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M

Michael N. Weedon

University of Exeter

105H指数
495论文数
7.4W被引数
收录论文 239
发表时间
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Prevalence and penetrance of heritable retinoblastoma in two adult population cohorts: implications for genomic newborn screening可遗传性视网膜母细胞瘤在两个成人人群队列中的患病率和外显率：对基因组新生儿筛查的启示
errEuropean Journal of Human Genetics
IF4.6
err2026-09-18
err0
errOAAI
errIsabella-Anna Lazaridi; Timothy Hall; Helen Hanson; James Fasham; Emma L. Baple; Michael N. Weedon; Caroline F. Wright; Leigh Jackson
err分享
err收藏
Genotype-first approach reveals monogenic lipodystrophy is underdiagnosed, with health and mortality risks基于基因分型的策略揭示单基因脂质营养不良被漏诊，存在健康和死亡风险
errEBioMedicine
IF10.8
err2026-04-18
err0
errOAAI
errLuke N. Sharp; Kevin Colclough; Jacques Murray Leech; Amy V. Evans; Andrew T. Hattersley; Michael N. Weedon; Rebecca J. Brown; Kashyap A. Patel
err分享
err收藏
Whole-genome sequencing analysis of anthropometric traits in 672,976 individuals reveals convergence between rare and common genetic associations672,976个体人体测量性状的全基因组测序分析揭示了罕见和常见遗传关联之间的趋同
errNature Communications
IF15.7
err2026-02-06
err0
errOAAI
errGareth Hawkes; Harrison I. W. Wright; Robin N. Beaumont; Kartik Chundru; Aimee Hanson; Leigh Jackson; Anna Murray; Kashyap Patel; Timothy M. Frayling; Caroline F. Wright; Andrew R. Wood; Michael N. Weedon
err分享
err收藏
Evaluating genotype-treatment interactions for high-risk medications in British general practice: a retrospective cohort study using UK Biobank评估英国全科实践中高风险药物基因型-治疗相互作用：一项利用英国生物银行数据的回顾性队列研究
errBritish Journal of General Practice
IF5.2
err2025-12-01
err0
errOAAI
errMokbel, Kinan; Weedon, Michael; Daniels, Rob; Moye, Victoria; Jackson, Leigh
err分享
err收藏
Population Prevalence, Penetrance, and Mortality for Genetically Confirmed MODY基因确诊的MODY（ maturity-onset diabetes of the young）的患病率、外显率和死亡率
errJOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
IF5.1
err2025-11-01
err0
errOAAI
errSharp, Luke N.; Colclough, Kevin; Murray Leech, Jacques; Cannon, Stuart J.; Laver, Thomas W.; Hattersley, Andrew T.; Weedon, Michael N.; Patel, Kashyap A.
err分享
err收藏
Streamlining large-scale genomic data management: Insights from the UK Biobank whole-genome sequencing data简化大规模基因组数据管理：来自UK Biobank全基因组测序数据的见解
errCell Genomics
IF9
err2025-09-18
err0
errOAAI
errXihao Li; Andrew R. Wood; Yuxin Yuan; Manrui Zhang; Yushu Huang; Gareth Hawkes; Robin N. Beaumont; Michael N. Weedon; Wenyuan Li; Xiaoyu Li; Xihong Lin; Zilin Li
err分享
err收藏
The role of interleukin-6 signalling in pleural infection: observational and genetic analyses白细胞介素-6信号在胸膜感染中的作用：观察性和遗传分析
erreBioMedicine
IF10.8
err2025-08-16
err0
PREAI
errAmerikos Argyriou; Alex Robbins; Rachel Scott; Jodie Chalmers; Harrison I.W. Wright; Robin N. Beaumont; Karen T. Elvers; Michael N. Weedon; Nick A. Maskell; David T. Arnold; Fergus W. Hamilton
err分享
err收藏
Clinical utility of self-reported sleep duration and insomnia symptoms in type 2 diabetes prediction自报睡眠时长和失眠症状在2型糖尿病预测中的临床效用
errDiabetologia
IF10.2
err2025-08-02
err0
errOAAI
errAlison K. Wright; Tianyi Huang; Matthew J. Carr; Arjun D. Premdayal; Sushant Saluja; Hassan S. Dashti; Simon G. Anderson; David W. Ray; Samuel E. Jones; Andrew R. Wood; Timothy M. Frayling; Michael N. Weedon; Jacqueline M. Lane; Richa Saxena; Junxi Liu; Jack Bowden; Deborah A. Lawlor; Susan Redline; Martin K. Rutter
err分享
err收藏
Utility of genome sequencing and group-enrichment to support splice variant interpretation in Marfan syndrome基因组测序和群体富集在支持马方综合征剪接变异解释中的应用价值
errGenetics in Medicine
IF6.2
err2025-06-02
err0
errOAAI
errSusan Walker; David J. Bunyan; Huw B. Thomas; Yesim Kesim; Christopher J. Kershaw; John Holloway; Htoo Wai; Michael Day; Cassandra L. Smith; Gareth Hawkes; Andrew R. Wood; Michael N. Weedon; Ed Blair; Stephanie L. Curtis; Catherine Fielden; Julie Evans; Rebecca Whittington; Sarah F. Smithson; Helen Cox; Paul Clift; Alistair T. Pagnamenta
err分享
err收藏
From Normal Variation in Sleep to Clinical Sleep Disorders: Genetic Insights from over One Million Individuals从正常睡眠变异到临床睡眠障碍：来自逾百万个体的遗传学见解
errSLEEP
IF4.9
err2025-05-19
err0
PREAI
errKunorozva, Lovemore; Maher, Matthew; Weedon, Michael; Wood, Andrew; Jones, Samuel; Abner, Erik; Saxena, Richa; Ollila, Hanna M.; Lane, Jacqueline M.
