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Familial Cancer|August 11, 2010
Frequency of extracolonic tumors in Brazilian families with Lynch syndrome: analysis of a hereditary colorectal cancer institutional registryFelipe Carneiro da Silva, Ligia Petrolini de Oliveira, Erika Monteiro Santos, et al.Cancers|August 26, 2023
A Breast Cancer Polygenic Risk Score Is Feasible for Risk Stratification in the Norwegian PopulationBayram Cevdet Akdeniz, Morten Mattingsdal, Mev Dominguez-Valentin, et al.JCO Global Oncology|May 20, 2026
Cancer Spectrum and Gene-Specific Patterns in Lynch Syndrome: Insights From 47 Families in a Brazilian Institutional CohortThiago Bassaneze, Fábio Oliveira Ferreira, Renata Lazari Sandoval, et al.Hereditary Cancer in Clinical Practice|January 27, 2018
Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindredsMev Dominguez-Valentin, D Gareth R Evans, Sigve Nakken, et al.Journal of Clinical Medicine|June 19, 2020
Spectrum and Frequency of Tumors, Cancer Risk and Survival in Chilean Families with Lynch Syndrome: Experience of the Implementation of a RegistryKarin Álvarez, Paulina Orellana, Marjorie De la Fuente, et al.Oral Oncology|August 2, 2011
Advances and applications of oral cancer basic researchSabrina Daniela da Silva, Alfio Ferlito, Robert P Takes, et al.Familial Cancer|November 13, 2017
Universal determination of microsatellite instability using BAT26 as a single marker in an Argentine colorectal cancer cohortMaría Laura González, Natalia Causada-Calo, Juan Pablo Santino, et al.Familial Cancer|April 30, 2024
A comprehensive characterization of the spectrum of MUTYH germline pathogenic variants in Latin AmericaPatricia Esperon, Florencia Neffa, Walter Pavicic, et al.Journal of Genetic Counseling|February 26, 2022
Patterns of germline and somatic testing after universal tumor screening for Lynch syndrome: A clinical practice survey of active members of the Collaborative Group of the Americas on Inherited Gastrointestinal CancerRachel Hodan, Linda Rodgers-Fouche, Sanjeevani Arora, et al.Scientific Reports|December 8, 2019
Results of multigene panel testing in familial cancer cases without genetic cause demonstrated by single gene testingMev Dominguez-Valentin, Sigve Nakken, Hélène Tubeuf, et al.Pageof 7