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

Integrating child mental health responses into recovery, development, and peacebuilding in fragile and conflict affected settings

将儿童心理健康应对措施纳入脆弱和受冲突影响地区的恢复、发展和和平建设中

Dominguez, Georgia B; Betancourt, Theresa S; Stark, Lindsay; Bah, Abdulai Jawo; Seth, Rajeev; Haddad, Joseph; Bhutta, Zulfiqar A

Uniform Amyloid Thresholds Across Populations

不同人群中淀粉样蛋白阈值的一致性

Vanderlip, Casey R; Gillen, Daniel L; Stark, Craig E L; Grill, Joshua D

Ether lipids influence cancer cell fate by modulating iron uptake.

醚脂通过调节铁的吸收来影响癌细胞的命运。

Mansell Ryan P, Müller Sebastian, Yang Jia-Shu, Innes-Gold Sarah, Das Sunny, Reinhardt Ferenc, Sigmund Kim Janina, Phadnis Vaishnavi V, Wan Zhengpeng, Stark Jillian, Hwang Daehee, Sindikubwabo Fabien, Syx Laurène, Servant Nicolas, Eaton Elinor Ng, Sampaio Julio L, Bell George W, Thiru Prathapan, Viravalli Amartya, Deik Amy, Clish Clary B, Hammond Paula T, Kamm Roger D, Cohen Adam E, Levental Ilya, Boehnke Natalie, Hsu Victor W, Levental Kandice R, Rodriguez Raphaël, Weinberg Robert A, Henry Whitney S

Skin Lipid-Microbe Interplay Links Staphylococcus hominis to Barrier Control in Adult Atopic Dermatitis

皮肤脂质-微生物相互作用将人葡萄球菌与成人特应性皮炎的屏障控制联系起来

Bhattacharyya, Madhumita; Lauffer, Felix; Jargosch, Manja; Frey, Kristina; Dadras, Mahsa Shahidi; Raunegger, Theresa; Wasserer, Sophia; Schmidt-Weber, Carsten B; Biedermann, Tilo; Eyerich, Kilian; Eyerich, Stefanie; Traidl-Hoffmann, Claudia; Klose, Christian; Reiger, Matthias; Garzorz-Stark, Natalie

Variants in DENND2B are associated with vulnerability for neurodevelopmental impairment, psychosis and catatonia

DENND2B基因变异与神经发育障碍、精神病和紧张症的易感性相关。

Murthy, Harsha; Hoang, Ny; Stark, Jamie C; Cui, Sunny; Pannia, Emanuela; Tsoi, Chung Ting; Harris, Simon; Ceolin, C'airah; Verhaeghe, Lauren; Scholten, Sydney; Baribeau, Danielle; Summers, Jane; Costain, Gregory; Selvanayagam, Thanuja; Howe, Jennifer L; Lewis, M E Suzanne; Brunet, Theresa; Rieger, Susanne; Rosenfeld, Jill A; Craigen, William J; Burrage, Lindsay C; Christie, Michelle R; Baldwin, Deborah; Wentzensen, Ingrid M; Keren, Boris; Cogne, Benjamin; Isidor, Bertrand; Afenjar, Alexandra; Elshafie, Reem M; Bastaki, Laila; Alkanderi, Sumaya; Myers, Kenneth A; Demarest, Scott; Angione, Katie; Abbott, Megan; Campeau, Philippe M; Dowling, James J; Mendoza-Londono, Roberto; Scherer, Stephen W; Deshwar, Ashish R; Vorstman, Jacob

Diagnostic Yield of Comprehensive Reanalysis After Nondiagnostic Short-Read Genome Sequencing in Infants With Unexplained Epilepsy

对不明原因癫痫婴儿进行非诊断性短读长基因组测序后进行全面重新分析的诊断率

Nguyen, Jimmy N H; Lachgar-Ruiz, Maria; Higginbotham, Edward J; Coleman, Matthew; Coleman, John; Shao, Wanqing; Scotchman, Elizabeth; Pritchard, Ashley J; Bell, Katrina M; Chitty, Lyn S; Christodoulou, John; De Fazio, Paul; Deshwar, Ashish R; Eltze, Christin; Griffiths, Anna J S; Hassell, Jane; Jain, Puneet; Kaliakatsos, Marios; Liang, Nicole S Y; Lombard, Patrick; Marshall, Christian R; Marx, Catherine; McRae, Lyndsey; Mulhern, Sarah; Paternoster, Ben; Perez Caballero, Ana; Pipko, Neta; Sidhu, Jashanpreet; Smith, Lacey; Stark, Zornitza; Trost, Brett; Wakeling, Emma; White, Susan M; Yoong, Michael; Chandler, Natalie J; Cross, J Helen; Scheffer, Ingrid E; Chau, Vann; Poduri, Annapurna; Howell, Katherine B; Stephenson, Sarah E M; McTague, Amy; Costain, Gregory; D'Gama, Alissa M

