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Assessing the relationship between monoallelic PRKN mutations and Parkinson's risk.
Lubbe SJ, Bustos BI, Hu J, Krainc D, Joseph T, Hehir J, Tan M, Zhang W, Escott-Price V, Williams NM, Blauwendraat C, Singleton AB, Morris HR; for International Parkinson’s Disease Genomics Consortium (IPDGC). Lubbe SJ, et al. Among authors: hu j. Hum Mol Genet. 2021 Mar 25;30(1):78-86. doi: 10.1093/hmg/ddaa273. Hum Mol Genet. 2021. PMID: 33448283 Free PMC article.
Gene-based burden analysis of damaging private variants in PRKN, PARK7 and PINK1 in Parkinson's disease cohorts of European descent.
Hu J, Waters CH, Spiegelman D, Fon EA, Yu E, Asayesh F, Krohn L, Saini P, Alcalay RN, Hassin-Baer S, Gan-Or Z, Krainc D, Zhang B, Bustos BI, Lubbe SJ; International Parkinson's Disease Genomics Consortium (IPDGC). Hu J, et al. Neurobiol Aging. 2022 Nov;119:136-138. doi: 10.1016/j.neurobiolaging.2022.07.012. Epub 2022 Jul 31. Neurobiol Aging. 2022. PMID: 36305379
P53 upregulation by USP7-engaging molecular glues.
Li Z, Wang Z, Zhong C, Zhang H, Liu R, An P, Ma Z, Lu J, Pan C, Zhang Z, Cao Z, Hu J, Xing D, Fei Y, Ding Y, Lu B. Li Z, et al. Among authors: hu j. Sci Bull (Beijing). 2024 Apr 11:S2095-9273(24)00251-2. doi: 10.1016/j.scib.2024.04.017. Online ahead of print. Sci Bull (Beijing). 2024. PMID: 38734583
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