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

A young progenitor for the most common planetary systems in the Galaxy

银河系中最常见行星系统的年轻前身

Livingston, John H; Petigura, Erik A; David, Trevor J; Masuda, Kento; Owen, James; Nesvorný, David; Batygin, Konstantin; de Leon, Jerome; Mori, Mayuko; Ikuta, Kai; Fukui, Akihiko; Watanabe, Noriharu; Orell Miquel, Jaume; Murgas, Felipe; Parviainen, Hannu; Korth, Judith; Libotte, Florence; Abreu García, Néstor; Gallardo, Pedro Pablo Meni; Narita, Norio; Pallé, Enric; Tamura, Motohide; Yonehara, Atsunori; Ridden-Harper, Andrew; Bieryla, Allyson; Trani, Alessandro A; Mamajek, Eric E; Ciardi, David R; Gorjian, Varoujan; Hillenbrand, Lynne A; Rebull, Luisa M; Newton, Elisabeth R; Mann, Andrew W; Vanderburg, Andrew; Stefánsson, Guðmundur; Mahadevan, Suvrath; Cañas, Caleb; Ninan, Joe; Higuera, Jesus; Todorov, Kamen; Désert, Jean-Michel; Pino, Lorenzo

A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions

GOLGA8A基因的重复扩增是伴有泛素阳性包涵体的非典型额颞叶变性的主要风险因素。

De Coster, Wouter; Van den Broeck, Marleen; Baker, Matt; Ghayal, Nikhil B; Wynants, Sarah; Batzler, Anthony; Pottier, Cyril; Alidadiani, Sara; Küçükali, Fahri; Jenkins, Gregory D; Policarpo, Rafaela; van Blitterswijk, Marka; DeJesus-Hernandez, Mariely; Soto-Beasley, Alexandra I; Faura, Júlia; Coopman, Elise; Hutten, Saskia; Mol, Merel O; Wallon, David; Sieben, Anne; Finger, Elizabeth C; Murray, Melissa E; Forrest, Shelley L; Tartaglia, Maria C; Troakes, Claire; van Rooij, Jeroen G J; Nguyen, Aivi T; Reichard, R Ross; Woodman, Natalie L; Nana, Alissa L; Weintraub, Sandra; Gefen, Tamar; De Vil, Bart; Bodi, Istvan; Lopez, Oscar L; Boluda, Susana; Belliard, Serge; Lebert, Florence; Marguet, Florent; Mao, Qinwen; Mesulam, Marsel M; Boxer, Adam L; Vandenbulcke, Mathieu; Suh, EunRan; Schaeverbeke, Jolien; Lambert, Jean-Charles; Scholz, Sonja W; Dalgard, Clifton L; Traynor, Bryan J; Gibbs, Raphael J; Schellenberg, Gerard D; Dormann, Dorothee; Joris, Geert; De Pooter, Tim; De Rijk, Peter; D'Hert, Svenn; Van Dongen, Jasper; van der Zee, Julie; Strazisar, Mojca; Gearing, Marla; Kukar, Thomas; Flanagan, Margaret; Engelborghs, Sebastiaan; Ghetti, Bernardino; Newell, Kathy L; King, Andrew; Roeber, Sigrun; Rosen, Howard J; Spina, Salvatore; Cras, Patrick; Ertekin-Taner, Nilüfer; Wszolek, Zbigniew K; Uitti, Ryan J; Cheshire, William P; Singer, Wolfgang; Herms, Jochen; Josephs, Keith A; Whitwell, Jennifer L; Petersen, Ronald C; Pasquier, Florence; Nicolas, Gaël; Castellani, Rudolph; Glass, Jonathan; Miller, Bruce L; Kovacs, Gabor G; Rissman, Robert A; Hiniker, Annie; Deramecourt, Vincent; Ang, Lee-Cyn; Lee-Way, Jin; Van Deerlin, Vivianna M; Dugger, Brittany N; Thal, Dietmar R; Grinberg, Lea T; Cruchaga, Carlos; Arzberger, Thomas; Munoz, David G; Keith, Julia; Zinman, Lorne; Rogaeva, Ekaterina; Lee, Edward B; Haggarty, Stephen J; Ansorge, Olaf; Husain, Masud; Halliday, Glenda M; Al-Sarraj, Safa; Ross, Owen A; Sleegers, Kristel; Vandenberghe, Rik; Boeve, Bradley F; Graff-Radford, Neill R; Kofler, Julia; White, Charles L 3rd; Lashley, Tammaryn; Neumann, Manuela; Biernacka, Joanna M; Seeley, William W; Seelaar, Harro; van Swieten, John C; Rohrer, Jonathan D; Dickson, Dennis W; Mackenzie, Ian R A; Rademakers, Rosa

