Peng Jin
Affiliations: | Emory School of Medicine |
Area:
Repeat instability, fragile X-related disorders, neuroepigeneticsGoogle:
"Peng Jin"Mean distance: (not calculated yet)
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Publications
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| Ye J, Huang Z, Li Q, et al. (2023) Transition of allele-specific DNA hydroxymethylation at regulatory loci is associated with phenotypic variation in monozygotic twins discordant for psychiatric disorders. Bmc Medicine. 21: 491 |
| Mei Z, Liu J, Schroeder JP, et al. (2023) Lowering Hippocampal miR-29a Expression Slows Cognitive Decline and Reduces Beta-Amyloid Deposition in 5×FAD Mice. Molecular Neurobiology |
| Mei Z, Liu J, Schroeder JP, et al. (2023) Lowering hippocampal miR-29a expression slows cognitive decline and reduces beta-amyloid deposition in 5xFAD mice. Research Square |
| Lin L, Liu X, Cheng X, et al. (2023) MicroRNA-650 Regulates the Pathogenesis of Alzheimer's Disease Through Targeting Cyclin-Dependent Kinase 5. Molecular Neurobiology |
| Liu Q, Zhang K, Kang Y, et al. (2022) Expression of expanded GGC repeats within causes behavioral deficits and neurodegeneration in a mouse model of neuronal intranuclear inclusion disease. Science Advances. 8: eadd6391 |
| Jin Y, Su K, Kong HE, et al. (2022) Cell-type specific DNA methylome signatures reveal epigenetic mechanisms for neuronal diversity and neurodevelopmental disorder. Human Molecular Genetics |
| Albizua I, Charen K, Shubeck L, et al. (2022) Descriptive analysis of seizures and comorbidities associated with fragile X syndrome. Molecular Genetics & Genomic Medicine. e2001 |
| Min S, Xu Q, Qin L, et al. (2022) Altered Hydroxymethylome in the substantia Nigra of Parkinson's disease. Human Molecular Genetics |
| Reyes Diaz JV, Jin Y, Garber K, et al. (2022) A homozygous exonic variant leading to exon skipping in ABCC8 as the cause of severe congenital hyperinsulinism. American Journal of Medical Genetics. Part A |
| Kong HE, Lim J, Linsalata A, et al. (2022) Identification of as a genetic modifier of fragile X-associated tremor/ataxia syndrome. Proceedings of the National Academy of Sciences of the United States of America. 119: e2118124119 |