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author Fellay, Jacques
Ge, Dongliang
Shianna, Kevin V.
Colombo, Sara
Ledergerber, Bruno
Cirulli, Elizabeth T.
Urban, Thomas J.
Zhang, Kunlin
Gumbs, Curtis E.
Smith, Jason P.
Castagna, Antonella
Cozzi-Lepri, Alessandro
De Luca, Andrea
Easterbrook, Philippa
Günthard, Huldrych F.
Mallal, Simon
Mussini, Cristina
Dalmau, Judith
Martinez-Picado, Javier
Miro, José M.
Obel, Niels
Wolinsky, Steven M.
Martinson, Jeremy J.
Detels, Roger
Margolick, Joseph B.
Jacobson, Lisa P.
Descombes, Patrick
Antonarakis, Stylianos E.
Beckmann, Jacques S.
O'Brien, Stephen J.
Letvin, Norman L.
McMichael, Andrew J.
Haynes, Barton F.
Carrington, Mary
Feng, Sheng
Telenti, Amalio
Goldstein, David B.
author_facet Fellay, Jacques
Ge, Dongliang
Shianna, Kevin V.
Colombo, Sara
Ledergerber, Bruno
Cirulli, Elizabeth T.
Urban, Thomas J.
Zhang, Kunlin
Gumbs, Curtis E.
Smith, Jason P.
Castagna, Antonella
Cozzi-Lepri, Alessandro
De Luca, Andrea
Easterbrook, Philippa
Günthard, Huldrych F.
Mallal, Simon
Mussini, Cristina
Dalmau, Judith
Martinez-Picado, Javier
Miro, José M.
Obel, Niels
Wolinsky, Steven M.
Martinson, Jeremy J.
Detels, Roger
Margolick, Joseph B.
Jacobson, Lisa P.
Descombes, Patrick
Antonarakis, Stylianos E.
Beckmann, Jacques S.
O'Brien, Stephen J.
Letvin, Norman L.
McMichael, Andrew J.
Haynes, Barton F.
Carrington, Mary
Feng, Sheng
Telenti, Amalio
Goldstein, David B.
author_sort Fellay, Jacques
collection PubMed
description To extend the understanding of host genetic determinants of HIV-1 control, we performed a genome-wide association study in a cohort of 2,554 infected Caucasian subjects. The study was powered to detect common genetic variants explaining down to 1.3% of the variability in viral load at set point. We provide overwhelming confirmation of three associations previously reported in a genome-wide study and show further independent effects of both common and rare variants in the Major Histocompatibility Complex region (MHC). We also examined the polymorphisms reported in previous candidate gene studies and fail to support a role for any variant outside of the MHC or the chemokine receptor cluster on chromosome 3. In addition, we evaluated functional variants, copy-number polymorphisms, epistatic interactions, and biological pathways. This study thus represents a comprehensive assessment of common human genetic variation in HIV-1 control in Caucasians.
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spelling pubmed-27912202009-12-30 Common Genetic Variation and the Control of HIV-1 in Humans Fellay, Jacques Ge, Dongliang Shianna, Kevin V. Colombo, Sara Ledergerber, Bruno Cirulli, Elizabeth T. Urban, Thomas J. Zhang, Kunlin Gumbs, Curtis E. Smith, Jason P. Castagna, Antonella Cozzi-Lepri, Alessandro De Luca, Andrea Easterbrook, Philippa Günthard, Huldrych F. Mallal, Simon Mussini, Cristina Dalmau, Judith Martinez-Picado, Javier Miro, José M. Obel, Niels Wolinsky, Steven M. Martinson, Jeremy J. Detels, Roger Margolick, Joseph B. Jacobson, Lisa P. Descombes, Patrick Antonarakis, Stylianos E. Beckmann, Jacques S. O'Brien, Stephen J. Letvin, Norman L. McMichael, Andrew J. Haynes, Barton F. Carrington, Mary Feng, Sheng Telenti, Amalio Goldstein, David B. PLoS Genet Research Article To extend the understanding of host genetic determinants of HIV-1 control, we performed a genome-wide association study in a cohort of 2,554 infected Caucasian subjects. The study was powered to detect common genetic variants explaining down to 1.3% of the variability in viral load at set point. We provide overwhelming confirmation of three associations previously reported in a genome-wide study and show further independent effects of both common and rare variants in the Major Histocompatibility Complex region (MHC). We also examined the polymorphisms reported in previous candidate gene studies and fail to support a role for any variant outside of the MHC or the chemokine receptor cluster on chromosome 3. In addition, we evaluated functional variants, copy-number polymorphisms, epistatic interactions, and biological pathways. This study thus represents a comprehensive assessment of common human genetic variation in HIV-1 control in Caucasians. Public Library of Science 2009-12-24 /pmc/articles/PMC2791220/ /pubmed/20041166 http://dx.doi.org/10.1371/journal.pgen.1000791 Text en This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Fellay, Jacques
Ge, Dongliang
Shianna, Kevin V.
Colombo, Sara
Ledergerber, Bruno
Cirulli, Elizabeth T.
Urban, Thomas J.
Zhang, Kunlin
Gumbs, Curtis E.
Smith, Jason P.
Castagna, Antonella
Cozzi-Lepri, Alessandro
De Luca, Andrea
Easterbrook, Philippa
Günthard, Huldrych F.
Mallal, Simon
Mussini, Cristina
Dalmau, Judith
Martinez-Picado, Javier
Miro, José M.
Obel, Niels
Wolinsky, Steven M.
Martinson, Jeremy J.
Detels, Roger
Margolick, Joseph B.
Jacobson, Lisa P.
Descombes, Patrick
Antonarakis, Stylianos E.
Beckmann, Jacques S.
O'Brien, Stephen J.
Letvin, Norman L.
McMichael, Andrew J.
Haynes, Barton F.
Carrington, Mary
Feng, Sheng
Telenti, Amalio
Goldstein, David B.
Common Genetic Variation and the Control of HIV-1 in Humans
title Common Genetic Variation and the Control of HIV-1 in Humans
title_full Common Genetic Variation and the Control of HIV-1 in Humans
title_fullStr Common Genetic Variation and the Control of HIV-1 in Humans
title_full_unstemmed Common Genetic Variation and the Control of HIV-1 in Humans
title_short Common Genetic Variation and the Control of HIV-1 in Humans
title_sort common genetic variation and the control of hiv-1 in humans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2791220/
https://www.ncbi.nlm.nih.gov/pubmed/20041166
http://dx.doi.org/10.1371/journal.pgen.1000791
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