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

WashU Epigenome Browser update 2019

WashU 表观基因组浏览器 2019 年更新

Li, Daofeng; Hsu, Silas; Purushotham, Deepak; Sears, Renee L; Wang, Ting

Tissue-specific DNA methylation is conserved across human, mouse, and rat, and driven by primary sequence conservation

组织特异性DNA甲基化在人类、小鼠和大鼠中均保守存在,并受一级序列保守性的驱动。

Zhou, Jia; Sears, Renee L; Xing, Xiaoyun; Zhang, Bo; Li, Daofeng; Rockweiler, Nicole B; Jang, Hyo Sik; Choudhary, Mayank N K; Lee, Hyung Joo; Lowdon, Rebecca F; Arand, Jason; Tabers, Brianne; Gu, C Charles; Cicero, Theodore J; Wang, Ting

Epigenomic annotation of genetic variants using the Roadmap Epigenome Browser

利用路线图表观基因组浏览器对遗传变异进行表观基因组注释

Zhou, Xin; Li, Daofeng; Zhang, Bo; Lowdon, Rebecca F; Rockweiler, Nicole B; Sears, Renee L; Madden, Pamela A F; Smirnov, Ivan; Costello, Joseph F; Wang, Ting

Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export.

XPR1基因突变会导致原发性家族性脑钙化,并伴有磷酸盐输出改变

Legati Andrea, Giovannini Donatella, Nicolas Gaël, López-Sánchez Uriel, Quintáns Beatriz, Oliveira João R M, Sears Renee L, Ramos Eliana Marisa, Spiteri Elizabeth, Sobrido María-Jesús, Carracedo Ángel, Castro-Fernández Cristina, Cubizolle Stéphanie, Fogel Brent L, Goizet Cyril, Jen Joanna C, Kirdlarp Suppachok, Lang Anthony E, Miedzybrodzka Zosia, Mitarnun Witoon, Paucar Martin, Paulson Henry, Pariente Jérémie, Richard Anne-Claire, Salins Naomi S, Simpson Sheila A, Striano Pasquale, Svenningsson Per, Tison François, Unni Vivek K, Vanakker Olivier, Wessels Marja W, Wetchaphanphesat Suppachok, Yang Michele, Boller Francois, Campion Dominique, Hannequin Didier, Sitbon Marc, Geschwind Daniel H, Battini Jean-Luc, Coppola Giovanni

A multiancestral genome-wide exome array study of Alzheimer disease, frontotemporal dementia, and progressive supranuclear palsy

一项针对阿尔茨海默病、额颞叶痴呆和进行性核上性麻痹的多祖先全基因组外显子组芯片研究

Chen, Jason A; Wang, Qing; Davis-Turak, Jeremy; Li, Yun; Karydas, Anna M; Hsu, Sandy C; Sears, Renee L; Chatzopoulou, Doxa; Huang, Alden Y; Wojta, Kevin J; Klein, Eric; Lee, Jason; Beekly, Duane L; Boxer, Adam; Faber, Kelley M; Haase, Claudia M; Miller, Josh; Poon, Wayne W; Rosen, Ami; Rosen, Howard; Sapozhnikova, Anna; Shapira, Jill; Varpetian, Arousiak; Foroud, Tatiana M; Levenson, Robert W; Levey, Allan I; Kukull, Walter A; Mendez, Mario F; Ringman, John; Chui, Helena; Cotman, Carl; DeCarli, Charles; Miller, Bruce L; Geschwind, Daniel H; Coppola, Giovanni

Decision tree analysis of genetic risk for clinically heterogeneous Alzheimer's disease

临床异质性阿尔茨海默病遗传风险的决策树分析

Yokoyama, Jennifer S; Bonham, Luke W; Sears, Renee L; Klein, Eric; Karydas, Anna; Kramer, Joel H; Miller, Bruce L; Coppola, Giovanni

An epigenetic signature in peripheral blood associated with the haplotype on 17q21.31, a risk factor for neurodegenerative tauopathy

外周血中与17q21.31单倍型相关的表观遗传特征,是神经退行性tau蛋白病的一个风险因素。

Li, Yun; Chen, Jason A; Sears, Renee L; Gao, Fuying; Klein, Eric D; Karydas, Anna; Geschwind, Michael D; Rosen, Howard J; Boxer, Adam L; Guo, Weilong; Pellegrini, Matteo; Horvath, Steve; Miller, Bruce L; Geschwind, Daniel H; Coppola, Giovanni

Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification

SLC20A2基因突变是家族性特发性基底节钙化的主要原因。

Hsu, Sandy Chan; Sears, Renee L; Lemos, Roberta R; Quintáns, Beatriz; Huang, Alden; Spiteri, Elizabeth; Nevarez, Lisette; Mamah, Catherine; Zatz, Mayana; Pierce, Kerrie D; Fullerton, Janice M; Adair, John C; Berner, Jon E; Bower, Matthew; Brodaty, Henry; Carmona, Olga; Dobricić, Valerija; Fogel, Brent L; García-Estevez, Daniel; Goldman, Jill; Goudreau, John L; Hopfer, Suellen; Janković, Milena; Jaumà, Serge; Jen, Joanna C; Kirdlarp, Suppachok; Klepper, Joerg; Kostić, Vladimir; Lang, Anthony E; Linglart, Agnès; Maisenbacher, Melissa K; Manyam, Bala V; Mazzoni, Pietro; Miedzybrodzka, Zofia; Mitarnun, Witoon; Mitchell, Philip B; Mueller, Jennifer; Novaković, Ivana; Paucar, Martin; Paulson, Henry; Simpson, Sheila A; Svenningsson, Per; Tuite, Paul; Vitek, Jerrold; Wetchaphanphesat, Suppachok; Williams, Charles; Yang, Michele; Schofield, Peter R; de Oliveira, João R M; Sobrido, María-Jesús; Geschwind, Daniel H; Coppola, Giovanni