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

Global Evaluation of Congenital Heart Disease-Associated Non-Coding Variants

全球先天性心脏病相关非编码变异评估

Peña-Martínez, Edwin G; Sharma, Shreya; Medina-Feliciano, Joshua G; Root, Elise; Parks, Lois G; Granitto, Marissa; Pomales-Matos, Diego A; Messon-Bird, Jean L; Barreiro-Rosario, Adriana C; Sanabria-Alberto, Leandro; Rivera-Madera, Alejandro; Rodríguez-Ríos, Jessica M; Velázquez-Roig, Rosalba; Figueroa-Rosado, Juan A; Noon, Mackenzie; Donmez, Omer A; Forney, Carmy; Hesse, Hayley K; Dunn, Katelyn A; Chen, Xiaoting; Hass, Matthew R; Lawson, Lucinda P; Weirauch, Matthew T; Kottyan, Leah C; Reilly, Steven K; Bhimsaria, Devesh; Rodríguez-Martínez, José A

A highly prevalent lupus risk haplotype increases IRF7-dependent induction of IFN-α, enhancing antiviral defense and exacerbating autoimmunity

一种高发的狼疮风险单倍型会增加IRF7依赖的IFN-α诱导,从而增强抗病毒防御并加剧自身免疫。

Virolainen, Samuel J; Creighton, Kathryn; Dashtiahangar, Maryam; Krishnamurthy, Durga; Parks, Lois; Forney, Carmy; Ampadu, Britney; Rudrapatna, Akshata N; Dunn, Katelyn A; Parameswaran, Sreeja; Hesse, Hayley K; Chen, Xiaoting; VonHandorf, Andrew; Edsall, Lee E; Yin, Cailing; Lynch, Arthur; Gittens, Olivia E; Diouf, Arame A; Jones, Sydney H; Hass, Matthew; Javier, Ellen; Donmez, Omer A; Keddari, Yasine; Danzinger, Oded; Seelamneni, Harsha; Namjou-Khales, Bahram; Ainsworth, Hannah C; Comeau, Mary E; Marion, Miranda C; Glenn, Stuart B; Nath, Swapan K; Freedman, Barry I; Tsao, Betty P; Kamen, Diane L; Brown, Elizabeth E; Gilkeson, Gary S; Alarcón, Graciela S; Reveille, John D; James, Judith A; Criswell, Lindsey A; Vilá, Luis M; Alarcón-Riquelme, Marta E; Petri, Michelle; Scofield, R Hal; Kimberly, Robert P; Ramsey-Goldman, Rosalind; Bae, Sang-Cheol; Graham, Deborah Cunninghame; Vyse, Timothy J; Guthridge, Joel M; Gaffney, Patrick M; Langefeld, Carl D; Kelly, Jennifer A; Kaufman, Kenneth M; Sivils, Kathy; Harley, John B; Shen, Nan; Lawson, Lucinda P; Baglaenko, Yuriy; Miraldi, Emily R; Rosenberg, Brad R; Siggers, Trevor; Waggoner, Stephen N; Weirauch, Matthew T; Kottyan, Leah C

Massively parallel analysis of genotype-dependent enhancer activity among atopic dermatitis genetic risk variants

对特应性皮炎遗传风险变异中基因型依赖性增强子活性的大规模并行分析

Shook, Molly S; Lu, Xiaoming; Chen, Xiaoting; Edsall, Lee E; Granitto, Marissa; Virolainen, Samuel J; Forney, Carmy; Donmez, Omer A; Parameswaran, Sreeja; Fadden, Catherine; Dexheimer, Phillip J; Jenkins, Seth; Grashel, Brittany; Kaufman, Kenneth M; Hershey, Gurjit Khurana; Martin, Lisa J; Satish, Latha; Weirauch, Matthew T; Kottyan, Leah C

Human cytomegalovirus infection coopts chromatin organization to diminish TEAD1 transcription factor activity.

