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

Whole-genome sequencing analysis of anthropometric traits in 672,976 individuals reveals convergence between rare and common genetic associations

对 672,976 名个体的全基因组测序分析显示,人体测量特征存在罕见和常见遗传关联,并揭示了二者之间的趋同性。

Hawkes, Gareth; Wright, Harrison I W; Beaumont, Robin N; Chundru, Kartik; Hanson, Aimee; Jackson, Leigh; Murray, Anna; Patel, Kashyap; Frayling, Timothy M; Wright, Caroline F; Wood, Andrew R; Weedon, Michael N

Genetics identifies obesity as a shared risk factor for co-occurring multiple long-term conditions

遗传学研究表明,肥胖是多种慢性疾病并存的共同风险因素。

Mounier, Ninon; Voller, Bethany; Masoli, Jane A H; Delgado, João; Dudbridge, Frank; Pilling, Luke C; Frayling, Timothy M; Bowden, Jack

Subclassification of obesity for precision prediction of cardiometabolic diseases

根据肥胖程度进行亚分类,以精确预测心血管代谢疾病

Coral, Daniel E; Smit, Femke; Farzaneh, Ali; Gieswinkel, Alexander; Tajes, Juan Fernandez; Sparsø, Thomas; Delfin, Carl; Bauvin, Pierre; Wang, Kan; Temprosa, Marinella; De Cock, Diederik; Blanch, Jordi; Fernández-Real, José Manuel; Ramos, Rafael; Ikram, M Kamran; Gomez, Maria F; Kavousi, Maryam; Panova-Noeva, Marina; Wild, Philipp S; van der Kallen, Carla; Adriaens, Michiel; van Greevenbroek, Marleen; Arts, Ilja; Le Roux, Carel; Ahmadizar, Fariba; Frayling, Timothy M; Giordano, Giuseppe N; Pearson, Ewan R; Franks, Paul W

Author Correction: Subclassification of obesity for precision prediction of cardiometabolic diseases

作者更正:肥胖症亚分类及其在心血管代谢疾病精准预测中的应用

Coral, Daniel E; Smit, Femke; Farzaneh, Ali; Gieswinkel, Alexander; Tajes, Juan Fernandez; Sparsø, Thomas; Delfin, Carl; Bauvin, Pierre; Wang, Kan; Temprosa, Marinella; De Cock, Diederik; Blanch, Jordi; Fernández-Real, José Manuel; Ramos, Rafael; Ikram, M Kamran; Gomez, Maria F; Kavousi, Maryam; Panova-Noeva, Marina; Wild, Philipp S; van der Kallen, Carla; Adriaens, Michiel; van Greevenbroek, Marleen; Arts, Ilja; Le Roux, Carel; Ahmadizar, Fariba; Frayling, Timothy M; Giordano, Giuseppe N; Pearson, Ewan R; Franks, Paul W

Whole-genome sequencing analysis identifies rare, large-effect noncoding variants and regulatory regions associated with circulating protein levels

全基因组测序分析可识别与循环蛋白水平相关的罕见、大效应非编码变异和调控区域。

Hawkes, Gareth; Chundru, Kartik; Jackson, Leigh; Patel, Kashyap A; Murray, Anna; Wood, Andrew R; Wright, Caroline F; Weedon, Michael N; Frayling, Timothy M; Beaumont, Robin N

A systematic analysis of the contribution of genetics to multimorbidity and comparisons with primary care data

对遗传因素在多种疾病共存中的作用进行系统分析,并与初级保健数据进行比较

Murrin, Olivia; Mounier, Ninon; Voller, Bethany; Tata, Linus; Gallego-Moll, Carlos; Roso-Llorach, Albert; Carrasco-Ribelles, Lucía A; Fox, Chris; Allan, Louise M; Woodward, Ruby M; Liang, Xiaoran; Valderas, Jose M; Khalid, Sara M; Dudbridge, Frank; Lamb, Sally E; Mancini, Mary; Farmer, Leon; Boddy, Kate; Bowden, Jack; Melzer, David; Frayling, Timothy M; Masoli, Jane A H; Pilling, Luke C; Violán, Concepción; Delgado, João

Clinical utility of self-reported sleep duration and insomnia symptoms in type 2 diabetes prediction

自我报告的睡眠时长和失眠症状在预测2型糖尿病中的临床应用价值

Wright, Alison K; Huang, Tianyi; Carr, Matthew J; Premdayal, Arjun D; Saluja, Sushant; Dashti, Hassan S; Anderson, Simon G; Ray, David W; Jones, Samuel E; Wood, Andrew R; Frayling, Timothy M; Weedon, Michael N; Lane, Jacqueline M; Saxena, Richa; Liu, Junxi; Bowden, Jack; Lawlor, Deborah A; Redline, Susan; Rutter, Martin K

Effects of childhood and adult height on later life cardiovascular disease risk estimated through Mendelian randomization

通过孟德尔随机化估计儿童期和成年期身高对晚年心血管疾病风险的影响

Richardson, Tom G; Urquijo, Helena; Howe, Laurence J; Hawkes, Gareth; DePaolo, John; Damrauer, Scott M; Frayling, Timothy M; Davey Smith, George

Using clustering of genetic variants in Mendelian randomization to interrogate the causal pathways underlying multimorbidity from a common risk factor

利用孟德尔随机化中的遗传变异聚类来探究由共同风险因素导致的多种疾病的因果通路

Liang, Xiaoran; Mounier, Ninon; Apfel, Nicolas; Khalid, Sara; Frayling, Timothy M; Bowden, Jack

Getting to GRIPS with MR-Egger: Modelling directional pleiotropy independently of allele coding

掌握 MR-Egger:独立于等位基因编码对方向性多效性进行建模

Dudbridge, Frank; Voller, Bethany; Woodward, Ruby M; Saxby, Katie L; Frayling, Timothy M; Pilling, Luke C; Bowden, Jack