

OAAI

Exploration of a Novel Noninvasive Prenatal Testing Approach for Monogenic Disorders Based on Fetal Nucleated Red Blood Cells

CLINICAL CHEMISTRY

IF6.3

2023-11-152

OA

Spermine and spermidine bind CXCR4 and inhibit CXCR4-but not CCR5-tropic HIV-1 infection

SCIENCE ADVANCES

IF12.5

2023-07-074

OAAI

Harms, Mirja; Smith, Nikaia; Han, Mingyu; Gross, Ruediger; von Maltitz, Pascal; Stuerzel, Christina; Ruiz-Blanco, Yasser B.; Almeida-Hernandez, Yasser; Rodriguez-Alfonso, Armando; Cathelin, Dominique; Caspar, Birgit; Tahar, Bouceba; Sayettat, Sophie; Bekaddour, Nassima; Vanshylla, Kanika; Kleipass, Franziska; Wiese, Sebastian; Staendker, Ludger; Klein, Florian; Lagane, Bernard; Boonen, Arnaud; Schols, Dominique; Benichou, Serge; Sanchez-Garcia, Elsa; Herbeuval, Jean-Philippe; Muench, Jan

Preimplantation genetic testing for hereditary hearing loss in Chinese population (Apr, 10.1007/s10815-023-02753-8, 2023)

JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

IF2.7

2023-04-240

OAAI

Preimplantation genetic testing for hereditary hearing loss in Chinese population

JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

IF2.7

2023-04-055

OAAI

Quantitative assessment of low-level parental mosaicism of SNVs and CNVs in Waardenburg syndrome

IF3.6

2022-12-281

PRE

Bifidobacterium lactis combined with Lactobacillus plantarum inhibit glioma growth in mice through modulating PI3K/AKT pathway and gut microbiota

乳酸双歧杆菌联合植物乳杆菌通过调控PI3K/AKT通路和肠道菌群抑制小鼠胶质瘤生长

FRONTIERS IN MICROBIOLOGY

IF4.5

2022-09-0629

OAAI

HIV-1 cell-to-cell spread overcomes the virus entry block of non-macrophage-tropic strains in macrophages

IF4.9

2022-05-2710

OAAI

Mechanisms of HIV-1 cell-to-cell transfer to myeloid cells

HIV-1细胞间转移至髓系细胞的机制

JOURNAL OF LEUKOCYTE BIOLOGY

IF3.1

2022-03-3112

OA

Analysis of genotype-phenotype relationships in 90 Chinese probands with Waardenburg syndrome

IF3.6

2021-06-1718

PREAI

Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss

JOURNAL OF MEDICAL GENETICS

IF3.7

2018-02-1616

OAAI