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

Sequencing and health data resource of children of African ancestry

非洲裔儿童的测序和健康数据资源

Kottyan, Leah C; Richards, Scott; Tracy, Morgan E; Lawson, Lucinda P; Kottyan, Isabelle C; Curwin, Annika; Cobb, Beth; Esslinger, Steve; Gerwe, Margaret; Morgan, James; Chandel, Alka; Travitz, Leksi; Huang, Yongbo; Black, Catherine; Sobowale, Agboade; Akintobi, Tinuke; Mitchell, Monica J; Beck, Andrew F; Unaka, Ndidi; Seid, Michael; Fairbanks, Sonja; Adams, Michelle; Mersha, Tesfaye B; Namjou, Bahram; Pauciulo, Michael W; Strawn, Jeffrey R; Ammerman, Robert T; Santel, Daniel; Pestian, John; Glauser, Tracy; Prows, Cynthia A; Martin, Lisa J; Muglia, Louis; Harley, John B; Chepelev, Iouri; Kaufman, Kenneth M

Pervasive Sharing of Causal Genetic Risk Factors Contributes to Clinical and Molecular Overlap between Sjögren's Disease and Systemic Lupus Erythematosus

广泛的致病遗传风险因素共享导致干燥综合征和系统性红斑狼疮在临床和分子水平上存在重叠

Chau, Karen; Raksadawan, Yanint; Allison, Kristen; Ice, John A; Scofield, Robert Hal; Chepelev, Iouri; Harley, Isaac T W

Epstein-Barr virus nuclear antigen 2 extensively rewires the human chromatin landscape at autoimmune risk loci

Epstein-Barr病毒核抗原2广泛重塑自身免疫风险位点的人类染色质结构

Hong, Ted; Parameswaran, Sreeja; Donmez, Omer A; Miller, Daniel; Forney, Carmy; Lape, Michael; Saint Just Ribeiro, Mariana; Liang, Jun; Edsall, Lee E; Magnusen, Albert F; Miller, William; Chepelev, Iouri; Harley, John B; Zhao, Bo; Kottyan, Leah C; Weirauch, Matthew T

Genome-wide chromatin occupancy of BRDT and gene expression analysis suggest transcriptional partners and specific epigenetic landscapes that regulate gene expression during spermatogenesis.

BRDT 的全基因组染色质占据情况和基因表达分析表明,转录伙伴和特定的表观遗传景观在精子发生过程中调控基因表达

Her Yoon Ra, Wang Li, Chepelev Iouri, Manterola Marcia, Berkovits Binyamin, Cui Kairong, Zhao Keji, Wolgemuth Debra J

The effect of inversion at 8p23 on BLK association with lupus in Caucasian population

8p23倒位对白种人群中BLK基因与狼疮关联的影响

Namjou, Bahram; Ni, Yizhao; Harley, Isaac T W; Chepelev, Iouri; Cobb, Beth; Kottyan, Leah C; Gaffney, Patrick M; Guthridge, Joel M; Kaufman, Kenneth; Harley, John B

Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner

17q21.31 处的常见倒位多态性以组织特异性方式影响多个基因的表达。

de Jong, Simone; Chepelev, Iouri; Janson, Esther; Strengman, Eric; van den Berg, Leonard H; Veldink, Jan H; Ophoff, Roel A

Detection of RNA editing events in human cells using high-throughput sequencing

利用高通量测序技术检测人类细胞中的RNA编辑事件

Chepelev, Iouri

A barrier-only boundary element delimits the formation of facultative heterochromatin in Drosophila melanogaster and vertebrates

仅有屏障的边界元件界定了果蝇和脊椎动物中兼性异染色质的形成。

Lin, Nianwei; Li, Xingguo; Cui, Kairong; Chepelev, Iouri; Tie, Feng; Liu, Bo; Li, Guangyao; Harte, Peter; Zhao, Keji; Huang, Suming; Zhou, Lei

Epigenome mapping in normal and disease States

正常和疾病状态下的表观基因组图谱

Maunakea, Alika K; Chepelev, Iouri; Zhao, Keji

Pol II and its associated epigenetic marks are present at Pol III-transcribed noncoding RNA genes

RNA聚合酶II及其相关的表观遗传标记存在于RNA聚合酶III转录的非编码RNA基因中。

Barski, Artem; Chepelev, Iouri; Liko, Dritan; Cuddapah, Suresh; Fleming, Alastair B; Birch, Joanna; Cui, Kairong; White, Robert J; Zhao, Keji