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

Malaria vaccine protection against intradermal or venous parasites: a randomized phase 2b human challenge trial

疟疾疫苗对皮内或静脉寄生虫的保护作用:一项随机 2b 期人体挑战试验

Kapulu, Melissa C; Orenge, Francesca; Kimani, Domtila; Kibwana, Elizabeth; Kibet, Hillary; Mutahi, Mary; Datoo, Mehreen S; Bellamy, Duncan; Musembi, Janet; Ngoto, Omar; Rashid, Hamisi; Akinyi, Stellamaris; Mwatasa, Mwaganyuma H; Nyamako, Lydia; Keter, Kelvias; Gatheru, Rose; Mutiso, Agnes; Musyoki, Jennifer; Mwacharo, Jedidah; Abebe, Yonas; James, Eric R; Billingsley, Peter F; Ngetsa, Caroline; Mosobo, Moses; Makale, Johnstone; Tawa, Brian; Wamae, Kevin; Ochola-Oyier, Lynette I; Lawrie, Alison; Ramos-Lopez, Fernando; Roberts, Rachel; Richie, Thomas L; Sim, B Kim Lee; Hoffman, Stephen L; Ewer, Katie J; Hill, Adrian V S; Hamaluba, Mainga; Bejon, Philip

Uncovering the role of LINE-1 in the evolution of lung adenocarcinoma

揭示LINE-1在肺腺癌演变中的作用

Zhang, Tongwu; Zhao, Wei; Wirth, Christopher; Díaz-Gay, Marcos; Yin, Jinhu; Cecati, Monia; Marchegiani, Francesca; Hoang, Phuc H; Leduc, Charles; Baine, Marina K; Travis, William D; Sholl, Lynette M; Joubert, Philippe; Sang, Jian; McElderry, John P; Antony, Michelle; Klein, Alyssa; Khandekar, Azhar; Hartman, Caleb; Rosenbaum, Jennifer; Colón-Matos, Frank J; Miraftab, Mona; Saha, Monjoy; Lee, Olivia W; Jones, Kristine M; Caporaso, Neil E; Wong, Maria Pik; Leung, Kin Chung; Hsiung, Chao Agnes; Chen, Chih-Yi; Edell, Eric S; Santamaría, Jacobo Martínez; Schabath, Matthew B; Yendamuri, Sai S; Manczuk, Marta; Lissowska, Jolanta; Świątkowska, Beata; Mukeria, Anush; Shangina, Oxana; Zaridze, David; Holcatova, Ivana; Mates, Dana; Milosavljevic, Sasa; Savic, Milan; Bossé, Yohan; Rothberg, Bonnie E Gould; Christiani, David C; Gaborieau, Valerie; Brennan, Paul; Liu, Geoffrey; Hofman, Paul; Homer, Robert; Yang, Soo-Ryum; Pesatori, Angela C; Consonni, Dario; Yang, Lixing; Zhu, Bin; Shi, Jianxin; Brown, Kevin; Rothman, Nathaniel; Chanock, Stephen J; Alexandrov, Ludmil B; Choi, Jiyeon; Cardelli, Maurizio; Lan, Qing; Nowak, Martin A; Wedge, David C; Landi, Maria Teresa

