Julie Metras

11 Third Hospital Drive
Singapore, 169610, Singapore

Last Updated: 09/26/2026

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Found 12 publications

Correction: follow-up, cancer risk and mortality in Peutz-Jeghers syndrome: data from the PRED-IdF network.

Correction: follow-up, cancer risk and mortality in Peutz-Jeghers syndrome: data from the PRED-IdF network.

Journal: European journal of human genetics : EJHG

Published: July 03, 2026

Impact of germline MMR gene variants on immune checkpoint inhibitors response in patients with MSI-H/dMMR digestive cancers: a retrospective cohort analysis.

Impact of germline MMR gene variants on immune checkpoint inhibitors response in patients with MSI-H/dMMR digestive cancers: a retrospective cohort analysis.

Journal: Hereditary cancer in clinical practice

Published: December 11, 2025

Follow-up, cancer risk and mortality in Peutz-Jeghers syndrome: Data from the PRED-IdF network.

Follow-up, cancer risk and mortality in Peutz-Jeghers syndrome: Data from the PRED-IdF network.

Journal: European journal of human genetics : EJHG

Published: November 27, 2025

Expert endoscopic surveillance in CDH1 pathogenic variant carriers seems safe, even after positive (pT1a) biopsies.

Expert endoscopic surveillance in CDH1 pathogenic variant carriers seems safe, even after positive (pT1a) biopsies.

Journal: Journal of medical genetics

Published: September 15, 2025

Occurrence of dMMR/MSI-H tumor during follow-up in Lynch syndrome patients treated with immune checkpoint inhibitors for metastatic digestive cancer between 2015 and 2024: a retrospective analysis of a monocentric prospective cohort study.

Occurrence of dMMR/MSI-H tumor during follow-up in Lynch syndrome patients treated with immune checkpoint inhibitors for metastatic digestive cancer between 2015 and 2024: a retrospective analysis of a monocentric prospective cohort study.

Journal: ESMO open

Published: January 06, 2025

Thirty-year compliance with a surveillance program for patients with familial adenomatous polyposis.

Thirty-year compliance with a surveillance program for patients with familial adenomatous polyposis.

Journal: Familial cancer

Published: October 15, 2024

Pathogenic germline variants in patients with early-onset colorectal cancer according to phenotype.

Pathogenic germline variants in patients with early-onset colorectal cancer according to phenotype.

Journal: European journal of human genetics : EJHG

Published: August 30, 2024

Updated European guidelines for clinical management of familial adenomatous polyposis (FAP), MUTYH-associated polyposis (MAP), gastric adenocarcinoma, proximal polyposis of the stomach (GAPPS) and other rare adenomatous polyposis syndromes: a joint EHTG-ESCP revision.

Updated European guidelines for clinical management of familial adenomatous polyposis (FAP), MUTYH-associated polyposis (MAP), gastric adenocarcinoma, proximal polyposis of the stomach (GAPPS) and other rare adenomatous polyposis syndromes: a joint EHTG-ESCP revision.

Journal: The British journal of surgery

Published: November 21, 2023

Lynch syndrome: influence of additional susceptibility variants on cancer risk.

Lynch syndrome: influence of additional susceptibility variants on cancer risk.

Journal: European journal of human genetics : EJHG

Published: October 12, 2022

Hereditary gastric cancer syndromes and their association with specific histological subtypes

Hereditary gastric cancer syndromes and their association with specific histological subtypes

Journal: Bulletin du cancer

Published: May 09, 2022

Preimplantation genetic testing in patients with genetic susceptibility to cancer.

Preimplantation genetic testing in patients with genetic susceptibility to cancer.

Journal: Familial cancer

Published: October 12, 2021

Impact of Appointment Waiting Time on Attendance Rates at a Clinical Cancer Genetics Service.

Impact of Appointment Waiting Time on Attendance Rates at a Clinical Cancer Genetics Service.

Journal: Journal of genetic counseling

Published: January 07, 2018

Showing 1-12 of 12

Last Updated: 09/26/2026