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

Unravelling the molecular mechanisms causal to type 2 diabetes across global populations and disease-relevant tissues

揭示全球人群和疾病相关组织中导致 2 型糖尿病的分子机制

期刊:Nature Metabolism
影响因子:20.8
doi:10.1038/s42255-025-01444-1
Bocher, Ozvan; Arruda, Ana Luiza; Yoshiji, Satoshi; Zhao, Chi; Huerta-Chagoya, Alicia; Su, Chen-Yang; Yin, Xianyong; Cammann, Davis; Taylor, Henry J; Chen, Jingchun; Suzuki, Ken; Mandla, Ravi; Yang, Ta-Yu; Matsuda, Fumihiko; Mercader, Josep M; Flannick, Jason; Meigs, James B; Wood, Alexis C; Vujkovic, Marijana; Voight, Benjamin F; Spracklen, Cassandra N; Rotter, Jerome I; Morris, Andrew P; Zeggini, Eleftheria
糖尿病
代谢
发表日期：2026
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Desiderata for a biomedical knowledge network: opportunities, challenges and future directions

构建生物医学知识网络的愿景：机遇、挑战与未来方向

期刊:Bioinformatics Advances
影响因子:2.8
doi:10.1093/bioadv/vbag036
Wu, Chunlei; Liu, Hongfang; Flannick, Jason; Musen, Mark A; Su, Andrew I; Hunter, Lawrence E; Powers, Thomas M; Wu, Cathy H
发表日期：2026
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A resource of "bottom-line" variant associations for 1,281 complex traits by integrating data across published genome-wide association studies

通过整合已发表的全基因组关联研究数据，我们获得了1281个复杂性状的“最终”变异关联资源。

期刊:
影响因子:
doi:10.21203/rs.3.rs-8585052/v1
Nguyen, Trang; Büyükgöl, Furkan; Smadbeck, Patrick; Massung, Jeffrey; Costanzo, Maria C; Ruiz, Monica; Dornbos, Peter; Yoshiji, Satoshi; Koesterer, Ryan; Nguyen, Thanh Long; Jang, Dongkeun; Hoang, Quy; Ji, Yue; McMahon, Aoife; Sengupta, Sebanti; Yin, Xianyong; Ryan, Brady; Welch, Ryan P; Treur, Jorien; Bezzina, Connie R; Abecasis, Goncalo; Boehnke, Michael; Burtt, Noël P; Flannick, Jason
发表日期：2026
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Realizing the promise of genome-wide association studies for effector gene prediction

实现全基因组关联研究在效应基因预测方面的潜力

期刊:Nature Genetics
影响因子:29
doi:10.1038/s41588-025-02210-5
Costanzo, Maria C; Harris, Laura W; Ji, Yue; McMahon, Aoife; Burtt, Noël P; Flannick, Jason
发表日期：2025
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Integrative proteogenomic analysis identifies COL6A3-derived endotrophin as a mediator of the effect of obesity on coronary artery disease

整合蛋白质基因组学分析发现，COL6A3衍生的内皮素是肥胖对冠状动脉疾病影响的介质。

期刊:Nature Genetics
影响因子:29
doi:10.1038/s41588-024-02052-7
Yoshiji, Satoshi; Lu, Tianyuan; Butler-Laporte, Guillaume; Carrasco-Zanini-Sanchez, Julia; Su, Chen-Yang; Chen, Yiheng; Liang, Kevin; Willett, Julian Daniel Sunday; Wang, Shidong; Adra, Darin; Ilboudo, Yann; Sasako, Takayoshi; Koyama, Satoshi; Nakao, Tetsushi; Forgetta, Vincenzo; Farjoun, Yossi; Zeberg, Hugo; Zhou, Sirui; Marks-Hultström, Michael; Machiela, Mitchell J; Kaalia, Rama; Dashti, Hesam; Claussnitzer, Melina; Flannick, Jason; Wareham, Nicholas J; Mooser, Vincent; Timpson, Nicholas J; Langenberg, Claudia; Richards, J Brent
肥胖
COL
代谢
发表日期：2025
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Accelerating Medicines Partnership in Type 2 Diabetes and Common Metabolic Diseases: Collaborating to Maximize the Value of Genetic and Genomic Data

