Pierre Vande Perre

Guidelines for reporting secondary findings of genome sequencing in cancer genes: the SFMPP recommendations

Pascal Pujol, Pierre Vande Perre, Laurence Faivre et al. · European Journal of Human Genetics · 2018 · 67 citations · Full text

Cancer Genes, Medicine, Next-generation Sequencing +10

An unusual phenotype occurs in 15% of mismatch repair-deficient tumors and is associated with non-colorectal cancers and genetic syndromes

Marion Jaffrelot, Nadim Farés, Anne Cécile Brunac et al. · Modern Pathology · 2021 · 59 citations · Full text

Germline mutation p.N363K in POLE is associated with an increased risk of colorectal cancer and giant cell glioblastoma

Pierre Vande Perre, Aurore Siegfried, Carole Corsini et al. · Familial Cancer · 2018 · 31 citations

Somatic Variant, Cancer Pathology, Cancer Risk +11

Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach

Sandrine M. Caputo, Lisa Golmard, Mélanie Léoné et al. · The American Journal of Human Genetics · 2021 · 29 citations · Full text

Genetic Analysis, Cosegregation Study, Allelic Variant +14

Psychosocial and clinical factors of probands impacting intrafamilial disclosure and uptake of genetic testing among families with <i>BRCA1/2</i> or MMR gene mutations

Nathalie Alegre, Pierre Vande Perre, Yves Jean Bignon et al. · Psycho-Oncology · 2019 · 16 citations · Full text