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

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

Development and Validation of a Type 1 Diabetes Multi-Ancestry Polygenic Score

1型糖尿病多祖源多基因评分的开发与验证

Deutsch, Aaron J; Bell, Andrew S; Michalek, Dominika A; Burkholder, Adam B; Nam, Stella; Kreienkamp, Raymond J; Sharp, Seth A; Huerta-Chagoya, Alicia; Mandla, Ravi; Nanjala, Ruth; Luo, Yang; Oram, Richard A; Florez, Jose C; Onengut-Gumuscu, Suna; Rich, Stephen S; Ng, Maggie C Y; Motsinger-Reif, Alison A; Manning, Alisa K; Mercader, Josep M; Udler, Miriam S

Associations of Combined Genetic and Lifestyle Risks With Incident Type 2 Diabetes in the UK Biobank

英国生物银行中遗传和生活方式风险因素与2型糖尿病发病率的关联

Zhao, Chi; Hatzikotoulas, Konstantinos; Balasubramanian, Raji; Bertone-Johnson, Elizabeth; Cai, Na; Huang, Lianyun; Huerta-Chagoya, Alicia; Janiczek, Margaret; Ma, Chaoran; Mandla, Ravi; Paluch, Amanda; Rayner, Nigel W; Southam, Lorraine; Sturgeon, Susan R; Suzuki, Ken; Taylor, Henry J; Vankim, Nicole; Yin, Xianyong; Lee, Chi Hyun; Collins, Francis; Spracklen, Cassandra N

Statistical uncertainty explains the poor agreement in polygenic scoring for type 2 diabetes

统计学上的不确定性解释了2型糖尿病多基因评分结果一致性较差的原因。

Mandla, Ravi; Li, Xinzhe; Shi, Zhuozheng; Abramowitz, Sarah A; Lapinska, Sandra; Levin, Michael G; Damrauer, Scott M; Pasaniuc, Bogdan

Genome-wide analysis implicates inner ear development in Ménière's disease

全基因组分析表明内耳发育与梅尼埃病有关

Shi, Zhuozheng; Mandla, Ravi; Li, Jingjing; Li, Xinzhe; Zhang, Zixuan Eleanor; Chen, Sixing; Lapinska, Sandra; Flynn-Carroll, Alexander O; Pasaniuc, Bogdan; Epstein, Douglas J; Mathieson, Iain

Author Correction: Rare variant analyses in 51,256 type 2 diabetes cases and 370,487 controls reveal the pathogenicity spectrum of monogenic diabetes genes

作者更正:对 51,256 例 2 型糖尿病患者和 370,487 例对照者的罕见变异分析揭示了单基因糖尿病基因的致病谱

Huerta-Chagoya, Alicia; Schroeder, Philip; Mandla, Ravi; Li, Jiang; Morris, Lowri; Vora, Maheak; Alkanaq, Ahmed; Nagy, Dorka; Szczerbinski, Lukasz; Madsen, Jesper G S; Bonàs-Guarch, Silvia; Mollandin, Fanny; Cole, Joanne B; Porneala, Bianca; Westerman, Kenneth; Li, Josephine H; Pollin, Toni I; Florez, Jose C; Gloyn, Anna L; Carey, David J; Cebola, Inês; Mirshahi, Uyenlinh L; Manning, Alisa K; Leong, Aaron; Udler, Miriam; Mercader, Josep M

Mendelian Randomization Suggests a Causal Link Between Glycemic Traits and Thoracic Aortic Structures and Diseases

孟德尔随机化表明血糖性状与胸主动脉结构和疾病之间存在因果关系

Daria, Tselmen; Iyer, Kruthika; Alkhairo, Hasan; Kho, Pik Fang; Suzuki, Ken; Hatzikotoulas, Konstantinos; Southam, Lorraine; Taylor, Henry J; Yin, Xianyong; Mandla, Ravi; Huerta-Chagoya, Alicia; Rayner, William N; Levin, Michael G; Damrauer, Scott M; Tsao, Philip S; Priest, James R; Klarin, Derek; Pirruccello, James; Echouffo Tcheugui, Justin B; Tcheandjieu, Catherine

Association of genetic scores related to insulin resistance with neurological outcomes in ancestrally diverse cohorts from the Trans-Omics for Precision Medicine (TOPMed) program

来自精准医学跨组学(TOPMed)计划的祖源多样性队列中,与胰岛素抵抗相关的遗传评分与神经系统结局的关联

Sarnowski, Chloé; Zhang, Yixin; Ammous, Farah; Shade, Lincoln M P; DiCorpo, Daniel; Jian, Xueqiu; Arnett, Donna K; Austin, Thomas R; Beiser, Alexa; Bis, Joshua C; Blangero, John; Boerwinkle, Eric; Bressler, Jan; Curran, Joanne E; DeCarli, Charles S; Doddapaneni, Harsha; Dupuis, Josée; Fardo, David W; Florez, Jose C; Gabriel, Stacey; Gibbs, Richard A; Glahn, David C; Gupta, Namrata; González, Hector M; González, Kevin A; Hatzikotoulas, Konstantinos; Hayden, Kathleen M; Heckbert, Susan R; Hidalgo, Bertha; Huerta-Chagoya, Alicia; Hughes, Timothy M; Kardia, Sharon L R; Kooperberg, Charles L; Launer, Lenore J; Longstreth, W T Jr; Mandla, Ravi; Mathias, Rasika A; Morris, Andrew P; Mosley, Thomas H; Nasrallah, Ilya M; Nyquist, Paul; Psaty, Bruce M; Qi, Qibin; Raffield, Laura M; Rayner, Nigel W; Reiner, Alexander P; Satizabal, Claudia L; Selvin, Elizabeth; Sevilla-Gonzalez, Magdalena D R; Smith, Albert V; Smith, Jennifer A; Smith, Kirk; Snively, Beverly M; Southam, Lorraine; Sofer, Tamar; Suzuki, Ken; Taylor, Henry J; Udler, Miriam S; Viaud-Martinez, Karine A; Wassertheil-Smoller, Sylvia; Wood, Alexis C; Yanek, Lisa R; Yin, Xianyong; Manning, Alisa K; Rotter, Jerome I; Rich, Stephen S; Meigs, James B; Fornage, Myriam; Seshadri, Sudha; Morrison, Alanna C

Correcting for Genomic Inflation Leads to Loss of Power in Large-Scale Genome-Wide Association Study Meta-Analysis

校正基因组膨胀会导致大规模全基因组关联研究荟萃分析的统计功效下降

Singh, Archit; Southam, Lorraine; Hatzikotoulas, Konstantinos; Rayner, Nigel W; Suzuki, Ken; Taylor, Henry J; Yin, Xianyong; Mandla, Ravi; Huerta-Chagoya, Alicia; Morris, Andrew P; Zeggini, Eleftheria; Bocher, Ozvan

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

Bocher, Ozvan; Arruda, Ana Luiza; Yoshiji, Satoshi; Zhao, Chi; Su, Chen-Yang; Yin, Xianyong; Cammann, Davis; Taylor, Henry J; Chen, Jingchun; Suzuki, Ken; Mandla, Ravi; Huerta-Chagoya, Alicia; 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