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

Effects of Sodium Glucose Cotransporter 2 Inhibitors by Diabetes Status and Level of Albuminuria: A Meta-Analysis

钠-葡萄糖协同转运蛋白2抑制剂对糖尿病状态和蛋白尿水平的影响:一项荟萃分析

Staplin, Natalie; Roddick, Alistair J; Neuen, Brendon L; Anker, Stefan D; Bhatt, Deepak L; Butler, Javed; Cherney, David Z; Docherty, Kieran F; Fletcher, Robert A; Inzucchi, Silvio E; Jardine, Meg; Mahaffey, Kenneth W; McGuire, Darren K; McMurray, John J V; Neal, Bruce; Packer, Milton; Patel, Siddharth M; Perkovic, Vlado; Sabatine, Marc S; Solomon, Scott; Vaduganathan, Muthiah; Wanner, Christoph; Wheeler, David C; Zannad, Faiez; Haynes, Richard; Heerspink, Hiddo J L; Herrington, William G

Phenome-wide analysis of copy number variants in 470,727 UK Biobank genomes

对英国生物银行470,727个基因组中的拷贝数变异进行全表型组分析

Zou, Xueqing Zoe; Hu, Fengyuan; Lou, Haiyi; Burren, Oliver S; Li, Xiaoyin; Megy, Karyn; Wheeler, Eleanor; Wu, Qiang; Atanur, Santosh S; Karpinski, Marcin; Loesch, Douglas; Fairhurst-Hunter, Zammy; Deevi, Sri V V; Oerton, Erin; Wen, Sean; Jiang, Xiao; Salvoro, Cecilia; Mitchell, Jonathan; Nag, Abhishek; Hollis, Ben; O'Neill, Amanda; Harrow, Jen; MacArthur, Stewart; Wasilewski, Sebastian; O'Dell, Sean; Tian, Lifeng; Smith, Katherine R; Del Angel, Guillermo; Fabre, Margarete; Dhindsa, Ryan S; Wang, Quanli; Petrovski, Slavé; Carss, Keren

Author Correction: Phenome-wide analysis of copy number variants in 470,727 UK Biobank genomes

作者更正:对英国生物银行470,727个基因组中的拷贝数变异进行全表型分析

Zou, Xueqing Zoe; Hu, Fengyuan; Lou, Haiyi; Burren, Oliver S; Li, Xiaoyin; Megy, Karyn; Wheeler, Eleanor; Wu, Qiang; Atanur, Santosh S; Karpinski, Marcin; Loesch, Douglas; Fairhurst-Hunter, Zammy; Deevi, Sri V V; Oerton, Erin; Wen, Sean; Jiang, Xiao; Salvoro, Cecilia; Mitchell, Jonathan; Nag, Abhishek; Hollis, Ben; O'Neill, Amanda; Harrow, Jen; MacArthur, Stewart; Wasilewski, Sebastian; O'Dell, Sean; Tian, Lifeng; Smith, Katherine R; Del Angel, Guillermo; Fabre, Margarete; Dhindsa, Ryan S; Wang, Quanli; Petrovski, Slavé; Carss, Keren

Stress controls heterochromatin inheritance via histone H3 ubiquitylation.

应激通过组蛋白H3泛素化控制异染色质遗传。

Bhatt Bharat, Wei Yi, Pradhan Ashis Kumar, Dhakshnamoorthy Jothy, Zofall Martin, Xiao Hua, Vijayakumari Drisya, Jain Shweta, Folco Hernan Diego, Qi Hongyun, Ball David A, Karpova Tatiana S, Wheeler David, Wong Jiemin, Grewal Shiv I S

Blocking RAN translation without altering repeat RNAs rescues C9ORF72-related ALS and FTD phenotypes

