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

An integrated view of the structure and function of the human 4D nucleome

人类4D核组结构和功能的综合视图

Dekker, Job; Oksuz, Betul Akgol; Zhang, Yang; Wang, Ye; Minsk, Miriam K; Kuang, Shuzhen; Yang, Liyan; Gibcus, Johan H; Krietenstein, Nils; Rando, Oliver J; Xu, Jie; Janssens, Derek H; Henikoff, Steven; Kukalev, Alexander; Andréa, Willemin; Winick-Ng, Warren; Kempfer, Rieke; Pombo, Ana; Yu, Miao; Kumar, Pradeep; Zhang, Liguo; Belmont, Andrew S; Sasaki, Takayo; van Schaik, Tom; Brueckner, Laura; Peric-Hupkes, Daan; van Steensel, Bas; Wang, Ping; Chai, Haoxi; Kim, Minji; Ruan, Yijun; Zhang, Ran; Quinodoz, Sofia A; Bhat, Prashant; Guttman, Mitchell; Zhao, Wenxin; Chien, Shu; Liu, Yuan; Venev, Sergey V; Plewczynski, Dariusz; Azcarate, Ibai Irastorza; Szabó, Dominik; Thieme, Christoph J; Szczepińska, Teresa; Chiliński, Mateusz; Sengupta, Kaustav; Conte, Mattia; Esposito, Andrea; Abraham, Alex; Zhang, Ruochi; Wang, Yuchuan; Wen, Xingzhao; Wu, Qiuyang; Yang, Yang; Liu, Jie; Boninsegna, Lorenzo; Yildirim, Asli; Zhan, Yuxiang; Chiariello, Andrea Maria; Bianco, Simona; Lee, Lindsay; Hu, Ming; Li, Yun; Barnett, R Jordan; Cook, Ashley L; Emerson, Daniel J; Marchal, Claire; Zhao, Peiyao; Park, Peter J; Alver, Burak H; Schroeder, Andrew J; Navelkar, Rahi; Bakker, Clara; Ronchetti, William; Ehmsen, Shannon; Veit, Alexander D; Gehlenborg, Nils; Wang, Ting; Li, Daofeng; Wang, Xiaotao; Nicodemi, Mario; Ren, Bing; Zhong, Sheng; Phillips-Cremins, Jennifer E; Gilbert, David M; Pollard, Katherine S; Alber, Frank; Ma, Jian; Noble, William S; Yue, Feng

Deep-learning prediction of gene expression from personal genomes

基于个人基因组的深度学习基因表达预测

Drusinsky, Shiron; Whalen, Sean; Pollard, Katherine S

The oligogenic inheritance test GCOD detects risk genes and their interactions in congenital heart defects

寡基因遗传检测 GCOD 可检测先天性心脏缺陷的风险基因及其相互作用。

Pittman, Maureen; Lee, Kihyun; Felix, Franco; Huang, Yu; Lam, Adrienne; Costa, Mauro W; Srivastava, Deepak; Pollard, Katherine S

Machine learning-predicted chromatin organization landscape across pediatric tumors

机器学习预测的儿童肿瘤染色质组织结构图谱

Gjoni, Ketrin; Zhang, Shu; Yan, Rachel E; Zhang, Bo; Miller, Daniel; Greenfield, Jeffrey P; Resnick, Adam; Dahmane, Nadia; Pollard, Katherine S

Gut microbiome-dependent IL-1 signaling is a mediator of ACVR1 (R206H) -driven heterotopic ossification

肠道微生物群依赖的IL-1信号传导是ACVR1(R206H)驱动的异位骨化的介质

Herzog, Hannah M; Fang, Camille; Lam, Liam; Jin, Katherine; Zamarioli, Ariane; Dinh, Ethan; Gupta, Chhedi Lal; Sharma, Aditi; Moody, Tania; Pierce, Jessica L; Hohl, Michael S; Takimoto, Sarah W; Lyalina, Svetlana; Wentworth, Kelly L; Yu, Kristie; Lu, Vivian F; Mamikunian, Isadora; Hunt, Natasha K; Lynch, Susan; Pollard, Katherine S; Hernandez, Christopher J; Perrien, Daniel S; Hsiao, Edward C