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa

U4 和 U6 snRNA 基因的新生突变和遗传性显性突变会导致视网膜色素变性。

Quinodoz, Mathieu; Rodenburg, Kim; Cvackova, Zuzana; Kaminska, Karolina; de Bruijn, Suzanne E; Iglesias-Romero, Ana Belén; Boonen, Erica G M; Ullah, Mukhtar; Zomer, Nick; Folcher, Marc; Bijon, Jacques; Holtes, Lara K; Tsang, Stephen H; Corradi, Zelia; Freund, K Bailey; Shliaga, Stefanida; Panneman, Daan M; Hitti-Malin, Rebekkah J; Ali, Manir; AlTalbishi, Ala'a; Andréasson, Sten; Ansari, Georg; Arno, Gavin; Astuti, Galuh D N; Ayuso, Carmen; Ayyagari, Radha; Banfi, Sandro; Banin, Eyal; Barakat, Tahsin Stefan; Barboni, Mirella T S; Bauwens, Miriam; Ben-Yosef, Tamar; Bernard, Virginie; Birch, David G; Biswas, Pooja; Blanco-Kelly, Fiona; Bocquet, Beatrice; Boon, Camiel J F; Branham, Kari; Bremond-Gignac, Dominique; Britten-Jones, Alexis Ceecee; Bujakowska, Kinga M; Burin des Roziers, Cyril; Cadena, Elizabeth L; Calzetti, Giacomo; Cancellieri, Francesca; Cattaneo, Luca; Chadderton, Naomi; Charbel Issa, Peter; Coutinho-Santos, Luísa; Daiger, Stephen P; De Baere, Elfride; De Bruyne, Marieke; de la Cerda, Berta; De Roach, John N; De Zaeytijd, Julie; Derks, Ronny; Dhaenens, Claire-Marie; Dudakova, Lubica; Duncan, Jacque L; Farrar, G Jane; Feltgen, Nicolas; Fenner, Beau J; Fernández-Caballero, Lidia; Ferraz Sallum, Juliana M; Gana, Simone; Garanto, Alejandro; Gardner, Jessica C; Gilissen, Christian; Gonzàlez-Duarte, Roser; Goto, Kensuke; Griffiths-Jones, Sam; Haack, Tobias B; Haer-Wigman, Lonneke; Hardcastle, Alison J; Hayashi, Takaaki; Héon, Elise; Hoefsloot, Lies H; Hoischen, Alexander; Holtan, Josephine P; Hoyng, Carel B; Ibanez, Manuel Benjamin B 4th; Inglehearn, Chris F; Iwata, Takeshi; Jensson, Brynjar O; Jones, Kaylie; Kalatzis, Vasiliki; Kamakari, Smaragda; Karali, Marianthi; Kellner, Ulrich; Klaver, Caroline C W; Knézy, Krisztina; Koenekoop, Robert K; Kohl, Susanne; Kominami, Taro; Kühlewein, Laura; Lamey, Tina M; Leibu, Rina; Leroy, Bart P; Liskova, Petra; Lopez, Irma; López-Rodríguez, Victor R de J; Mahieu, Quinten; Mahroo, Omar A; Manes, Gaël; Mansard, Luke; Martín-Gutiérrez, M Pilar; Martins, Nelson; Mauring, Laura; McKibbin, Martin; McLaren, Terri L; Meunier, Isabelle; Michaelides, Michel; Millán, José M; Mizobuchi, Kei; Mukherjee, Rajarshi; Nagy, Zoltán Zsolt; Neveling, Kornelia; Ołdak, Monika; Oorsprong, Michiel; Pan, Yang; Papachristou, Anastasia; Percesepe, Antonio; Pfau, Maximilian; Pierce, Eric A; Place, Emily; Ramesar, Raj; Ramond, Francis; Rasquin, Florence Andrée; Rice, Gillian I; Roberts, Lisa; Rodríguez-Hidalgo, María; Ruiz-Ederra, Javier; Sabir, Ataf H; Sajiki, Ai Fujita; Sánchez-Barbero, Ana Isabel; Sarma, Asodu Sandeep; Sangermano, Riccardo; Santos, Cristina M; Scarpato, Margherita; Scholl, Hendrik P N; Sharon, Dror; Signorini, Sabrina G; Simonelli, Francesca; Sousa, Ana Berta; Stefaniotou, Maria; Stefansson, Kari; Stingl, Katarina; Suga, Akiko; Sulem, Patrick; Sullivan, Lori S; Szabó, Viktória; Szaflik, Jacek P; Taurina, Gita; Thiadens, Alberta A H J; Toomes, Carmel; Tran, Viet H; Tsilimbaris, Miltiadis K; Tsoka, Pavlina; Vaclavik, Veronika; Vajter, Marie; Valeina, Sandra; Valente, Enza Maria; Valentine, Casey; Valero, Rebeca; Valleix, Sophie; van Aerschot, Joseph; van den Born, L Ingeborgh; Van Heetvelde, Mattias; Verhoeven, Virginie J M; Vincent, Andrea L; Webster, Andrew R; Whelan, Laura; Wissinger, Bernd; Yioti, Georgia G; Yoshitake, Kazutoshi; Zenteno, Juan C; Zeuli, Roberta; Zuleger, Theresia; Landau, Chaim; Jacob, Allan I; Lin, Siying; Cremers, Frans P M; Lee, Winston; Ellingford, Jamie M; Stanek, David; Roosing, Susanne; Rivolta, Carlo

