Afane Brahimi

Lille, 59000, France

Last Updated: 09/26/2026

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Found 10 publications

High-grade gliomas and Lynch syndrome: A retrospective descriptive study with a literature review.

High-grade gliomas and Lynch syndrome: A retrospective descriptive study with a literature review.

Journal: Neuro-oncology practice

Published: March 09, 2026

MLH1 Constitutional Epimutation Screening Requires Highly Sensitive Assays to Identify Lynch Syndrome Patients With Very Low Mosaic Methylation Level.

MLH1 Constitutional Epimutation Screening Requires Highly Sensitive Assays to Identify Lynch Syndrome Patients With Very Low Mosaic Methylation Level.

Journal: Human mutation

Published: November 29, 2024

Germline Pathogenic DROSHA Variants Are Linked to Pineoblastoma and Wilms Tumor Predisposition.

Germline Pathogenic DROSHA Variants Are Linked to Pineoblastoma and Wilms Tumor Predisposition.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research

Published: August 27, 2024

Postzygotic mosaicism of SMARCB1 variants in patients with rhabdoid tumors: A not-so-rare condition exposing to successive tumors.

Postzygotic mosaicism of SMARCB1 variants in patients with rhabdoid tumors: A not-so-rare condition exposing to successive tumors.

Journal: Neuro-oncology

Published: August 02, 2024

AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancer.

AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancer.

Journal: Genes, chromosomes & cancer

Published: September 26, 2022

The Frequency of Germline BRCA and Non-BRCA HR-Gene-Variants in a Cohort of Pancreatic Cancer Patients.

The Frequency of Germline BRCA and Non-BRCA HR-Gene-Variants in a Cohort of Pancreatic Cancer Patients.

Journal: Digestive diseases and sciences

Published: May 06, 2022

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

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

Journal: American journal of human genetics

Published: June 15, 2021

Familial adenomatous polyposis associated craniopharyngioma secondary to both germline and somatic mutations in the APC gene.

Familial adenomatous polyposis associated craniopharyngioma secondary to both germline and somatic mutations in the APC gene.

Journal: Acta neuropathologica

Published: July 31, 2020

Cost-effectiveness evaluation of pre-counseling telephone interviews before face-to-face genetic counseling in cancer genetics.

Cost-effectiveness evaluation of pre-counseling telephone interviews before face-to-face genetic counseling in cancer genetics.

Journal: Familial cancer

Published: October 29, 2017

Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palate.

Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palate.

Journal: European journal of human genetics : EJHG

Published: October 21, 2014

Showing 1-10 of 10

Last Updated: 09/26/2026