Zhenwei Liu

Chemistry

H指数:16

被引数:774

个人简介

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Tunable persistent luminescence nanoparticles for profiling bacterial extracellular azoreductase activity and antibiotic susceptibility

可调谐长余辉纳米颗粒用于表征细菌胞外偶氮还原酶活性和抗生素敏感性

Analytical and Bioanalytical Chemistry

IF3.8

2026-05-120

PRE

Divergent Total Syntheses of (-)-Galanthamine, (-)-Narwedine, (-)-Lycoraminone and (-)-Lycoramine, and Formal Syntheses of (-)-Morphine and (-)-Codeine

ORGANIC LETTERS

IF5

2026-01-090

PRE

Multi-omics integration reveals gut microbiota dysbiosis and metabolic alterations of cerebrospinal fluid in children with epilepsy

多组学整合揭示了癫痫患儿肠道微生物群失调和脑脊液代谢改变

Frontiers in Microbiology

IF4.5

2025-09-220

OAAI

Passive head-up tilt positioning as an early mobilization strategy in neurocritical care: a prospective-retrospective controlled study

被动头高位倾斜定位作为神经危重症护理中的早期活动策略：一项前瞻性-回顾性对照研究

Frontiers in Neurology

IF2.8

2025-08-170

Increased RNA editing sites revealed as potential novel biomarkers for diagnosis in primary Sjogren's syndrome

JOURNAL OF AUTOIMMUNITY

IF7

2023-07-016

PRE

Realizing near-infrared mechanophosphorescence from an organic host/guest system

JOURNAL OF MATERIALS CHEMISTRY C

IF5.1

2023-01-011

PRE

Microbiota dysbiosis in primary Sjogren's syndrome and the ameliorative effect of hydroxychloroquine

CELL REPORTS

IF6.9

2022-09-0122

Metagenomic Analysis Reveals A Possible Association Between Respiratory Infection and Periodontitis

GENOMICS PROTEOMICS & BIOINFORMATICS

IF7.9

2021-07-092

OAAI

Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autism

先证者中多个从头编码变体的非随机发生表明自闭症中存在寡基因模型

GENETICS IN MEDICINE

IF6.2

2020-01-0125

OAAI

Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autism (vol 21, pg 1, 2019)

GENETICS IN MEDICINE

IF6.2

2019-11-011

OAAI

Elevated CCL19/CCR7 Expression During the Disease Process of Primary Sjogren's Syndrome

FRONTIERS IN IMMUNOLOGY

IF5.9

2019-04-2424

OAAI

A de novo pathogenic CSNK1E mutation identified by exome sequencing in family trios with epileptic encephalopathy

通过外显子组测序在患有癫痫性脑病的家族三人组中鉴定到的从头致病性CSNK1E突变

HUMAN MUTATION

IF3.7

2018-12-088

OAAI

Prevalence of Common Respiratory Viral Infections and Identification of Adenovirus in Hospitalized Adults in Harbin, China 2014 to 2017

FRONTIERS IN MICROBIOLOGY

IF4.5

2018-11-279

OAAI

64Cu-Labeled multifunctional dendrimers for targeted tumor PET imaging

NANOSCALE

IF5.1

2018-01-0139

OAAI

Identification of de novo germline mutations and causal genes for sporadic diseases using trio-based whole-exome/genome sequencing

BIOLOGICAL REVIEWS

IF11.7

2017-11-2029

PREAI

Trio-based exome sequencing arrests de novo mutations in early-onset high myopia

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

IF9.1

2017-04-0373

OAAI

Whole-exome sequencing identifies a novel de novo mutation in DYNC1H1 in epileptic encephalopathies

SCIENTIFIC REPORTS

IF3.9

2017-03-2124

OAAI

mirDNMR: a gene-centered database of background de novo mutation rates in human

NUCLEIC ACIDS RESEARCH

IF13.1

2016-10-3013

OAAI

mirVAFC: A Web Server for Prioritizations of Pathogenic Sequence Variants from Exome Sequencing Data via Classifications

mirVAFC: 一个网络服务器，用于通过分类从外显子组测序数据中优先考虑致病序列变异

HUMAN MUTATION

IF3.7

2016-10-138

OAAI

Therapeutic effect of human umbilical cord mesenchymal stem cells modified by angiotensin-converting enzyme 2 gene on bleomycin-induced lung fibrosis injury

MOLECULAR MEDICINE REPORTS

IF3.5

2014-12-0165

OAAI

Zhenwei Liu

个人简介

教育背景

工作经历

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