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Cohort Profile: Extended Cohort for E-health, Environment and DNA (EXCEED).

作者信息

John Catherine, Reeve Nicola F, Free Robert C, Williams Alexander T, Ntalla Ioanna, Farmaki Aliki-Eleni, Bethea Jane, Barton Linda M, Shrine Nick, Batini Chiara, Packer Richard, Terry Sarah, Hargadon Beverley, Wang Qingning, Melbourne Carl A, Adams Emma L, Bee Catherine E, Harrington Kyla, Miola José, Brunskill Nigel J, Brightling Christopher E, Barwell Julian, Wallace Susan E, Hsu Ron, Shepherd David J, Hollox Edward J, Wain Louise V, Tobin Martin D

机构信息

Department of Health Sciences, University of Leicester, Leicester, UK.

NIHR Leicester Biomedical Research Centre, University of Leicester, Leicester, UK.

出版信息

Int J Epidemiol. 2019 Jun 1;48(3):678-679j. doi: 10.1093/ije/dyz073.

DOI:10.1093/ije/dyz073
PMID:31062032
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6659362/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fde7/6659362/040c2bbcbcfc/dyz073f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fde7/6659362/68a3c44f93fa/dyz073f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fde7/6659362/f5b9d48782d5/dyz073f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fde7/6659362/040c2bbcbcfc/dyz073f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fde7/6659362/68a3c44f93fa/dyz073f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fde7/6659362/f5b9d48782d5/dyz073f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fde7/6659362/040c2bbcbcfc/dyz073f3.jpg

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New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.新的肺功能遗传信号突出了多种血统中的途径和慢性阻塞性肺疾病的关联。
Nat Genet. 2019 Mar;51(3):481-493. doi: 10.1038/s41588-018-0321-7. Epub 2019 Feb 25.
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Retention strategies in longitudinal cohort studies: a systematic review and meta-analysis.纵向队列研究中的保留策略：系统评价和荟萃分析。
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Pilot Feasibility Stud. 2024 Sep 13;10(1):120. doi: 10.1186/s40814-024-01546-9.
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Genome-wide association study of thyroid-stimulating hormone highlights new genes, pathways and associations with thyroid disease.全基因组关联研究甲状腺刺激素强调了新的基因、途径以及与甲状腺疾病的关联。
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Identification and characterisation of a rare variant underlying hereditary non-alcoholic fatty liver disease.遗传性非酒精性脂肪性肝病潜在罕见变异的鉴定与特征分析。
JHEP Rep. 2023 Apr 23;5(8):100764. doi: 10.1016/j.jhepr.2023.100764. eCollection 2023 Aug.
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Genetic Associations and Architecture of Asthma-COPD Overlap.哮喘-COPD 重叠的遗传关联和结构。
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