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

Prospective evaluation of artificial intelligence integration into breast cancer screening in multiple workflow settings: the GEMINI study

在多种工作流程环境下对人工智能集成到乳腺癌筛查中的前瞻性评估:GEMINI 研究

de Vries, Clarisse Florence; Lip, Gerald; Staff, Roger Todd; Dymiter, Jaroslaw Artur; Tse, Benjamin; Ng, Annie; Fox, Georgia; Oberije, Cary; Anderson, Lesley Ann

US Food and Drug Administration Approval of Biologic Drugs for Use in Children and Adolescents

美国食品药品监督管理局批准生物制剂用于儿童和青少年

Lyu, Ning; Schneeweiss, Sebastian; Bourgeois, Florence T; Savage, Timothy J

Large outbreak of group B invasive meningococcal disease in young adults in South East England, March 2026

2026年3月,英格兰东南部爆发大规模B组侵袭性脑膜炎球菌病疫情,感染对象为年轻成人。

Phillips, Andrew; Smith, Jennifer; Bansi-Matharu, Loveleen; Sikwese, Kenly; Kityo, Cissy; Flexner, Charles; Vitoria, Marco; Ford, Nathan; Doherty, Meg; Panos, Zack; Ripin, David; Hickey, Matthew; Havlir, Diane; Gandhi, Monica; Reid, Michael; Revill, Paul; I’Anson, Jessica; Anderson, Charlotte; Arora, Shona; Borrow, Ray; Bray, Neil; Campbell, Helen; Campbell, Colin NJ; Chand, Meera; Clark, Stephen A; Crook, Paul; Edeghere, Obaghe; Glass, Stephen; Ghosh, Anjan; Groves, Natalie; Halford, Florence; Hewitt, Kirsty; Hopkins, Susan; Hornigold, Rachael; Jarratt, Reece; Kliner, Merav; Kouppa, Nefeli; Ladhani, Shamez N; Lucidarme, Jay; Luxmi, Shobha; Maiden, Martin CJ; Matthews, Eve; Mearkle, Rachel; Mirrielees, Charlotte; Morgan, Jaime; Moses, Samuel; Myers, Rich; Oswald, Grace; Riley, Steven; Roberts, David J; Rodrigues, Charlene MC; Sawyer, Clare; Strutt, Matthew; Waller, Ed; Welfare, William; Mannes, Trish

Latent transition analysis for longitudinal studies of post-acute infection syndromes

潜在转换分析在急性感染后综合征纵向研究中的应用

Gusinow, Roy; Górska, Anna; Canziani, Lorenzo Maria; Lopes-Rafegas, Iris; Alvarez Garavito, Carolina; Tami, Adriana; Gentilotti, Elisa; Sicuri, Elisa; Laouénan, Cédric; Ghosn, Jade; Florence, Aline-Marie; Lahfej, Nadhem; Mazzaferri, Fulvia; Del Piccolo, Lidia; Giannella, Maddalena; Toschi, Alice; Di Chiara, Michela; Caponcello, Maria Giulia; Palacios-Baena, Zaira R; Wold, Karin I; Rossi, Elisa; Tacconelli, Evelina; Hasenauer, Jan

Neoadjuvant immune checkpoint blockade before chemoradiation for cervical squamous carcinoma (GINECO window-of-opportunity COLIBRI study): a phase II trial

宫颈鳞状细胞癌新辅助放化疗前免疫检查点阻断治疗(GINECO 机会窗口 COLIBRI 研究):一项 II 期试验

Ray-Coquard, Isabelle; Kaminsky-Forrett, Marie-Christine; Ohkuma, Ryotaro; de Montfort, Aymeric; Joly, Florence; Treilleux, Isabelle; Ghamry-Barrin, Sarah; Bello-Roufai, Diana; Saintigny, Pierre; Angelergues, Antoine; Michon, Lucas; Hardy-Bessard, Anne-Claire; Attignon, Valéry; Auclair, Jessie; Chemin, Gabriel; Lainé, Alexandra; Péré, Hélène; Veyer, David; Savoye, Aude-Marie; Berthet, Justine; Caux, Christophe; Lecuru, Fabrice; Dubois, Bertrand; Bétrian, Sarah

Automated mapping of DNA replication fork progression in human cells with ForkML

利用 ForkML 实现人类细胞中 DNA 复制叉进程的自动映射

Rojat, Victoria; Ciardo, Diletta; Tourancheau, Alan; Proux, Florence; Jean, Etienne; Arbona, Jean-Michel; Audit, Benjamin; Millot, Gael A; Bonhomme, Frédéric; Arimondo, Paola B; Hyrien, Olivier; Le Tallec, Benoît