Angélina Legros

发表

BRCA1 allele-specific expression in genetic predisposed breast/ovarian cancer

T. Frebourg, B. Clarisse, F. Joly, 2017, Familial Cancer.

Next-generation sequencing for the diagnosis of hereditary breast and ovarian cancer using genomic capture targeting multiple candidate genes

T. Frebourg, Baptiste Brault, P. Berthet, 2014, European Journal of Human Genetics.

Landscape of pathogenic variations in a panel of 34 genes and cancer risk estimation from 5131 HBOC families

T. Frebourg, Baptiste Brault, P. Berthet, 2018, Genetics in Medicine.

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

F. Révillion, R. Lidereau, N. Sevenet, 2021, American journal of human genetics.

Detecting splicing patterns in genes involved in hereditary breast and ovarian cancer

C. Houdayer, T. Frebourg, Baptiste Brault, 2017, European Journal of Human Genetics.

Two novel variants in the 3′UTR of the BRCA1 gene in familial breast and/or ovarian cancer

S. Lheureux, L. Poulain, P. Berthet, 2011, Breast Cancer Research and Treatment.

Assessment of branch point prediction tools to predict physiological branch points and their alteration by variants

A. Spurdle, N. Sevenet, C. Houdayer, 2019, BMC Genomics.

Landscape of pathogenic variations in a panel of 34 genes and cancer risk estimation from 5131 HBOC families

T. Frebourg, Baptiste Brault, P. Berthet, 2018, Genetics in Medicine.

Genetic profiles of cervical tumors by high-throughput sequencing for personalized medical care

A. Nicolas, X. Sastre, T. Frebourg, 2015, Cancer medicine.

OutLyzer: software for extracting low-allele-frequency tumor mutations from sequencing background noise in clinical practice

Dominique Vaur, Sophie Krieger, Baptiste Brault, 2016, Oncotarget.

Two novel variants in the 3’UTR of the gene in familial breast and/or ovarian cancer

L. Poulain, P. Berthet, S. Krieger, 2023 .