A Prognostic Signature for Lung Adenocarcinoma in Patients Who Have Never Smoked

从未吸烟者肺腺癌患者的预后特征

Zhao, Wei; Zhang, Tongwu; Hua, Xing; Hoang, Phuc H; Miraftab, Mona; Saha, Monjoy; McElderry, John P; Sang, Jian; Lee, Olivia W; Hartman, Caleb; Khandekar, Azhar; Sharma, Sunandini; Colón-Matos, Frank J; Anyaso-Samuel, Samuel; Wang, Difei; Jones, Kristine; Hutchinson, Amy; Hicks, Belynda; Rosenbaum, Jennifer; Zhong, Xiaoming; Yang, Yang; Pesatori, Angela C; Consonni, Dario; Christiani, David C; Leung, Kin Chung; Wong, Maria Pik; Manczuk, Marta; Lissowska, Jolanta; Świątkowska, Beata; Mukeria, Anush; Shangina, Oxana; Zaridze, David; Holcatova, Ivana; Mates, Dana; Milosavljevic, Sasa; Ognjanovic, Simona; Savic, Milan; Kontic, Milica; Gaborieau, Valerie; Brennan, Paul; Arrieta, Oscar; Bossé, Yohan; Edell, Eric S; Schabath, Matthew B; Hofman, Paul; Mas, Luis; Yendamuri, Sai S; Chen, Chih-Yi; Chang, I-Shou; Hsiung, Chao Agnes; Liu, Geoffrey; Martinez Santamaría, Jacobo; Gould Rothberg, Bonnie E; Mutreja, Karun; Lawrence, Scott; Rothman, Nathaniel; Alexandrov, Ludmil B; Leduc, Charles; Baine, Marina K; Joubert, Philippe; Sholl, Lynette M; Travis, William D; Homer, Robert; Lan, Qing; Chanock, Stephen J; Yang, Lixing; Yang, Soo-Ryum; Shi, Jianxin; Landi, Maria Teresa

