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

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

Long-Term Mpox Sequelae 11 to 18 Months After Acute Illness : A Cohort Study in Two U.S. Cities

急性感染后11至18个月的长期痘后遗症:美国两座城市的队列研究

Cholli, Preetam A; Zucker, Jason; Vigil, Karen J; Minhaj, Faisal S; Weidle, Paul J; Taylor, Melanie M; Gray, Brett; Haberling, Dana L; Ajmal, Agha; Rao, Agam K; Cantos, Anyelina; Guagliardo, Sarah Anne J; Flanagan, Max; Rodriguez, Gilhen H; Tamí-Maury, Irene; O'Connor, Siobhán M

Locally Ablative Therapies in Oligometastatic Breast Cancer

寡转移性乳腺癌的局部消融治疗

Nierenberg, Tori C; Thomas, Samantha M; Halliday, Ian; van den Bruele, Astrid Botty; Wang, Ton; Rosenberger, Laura H; Flanagan, Meghan R; DiLalla, Gayle A; Hwang, E Shelley; Plichta, Jennifer K

A novel Kupffer cell-targeting nanoparticle system to Mitigate alcohol-associated liver disease.

一种新型的库普弗细胞靶向纳米颗粒系统,用于缓解酒精相关性肝病。

Unagolla Janitha M, Flanagan Riley, Perera Kalindu, Kim Youbin, Soloff Curtis, Kaye Emily, Slitt Angela, Menon Jyothi U

Loss of function variants in the primate-specific gene ZNF808 cause neonatal, transient and adult-onset diabetes

灵长类特异性基因 ZNF808 的功能缺失变异会导致新生儿糖尿病、暂时性糖尿病和成人发病型糖尿病。

Russ-Silsby, James; Colclough, Kevin; Johnson, Matthew B; Wakeling, Matthew N; Owens, Nick D L; Amaratunga, Shenali A; Flanagan, Sarah E; Patel, Kashyap A; Hattersley, Andrew T; De Franco, Elisa

Genetics and Genomics in Sickle Cell Disease in Africa

非洲镰状细胞病的遗传学和基因组学

Nkya, Siana; Makani, Julie; Flanagan, Jonathan M

Investigating the Frequency and Outcome of Central Vein Sign and Paramagnetic Rim Lesions in Children With MOGAD

探讨MOGAD患儿中心静脉征和顺磁性环状病变的发生频率和预后

Nistri, Riccardo; Cacciaguerra, Laura; Sacco, Simone; Virupakshaiah, Akash; De Meo, Ermelinda; Papinutto, Nico; Henry, Roland G; Meirson, Hadas; Hemingway, Cheryl; Rossor, Thomas; Wassmer, Evangeline; Bensira, Liat; Pratt, Li-Tal; Biswas, Asthik; Sudhakar, Sniya; Mankad, Kshitij; Chen, John J; Pittock, Sean J; Barkhof, Frederik; Ciccarelli, Olga; Waubant, Emmanuelle; Flanagan, Eoin P; Hacohen, Yael

Incidence and Outcomes of Atrial Fibrillation and Systolic Dysfunction in Patients Receiving Mavacamten for Obstructive Hypertrophic Cardiomyopathy: A Multicenter Study

接受马伐卡坦治疗的梗阻性肥厚型心肌病患者发生房颤和收缩功能障碍的概率及预后:一项多中心研究

Nguyen, Olives; Wiedrick, Jack; Massera, Daniele; Adlestein, Elizabeth; Frejat, Sumar; Castrichini, Matteo; Alsidawi, Said; Giudicessi, John R; Geske, Jeffrey B; Carrick, Richard T; Madrazo, Jose; Dellise, Nicole; Zenker, Mark A; Boyle, Thomas A; Reza, Nosheen; Owens, Anjali Tiku; Frankel, David S; Hundal, Prabhjot; Tajik, Jamil; Galazka, Patrycja; Lewontin, Myra; Ayers, Michael; Wong, Timothy; Flanagan, Michael; Mitter, Sumeet Singh; Kanwal, Arjun; Bilen, Ozlem; Baghdadi, Sarah; Shah, Hirak; Kvapil, Jared; Roldan, Paola; Berenbom, Loren; Jesurum, Jill; Tootill, Denise; Siqueira-Benzow, Alice; Harper, Mariko; Saleh, Danish; Choudhury, Lubna; Valenta, Isabela; Lang, Melissa; Phelan, Dermot M; Prizand, Dmitry; Lakdawala, Neal; Ho, Carolyn Y; Liang, Lusha W; Weiner, Shepard D; Ravi, Sririam; Abuzaid, Ahmed Sami; Makkiya, Mohammed; Markowitz, Jeremy S; Sherrid, Mark; Masri, Ahmad

Bi-allelic variants in the non-protein-coding minor spliceosome components RNU6ATAC and RNU4ATAC cause syndromic monogenic autoimmune diabetes

非蛋白质编码的次要剪接体组分 RNU6ATAC 和 RNU4ATAC 的双等位基因变异会导致综合征型单基因自身免疫性糖尿病

Johnson, Matthew B; Russ-Silsby, James; Blair, Paul A; Govier, Molly; Bonfield, Georgia; Domingo-Vila, Clara; Wakeling, Matthew N; Oram, Richard A; Flanagan, Sarah E; Tree, Timothy I M; Patel, Kashyap A; Hattersley, Andrew T; De Franco, Elisa

MRI characteristics during attack and remission distinguish patients with MOG antibody-associated disease from multiple sclerosis

发作期和缓解期的MRI特征可以区分MOG抗体相关疾病患者和多发性硬化症患者。

Syc-Mazurek, Stephanie B; Cacciaguerra, Laura; Tajfirouz, Deena A; Redenbaugh, Vyanka; Krecke, Karl N; Thakolwiboon, Smathorn; Dinoto, Alessandro; Madhavan, Ajay; Tillema, Jan-Mendelt; Lopez-Chiriboga, A Sebastian; Valencia-Sanchez, Cristina; Sechi, Elia; Chen, John J; Pittock, Sean J; Flanagan, Eoin P