Fine-mapping of genetic loci driving spontaneous clearance of hepatitis C virus infection
Fine-mapping of genetic loci driving spontaneous clearance of hepatitis C virus infection
Approximately three quarters of acute hepatitis C (HCV) infections evolve to a chronic state, while one quarter are spontaneously cleared. Genetic predispositions strongly contribute to the development of chronicity. We have conducted a genome-wide association study to identify genomic variants underlying HCV spontaneous clearance using ImmunoChip in European and African ancestries. We confirmed two previously reported significant associations, in the IL28B/IFNL4 and the major histocompatibility complex (MHC) regions, with spontaneous clearance in the European population. We further fine-mapped the association in the MHC to a region of about 50 kilo base pairs, down from 1 mega base pairs in the previous study. Additional analyses suggested that the association in MHC is stronger in samples from North America than those from Europe
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Huang, Hailiang
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Duggal, Priya
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Thio, Chloe L.
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Latanich, Rachel
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Goedert, James J.
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Mangia, Alessandra
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Cox, Andrea L.
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Kirk, Gregory D.
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Mehta, Shruti
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Aneja, Jasneet
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Alric, Laurent
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Donfield, Sharyne M.
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Cramp, Matthew E.
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Khakoo, Salim
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Tobler, Leslie H.
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Busch, Michael
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Alexander, Graeme J.
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Rosen, Hugo R.
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Edlin, Brian R.
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Segal, Florencia P.
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Lauer, Georg M.
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Thomas, David L.
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Daly, Mark J.
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Chung, Raymond T.
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Kim, Arthur Y.
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Huang, Hailiang
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Duggal, Priya
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Thio, Chloe L.
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Latanich, Rachel
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Goedert, James J.
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Mangia, Alessandra
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Cox, Andrea L.
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Kirk, Gregory D.
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Mehta, Shruti
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Aneja, Jasneet
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Alric, Laurent
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Donfield, Sharyne M.
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Cramp, Matthew E.
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Khakoo, Salim
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Tobler, Leslie H.
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Busch, Michael
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Alexander, Graeme J.
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Rosen, Hugo R.
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Edlin, Brian R.
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Segal, Florencia P.
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Lauer, Georg M.
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Thomas, David L.
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Daly, Mark J.
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Chung, Raymond T.
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Kim, Arthur Y.
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