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Mev Dominguez-Valentin

University of Oslo

4

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Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database (Genetics in Medicine, (2020), 22, 1, (15-25), 10.1038/s41436-019-0596-9)

2020 Genetics in Medicine
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Causes for Frequent Pathogenic BRCA1 Variants Include Low Penetrance in Fertile Ages, Recurrent De-Novo Mutations and Genetic Drift

2019 Cancers
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Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report

2019 Hereditary Cancer in Clinical Practice
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A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America

2017 BMC Cancer
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