Denis Boidin

Evidence of constitutional MLH1 epimutation associated to transgenerational inheritance of cancer susceptibility

M. Crépin, F. Escande, M. Mathieu, 2012, Human mutation.

Characterisation of heterozygous PMS2 variants in French patients with Lynch syndrome

T. Frebourg, Qing Wang, K. Cassinari, 2020, Journal of Medical Genetics.

MSH2 c.1022T>C, p.Leu341Pro is a founder pathogenic variation and a major cause of Lynch syndrome in the North of France

F. Vasseur, S. Cattan, M. Buisine, 2020, Genes, chromosomes & cancer.