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

Professionalism Milestones Assessments Used by Emergency Medicine Residency Programs: A Cross-sectional Survey

急诊医学住院医师培训项目使用的专业素养里程碑评估:一项横断面调查

Stehman, Christine R; Hochman, Steven; Fernández-Frackelton, Madonna; Volz, Emilio G; Domingues, Rui; Love, Jeffrey N; Soares, William

Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility

CXCR4基因变异与幼年特发性关节炎易感性相关

Finkel, Terri H; Li, Jin; Wei, Zhi; Wang, Wei; Zhang, Haitao; Behrens, Edward M; Reuschel, Emma L; Limou, Sophie; Wise, Carol; Punaro, Marilynn; Becker, Mara L; Munro, Jane E; Flatø, Berit; Førre, Øystein; Thompson, Susan D; Langefeld, Carl D; Glass, David N; Glessner, Joseph T; Kim, Cecilia E; Frackelton, Edward; Shivers, Debra K; Thomas, Kelly A; Chiavacci, Rosetta M; Hou, Cuiping; Xu, Kexiang; Snyder, James; Qiu, Haijun; Mentch, Frank; Wang, Kai; Winkler, Cheryl A; Lie, Benedicte A; Ellis, Justine A; Hakonarson, Hakon

Social media guidelines and best practices: recommendations from the Council of Residency Directors Social Media Task Force

社交媒体指南和最佳实践:住院医师项目主任委员会社交媒体工作组的建议

Pillow, Malford T; Hopson, Laura; Bond, Michael; Cabrera, Daniel; Patterson, Leigh; Pearson, David; Sule, Harsh; Ankel, Felix; Fernández-Frackelton, Madonna; Hall, Ronald V; Kegg, Jason A; Norris, Donald; Takenaka, Katrin

Large sample size, wide variant spectrum, and advanced machine-learning technique boost risk prediction for inflammatory bowel disease

大样本量、广泛的变异谱和先进的机器学习技术提高了炎症性肠病风险预测的准确性。

Wei, Zhi; Wang, Wei; Bradfield, Jonathan; Li, Jin; Cardinale, Christopher; Frackelton, Edward; Kim, Cecilia; Mentch, Frank; Van Steen, Kristel; Visscher, Peter M; Baldassano, Robert N; Hakonarson, Hakon

The missense variation landscape of FTO, MC4R, and TMEM18 in obese children of African Ancestry

非洲裔肥胖儿童中FTO、MC4R和TMEM18的错义变异图谱

Deliard, Sandra; Panossian, Saarene; Mentch, Frank D; Kim, Cecilia E; Hou, Cuiping; Frackelton, Edward C; Bradfield, Jonathan P; Glessner, Joseph T; Zhang, Haitao; Wang, Kai; Sleiman, Patrick M A; Chiavacci, Rosetta M; Berkowitz, Robert I; Hakonarson, Hakon; Zhao, Jianhua; Grant, Struan F A

Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis

评估 FUS/TLS 相关基因 EWSR1 在肌萎缩侧索硬化症中的作用

Julien Couthouis, Michael P Hart, Renske Erion, Oliver D King, Zamia Diaz, Tadashi Nakaya, Fadia Ibrahim, Hyung-Jun Kim, Jelena Mojsilovic-Petrovic, Saarene Panossian, Cecilia E Kim, Edward C Frackelton, Jennifer A Solski, Kelly L Williams, Dana Clay-Falcone, Lauren Elman, Leo McCluskey, Robert Gree

