Yongnian Shen
Overview
Explore the profile of Yongnian Shen including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
52
Citations
503
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Chang G, Ying L, Zhang Q, Feng B, Yao R, Ding Y, et al.
BMC Endocr Disord
. 2024 Jan;
24(1):8.
PMID: 38212772
Background: ABCC8 variants can cause hyperinsulinemia by activating or deactivating gene expression. This study used targeted exon sequencing to investigate genetic variants of ABCC8 and the associated phenotypic features in...
2.
Chang G, Li Q, Li N, Li G, Li J, Ding Y, et al.
BMC Endocr Disord
. 2022 Mar;
22(1):70.
PMID: 35296306
Background: The GNAS gene on chromosome 20q13.3, encodes the alpha-subunit of the stimulatory G protein, which is expressed in most tissues and regulated through reciprocal genomic imprinting. Disorders of GNAS...
3.
Li X, Yao R, Chang G, Li Q, Song C, Li N, et al.
J Clin Endocrinol Metab
. 2021 Dec;
107(4):972-985.
PMID: 34850017
Context: Data and studies based on exome sequencing for the genetic evaluation of short stature are limited, and more large-scale studies are warranted. Some factors increase the likelihood of a...
4.
Yin L, Mao Y, Zhou Y, Shen Y, Chen H, Zhou W, et al.
Clin Rheumatol
. 2021 Oct;
41(3):877-888.
PMID: 34674084
Objectives: Most patients with progressive pseudorheumatoid dysplasia (PPRD) are initially misdiagnosed because of disease rarity and lack of awareness by most clinicians. The purpose of this study was to provide...
5.
Li Q, Chang G, Yin L, Li J, Huang X, Shen Y, et al.
Sci Rep
. 2020 Dec;
10(1):21224.
PMID: 33277604
Cornelia de Lange Syndrome (CdLS) is a rare genetic disorder, which causes a range of physical, cognitive, and medical challenges. To retrospectively analyze the clinical characteristics and genetic variations of...
6.
Li Q, Li J, Chang G, Ding Y, Wang Y, Shen Y, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
. 2020 Aug;
37(9):1018-1020.
PMID: 32820520
Objective: To explore the clinical characteristics and genetic basis for an infant featuring combined pituitary hormone deficiency. Methods: Clinical data and results of DNA sequencing of the child were analyzed....
7.
Xu Y, Wang Y, Li N, Yao R, Li G, Li J, et al.
Eur J Endocrinol
. 2019 Jul;
181(3):311-323.
PMID: 31277073
Context: Diagnosis of non-chromosomal type disorders of sex development (DSD) has long been challenging. There is still no research on overview of a large Chinese DSD cohort. Objective: To determine...
8.
Zheng H, He Y, Kan S, Li D, Lv G, Shen Y, et al.
Mycoses
. 2019 Jan;
62(4):384-390.
PMID: 30663811
Background: The infection rate for dematiaceous fungi has increased rapidly over the most recent decades. However, the treatment for such infections has been lacking in empirical support with oral antifungal...
9.
Gao Y, Liang G, Wang Q, She X, Shi D, Shen Y, et al.
Mycopathologia
. 2019 Jan;
184(1):1-12.
PMID: 30600418
Objective: The immunological mechanisms behind different mucosa against candidiasis are largely unknown. In this study, we investigate the natural protective mechanisms and local cytokine responses of C. albicans-infected oral and...
10.
Yang H, Cai Q, Gao Z, Lv G, Shen Y, Liu W, et al.
Mycopathologia
. 2018 Jun;
183(5):815-820.
PMID: 29946995
We report a case of subcutaneous infection caused by Exophiala oligosperma. Erythematous ulcerated plaque with exudate was major clinical features. Histopathological examination showed yeast-like cells and fungal hyphae. Mycological and...