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Selective Research Papers

Home Publications Selective Research Papers

Zou Z; Wei J; Chen Y; Kang Y; Shi H; Yang F; Shi Z; Chen S; Zhou Y; Sepich-Poore C; Zhuang X; Zhou X; Jiang H; Wen Z; Jin P; Luo C; He C. FMRP phosphorylation modulates neuronal translation through YTHDF1. Mol Cell . 2023 Dec 7;83(23):4304-4317.e8. doi: 10.1016/j.molcel.2023.10.028. Epub 2023 Nov 9. PMID: 37949069

December 7, 2023

Liu Q, Zhang K, Kang Y, Li Y, Deng P, Li Y, Tian Y, Sun Q, Tang Y, Xu K, Zhou Y, Wang JL, Guo J, Li JD, Xia K, Meng Q, Allen EG, Wen Z, Li Z, Jiang H, Shen L, Duan R, Yao B, Tang B*, Jin P*, Pan Y*. (2022) Expression of expanded GGC repeats within NOTCH2NLC causes behavioral deficits and neurodegeneration in a mouse model of neuronal intranuclear inclusion disease. Science Advances 8(47):eadd6391. Epub 20221123. doi: 10.1126/sciadv.add6391. PubMed PMID: 36417528. (*: Co-Corresponding authors)

November 25, 2022

Kong HE; Lim J; Linsalata A; Kang Y; Malik I; Allen EG; Cao Y; Shubeck L; Johnston R; Huang Y; Gu Y; Guo X; Zwick ME; Qin Z; Wingo TS; Juncos J; Nelson DL; Epstein MP; Cutler DJ; Todd PK; Sherman SL; Warren ST; Jin P. Identification of PSMB5 as a genetic modifier of fragile X-associated tremor/ataxia syndrome. Proc Natl Acad Sci U S A . 2022 May 31;119(22):e2118124119. doi: 10.1073/pnas.2118124119. Epub 2022 May 26. PMID: 35617426

May 31, 2022

Kang Y, Zhou Y, Li Y, Han Y, Xu J, Niu W, Li Z, Liu S, Feng H, Huang W, Duan R, Xu T, Raj N, Zhang F, Dou J, Xu C, Wu H, Bassell GJ, Warren ST, Allen EG, Jin P*, Wen Z*. (2021) A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies. Nat Neurosci . 2021 Oct;24(10):1377-1391. doi: 10.1038/s41593-021-00913-6. Epub 2021 Aug 19. PMID: 34413513

October 24, 2021

Kim H, Kang Y, Li Y, Chen L, Lin L, Johnson ND, Zhu D, Robinson MH, McSwain L, Barwick BG, Yuan X, Liao X, Zhao J, Zhang Z, Shu Q, Chen J, Allen EG, Kenney AM, Castellino RC, Van Meir EG, Conneely KN, Vertino PM, Jin P*, Li J*. (2021) Ten-eleven translocation protein 1 modulates medulloblastoma progression. Genome Biology, 22(1):125. (*: Co-Corresponding authors)

April 29, 2021

Shafik AM; Zhang F; Guo Z; Dai Q; Pajdzik K; Li Y; Kang Y; Yao B; Wu H; He C; Allen EG; Duan R; Jin P. N6-methyladenosine dynamics in neurodevelopment and aging, and its potential role in Alzheimer’s disease. Genome Biol . 2021 Jan 5;22(1):17. doi: 10.1186/s13059-020-02249-z. PMID: 33402207

January 5, 2021

Tian Y, Wang JL, Huang W, Zeng S, Jiao B, Liu Z, Chen Z, Li Y, Wang Y, Min HX, Wang XJ, You Y, Zhang RX, Chen XY, Yi F, Zhou YF, Long HY, Zhou CJ, Hou X, Wang JP, Xie B, Liang F, Yang ZY, Sun QY, Allen EG, Shafik AM, Kong HE, Guo JF, Yan XX, Hu ZM, Xia K, Jiang H, Xu HW, Duan RH, Jin P*, Tang BS, Shen L*. (2019) Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders. American Journal of Human Genetics,105: 166-176. (*: Co-Corresponding authors)

May 27, 2019

Cheng Y, Sun M, Chen L, Li Y, Lin L, Yao B, Li Z, Wang Z, Chen J, Miao Z, Xin N, Huang L, Allen EG, Wu H, Xu X, Jin P. (2018) Distinct roles of Ten-eleven translocation protein 1 and 2 in response to environmental stress. Cell Reports, 25: 3194-3203.

January 29, 2019

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Emory University School of Medicine
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