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Medcomm|March 17, 2023
Increased RTN3 phenocopies nonalcoholic fatty liver disease by inhibiting the AMPK-IDH2 pathwayHao Huang, Shuai Guo, Ya-Qin Chen, et al.
Medicine|November 15, 2025
A novel DCC truncating mutation leads to rare congenital mirror movements and corpus callosum agenesis: A case reportGao-Hui Cao, Ai-Qian Zhang, Yi Dong, et al.
Frontiers in Genetics|May 14, 2023
Case report: A novel mutation of RecQ-like helicase 5 in a Chinese family with early myocardial infarction, coronary artery disease, and stroke hemiplegiaYi Tang, Qian Wang, Wei-Kai Zhang, et al.
BMC Medical Genetics|November 8, 2019
Identification of a novel mutation of NOG in family with proximal symphalangism and early genetic counselingCong Ma, Lv Liu, Fang-Na Wang, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry|June 24, 2026
Gut Microbiota from GAD patients with divergent early pharmacological responses transmits anxiety-like behaviors and distinct metabolic profiles in recipient miceHong He, Li-Zhi Liu, Hui-Feng Duan, et al.
Biomed Research International|May 7, 2021
Whole-Exome Sequencing Identifies a Novel TRPM4 Mutation in a Chinese Family with Atrioventricular BlockYi Dong, Ran Du, Liang-Liang Fan, et al.
Medcomm|February 6, 2024
Correction to: Increased RTN3 phenocopies nonalcoholic fatty liver disease by inhibiting the AMPK-IDH2 pathwayHao Huang, Shuai Guo, Ya-Qin Chen, et al.
Frontiers in Pediatrics|July 22, 2026
Whole exome sequencing identified a novel compound heterozygous mutation of nephrocystin 4 in a child with nephronophthisis-a rare case reportWang Li, Gao-Hui Cao, Nan-Nan Li, et al.
Cardiology in the Young|February 7, 2018
Whole-exome sequencing identifies a Novel SCN5A mutation (C335R) in a Chinese family with arrhythmiaHao Huang, Dong-Bo Ding, Liang-Liang Fan, et al.
Applied Biochemistry and Biotechnology|April 8, 2015
Novel mutations of low-density lipoprotein receptor gene in China patients with familial hypercholesterolemiaLiang-liang Fan, Min-jie Lin, Ya-qin Chen, et al.
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