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Page 1
Relaxed Selection During a Recent Human Expansion.
Peischl S, Dupanloup I, Foucal A, Jomphe M, Bruat V, Grenier JC, Gouy A, Gilbert KJ, Gbeha E, Bosshard L, Hip-Ki E, Agbessi M, Hodgkinson A, Vézina H, Awadalla P, Excoffier L. Peischl S, et al. Among authors: gbeha e. Genetics. 2018 Feb;208(2):763-777. doi: 10.1534/genetics.117.300551. Epub 2017 Nov 29. Genetics. 2018. PMID: 29187508 Free PMC article.
Gene-by-environment interactions in urban populations modulate risk phenotypes.
Favé MJ, Lamaze FC, Soave D, Hodgkinson A, Gauvin H, Bruat V, Grenier JC, Gbeha E, Skead K, Smargiassi A, Johnson M, Idaghdour Y, Awadalla P. Favé MJ, et al. Among authors: gbeha e. Nat Commun. 2018 Mar 6;9(1):827. doi: 10.1038/s41467-018-03202-2. Nat Commun. 2018. PMID: 29511166 Free PMC article.
An X-linked haplotype of Neandertal origin is present among all non-African populations.
Yotova V, Lefebvre JF, Moreau C, Gbeha E, Hovhannesyan K, Bourgeois S, Bédarida S, Azevedo L, Amorim A, Sarkisian T, Avogbe PH, Chabi N, Dicko MH, Kou' Santa Amouzou ES, Sanni A, Roberts-Thomson J, Boettcher B, Scott RJ, Labuda D. Yotova V, et al. Among authors: gbeha e. Mol Biol Evol. 2011 Jul;28(7):1957-62. doi: 10.1093/molbev/msr024. Epub 2011 Jan 25. Mol Biol Evol. 2011. PMID: 21266489
Genomic architecture of sickle cell disease in West African children.
Quinlan J, Idaghdour Y, Goulet JP, Gbeha E, de Malliard T, Bruat V, Grenier JC, Gomez S, Sanni A, Rahimy MC, Awadalla P. Quinlan J, et al. Among authors: gbeha e. Front Genet. 2014 Feb 14;5:26. doi: 10.3389/fgene.2014.00026. eCollection 2014. Front Genet. 2014. PMID: 24592274 Free PMC article.
Evidence for additive and interaction effects of host genotype and infection in malaria.
Idaghdour Y, Quinlan J, Goulet JP, Berghout J, Gbeha E, Bruat V, de Malliard T, Grenier JC, Gomez S, Gros P, Rahimy MC, Sanni A, Awadalla P. Idaghdour Y, et al. Among authors: gbeha e. Proc Natl Acad Sci U S A. 2012 Oct 16;109(42):16786-93. doi: 10.1073/pnas.1204945109. Epub 2012 Sep 4. Proc Natl Acad Sci U S A. 2012. PMID: 22949651 Free PMC article.
Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans.
Casals F, Hodgkinson A, Hussin J, Idaghdour Y, Bruat V, de Maillard T, Grenier JC, Gbeha E, Hamdan FF, Girard S, Spinella JF, Larivière M, Saillour V, Healy J, Fernández I, Sinnett D, Michaud JL, Rouleau GA, Haddad E, Le Deist F, Awadalla P. Casals F, et al. Among authors: gbeha e. PLoS Genet. 2013;9(9):e1003815. doi: 10.1371/journal.pgen.1003815. Epub 2013 Sep 26. PLoS Genet. 2013. PMID: 24086152 Free PMC article.
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