How Functional Variants Reconfigure the Rac2 Conformational Landscape

功能性变异如何重塑 Rac2 构象格局

Gjoni, Ketrin; Zhang, Shu; Yan, Rachel E; Zhang, Bo; Miller, Daniel; Resnick, Adam; Dahmane, Nadia; Pollard, Katherine S; Ruffle, James; Mohinta, Samia; Pombo, Guilherme; Gray, Robert; Kopanitsa, Valeriya; Lee, Faith; Brandner, Sebastian; Hyare, Harpreet; Nachev, Parashkev; Otani, Ryohei; Mukasa, Akitake; Uzuka, Takeo; Higuchi, Fumi; Matsuda, Hadzki; Tanaka, Shota; Kim, Phyo; Ueki, Keisuke; Arakawa, Yoshiki; Liu, Bin; Yokogawa, Ryuta; Tokunaga, Shinya; Hattori, Etsuko; Fukui, Nobuyuki; Terada, Yukinori; Matsui, Yasuzumi; Tannji, Masahiro; Mineharu, Yohei; Miyamoto, Susumu; Aram, Modrek S; Themasap, Khan N; Sumru Bayin, N; Zhang, Guoan; Thomas, Neubert; Dimitris, Placantonakis G; Haspel, Nurit; Jang, Hyunbum; Nussinov, Ruth

Author Correction: Myocardial reprogramming by HMGN1 underlies heart defects in trisomy 21

作者更正:HMGN1介导的心肌重编程是21三体综合征心脏缺陷的根本原因

Ranade, Sanjeev S; Li, Feiya; Whalen, Sean; Pelonero, Angelo; Ye, Lin; Huang, Yu; Brand, Abigail; Nishino, Tomohiro; Mital, Rahul; Boileau, Ryan M; Koback, Frances; Padmanabhan, Arun; Yu, Victoria; Cimarosti, Bastien; Presas-Ramos, Diana; Merriman, Alexander F; Wallace, Langley Grace; Nguyen, Annie; Poulis, Nikolaos; Costa, Mauro W; Gifford, Casey A; Pollard, Katherine S; Srivastava, Deepak

Structural variants in human congenital heart disease disrupt distal genomic regulatory contacts of developmental genes.

人类先天性心脏病中的结构变异会破坏发育基因的远端基因组调控联系。

Lee Jodi, Wu Jingshing, Pittman Maureen, Grant Zoe L, Kuang Shuzhen, Quiat Daniel, Morton Sarah U, Fudenberg Geoff, Traglia Michela, Hayes Kelly A, Kumar Ritu, Bruneau Benoit G, Pollard Katherine S

Myocardial reprogramming by HMGN1 underlies heart defects in trisomy 21.

HMGN1介导的心肌重编程是21三体综合征心脏缺陷的根本原因。

Ranade Sanjeev S, Li Feiya, Whalen Sean, Pelonero Angelo, Ye Lin, Huang Yu, Brand Abigail, Nishino Tomohiro, Mital Rahul, Boileau Ryan M, Koback Frances, Padmanabhan Arun, Yu Victoria, Cimarosti Bastien, Presas-Ramos Diana, Merriman Alexander F, Wallace Langley Grace, Nguyen Annie, Poulis Nikolaos, Costa Mauro W, Gifford Casey A, Pollard Katherine S, Srivastava Deepak

Comparing chromatin contact maps at scale: methods and insights

大规模比较染色质接触图谱:方法与见解

Gjoni, Ketrin; Gunsalus, Laura M; Kuang, Shuzhen; McArthur, Evonne; Pittman, Maureen; Capra, John A; Pollard, Katherine S