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

Childhood brain tumors instruct cranial hematopoiesis and immunotolerance.

儿童脑肿瘤会影响颅内造血和免疫耐受。

Cooper Elizabeth, Posner David A, Lee Colin Y C, Hu Linda, Bonner Sigourney, Taylor Jessica T, Baldwin Oscar, Jimenez-Guerrero Rocio, Masih Katherine E, Rahrmann Katherine Wickham, Eigenbrood Jason, Ngo Gina, Franklin Valar Nila Roamio, D'Santos Clive S, Mair Richard, Santarius Thomas, Craven Claudia, Jalloh Ibrahim, Moreno Vicente Julia, Halim Timotheus Y F, Wang Li, Kreigstien Arnold R, Wainwright Brandon, Swartling Fredrik J, Khan Javed, Clatworthy Menna R, Gilbertson Richard J

Genetic Diagnosis and Discovery Enabled by Large Language Models

大型语言模型助力基因诊断与发现

Tu, Tao; Saab, Khaled; Liu, Weida; Fang, Zhouqing; Cheng, Zhuanfen; Spasic, Svetolik; Djurisic, Maja; Mohri, Hiroaki; Ren, Wenlong; Palepu, Anil; Gottweis, Juraj; Karthikesalingam, Alan; Kulkarni, Kavita; Pawlosky, Annalisa; Bonner, Devon; Kravets, Elijah; Marwaha, Shruti; Mendez, Hector R; Wheeler, Matthew T; Bernstein, Jonathan A; Tsai, Cheng-Yu; Wu, Chen-Chi; Stankovic, Konstantina M; Natarajan, Vivek; Peltz, Gary

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

Biallelic LAMP3 variants in 5 families with interstitial lung disease: Evidence of a disease-gene association.

个间质性肺病家族中的双等位基因 LAMP3 变异:疾病基因关联的证据。

Keehan Laura A, Ono-Minagi Hitomi, Hadhud Mohamad, Rips Jonathan, Hinds Daniel M, Fischer Anthony J, Bartlett Jennifer A, McCray Paul B, Qawasmi Nada, Nathan Nadia, Louvrier Camille, Desroziers Tifenn, Damme Markus, Griese Matthias, Wegner Daniel J, Cole F Sessions, Wambach Jennifer A, Wheeler Matthew T, Burbelo Peter D, Bonner Devon E, Bernstein Jonathan A, Chiorini John A, Breuer Oded, Milla Carlos

Child Vaccination Status and Behavioral and Social Drivers of Vaccination Among Their Caregivers in the Philippines: Cross-Sectional Survey Study Comparison of Household, Mobile, and Online Modes

菲律宾儿童疫苗接种状况及其照护者疫苗接种行为和社会驱动因素:家庭、移动和在线模式的横断面调查研究比较

Bonner, Kimberly E; Hipol, Mikka; Sy, Dominique; Royono, Rivandra; Johnson, Douglas; Del Rosario, Isabel; Redfern, Alice; Biel-Romualdo, Darahlyn; Wong, Man Kai; Lam, Eugene; Kulkarni, Shibani; Ward, Kirsten; Lacson, Romel; Chen, Meng-Yu; Miraflor, James Matthew; Pacial, Devon Ray; Bunoan, Rowena; Catan, Hugo; Shragai, Talya

Digital Educational Strategies to Implement Evidence-Based Care for Atherosclerotic Cardiovascular Disease

数字化教育策略在动脉粥样硬化性心血管疾病循证治疗中的应用

Zeng, Aileen; Bonner, Carissa; Chow, Clara K; Godinho, Myron A; Laranjo, Liliana; Nickel, Brooke; Zaman, Sarah; O'Hagan, Edel

De novo heterozygous variants of the RSF1 gene are responsible for a syndromic neurodevelopmental disorder

RSF1基因的新生杂合变异是导致综合征性神经发育障碍的原因。

Jost, Céline; Busa, Tiffany; Wegner, Daniel; Shinawi, Marwan; Schaefer, Elise; Piton, Amélie; Schluth-Bolard, Caroline; Charles, Perrine; Keren, Boris; Mayerhanser, Katharina; Brunet, Theresa; Schatz, Ulrich; Neil, Jennifer E; Walsh, Christopher A; Sisco, Kathleen; J Paul, Alexander; Lee, Chung; Dykzeul, Natalie; Bonner, Devon; Bernstein, Jonathan A; Sutcliffe, Erin; Wentzensen, Ingrid M; Froehlich, Catherine; Liebler, Kaleigh; Galvin Parton, Patricia; Weiss-Burns, Jody; Sagnol, Chloé; Delanne, Julian; Racine, Caroline; Thauvin-Robinet, Christel; Safraou, Hana; Tran Mau-Them, Frédéric; Duffourd, Yannis; Bruel, Ange-Line; Faivre, Laurence

Role of the protease-activated receptor 2 in multi-walled carbon nanotube-induced macrophage polarization ex vivo and airway fibrosis in murine allergic lung disease in vivo.

蛋白酶激活受体 2 在多壁碳纳米管诱导的巨噬细胞离体极化和小鼠过敏性肺病体内气道纤维化中的作用。

Tisch Logan J, Bartone Ryan D, Antoniak Silvio, Bonner James C

Bi-allelic RNU6ATAC variants cause a minor spliceopathy characterized by transcriptome-wide minor intron retention and multisystem manifestations

RNU6ATAC双等位基因变异会导致一种轻微的剪接病,其特征是转录组范围内的次要内含子保留和多系统表现。

Mendez, Rodrigo; Arriaga, Taylor M; Ma, Jialan; Bonner, Devon E; Emami, Sara; Levy, Rebecca J; Alsagheir, Afaf; Alhaddad, Bader; Bakur, Khadijah; Ungar, Rachel A; Matalon, Dena R; Miller, Alexander M; Nguyen, Jonathan; Smith, Kevin S; Scott, Stuart A; Liao, Linda; Ng, Zena; Marwaha, Shruti; Ward, Alistair; Novacic, Danica; Alkuraya, Fowzan S; Bernstein, Jonathan A; Ganesh, Vijay S; O'Donnell-Luria, Anne; Montgomery, Stephen B; Wheeler, Matthew T

Kinetics of Biomarkers for Therapeutic Assessment in Swiss Mice Infected with a Virulent Trypanosoma cruzi Strain

瑞士小鼠感染强毒性克氏锥虫株后,生物标志物动力学在治疗评估中的应用

Alves-Rosa, María Fernanda; Dorta, Doriana; Prescilla-Ledezma, Alexa; Carrasco, Jafeth; Bonner, Leighanne; Tamayo, Jon J; Ng, Michelle G; Vega, Adelenis; Morales, Melany; Beltran, Davis; De Jesús, Rosa; Spadafora, Carmenza