人类巨细胞病毒感染会利用染色质组织来降低 TEAD1 转录因子的活性

Sayeed Khund, Parameswaran Sreeja, Beucler Matthew J, Edsall Lee E, VonHandorf Andrew, Crowther Audrey, Donmez Omer A, Hass Matthew R, Richards Scott, Forney Carmy R, Hesse Hayley K, Jones Sydney H, Dunn Katelyn A, Wright Jay, Leong Merrin Man Long, Murray-Nerger Laura A, Yechoor Vijay, Gewurz Ben E, Kaufman Kenneth M, Harley John B, Zhao Bo, Miller William E, Kottyan Leah C, Weirauch Matthew T

Genome-wide discovery of multiple sclerosis genetic risk variant allelic regulatory activity

全基因组范围内发现多发性硬化症遗传风险变异等位基因调控活性

Granitto, Marissa; Parks, Lois; Shook, Molly S; Forney, Carmy; Chen, Xiaoting; Edsall, Lee E; Donmez, Omer A; Parameswaran, Sreeja; Fisher, Kristen S; Zabeti, Aram; Lawson, Lucinda P; Weirauch, Matthew T; Kottyan, Leah C

Systematic investigation reveals extensive Epstein-Barr virus transcriptional regulation of the human genome

系统性研究揭示了 Epstein-Barr 病毒对人类基因组广泛的转录调控作用

Dexheimer, Phillip J; Hass, Matthew R; Edsall, Lee E; Diouf, Arame A; Jones, Sydney H; Donmez, Omer; Yin, Cailing; Dunn, Katelyn A; Forney, Carmy; Hesse, Hayley K; VonHandorf, Andrew; Chen, Xiaoting; Parameswaran, Sreeja; Gittens, Olivia E; Viel, Kenyatta C M F; Razavi, Rozita; Gewurz, Benjamin E; Zhao, Bo; Lawson, Lucinda P; Hughes, Timothy R; Kottyan, Leah C; Weirauch, Matthew T

Systematic identification of genotype-dependent enhancer variants in eosinophilic esophagitis

嗜酸性食管炎中基因型依赖性增强子变异的系统鉴定

Molly S Shook, Xiaoming Lu, Xiaoting Chen, Sreeja Parameswaran, Lee Edsall, Michael P Trimarchi, Kevin Ernst, Marissa Granitto, Carmy Forney, Omer A Donmez, Arame A Diouf, Andrew VonHandorf, Marc E Rothenberg, Matthew T Weirauch, Leah C Kottyan

Macrophage memories of early-life injury drive neonatal nociceptive priming

巨噬细胞对早期生活损伤的记忆驱动新生儿伤害性感受启动

Adam J Dourson,Adewale O Fadaka,Anna M Warshak,Aditi Paranjpe,Benjamin Weinhaus,Luis F Queme,Megan C Hofmann,Heather M Evans,Omer A Donmez,Carmy Forney,Matthew T Weirauch,Leah C Kottyan,Daniel Lucas,George S Deepe Jr,Michael P Jankowski

Filaggrin loss-of-function variants are associated with atopic dermatitis phenotypes in a diverse, early-life prospective cohort

在一项针对不同年龄段早期人群的前瞻性队列研究中,丝聚蛋白功能缺失变异与特应性皮炎表型相关。

Virolainen, Samuel J; Satish, Latha; Biagini, Jocelyn M; Chaib, Hassan; Chang, Wan Chi; Dexheimer, Phillip J; Dixon, Michael R; Dunn, Katelyn; Fletcher, David; Forney, Carmy; Granitto, Marissa; Hestand, Matthew S; Hurd, Makenna; Kauffman, Kenneth; Lawson, Lucinda; Martin, Lisa J; Peña, Loren Dm; Phelan, Kieran J; Shook, Molly; Weirauch, Matthew T; Khurana Hershey, Gurjit K; Kottyan, Leah C

Genome-wide epigenetic profiling and transcriptome analysis in pediatric Obstructive Sleep Apnea: A focus on Black female children

儿童阻塞性睡眠呼吸暂停的全基因组表观遗传谱分析和转录组分析:以黑人女童为例

Koritala, Bala S C; Parameswaran, Sreeja; Donmez, Omer A; Forney, Carmy; Rowden, Hope; Moore, Charles A; Duggins, Angela L; Sestito, Alexandra; Leader, Brittany A; Weirauch, Matthew T; Kottyan, Leah C; Smith, David F