阻断 RAN 翻译而不改变重复 RNA 可挽救 C9ORF72 相关 ALS 和 FTD 表型

Jiang, Xin; Schaeffer, Laure; Patni, Divya; Russo, Tommaso; Lee, Chao-Zong; Aguilar, Corey; Marques, Christine; Jansen-West, Karen; Hruska-Plochan, Marian; Ray-Soni, Ananya; Lim, Su Min; Held, Aaron; Yue, Mei; Castellanos Otero, Paula; Aryal, Sandeep; Beaussant, Hortense D A M; Basu, Himanish; Takakuwa, Hiro; Daughrity, Lillian M; Ramesh, Nandini; Da Costa, Paulo; A A Quadros, Ana Rita; Nolan, Matthew; Reyes, Charles Jourdan F; Wheeler, Hayden; Moran, Laura C; Griesman, Grant; Wymann, Benjamin; Trombetta, Bianca A; Lopez-De-Silanes, Emma Sofia; Canori, Michael; Krishnan, Gopinath; Vieira Souza Da Silva, Yasmim; Eriani, Gilbert; Albers, Mark W; Arnold, Steven E; Song, Yuyu; Jain, Ankur; Chiu, Isaac M; Zhang, Yong-Jie; Gao, Fen-Biao; Wainger, Brian J; Polymenidou, Magdalini; Petrucelli, Leonard; Martin, Franck; Lagier-Tourenne, Clotilde

Ontogeny Dictates Oncogenic Potential, Lineage Hierarchy, and Therapy Response in Pediatric Leukemia

儿童白血病中,个体发育决定致癌潜能、谱系层级和治疗反应

Wang, Ke; Saniei, Shayan; Poddar, Nikita; Martinez, Isabella G; Chao, Clifford; Autar, Subrina; Fiore, Persephone; Carcamo, Saul; Sreenath, Meghana; Peplinski, Jack H; Ries, Rhonda E; Mei, Anna Huo-Chang; Rahman, Noshin Azra; Mekerishvili, Levan; Quijada-Álamo, Miguel; Freed, Grace; Zhang, Mimi; Lachman, Katherine; Diaz, Zayna; Gonzalez, Manuel M; Zhang, Jing; Pham, Giang; Filipescu, Dan; Berisa, Mirela; Balestra, Tommaso; Wheeler, Noelle; Reisz, Julie A; D'Alessandro, Angelo; Puleston, Daniel J; Bernstein, Emily; Chipuk, Jerry E; Wunderlich, Mark; Tasian, Sarah K; Marcellino, Bridget K; Glass, Ian A; Sturgeon, Christopher M; Landau, Dan A; Chen, Zhihong; Papapetrou, Eirini P; Izzo, Franco; Meshinchi, Soheil; Hasson, Dan; Wagenblast, Elvin

Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorder

RNU2-2基因的双等位基因变异会导致最常见的已知隐性遗传性神经发育障碍。

Greene, Daniel; Mendez, Rodrigo; Lees, Jon; Barbosa, Mafalda; Bruselles, Alessandro; Chiriatti, Luigi; Ferraro, Federico; Mancini, Cecilia; Schot, Rachel; Sleutels, Frank; Bertini, Enrico; Bonner, Devon E; Bouman, Arjan; Brooks, Alice S; Cassini, Thomas A; Ezell, Kimberly M; Gomez-Ospina, Natalia; Kleefstra, Tjitske; O'Donoghue, Michael; Rives, Lynette; Shashi, Vandana; Spillmann, Rebecca C; Wafik, Mohamed; Freson, Kathleen; Barakat, Tahsin Stefan; Tartaglia, Marco; Bernstein, Jonathan A; Mumford, Andrew D; Wheeler, Matthew T; Turro, Ernest

Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes

非编码RNA基因RNU4-2的双等位基因变异会导致一种隐性遗传的神经发育综合征,并伴有明显的白质改变。

Rius, Rocio; Blakes, Alexander J M; Chen, Yuyang; De Jonghe, Joachim; Lecoquierre, François; Dawes, Ruebena; Cogne, Benjamin; Kim, Hyung Chul; Alvi, Javeria R; Amblard, Florence; Ansari, Morad; Arlt, Annabelle; Austin-Tse, Christina; Baer, Sarah; Balasubramanian, Meena; Balton, Elsa V; Barcia, Giulia; Beleza-Meireles, Ana; Bernstein, Jonathan A; Beygo, Jasmin; Blanc, Pierre; Bramswig, Nuria C; Braun, Frederik; Buchzik, Daniel; Calame, Daniel G; Campbell, Jamie; Coutton, Charles; Cunningham, Chloe A; Dargie, Nitsuh; Depienne, Christel; Dipple, Katrina M; Dieux, Anne; Dixit, Abhijit; Dreyer, Lauren; Du, Haowei; El Chehadeh, Salima; Field, Michael; Ewans, Lisa J; Geiger, Vanessa; Gibbs, Richard A; Glass, Ian; Grunewald, Olivier; Gueguen, Paul; Haack, Tobias B; Hadj Abdallah, Hamza; Harbuz, Radu; Helbig, Ingo; Horvath, Judit; Hustinx, Alexander; Isidor, Bertrand; Jacquemont, Marie-Line; Jamie, Fraser; Jeanne, Médéric; Kessler, Riley; Klinkhammer, Hannah; Korenke, G Christoph; Kotzaeridou, Urania; Krawitz, Peter; Laurie, Steven; Leventer, Richard J; Levy, Rebecca J; Lupski, James R; Marijon, Pierre; McGinnis, Kaitlin E; Mendez, Rodrigo; Messaoud, Olfa; Nava, Caroline; Nizard, Mevyn; O'Donnell-Luria, Anne; O'Leary, Melanie C; Olivieri, Simone; Parida, Amitav; Pehlivan, Davut; Prentice, Anna Jenne; Posey, Jennifer E; Reuter, Chloe M; Satre, Véronique; Schluth-Bolard, Caroline; Smol, Thomas; Sultan, Tipu; Taylor, John; Thauvin-Robinetvin, Christel; Thevenon, Julien; Uebergang, Eloise; Ueberberg, Sandra; Vincent-Delorme, Catherine; Wassmer, Evangeline; Westwood, Emma; Wheeler, Matthew T; Gulec, Elif Yilmaz; Vanderver, Adeline; Vossough, Arastoo; Sanders, Stephan J; Banka, Siddharth; Findlay, Gregory M; MacArthur, Daniel G; Simons, Cas; Whiffin, Nicola

Large-scale testing of antimicrobial lethality at single-cell resolution predicts mycobacterial infection outcomes

大规模单细胞分辨率的抗菌药物致死率测试可预测分枝杆菌感染结果。

Jovanovic, Alexander; Bright, Frederick K; Sadeghi, Ahmad; Wicki, Basil; Caño Muñiz, Santiago E; Giannini, Greta C; Toprak, Sara; Sauteur, Loïc; Rodoni, Anna; Wüst, Andreas; Lupien, Andréanne; Borrell, Sonia; Grogono, Dorothy M; Wheeler, Nicole E; Dehio, Philippe; Nemeth, Johannes; Pargger, Hans; Thomson, Rachel; Bell, Scott C; Gagneux, Sebastien; Bryant, Josephine M; Peng, Tingying; Diacon, Andreas H; Floto, R Andres; Abanto, Michael; Boeck, Lucas

Notes from the Field: Wastewater Surveillance for Measles Virus During a Measles Outbreak - Colorado, August 2025

现场笔记:2025年8月科罗拉多州麻疹疫情期间的废水麻疹病毒监测

Jensen, Grace M; Gidfar, Cyrus; Weisbeck, Kirsten; Barnes, Meghan; Minnerath, Erin; Matzinger, Shannon; Wheeler, Allison