Back to Authors

Michelli, Rodrigo D.

A5028313384 | I4210093009

Mayo Clinic

Hospital de Câncer de Barretos

Citations 2

Whole‐exome sequencing of non‐ BRCA1/BRCA2 mutation carrier cases at high‐risk for hereditary breast/ovarian cancer

Human Mutation | December 18, 2020 | Volume: 42 | Issue: 3 | Pages: 290-299

10.1002/humu.24158 | PMID 33326660

Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

Human Mutation | May 27, 2019 | Volume: 40 | Issue: 9 | Pages: 1557-1578

10.1002/humu.23818 | PMID 31131967