加速药物研发伙伴关系在 2 型糖尿病和常见代谢疾病领域的应用：携手合作，最大限度地发挥遗传和基因组数据的价值

期刊:Diabetes
影响因子:7.5
doi:10.2337/db25-0042
Costanzo, Maria C; Akolkar, Beena; Claussnitzer, Melina; Florez, Jose C; Gloyn, Anna L; Grant, Struan F A; Kaestner, Klaus H; Manning, Alisa K; Mohlke, Karen L; Parker, Stephen C J; Titchenell, Paul M; Udler, Miriam S; Jones, Melissa A; Kamphaus, Tania N; Fischer, Rachel A; McCarthy, Mark I; Miller, Melissa R; Boehnke, Michael; Flannick, Jason; Burtt, Noël P
糖尿病
代谢
发表日期：2025
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An Alternatively Translated Isoform of PPARG Suggests AF-1 Domain Inhibition as an Insulin Sensitization Target.

PPARG 的另一种翻译同工型表明 AF-1 结构域抑制可作为胰岛素增敏靶点

期刊:Diabetes
影响因子:7.5
doi:10.2337/db24-0497
Du Xiaomi, Mendez-Lara Karen, Hu Siqi, Diao Rachel, Bhavimani Guru, Hernandez Ruben, Glass Kimberly, De Arruda Saldanha Camila, Flannick Jason, Heinz Sven, Majithia Amit R
信号转导
发表日期：2025
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Common and rare genetic variants explain distinct diagnostic variance in pediatric attention deficit hyperactivity disorder

常见和罕见的基因变异解释了儿童注意力缺陷多动障碍的不同诊断差异

期刊:Genetics in Medicine
影响因子:6.2
doi:10.1016/j.gim.2025.101598
Arnett, Anne B; Koesterer, Ryan; Tovar, Paulina Gonzalez; O'Connell, Mia; Patel, Soleha; Zhang, Han; French, Courtney E; Rockowitz, Shira; Flannick, Jason; Doan, Ryan
发表日期：2025
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Erratum: The Neurodegenerative Disease Knowledge Portal: Propelling Discovery Through the Sharing of Neurodegenerative Disease Genomic Resources

更正：神经退行性疾病知识门户：通过共享神经退行性疾病基因组资源推动发现

期刊:Neurology-Genetics
影响因子:3.7
doi:10.1212/NXG.0000000000200273
Dilliott, Allison A; Costanzo, Maria C; Bandres-Ciga, Sara; Blauwendraat, Cornelis; Casey, Bradford; Hoang, Quy; Iwaki, Hirotaka; Jang, Dongkeun; Kim, Jonggeol Jeffrey; Leonard, Hampton L; Levine, Kristin S; Makarious, Mary; Nguyen, Trang T; Rouleau, Guy A; Singleton, Andrew B; Smadbeck, Patrick; Solle, J; Vitale, Dan; Nalls, Mike; Flannick, Jason; Burtt, Noël P; Farhan, Sali M K
神经科学
发表日期：2025
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The Neurodegenerative Disease Knowledge Portal: Propelling Discovery Through the Sharing of Neurodegenerative Disease Genomic Resources

神经退行性疾病知识门户：通过共享神经退行性疾病基因组资源推动发现

期刊:Neurology-Genetics
影响因子:3.7
doi:10.1212/NXG.0000000000200246
Dilliott, Allison A; Costanzo, Maria C; Bandres-Ciga, Sara; Blauwendraat, Cornelis; Casey, Bradford; Hoang, Quy; Iwaki, Hirotaka; Jang, Dongkeun; Kim, Jonggeol Jeffrey; Leonard, Hampton L; Levine, Kristin S; Makarious, Mary; Nguyen, Trang T; Rouleau, Guy A; Singleton, Andrew B; Smadbeck, Patrick; Solle, J; Vitale, Dan; Nalls, Mike; Flannick, Jason; Burtt, Noël P; Farhan, Sali M K
神经科学
发表日期：2025
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