Smooth Muscle LRRC8A Knockout Preserves Vascular Function in Ang II Hypertension

平滑肌LRRC8A基因敲除可维持血管紧张素II高血压患者的血管功能

Choi, Hyehun; Panja, Sourav; Nguyen, Hong-Ngan; Stark, Ryan J; Lamb, Fred S

Variant interpretation training for the genomics era: Learning outcomes to inform professional competencies and education

基因组学时代的变异解读培训:以学习成果为基础的专业能力和教育

Nisselle, Amy; Liddicoat, Douglas; Cliffe, Corrina; Gallacher, Lyndon; Martyn, Melissa; Hodgson, Jan; Baker, Naomi L; Beshay, Victoria; Fanjul-Fernandez, Miriam; Fellowes, Andrew P; Lunke, Sebastian; Phelan, Dean G; Roesley, Ain; Stark, Zornitza; Tan, Tiong Yang; Thompson, Bryony; Gaff, Clara L; Thorne, Natalie

De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.

KDM2A基因的新生变异会导致综合征性神经发育障碍。

Anderson Eric N, Drukewitz Stephan, Kour Sukhleen, Chimata Anuradha V, Rajan Deepa S, Schönnagel Senta, Stals Karen L, Donnelly Deirdre, O'Sullivan Siobhan, Mantovani John F, Tan Tiong Y, Stark Zornitza, Zacher Pia, Chatron Nicolas, Monin Pauline, Drunat Severine, Vial Yoann, Latypova Xenia, Levy Jonathan, Verloes Alain, Carter Jennefer N, Bonner Devon E, Shankar Suma P, Bernstein Jonathan A, Cohen Julie S, Comi Anne, Carere Deanna Alexis, Dyer Lisa M, Mullegama Sureni V, Sanchez-Lara Pedro A, Grand Katheryn, Kim Hyung-Goo, Ben-Mahmoud Afif, Gospe Sidney M Jr, Belles Rebecca S, Bellus Gary, Lichtenbelt Klaske D, Oegema Renske, Rauch Anita, Ivanovski Ivan, Mau-Them Frederic Tran, Garde Aurore, Rabin Rachel, Pappas John, Bley Annette E, Bredow Janna, Wagner Timo, Decker Eva, Bergmann Carsten, Domenach Louis, Margot Henri, Lemke Johannes R, Abou Jamra Rami, Hentschel Julia, Mefford Heather, Singh Amit, Pandey Udai Bhan, Platzer Konrad

Plasma GFAP outperforms CSF GFAP in detecting amyloid pathology and is associated with increased risk of clinical progression in early Alzheimer's disease

血浆GFAP在检测淀粉样蛋白病理方面优于脑脊液GFAP,并且与早期阿尔茨海默病临床进展风险增加相关。

Cetindag, Arda C; Schipke, Carola G; Esselmann, Hermann; Kruse, Niels; Wiltfang, Jens; Schneider, Anja; Fliessbach, Klaus; Miklitz, Carolin; Maier, Franziska; Buerger, Katharina; Janowitz, Daniel; Ewers, Michael; Stöcklein, Sophia; Perneczky, Robert; Rauchmann, Boris-Stephan; Kurz, Carolin; Teipel, Stefan; Kilimann, Ingo; Goerss, Doreen; Laske, Christoph; Sodenkamp, Sebastian; Najafpour, Elham; Wagner, Michael; Roeske, Sandra; Frommann, Ingo; Stark, Melina; Brosseron, Frederic; Ramirez, Alfredo; Kleineidam, Luca; Priller, Josef; Spruth, Eike Jakob; Gemenetzi, Maria; Altenstein, Slawek; Düzel, Emrah; Glanz, Wenzel; Incesoy, Enise I; Butryn, Michaela; Bauer, Chris; Jessen, Frank; Peters, Oliver