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

Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies

对snRNA基因的系统分析揭示了显性和隐性发育性脑病和癫痫性脑病中常见的RNU2-2变异。

Leitão, Elsa; Santini, Amandine; Cogne, Benjamin; Essid, Miriam; Athanasiadou, Maria; LaFlamme, Christy W; Marijon, Pierre; Bernard, Virginie; Jousselin, Kevin; Chatron, Nicolas; Barcia, Giulia; Keren, Boris; Mignot, Cyril; Charles, Perrine; Besnard, Thomas; Paluch, Robin; de Sainte Agathe, Jean-Madeleine; Almanza Fuerte, Edith P; Sengupta, Soham; Milh, Mathieu; Ramond, Francis; Allan, Talia; An, Isabelle; Araujo, Camila; Arpin, Stéphanie; Austin-Tse, Christina; Auvin, Stéphane; Baer, Sarah; Bahi-Buisson, Nadia; Bak, Mads; Barth, Magalie; Baulac, Stéphanie; Bednarek-Weirauch, Nathalie; Begemann, Matthias; Bennett, Mark F; Bensabath, Uriel; Bézieau, Stéphane; Bhouri, Rakia; Biehler, Margaux; Hammer, Trine Bjørg; Bogoin, Julie; Bonanno, Emilie; Boussion, Simon; Bris, Céline; Brosseau-Beauvir, Adelaide; Bruel, Ange-Line; Briand-Suleau, Audrey; Buratti, Julien; Celse, Tristan; Chambon, Pascal; Chemaly, Nicole; Chesneau, Bertrand; Colin, Estelle; Colmard, Maxime; Colson, Cindy; Conrad, Solène; Courtin, Thomas; Creveaux, Isabelle; Cullier, Anne-Charlotte; Dang, Louis T; de Saint Martin, Anne; de Vanssay de Blavous Legendre, Caroline; Demeer, Bénédicte; Denommé-Pichon, Anne-Sophie; Diekhoff, Philine; DiTroia, Stephanie; Doco-Fenzy, Martine; Dubourg, Christèle; Dubucs, Charlotte; Ducreux, Stéphanie; Dufour, Louis; Duquet, Romain; Durand, Benjamin; El Chehadeh, Salima; Elbracht, Miriam; Faivre, Laurence; Faoucher, Marie; Faudet, Anne; Forlani, Sylvie; Fradin, Mélanie; Gaignard, Pauline; Ganne, Benjamin; Garde, Aurore; Géraud, Justine; Gill, Deepak; Goldenberg, Alice; Grabli, David; Grisel, Coraline; Gueden, Sophie; Gueguen, Paul; Guerrot, Anne-Marie; Guichet, Agnès; Haack, Tobias B; Härting, Nina; Häusler, Martin Georg; Heide, Solveig; Herget, Theresia; Héron, Bénédicte; Héron, Delphine; Herwig, Johanna; Heulin, Mathilde; Holling, Tess; Houdayer, Clara; Isidor, Bertrand; Jacquette, Aurélia; Januel, Louis; Jean-Marçais, Nolwenn; Kaiser, Frank J; Kaya, Sabine; King, Chontelle; Konyukh, Marina; Kraft, Florian; Krause, Jeremias; Kirstetter, Rémi; Kuechler, Alma; Kurth, Ingo; Kutsche, Kerstin; Labalme, Audrey; Laloy, Jean-Serene; Laugel, Vincent; Le Bricquir, Floriane; Lèbre, Anne-Sophie; Lebrun, Marine; Leguern, Eric; Levy, Jonathan; Lieffering, Nico; Lyonnet, Stanislas; Lüthy, Kevin; Macdonald, Sian M W; Mansour-Hendili, Lamisse; Maraval, Julien; Marquardt, Iris; Mattausch, Carolin; Mercier, Sandra; Messaoud, Olfa; Morel, Godelieve; Mortreux, Jérémie; Munnich, Arnold; Nabbout, Rima; Nambot, Sophie; Navarro, Vincent; Neale, Ashana; Nguyen, Laetitia; Nizon, Mathilde; Nowak, Frédérique; O'Leary, Melanie C; Odent, Sylvie; Ojeda, Naomi Meave; Olin, Valérie; Olivieri, Simone; Õunap, Katrin; Pais, Lynn S; Panagiotakaki, Eleni; Patat, Olivier; Perrin-Sabourin, Laurence; Petit, Florence; Philippe, Christophe; Piton, Amélie; Planes, Marc; Poirsier, Céline; Pouzet, Antoine; Prouteau, Clément; Quéméner-Redon, Sylvia; Renaud, Mathilde; Richard, Anne-Claire; Rio, Marlène; Rivier, Clotilde; Robin-Renaldo, Florence; Rollier, Paul; Rossi, Massimiliano; Roubertie, Agathe; Ruault, Valentin; Rupin-Mas, Maïlys; Saugier-Veber, Pascale; Saunier, Aline; Saneto, Russell; Sarrazin, Elisabeth; Sarret, Catherine; Schaefer, Elise; Schluth-Bolard, Caroline; Schneider, Amy; Schumann, Isabell; Seplyarskiy, Vladimir B; Spranger, Stephanie; Smol, Thomas; Sturm, Marc; Sunyaev, Shamil R; Sperelakis-Beedham, Brian; Stenton, Sarah L; Stock, Friedrich; Tharreau, Mylène; Torun, Deniz; Toulouse, Joseph; Thiyagarajah, Harshini; Valence, Stéphanie; Valleix, Sophie; Van-Gils, Julien; Villard, Laurent; Ville, Dorothée; Villeneuve, Nathalie; Vitobello, Antonio; Waernessyckle, Aurélie; Wagner, Jan; Weber, Yvonne; Wieczorek, Dagmar; Witkowski, Tom; Yadavilli, Manya; Yammine, Tony; Zaafrane-Khachnaoui, Khaoula; Zaki, Maha S; Ziegler, Alban; Bramswig, Nuria C; Lermine, Alban; Nicolas, Gael; Gleeson, Joseph G; Sadleir, Lynette G; Hildebrand, Michael S; Scheffer, Ingrid E; Whiffin, Nicola; O'Donnell-Luria, Anne; Mefford, Heather C; Blanc, Pierre; Thevenon, Julien; Charbonnier, Camille; Charenton, Clément; Depienne, Christel; Lesca, Gaetan; Nava, Caroline

