Ying Sheng

Vanderbilt University

H指数:26

被引数:6,244

个人简介

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教育背景

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工作经历

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荣誉奖项

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Associations Between Potassium Channel Genes and the Occurrence of Palpitations in Women Prior to Breast Cancer Surgery

钾通道基因与乳腺癌手术前女性心悸发生之间的关系

SEMINARS IN ONCOLOGY NURSING

IF2.3

2025-12-010

OAAI

The deubiquitinase OTUD4 suppresses TAK1 kinase-dependent NF-κB signaling and inflammation

去泛素化酶OTUD4抑制TAK1激酶依赖的NF-κB信号通路和炎症

Journal of Biological Chemistry

IF3.9

2025-10-070

OAAI

USP7 promotes temozolomide resistance by stabilizing MGMT in glioblastoma

USP7通过稳定MGMT促进胶质母细胞瘤对替莫唑胺的耐药性

Cell Death & Disease

IF9.6

2025-08-200

Global research trends and frontiers in patent foramen ovale closure: a comprehensive bibliometric analysis (2004–2024)

全球房间隔缺损封堵术的研究趋势与前沿：一项全面的文献计量分析（2004–2024）

Frontiers in Neurology

IF2.8

2025-07-230

Patterns of Lifestyle Risk Behaviors for Cardiovascular Disease in Family Caregivers: A Latent Class Analysis

心血管疾病家庭照护者的生活方式风险行为模式：一项潜在类别分析

CIRCULATION

IF38.6

2024-11-120

PRE

Publisher Correction: A 39 kb structural variant causing Lynch syndrome detected by optical genome mapping and nanopore sequencing

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2024-01-041

OAAI

A 39 kb structural variant causing Lynch Syndrome detected by optical genome mapping and nanopore sequencing

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2023-11-295

OAAI

Preliminary Results of the Sit Less Program for Patients With Coronary Artery Disease: A Pilot Randomized Controlled Trial

CIRCULATION

IF38.6

2023-11-070

PRE

The miR156b-GmSPL2b module mediates male fertility regulation of cytoplasmic male sterility-based restorer line under high-temperature stress in soybean

miR156b-GmSPL2b模块介导高温胁迫下大豆细胞质雄性不育恢复系的雄性育性调节

PLANT BIOTECHNOLOGY JOURNAL

IF10.5

2023-04-148

Phenomenological 2D and 3D Models of Ductile Fracture for Girth Weld of X80 Pipeline

BUILDINGS

IF3.1

2023-01-181

Circ_0000647 promotes cell injury by modulating miR-126-5p/TRAF3 axis in oxygen-glucose deprivation and reperfusion-induced SK-N-SH cell model

INTERNATIONAL IMMUNOPHARMACOLOGY

IF4.7

2022-03-0119

PRE

ZBTB11 dysfunction: spectrum of brain abnormalities, biochemical signature and cellular consequences

BRAIN

IF11.7

2022-02-016

OAAI

A novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge-Weber syndrome

HUMAN MOLECULAR GENETICS

IF3.2

2021-06-1426

OAAI

Benefits of clinical criteria and high-throughput sequencing for diagnosing children with syndromic craniosynostosis

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2020-12-0720

OAAI

Association of pubovisceral muscle tear with functional capacity of urethral closure: evaluating maternal recovery from labor and delivery

AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY

IF8.4

2020-06-017

OAAI

Coexistence of Congenital Adrenal Hyperplasia and Autoimmune Addison's Disease

先天性肾上腺皮质增生症与自身免疫性Addison病并存

FRONTIERS IN ENDOCRINOLOGY

IF4.6

2019-09-272

OAAI

Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis

BRAIN

IF11.7

2019-03-0723

OAAI

Down-regulation of exosomal miR-106b-5p derived from cholesteatoma perimatrix fibroblasts promotes angiogenesis in endothelial cells by overexpression of Angiopoietin 2

CELL BIOLOGY INTERNATIONAL

IF3.1

2018-06-2920

PREAI

Whole-exome sequencing for diagnosis of hereditary ichthyosis

JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY

IF8

2018-03-0924

PREAI

Homozygous KIDINS220 loss-of-function variants in fetuses with cerebral ventriculomegaly and limb contractures

HUMAN MOLECULAR GENETICS

IF3.2

2017-07-0727

OAAI

Ying Sheng

个人简介

教育背景

工作经历

荣誉奖项

研究方向