Publications by authors named "Rodrigo D Michelli"

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Whole-exome sequencing of non-BRCA1/BRCA2 mutation carrier cases at high-risk for hereditary breast/ovarian cancer.
Paula S Felicio, Rebeca S Grasel, Natalia Campacci, Andre E de Paula, Henrique C R Galvão, Rodrigo D Michelli

Hum Mutat· March 2021

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Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification.
Michael T Parsons, Emma Tudini, Hongyan Li, Eric Hahnen, Barbara Wappenschmidt, Rodrigo D Michelli

Hum Mutat· September 2019

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Identification of hereditary cancer in the general population: development and validation of a screening questionnaire for obtaining the family history of cancer.
Natalia Campacci, Juliana O de Lima, André L Carvalho, Rodrigo D Michelli, Rafael Haikel

Cancer Med· December 2017

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A TP53 founder mutation, p.R337H, is associated with phyllodes breast tumors in Brazil.
Juliana Giacomazzi, Patricia Koehler-Santos, Edenir Inez Palmero, Marcia S Graudenz, Luis Fernando Rivero, Rodrigo Depieri Michelli

Virchows Arch· July 2013

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