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Recurrent structural variation, clustered sites of selection, and disease risk for the complement factor H (CFH) gene family

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dc.contributor.authorCantsilieris, Stuart
dc.contributor.authorNelson, Bradley J.
dc.contributor.authorHuddleston, John
dc.contributor.authorBaker, Carl
dc.contributor.authorHarshman, Lana
dc.contributor.authorPenewit, Kelsi
dc.contributor.authorMunson, Katherine M.
dc.contributor.authorSorensen, Melanie
dc.contributor.authorWelch, Anne Marie E.
dc.contributor.authorDang, Vy
dc.contributor.authorGrassmann, Felix
dc.contributor.authorRichardson, Andrea J.
dc.contributor.authorGuymer, Robyn H.
dc.contributor.authorGraves-Lindsay, Tina A.
dc.contributor.authorWilson, Richard K.
dc.contributor.authorWeber, Bernhard H.F.
dc.contributor.authorBaird, Paul N.
dc.contributor.authorAllikmets, Rando
dc.contributor.authorEichler, Evan E.
dc.contributor.institutionUniversity of Aberdeen.Medical Sciencesen
dc.date.accessioned2020-06-30T10:10:01Z
dc.date.available2020-06-30T10:10:01Z
dc.date.issued2018-05-08
dc.descriptionData deposition: The data reported in this paper have been deposited as a National Center for Biotechnology Information BioProject (accession no. PRJNA401648). Author contributions: S.C. and E.E.E. designed research; S.C., C.B., L.H., K.P., K.M.M., M.S., A.E.W., V.D., T.A.G.-L., and R.K.W. performed research; S.C., J.H., C.B., L.H., K.P., K.M.M., M.S., A.E.W., V.D., F.G., A.J.R., R.H.G., T.A.G.-L., R.K.W., B.H.F.W., P.N.B., R.A., and E.E.E. contributed new reagents/analytic tools; S.C., B.J.N., J.H., and E.E.E. analyzed data; and S.C., B.J.N., and E.E.E. wrote the paper.en
dc.description.statusPeer revieweden
dc.format.extent10
dc.format.extent1448773
dc.identifier170735933
dc.identifierebfe5d19-2a55-45c4-8533-f51f73a5bdbd
dc.identifier85046691982
dc.identifier29686068
dc.identifier.citationCantsilieris, S, Nelson, B J, Huddleston, J, Baker, C, Harshman, L, Penewit, K, Munson, K M, Sorensen, M, Welch, A M E, Dang, V, Grassmann, F, Richardson, A J, Guymer, R H, Graves-Lindsay, T A, Wilson, R K, Weber, B H F, Baird, P N, Allikmets, R & Eichler, E E 2018, 'Recurrent structural variation, clustered sites of selection, and disease risk for the complement factor H (CFH) gene family', Proceedings of the National Academy of Sciences of the United States of America, vol. 115, no. 19, pp. E4433-E4442. https://doi.org/10.1073/pnas.1717600115en
dc.identifier.doi10.1073/pnas.1717600115
dc.identifier.iss19en
dc.identifier.issn0027-8424
dc.identifier.otherORCID: /0000-0003-1390-7528/work/76609388
dc.identifier.urihttps://hdl.handle.net/2164/14610
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=85046691982&partnerID=8YFLogxKen
dc.identifier.urlhttp://www.pnas.org/lookup/suppl/doi:10.1073/pnas.1717600115/-/DCSupplementalen
dc.identifier.vol115en
dc.language.isoeng
dc.relation.ispartofProceedings of the National Academy of Sciences of the United States of Americaen
dc.subjectSDG 3 - Good Health and Well-beingen
dc.subjectAge-related macular degenerationen
dc.subjectAMDen
dc.subjectCFH gene familyen
dc.subjectNatural selectionen
dc.subjectStructural variationen
dc.subjectR Medicineen
dc.subjectGeneralen
dc.subject.lccRen
dc.titleRecurrent structural variation, clustered sites of selection, and disease risk for the complement factor H (CFH) gene familyen
dc.typeJournal articleen

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