Recurrent structural variation, clustered sites of selection, and disease risk for the complement factor H (CFH) gene family
Stuart Cantsilieris, Bradley J Nelson, John Huddleston, Carl Baker, Lana Harshman, Kelsi Penewit, Katherine M Munson, Melanie Sorensen, AnneMarie E Welch, Vy Dang, Felix Grassmann, Andrea J Richardson, Robyn H Guymer, Tina A Graves-Lindsay, Richard K Wilson, Bernhard HF Weber, Paul N Baird, Rando Allikmets, Evan E Eichler
Proceedings of the National Academy of Sciences | NATL ACAD SCIENCES | Published : 2018
Awarded by US NIH
Awarded by National Health and Medical Research Council (NHMRC) C. J. Martin Biomedical Fellowship
Awarded by NHMRC Senior Research Fellowship
Awarded by NIH
We thank T. Brown for assistance with manuscript preparation. This work was supported, in part, by grants from the US NIH (Grant R01HG002385 to E.E.E. and Grant U41HG007635 to R.K.W. and E.E.E.). S.C. was supported by a National Health and Medical Research Council (NHMRC) C. J. Martin Biomedical Fellowship (1073726). P.N.B. was supported by an NHMRC Senior Research Fellowship (APP1138585). The Centre for Eye Research Australia receives operational infrastructure support from the Victorian Government. R.A. was supported, in part, by NIH Grants R01-EY013435 and P30-EY019007 and by an unrestricted grant from Research to Prevent Blindness to the Department of Ophthalmology, Columbia University. E.E.E. is an Investigator of the Howard Hughes Medical Institute.