日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

A Common PD-Risk GBA1 Variant Disrupts LIMP2 Interaction, Impairs Glucocerebrosidase Function, and Drives Lysosomal and Mitochondrial Dysfunction.

常见的帕金森病风险 GBA1 变异会破坏 LIMP2 相互作用,损害葡萄糖脑苷脂酶功能,并导致溶酶体和线粒体功能障碍

Davis Oliver B, Kung Jennifer E, Davis Sonnet S, Ghosh Rajarshi, Andrews Shan V, Gould Neal S, Kluss Jillian H, Thomsen Elliot, Agam Maayan, Coan John P, Maloney Michael T, Nguyen Ann H, Nguyen Hoang N, Propson Nicholas E, Lozano Edwin I, Yuan Tianao, Xa Kaitlin, Sperberg R Andres Parra, Jain Shourya, Lawrence Roger, Ullman Julie C, Balasundar Srijana, Benton H Paul, Petkovic Maja, Qerqez Ahlam N, Wang Xiang, Zhu Sha, Di Paolo Gilbert, Kariolis Mihalis S, Mahon Cathal S, Arguello Annie, Vocadlo David J, Cookson Mark R, Suh Jung H, Rougé Lionel, Henry Anastasia G

Global endometrial DNA methylation analysis reveals insights into mQTL regulation and associated endometriosis disease risk and endometrial function

全球子宫内膜DNA甲基化分析揭示了mQTL调控及其与子宫内膜异位症疾病风险和子宫内膜功能相关的机制

Mortlock, Sally; Houshdaran, Sahar; Kosti, Idit; Rahmioglu, Nilufer; Nezhat, Camran; Vitonis, Allison F; Andrews, Shan V; Grosjean, Parker; Paranjpe, Manish; Horne, Andrew W; Jacoby, Alison; Lager, Jeannette; Opoku-Anane, Jessica; Vo, Kim Chi; Manvelyan, Evelina; Sen, Sushmita; Ghukasyan, Zhanna; Collins, Frances; Santamaria, Xavier; Saunders, Philippa; Kober, Kord; McRae, Allan F; Terry, Kathryn L; Vallvé-Juanico, Júlia; Becker, Christian; Rogers, Peter A W; Irwin, Juan C; Zondervan, Krina; Montgomery, Grant W; Missmer, Stacey; Sirota, Marina; Giudice, Linda

Large-scale placenta DNA methylation integrated analysis reveals fetal sex-specific differentially methylated CpG sites and regions

大规模胎盘DNA甲基化整合分析揭示了胎儿性别特异性差异甲基化的CpG位点和区域

Andrews, Shan V; Yang, Irene J; Froehlich, Karolin; Oskotsky, Tomiko; Sirota, Marina

Estimation of Eosinophil Cells in Cord Blood with References Based on Blood in Adults via Bayesian Measurement Error Modeling

基于成人血液参考值的脐带血嗜酸性粒细胞估计:贝叶斯测量误差模型

Jiang, Yu; Zhang, Hongmei; Andrews, Shan V; Arshad, Hasan; Ewart, Susan; Holloway, John W; Fallin, M Daniele; Bakulski, Kelly M; Karmaus, Wilfried

Case-control meta-analysis of blood DNA methylation and autism spectrum disorder

血液DNA甲基化与自闭症谱系障碍的病例对照荟萃分析

Andrews, Shan V; Sheppard, Brooke; Windham, Gayle C; Schieve, Laura A; Schendel, Diana E; Croen, Lisa A; Chopra, Pankaj; Alisch, Reid S; Newschaffer, Craig J; Warren, Stephen T; Feinberg, Andrew P; Fallin, M Daniele; Ladd-Acosta, Christine

Cross-tissue integration of genetic and epigenetic data offers insight into autism spectrum disorder

跨组织整合遗传和表观遗传数据有助于深入了解自闭症谱系障碍

Andrews, Shan V; Ellis, Shannon E; Bakulski, Kelly M; Sheppard, Brooke; Croen, Lisa A; Hertz-Picciotto, Irva; Newschaffer, Craig J; Feinberg, Andrew P; Arking, Dan E; Ladd-Acosta, Christine; Fallin, M Daniele

"Gap hunting" to characterize clustered probe signals in Illumina methylation array data

利用“间隙搜索”来表征Illumina甲基化芯片数据中聚集的探针信号

Andrews, Shan V; Ladd-Acosta, Christine; Feinberg, Andrew P; Hansen, Kasper D; Fallin, M Daniele

DNA methylation of cord blood cell types: Applications for mixed cell birth studies

脐带血细胞类型的DNA甲基化:在混合细胞出生研究中的应用

Bakulski, Kelly M; Feinberg, Jason I; Andrews, Shan V; Yang, Jack; Brown, Shannon; L McKenney, Stephanie; Witter, Frank; Walston, Jeremy; Feinberg, Andrew P; Fallin, M Daniele