err分享
err收藏
Genome-wide association analysis of composite sleep health scores in 413,904 individuals
errCOMMUNICATIONS BIOLOGY
IF5.1
err2025-01-24
err0
errOAAI
errGoodman, Matthew O.; Faquih, Tariq; Paz, Valentina; Nagarajan, Pavithra; Lane, Jacqueline M.; Spitzer, Brian; Maher, Matthew; Chung, Joon; Cade, Brian E.; Purcell, Shaun M.; Zhu, Xiaofeng; Noordam, Raymond; Phillips, Andrew J. K.; Kyle, Simon D.; Spiegelhalder, Kai; Weedon, Michael N.; Lawlor, Deborah A.; Rotter, Jerome I.; Taylor, Kent D.; Isasi, Carmen R.; Sofer, Tamar; Dashti, Hassan S.; Rutter, Martin K.; Redline, Susan; Saxena, Richa; Wang, Heming
err分享
err收藏
Accurate and cost-effective generation of a genetic risk score direct from blood lysates直接从血液裂解物中准确且经济高效地生成遗传风险评分
errJOURNAL OF TRANSLATIONAL MEDICINE
IF7.5
err2024-12-20
err0
errOAAI
errLocke, Jonathan M.; Spurrier, Benjamin; Laver, Thomas W.; Houghton, Jayne A. L.; Colclough, Kevin; Weedon, Michael N.; Oram, Richard A.
err分享
err收藏
Type 1 Diabetes Genetic Risk Contributes to Phenotypic Presentation in Monogenic Autoimmune Diabetes1型糖尿病遗传风险有助于单基因自身免疫性糖尿病的表型呈现
errDIABETES
IF7.5
err2024-11-12
err1
PREAI
errLuckett, Amber M.; Hawkes, Gareth; Green, Harry D.; De Franco, Elisa; Hagopian, William A.; Roep, Bart O.; Weedon, Michael N.; Oram, Richard A.; Johnson, Matthew B.
err分享
err收藏
Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height333,100个体的全基因组测序揭示了罕见的非编码单一变异和与身高的聚集关联
errNATURE COMMUNICATIONS
IF15.7
err2024-10-03
err2
errOAAI
errHawkes, Gareth; Beaumont, Robin N.; Li, Zilin; Mandla, Ravi; Li, Xihao; Albert, Christine M.; Arnett, Donna K.; Ashley-Koch, Allison E.; Ashrani, Aneel A.; Barnes, Kathleen C.; Boerwinkle, Eric; Brody, Jennifer A.; Carson, April P.; Chami, Nathalie; Chen, Yii-Der Ida; Chung, Mina K.; Curran, Joanne E.; Darbar, Dawood; Ellinor, Patrick T.; Fornage, Myrian; Gordeuk, Victor R.; Guo, Xiuqing; He, Jiang; Hwu, Chii-Min; Kalyani, Rita R.; Kaplan, Robert; Kardia, Sharon L. R.; Kooperberg, Charles; Loos, Ruth J. F.; Lubitz, Steven A.; Minster, Ryan L.; Naseri, Take; Viali, Satupa'itea; Mitchell, Braxton D.; Murabito, Joanne M.; Palmer, Nicholette D.; Psaty, Bruce M.; Redline, Susan; Shoemaker, M. Benjamin; Silverman, Edwin K.; Telen, Marilyn J.; Weiss, Scott T.; Yanek, Lisa R.; Zhou, Hufeng; Liu, Ching-Ti; North, Kari E.; Justice, Anne E.; Locke, Jonathan M.; Owens, Nick; Murray, Anna; Patel, Kashyap; Frayling, Timothy M.; Wright, Caroline F.; Wood, Andrew R.; Lin, Xihong; Manning, Alisa; Weedon, Michael N.
