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Paper Details

Recurrent structural variation, clustered sites of selection, and disease risk for the complement factor H (<i>CFH</i>) gene family.
Proc Natl Acad Sci U S A
37
2018
360-kbp locus, 4, AHUS, AMD, CFH, CFH-related, CFHR, CFHR fusion genes, CFHR gene promoter, CFHR genes, CFHR1, CFHR2, CFHR3, CFHR3 7-13 Mya, CFHR4 25-, CFHR4 25-35 Mya, N, age-related macular degeneration, ancestral CFHR gene promoter, atypical hemolytic uremic syndrome, complement factor H, complement factor H (CFH) gene family, exons 8 and 9, functional domains, gene family, genetic disease, genetic diseases, human, patients
Author NameAffiliation
Carl BakerUniversity of Washington School of Medicine
Carl BakerUniversity of Washington School of Medicine
Felix GrassmannInstitute of Human Genetics, University of Regensburg
Andrea J RichardsonUniversity of Melbourne, Royal Victorian Eye and Ear Hospital
Robyn H GuymerUniversity of Melbourne, Royal Victorian Eye and Ear Hospital
Tina GravesMcDonnell Genome Institute at Washington University
Tina GravesMcDonnell Genome Institute at Washington University
Richard K WilsonInstitute for Genomic Medicine, Nationwide Children's Hospital
Richard K WilsonThe Ohio State University College of Medicine
Richard K WilsonInstitute for Genomic Medicine, Nationwide Children's Hospital
Richard K WilsonThe Ohio State University College of Medicine
Paul N BairdUniversity of Melbourne, Royal Victorian Eye and Ear Hospital
Rando AllikmetsColumbia University
Rando AllikmetsColumbia University
Evan E EichlerUniversity of Washington School of Medicine
Evan E EichlerHoward Hughes Medical Institute, University of Washington
Evan E EichlerUniversity of Washington School of Medicine
Evan E EichlerHoward Hughes Medical Institute, University of Washington
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