Determinants of transthyretin levels and their association with adverse clinical outcomes among UK Biobank participants
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DOI: 10.1038/s41467-024-50231-1
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- Cristopher V. Van Hout & Ioanna Tachmazidou & Joshua D. Backman & Joshua D. Hoffman & Daren Liu & Ashutosh K. Pandey & Claudia Gonzaga-Jauregui & Shareef Khalid & Bin Ye & Nilanjana Banerjee & Alexand, 2020. "Exome sequencing and characterization of 49,960 individuals in the UK Biobank," Nature, Nature, vol. 586(7831), pages 749-756, October.
- Benjamin B. Sun & Joshua Chiou & Matthew Traylor & Christian Benner & Yi-Hsiang Hsu & Tom G. Richardson & Praveen Surendran & Anubha Mahajan & Chloe Robins & Steven G. Vasquez-Grinnell & Liping Hou & , 2023. "Plasma proteomic associations with genetics and health in the UK Biobank," Nature, Nature, vol. 622(7982), pages 329-338, October.
- Joshua D. Backman & Alexander H. Li & Anthony Marcketta & Dylan Sun & Joelle Mbatchou & Michael D. Kessler & Christian Benner & Daren Liu & Adam E. Locke & Suganthi Balasubramanian & Ashish Yadav & Ni, 2021. "Exome sequencing and analysis of 454,787 UK Biobank participants," Nature, Nature, vol. 599(7886), pages 628-634, November.
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