err分享
err收藏
DISCOVERY OF NOVEL GENES ASSOCIATED WITH SLEEP AND CIRCADIAN RHYTHM PHENOTYPES AND DISORDERS VIA WHOLE-EXOME SEQUENCING
errEUROPEAN NEUROPSYCHOPHARMACOLOGY
IF6.7
err2024-10-01
err0
PREAI
errZhang, Yingzhe; Chen, Chia-Yen; Maher, Matthew; Valliere, Jesse; Kunorozva, Lovemore; Jones, Samuel; Wood, Andrew; Weedon, Michael; Ge, Tian; Lane, Jacqueline M.; Saxena, Richa; Ollila, Hanna M.
err分享
err收藏
Colorectal cancer risk stratification using a polygenic risk score in symptomatic primary care patients-a UK Biobank retrospective cohort study在有症状的初级保健患者中使用多基因风险评分进行结直肠癌风险分层-英国Biobank回顾性队列研究
errEUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
err2024-08-01
err1
errOAAI
errMallabar-Rimmer, Bethan; Merriel, Samuel W. D.; Webster, Amy P.; Jackson, Leigh; Wood, Andrew R.; Barclay, Matthew; Tyrrell, Jessica; Ruth, Katherine S.; Thirlwell, Christina; Oram, Richard; Weedon, Michael N.; Bailey, Sarah E. R.; Green, Harry D.
err分享
err收藏
Guidance for estimating penetrance of monogenic disease-causing variants in population cohorts
errNATURE GENETICS
IF31.8
err2024-07-29
err0
PREAI
errWright, Caroline F.; Sharp, Luke N.; Jackson, Leigh; Murray, Anna; Ware, James S.; MacArthur, Daniel G.; Rehm, Heidi L.; Patel, Kashyap A.; Weedon, Michael N.
err分享
err收藏
The role of accelerometer-derived sleep traits on glycated haemoglobin and glucose levels: a Mendelian randomization study加速度计衍生的睡眠特征对糖化血红蛋白和葡萄糖水平的作用: 一项孟德尔随机化研究
errSCIENTIFIC REPORTS
IF3.9
err2024-06-28
err0
errOAAI
errLiu, Junxi; Richmond, Rebecca C.; Anderson, Emma L.; Bowden, Jack; Barry, Ciarrah-Jane S.; Dashti, Hassan S.; Daghlas, Iyas S.; Lane, Jacqueline M.; Kyle, Simon D.; Vetter, Celine; Morrison, Claire L.; Jones, Samuel E.; Wood, Andrew R.; Frayling, Timothy M.; Wright, Alison K.; Carr, Matthew J.; Anderson, Simon G.; Emsley, Richard A.; Ray, David W.; Weedon, Michael N.; Saxena, Richa; Rutter, Martin K.; Lawlor, Deborah A.
err分享
err收藏
Associations between diabetes-related genetic risk scores and residual beta cell function in type 1 diabetes: the GUTDM1 study1型糖尿病中糖尿病相关遗传风险评分与残余 β 细胞功能之间的关联: GUTDM1研究
errDIABETOLOGIA
IF10.2
err2024-06-26
err0
errOAAI
errSnethlage, Coco M. Fuhri; Balvers, Manon; Ferwerda, Bart; Rampanelli, Elena; de Groen, Pleun; Roep, Bart O.; Herrema, Hilde; McDonald, Timothy J.; van Raalte, Daniel H.; Weedon, Michael N.; Oram, Richard A.; Nieuwdorp, Max; Hanssen, Nordin M. J.
err分享
err收藏
Whole-Genome Sequencing Identifies a Rare Noncoding Variant Proximal to METRN Associated with HbA1c Levels
errDIABETES
IF7.5
err2024-06-14
err0
PREAI
errHawkes, Gareth; Patel, Kashyap A.; Barroso, Ines; Frayling, Timothy M.; Manning, Alisa; Weedon, Michael N.
err分享
err收藏

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