Jia Geng
Overview
Explore the profile of Jia Geng including associated specialties, affiliations and a list of published articles.
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Articles
113
Citations
962
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0
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Recent Articles
1.
Cheng H, Wang X, Zhong M, Geng J, Li W, Pei K, et al.
Adv Sci (Weinh)
. 2025 Mar;
:e2408891.
PMID: 40089864
Effective research and clinical application in audiology and hearing loss (HL) require the integration of diverse data, yet the absence of a dedicated database impedes understanding and insight extraction in...
2.
Zhao C, Mou X, Zhang Q, Chen C, Zhu Y, Hong L, et al.
Biosens Bioelectron
. 2025 Feb;
276:117250.
PMID: 39955838
Modifying transmembrane channels is essential for enhancing functionality. Current modification methods often require chemical reactions or protein engineering, which can increase technical complexity and workload. The inner transmembrane region of...
3.
Dong B, Li Y, Ai F, Geng J, Tang T, Peng W, et al.
Front Genet
. 2025 Jan;
15:1523304.
PMID: 39872005
Background: Patent foramen ovale (PFO) is a congenital defect between the atria, resulting in abnormal hemodynamics. We conducted a genome-wide association study (GWAS) to identify common genetic variants associated with...
4.
Yang T, Dong Y, Zhang M, Feng J, Fu S, Xiao P, et al.
Exp Hematol Oncol
. 2025 Jan;
14(1):2.
PMID: 39754190
Background: Sequential CD19 and CD22 chimeric antigen receptor (CAR)-T cell therapy offers a promising approach to antigen-loss relapse in relapsed/refractory (R/R) B-cell acute lymphoblastic leukemia (B-ALL); however, research in adults...
5.
Chen Y, Xie S, Geng J, Li Z, Yang Y, Wang S
J Dermatol
. 2024 Oct;
52(3):531-535.
PMID: 39436000
Biallelic variants in the LSS gene have been reported in individuals affected by alopecia-intellectual disability syndrome 4, cataract 44, hypotrichosis 14, and palmoplantar keratoderma-congenital alopecia syndrome type 2. The present...
6.
Chen Y, Geng J, Xiao Y, Zhou X, Li M, Li W
J Dermatol
. 2024 Oct;
52(3):526-530.
PMID: 39377561
Peeling skin syndrome type 1 (PSS1) is an autosomal recessive genodermatosis caused by the CDSN gene loss-of-function mutation and characterized by widespread superficial skin peeling and erythroderma with unbearable pruritus....
7.
Long X, Xiong W, Wang X, Geng J, Zhong M, Huang Y, et al.
BMC Med Genomics
. 2024 Aug;
17(1):203.
PMID: 39123271
Background: A comprehensive understanding of the genetic basis of rare diseases and their regulatory mechanisms is essential for human molecular genetics. However, the genetic mutant spectrum of pathogenic genes within...
8.
Chi P, Wang X, Li J, Yang H, Li K, Zhang Y, et al.
Cell Res
. 2024 Jun;
34(10):743-745.
PMID: 38942816
No abstract available.
9.
Song D, Geng J, Yi Q, Liu H, Wang S, Jiang X
Indian J Dermatol Venereol Leprol
. 2024 Jun;
:1-3.
PMID: 38841935
No abstract available.
10.
Sun K, Pu L, Chen C, Chen M, Li K, Li X, et al.
Nucleic Acids Res
. 2024 Mar;
52(7):e39.
PMID: 38477342
CRISPR-Cas systems with dual functions offer precise sequence-based recognition and efficient catalytic cleavage of nucleic acids, making them highly promising in biosensing and diagnostic technologies. However, current methods encounter challenges...