Fei Yin

Central South University — China

Biochemistry, Genetics and Molecular Biology · Life Sciences

31h-index3.6kcitations188works2.42yr avg
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Research Topics

Genetics and Neurodevelopmental Disorders(49), Epilepsy research and treatment(33), Neuroscience and Neuropharmacology Research(21), Genomics and Rare Diseases(20), MicroRNA in disease regulation(14)

Publications188 total

Biallelic FOXRED1 mutations cause infantile mitochondrial encephalopathy with complex I disassembly and basal ganglia degeneration
Mitochondrion·2025
[A case of Harel-Yoon syndrome with seizures caused by an <i>ATAD3A</i> variant].
PubMed·2025Open Access
Isolated Central Nervous System FHL3 in an Asian Pediatric Patient: A Case Report and Literature Review
Journal of Inflammation Research·2025Open Access
Long-term Omega-3 polyunsaturated fatty acid supplementation improves meningeal lymphatic function during brain aging in mice
Journal of Lipid Research·2025Open Access
Functional characterization and in vitro pharmacological rescue of a novel KCNA2 variant associated with developmental and epileptic encephalopathy
Neuroscience·2025
Research on rotational dynamics and protective capabilities of variable density flat chambers
Journal of Physics Conference Series·2025Open Access
The Role of Estrogen in Mitochondrial Disease
Cellular and Molecular Neurobiology·2025· 17 citedOpen Access
The genetic spectrum features of 2261 Chinese children with epilepsy and intellectual disability
BMC Medicine·2025· 1 citedOpen Access
ICME 2025 Generalizable HDR and SDR Video Quality Measurement Grand Challenge
arXiv (Cornell University)·2025Open Access
[Clinical characteristics of epilepsy with intellectual disability associated with <i>SETD1B</i> gene in three pediatric cases and a literature review].
PubMed·2025Open Access
Global spatiotemporal distribution characteristics and regional risk stratification model of acute myeloid leukaemia based on molecular genetics and cytogenetic features
British Journal of Haematology·2025Open Access
Anti-GAD65 Antibodies Related Refractory Epilepsy Successfully Treated with Tocilizumab: A Case Report and Systematic Literature Review
ImmunoTargets and Therapy·2025· 3 citedOpen Access
The utilization of the multimodal immunotherapy for the opsoclonus–myoclonus syndrome can reduce relapses and permanent neurological sequelae
˜The œItalian Journal of Pediatrics/Italian journal of pediatrics·2025Open Access
Anti-GluK2 Encephalitis in an Asian Child: A Case Report and Literature Review
ImmunoTargets and Therapy·2024· 2 citedOpen Access
Key role of ERβ in estrogenic regulation of neuronal mitochondrial function
Alzheimer s & Dementia·2024· 1 citedOpen Access
Treatment of juvenile myasthenia gravis with tacrolimus: A cohort study
European Journal of Neurology·2024· 2 citedOpen Access
[Developmental and epileptic encephalopathy 33 caused by <i>EEF1A2</i> gene mutation: a case report].
PubMed·2024Open Access
Mutations in <scp><i>CLCN6</i></scp> as a Novel Genetic Cause of Neuronal Ceroid Lipofuscinosis in Patients and a Murine Model
Annals of Neurology·2024· 7 citedOpen Access
Roles of KCNA2 in Neurological Diseases: from Physiology to Pathology
Molecular Neurobiology·2024· 12 cited
Targeted sequencing identifies risk variants in 202 candidate genes for neurodevelopmental disorders
Gene·2023· 1 cited
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Frequent Co-authors

Jing Peng(36), Fang He(22), Lifen Yang(18), Miriam Kessi(10), Nan Pang(9), Ahmed Omran(9), Xiaolu Deng(8), Huimin Kong(8), Ciliu Zhang(8), Liwen Wu(7), Na Gan(6), Chen Chen(5), Juan Xiong(5), Muhammad Usman Ashhab(4), Baiyu Chen(4), Ahmed Arafat(4), Shiqi Guang(3), Guoli Wang(3), Liwen Wu(3), Ying Wang(3)