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Fletta eftir efnisorði "Biological Specimen Banks"

Fletta eftir efnisorði "Biological Specimen Banks"

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    Adverse health consequences of undiagnosed hearing loss at middle age : A prospective cohort study with the UK Biobank 
    Xu, Shishi; Hou, Can; Han, Xin; Hu, Yao; Yang, Huazhen; Shang, Yanan; Chen, Wenwen; Zeng, Yu; Ying, Zhiye; Sun, Yajing; Qu, Yuanyuan; Lu, Yu; Fang, Fang; Valdimarsdóttir, Unnur A.; Song, Huan (2023-08)
    Objectives: Hearing impairment is common in the middle-aged population but remains largely undiagnosed and untreated. The knowledge about to what extent and how hearing impairment matters for health is currently lacking. Thus, we aimed to comprehensively ...
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    Cardiovascular-related deaths at the beginning of the COVID-19 outbreak : A prospective analysis based on the UK Biobank 
    Wang, Junren; Zhu, Jianwei; Yang, Huazhen; Hu, Yao; Sun, Yajing; Ying, Zhiye; Qu, Yuanyuan; Valdimarsdottir, Unnur; Fang, Fang; Song, Huan (2021-06-04)
    Objective To assess the impact of the COVID-19 outbreak on cardiovascular disease (CVD) related mortality and hospitalisation. Design Community-based prospective cohort study. Setting The UK Biobank. Participants 421 372 UK Biobank participants who ...
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    COVID-19 and risk of subsequent life-threatening secondary infections : a matched cohort study in UK Biobank 
    Hou, Can; Hu, Yihan; Yang, Huazhen; Chen, Wenwen; Zeng, Yu; Ying, Zhiye; Hu, Yao; Sun, Yajing; Qu, Yuanyuan; Gottfreðsson, Magnús; Valdimarsdóttir, Unnur Anna; Song, Huan (2021-11-16)
    BACKGROUND: With the increasing number of people infected with and recovered from coronavirus disease 2019 (COVID-19), the extent of major health consequences of COVID-19 is unclear, including risks of severe secondary infections. METHODS: Based on ...
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    COVID-19 related outcomes among individuals with neurodegenerative diseases : a cohort analysis in the UK biobank 
    Hu, Yihan; Yang, Huazhen; Hou, Can; Chen, Wenwen; Zhang, Hanyue; Ying, Zhiye; Hu, Yao; Sun, Yajing; Qu, Yuanyuan; Feychting, Maria; Valdimarsdóttir, Unnur Anna; Song, Huan; Fang, Fang (2022-01-07)
    Background: An increased susceptibility to COVID-19 has been suggested for individuals with neurodegenerative diseases, but data are scarce from longitudinal studies. Methods: In this community-based cohort study, we included 96,275 participants of the ...
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    Large-scale plasma proteomics comparisons through genetics and disease associations 
    Eldjarn, Grimur Hjorleifsson; Ferkingstad, Egil; Lund, Sigrun H.; Helgason, Hannes; Magnusson, Olafur Th; Gunnarsdottir, Kristbjorg; Olafsdottir, Thorunn A.; Halldorsson, Bjarni V.; Olason, Pall I.; Zink, Florian; Gudjonsson, Sigurjon A.; Sveinbjornsson, Gardar; Magnusson, Magnus I.; Helgason, Agnar; Oddsson, Asmundur; Halldorsson, Gisli H.; Magnusson, Magnus K.; Sævarsdóttir, Sædís; Eiriksdottir, Thjodbjorg; Masson, Gisli; Stefansson, Hreinn; Jonsdottir, Ingileif; Holm, Hilma; Rafnar, Thorunn; Melsted, Pall; Saemundsdottir, Jona; Norddahl, Gudmundur L.; Thorleifsson, Gudmar; Ulfarsson, Magnus O.; Gudbjartsson, Daniel F.; Thorsteinsdottir, Unnur; Sulem, Patrick; Stefansson, Kari (2023-10-04)
    High-throughput proteomics platforms measuring thousands of proteins in plasma combined with genomic and phenotypic information have the power to bridge the gap between the genome and diseases. Here we performed association studies of Olink Explore ...
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    The role of genetic predisposition in cardiovascular risk after cancer diagnosis : a matched cohort study of the UK Biobank 
    Yang, Huazhen; Zeng, Yu; Chen, Wenwen; Sun, Yajing; Hu, Yao; Ying, Zhiye; Wang, Junren; Qu, Yuanyuan; Fang, Fang; Valdimarsdóttir, Unnur A.; Song, Huan (2022-08-24)
    Background: Evidence is scarce regarding the potential modifying role of disease susceptibility on the association between a prior cancer diagnosis and cardiovascular disease (CVD). Methods: We conducted a matched cohort study of UK Biobank including ...
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    The sequences of 150,119 genomes in the UK Biobank 
    DBDS Genetic Consortium (2022-07-20)
    Detailed knowledge of how diversity in the sequence of the human genome affects phenotypic diversity depends on a comprehensive and reliable characterization of both sequences and phenotypic variation. Over the past decade, insights into this relationship ...