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Paper Details

Protective coding variants in CFH and PELI3 and a variant near CTRB1 are associated with age-related macular degenerationâ¿ .
Hum Mol Genet
14
2016
AMD, APOH genes, C3, C9, CFH, CFH R1210C, COL4A3, COL4A3 and APOH genes, CTRB1, HumanExome, Illumina Infinium HumanExome BeadChip, PELI3, R1210C, advanced AMD, age-related macular degeneration, high-density lipoprotein, low-frequency protective variants, non, protective loci, rare variants, rs8056814, vision
Author NameAffiliation
Yi YuTufts Medical Center
Eric H SouiedCreteil Universite Paris Est
Soumya RaychaudhuriBroad Institute
Soumya RaychaudhuriUniversity of Manchester
Soumya RaychaudhuriBrigham and Women's Hospital
Soumya RaychaudhuriBrigham and Women's Hospital
Soumya RaychaudhuriPartners HealthCare Center for Personalized Genetic Medicine
Soumya RaychaudhuriBroad Institute
Soumya RaychaudhuriPartners HealthCare Center for Personalized Genetic Medicine
Soumya RaychaudhuriBrigham and Women's Hospital
Soumya RaychaudhuriBrigham and Women's Hospital
Soumya RaychaudhuriUniversity of Manchester
Mark J DalyBroad Institute
Mark J DalyMassachusetts General Hospital
Mark J DalyPartners HealthCare Center for Personalized Genetic Medicine
Mark J DalyBroad Institute
Mark J DalyPartners HealthCare Center for Personalized Genetic Medicine
Mark J DalyMassachusetts General Hospital
Johanna M SeddonTufts Medical Center
Johanna M SeddonTufts University School of Medicine
Johanna M SeddonTufts University
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