γδ T cell-derived IL-4 initiates CD8(+) T cell immunity

γδ T 细胞衍生的 IL-4 启动 CD8(+) T 细胞免疫

Le, Shirley; Dooley, Nick; Murphy, Declan; Liu, Shangyi; Gandolfo, Luke C; Ge, Zhengyu; May, Rose; Cozijnsen, Anton; Burn, Thomas N; Jennison, Charlie; Bachem, Annabell; Xu, Calvin; Koay, Hui-Fern; Schröder, Jan; Oyong, Damian; Nalubega, Mayimuna; Kenangalem, Enny; Gras, Stephanie; Cockburn, Ian A; Bedoui, Sammy; Mackay, Laura K; McFadden, Geoffrey I; Fernandez-Ruiz, Daniel; Boyle, Michelle; Heath, William R; Beattie, Lynette

Ancestry-Associated Performance Variability of Open-Source AI Models for EGFR Prediction in Lung Cancer

肺癌EGFR预测开源AI模型的祖源相关性性能差异

Rakaee, Mehrdad; Nassar, Amin H; Tafavvoghi, Masoud; Jabar, Falah; Bou Farhat, Elias; Adib, Elio; Andersen, Sigve; Busund, Lill-Tove Rasmussen; Pøhl, Mette; Helland, Åslaug; Gusev, Alexander; Ricciuti, Biagio; Sholl, Lynette M; Donnem, Tom; Kwiatkowski, David J

Human TET2-Mutant Clonal Hematopoiesis Expansion Is Driven by Distinct Inflammatory Signaling Responses in Stem Cells Versus Myeloid Progeny.

人类 TET2 突变克隆造血扩增是由干细胞与髓系子代细胞中不同的炎症信号反应驱动的。

Huerga Encabo Hector, D'Agostino Giuseppe, Sturgess Katherine, Lord Alice E, Jong Eric D, Ferrelli Alessandra, Sharma Aneesh, Mian Syed A, Habel Khadidja, Llorian-Sopena Miriam, Ramesh Amirtha Priya, Mohamad Nor Fatihah, Foissner Helene, Garcia-Albornoz Manuel, Graver Lynette, Papazoglou Despoina, Ngo Steven, Anjos-Afonso Fernando, Ariza-McNaughton Linda, Ficz Gabriella, Bonnet Dominique

Neurodegenerative Diseases in Male Former First-Class New Zealand Rugby Players

新西兰前一级橄榄球男运动员的神经退行性疾病

Anns, Francesca; Quarrie, Kenneth L; Milne, Barry J; Li, Chao; Gardner, Andrew J; Murphy, Ian R; Verhagen, Evert; Wright, Craig; Morton, Susan M B; Lumley, Thomas; Tippett, Lynette; D'Souza, Stephanie

Multi-ancestry transcriptome prediction with functionally informed variants in TOPMed MESA improves performance of transcriptome-wide association studies

利用TOPMed MESA中功能性变异进行多祖先转录组预测可提高全转录组关联研究的性能

Hu, Xiaowei; Araujo, Daniel S; Khunsriraksakul, Chachrit; Wang, Lida; Sun, Quan; Wen, Jia; Zhou, Lingbo; Ekunwe, Lynette; Lange, Leslie A; Lange, Ethan M; Montgomery, Stephen B; Reiner, Alexander P; Aguet, Francois; Ardlie, Kristin G; Lappalainen, Tuuli; Gignoux, Christopher R; Burchard, Esteban G; Taylor, Kent D; Guo, Xiuqing; Rotter, Jerome I; Rich, Stephen S; Cornell, Elaine; Durda, Peter; Tracy, Russell P; Liu, Yongmei; Johnson, W Craig; Papanicolaou, George P; Perera, Minoli A; Cho, Michael H; Liu, Dajiang J; Raffield, Laura M; Li, Yun; Wheeler, Heather E; Im, Hae Kyung; Manichaikul, Ani