Marco Olivares-Jimenez

Mexico City, DIF, Mexico

Last Updated: 09/26/2026

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Found 13 publications

Cancer spectrum in Mexican patients with the CHEK2 p.(Leu236Pro) variant: a retrospective study.

Cancer spectrum in Mexican patients with the CHEK2 p.(Leu236Pro) variant: a retrospective study.

Journal: Familial cancer

Published: April 08, 2025

Prevalence of pathogenic or likely pathogenic germline variants in cancer predisposition genes among selected patients with lung adenocarcinoma: The GERMLUNG study.

Prevalence of pathogenic or likely pathogenic germline variants in cancer predisposition genes among selected patients with lung adenocarcinoma: The GERMLUNG study.

Journal: Lung cancer (Amsterdam, Netherlands)

Published: March 27, 2024

First family with Perry syndrome from Mexico.

First family with Perry syndrome from Mexico.

Journal: Biomedical reports

Published: January 29, 2024

Case report: A familial B-acute lymphoblastic leukemia associated with a new germline pathogenic variant in PAX5. The first report in Mexico.

Case report: A familial B-acute lymphoblastic leukemia associated with a new germline pathogenic variant in PAX5. The first report in Mexico.

Journal: Frontiers in oncology

Published: December 13, 2023

IKZF1plus is a frequent biomarker of adverse prognosis in Mexican pediatric patients with B-acute lymphoblastic leukemia.

IKZF1plus is a frequent biomarker of adverse prognosis in Mexican pediatric patients with B-acute lymphoblastic leukemia.

Journal: Frontiers in oncology

Published: November 13, 2023

Mutational Landscape of CEBPA in Mexican Pediatric Acute Myeloid Leukemia Patients: Prognostic Implications.

Mutational Landscape of CEBPA in Mexican Pediatric Acute Myeloid Leukemia Patients: Prognostic Implications.

Journal: Frontiers in pediatrics

Published: March 19, 2022

Uterus infantilis: a novel phenotype associated with AARS2 new genetic variants. A case report.

Uterus infantilis: a novel phenotype associated with AARS2 new genetic variants. A case report.

Journal: Frontiers in neurology

Published: February 18, 2022

Corrigendum: ALG1-CDG Caused by Non-Functional Alternative Splicing Involving a Novel Pathogenic Complex Allele.

Corrigendum: ALG1-CDG Caused by Non-Functional Alternative Splicing Involving a Novel Pathogenic Complex Allele.

Journal: Frontiers in genetics

Published: September 15, 2021

ALG1-CDG Caused by Non-functional Alternative Splicing Involving a Novel Pathogenic Complex Allele.

ALG1-CDG Caused by Non-functional Alternative Splicing Involving a Novel Pathogenic Complex Allele.

Journal: Frontiers in genetics

Published: July 21, 2021

Non-functional alternative splicing caused by a Latino pathogenic variant in a case of PMM2-CDG.

Non-functional alternative splicing caused by a Latino pathogenic variant in a case of PMM2-CDG.

Journal: Molecular genetics and metabolism reports

Published: April 30, 2021

Identification through exome sequencing of the first PMM2-CDG individual of Mexican mestizo origin.

Identification through exome sequencing of the first PMM2-CDG individual of Mexican mestizo origin.

Journal: Molecular genetics and metabolism reports

Published: July 20, 2020

Profiling FLT3 Mutations in Mexican Acute Myeloid Leukemia Pediatric Patients: Impact on Overall Survival.

Profiling FLT3 Mutations in Mexican Acute Myeloid Leukemia Pediatric Patients: Impact on Overall Survival.

Journal: Frontiers in pediatrics

Published: April 14, 2020

Showing 1-12 of 13

Last Updated: 09/26/2026