Fine mapping of 2q35 high-risk neuroblastoma locus reveals independent functional risk variants and suggests full-length BARD1 as tumor-suppressor

A previous genome-wide association study (GWAS) identified common variation at the BARD1 locus as being highly associated with susceptibility to high-risk neuroblastoma, but the mechanisms underlying this association have been not extensively investigated. Here, we performed a fine mapping analysis...

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Publié dans:Int J Cancer
Auteurs principaux: Cimmino, Flora, Avitabile, Marianna, Diskin, Sharon J, Vaksman, Zalman, Pignataro, Piero, Formicola, Daniela, Cardinale, Antonella, Testori, Alessandro, Koster, Jan, de Torres, Carmen, Devoto, Marcella, Maris, John M, Iolascon, Achille, Capasso, Mario
Format: Artigo
Langue:Inglês
Publié: 2018
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Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC6258207/
https://ncbi.nlm.nih.gov/pubmed/30132831
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ijc.31822
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