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

对大量基因中心关联研究的荟萃分析揭示了与身高相关的常见和罕见变异

Lanktree, Matthew B; Guo, Yiran; Murtaza, Muhammed; Glessner, Joseph T; Bailey, Swneke D; Onland-Moret, N Charlotte; Lettre, Guillaume; Ongen, Halit; Rajagopalan, Ramakrishnan; Johnson, Toby; Shen, Haiqing; Nelson, Christopher P; Klopp, Norman; Baumert, Jens; Padmanabhan, Sandosh; Pankratz, Nathan; Pankow, James S; Shah, Sonia; Taylor, Kira; Barnard, John; Peters, Bas J; Maloney, Cliona M; Lobmeyer, Maximilian T; Stanton, Alice; Zafarmand, M Hadi; Romaine, Simon P R; Mehta, Amar; van Iperen, Erik P A; Gong, Yan; Price, Tom S; Smith, Erin N; Kim, Cecilia E; Li, Yun R; Asselbergs, Folkert W; Atwood, Larry D; Bailey, Kristian M; Bhatt, Deepak; Bauer, Florianne; Behr, Elijah R; Bhangale, Tushar; Boer, Jolanda M A; Boehm, Bernhard O; Bradfield, Jonathan P; Brown, Morris; Braund, Peter S; Burton, Paul R; Carty, Cara; Chandrupatla, Hareesh R; Chen, Wei; Connell, John; Dalgeorgou, Chrysoula; Boer, Anthonius de; Drenos, Fotios; Elbers, Clara C; Fang, James C; Fox, Caroline S; Frackelton, Edward C; Fuchs, Barry; Furlong, Clement E; Gibson, Quince; Gieger, Christian; Goel, Anuj; Grobbee, Diederik E; Hastie, Claire; Howard, Philip J; Huang, Guan-Hua; Johnson, W Craig; Li, Qing; Kleber, Marcus E; Klein, Barbara E K; Klein, Ronald; Kooperberg, Charles; Ky, Bonnie; Lacroix, Andrea; Lanken, Paul; Lathrop, Mark; Li, Mingyao; Marshall, Vanessa; Melander, Olle; Mentch, Frank D; Meyer, Nuala J; Monda, Keri L; Montpetit, Alexandre; Murugesan, Gurunathan; Nakayama, Karen; Nondahl, Dave; Onipinla, Abiodun; Rafelt, Suzanne; Newhouse, Stephen J; Otieno, F George; Patel, Sanjey R; Putt, Mary E; Rodriguez, Santiago; Safa, Radwan N; Sawyer, Douglas B; Schreiner, Pamela J; Simpson, Claire; Sivapalaratnam, Suthesh; Srinivasan, Sathanur R; Suver, Christine; Swergold, Gary; Sweitzer, Nancy K; Thomas, Kelly A; Thorand, Barbara; Timpson, Nicholas J; Tischfield, Sam; Tobin, Martin; Tomaszewski, Maciej; Verschuren, W M Monique; Wallace, Chris; Winkelmann, Bernhard; Zhang, Haitao; Zheng, Dongling; Zhang, Li; Zmuda, Joseph M; Clarke, Robert; Balmforth, Anthony J; Danesh, John; Day, Ian N; Schork, Nicholas J; de Bakker, Paul I W; Delles, Christian; Duggan, David; Hingorani, Aroon D; Hirschhorn, Joel N; Hofker, Marten H; Humphries, Steve E; Kivimaki, Mika; Lawlor, Debbie A; Kottke-Marchant, Kandice; Mega, Jessica L; Mitchell, Braxton D; Morrow, David A; Palmen, Jutta; Redline, Susan; Shields, Denis C; Shuldiner, Alan R; Sleiman, Patrick M; Smith, George Davey; Farrall, Martin; Jamshidi, Yalda; Christiani, David C; Casas, Juan P; Hall, Alistair S; Doevendans, Pieter A; Christie, Jason D; Berenson, Gerald S; Murray, Sarah S; Illig, Thomas; Dorn, Gerald W 2nd; Cappola, Thomas P; Boerwinkle, Eric; Sever, Peter; Rader, Daniel J; Reilly, Muredach P; Caulfield, Mark; Talmud, Philippa J; Topol, Eric; Engert, James C; Wang, Kai; Dominiczak, Anna; Hamsten, Anders; Curtis, Sean P; Silverstein, Roy L; Lange, Leslie A; Sabatine, Marc S; Trip, Mieke; Saleheen, Danish; Peden, John F; Cruickshanks, Karen J; März, Winfried; O'Connell, Jeffrey R; Klungel, Olaf H; Wijmenga, Cisca; Maitland-van der Zee, Anke Hilse; Schadt, Eric E; Johnson, Julie A; Jarvik, Gail P; Papanicolaou, George J; Grant, Struan F A; Munroe, Patricia B; North, Kari E; Samani, Nilesh J; Koenig, Wolfgang; Gaunt, Tom R; Anand, Sonia S; van der Schouw, Yvonne T; Soranzo, Nicole; Fitzgerald, Garret A; Reiner, Alex; Hegele, Robert A; Hakonarson, Hakon; Keating, Brendan J

Common variants at 5q22 associate with pediatric eosinophilic esophagitis

5q22 上的常见变异与儿童嗜酸性食管炎相关

Rothenberg, Marc E; Spergel, Jonathan M; Sherrill, Joseph D; Annaiah, Kiran; Martin, Lisa J; Cianferoni, Antonella; Gober, Laura; Kim, Cecilia; Glessner, Joseph; Frackelton, Edward; Thomas, Kelly; Blanchard, Carine; Liacouras, Chris; Verma, Ritu; Aceves, Seema; Collins, Margaret H; Brown-Whitehorn, Terri; Putnam, Phil E; Franciosi, James P; Chiavacci, Rosetta M; Grant, Struan F A; Abonia, J Pablo; Sleiman, Patrick M A; Hakonarson, Hakon

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

注意力缺陷多动障碍中发现的罕见结构变异主要与神经发育基因相关。

Elia, J; Gai, X; Xie, H M; Perin, J C; Geiger, E; Glessner, J T; D'arcy, M; deBerardinis, R; Frackelton, E; Kim, C; Lantieri, F; Muganga, B M; Wang, L; Takeda, T; Rappaport, E F; Grant, S F A; Berrettini, W; Devoto, M; Shaikh, T H; Hakonarson, H; White, P S

A genome-wide study reveals copy number variants exclusive to childhood obesity cases

全基因组研究揭示了儿童肥胖病例特有的拷贝数变异

Glessner, Joseph T; Bradfield, Jonathan P; Wang, Kai; Takahashi, Nagahide; Zhang, Haitao; Sleiman, Patrick M; Mentch, Frank D; Kim, Cecilia E; Hou, Cuiping; Thomas, Kelly A; Garris, Maria L; Deliard, Sandra; Frackelton, Edward C; Otieno, F George; Zhao, Jianhua; Chiavacci, Rosetta M; Li, Mingyao; Buxbaum, Joseph D; Berkowitz, Robert I; Hakonarson, Hakon; Grant, Struan F A