Mariam Ibáñez

Professor

Universidad CEU Cardenal Herrera

Spain

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About

Mariam Ibáñez is a Professor at CEU Universidad Cardenal Herrera in Spain. Her research areas include next-generation sequencing applications in hematological malignancies, particularly focusing on chronic lymphocytic leukemia and myelodysplastic syndromes. She has authored several significant articles detailing the detection of gene mutations and chromosomal abnormalities in various blood disorders.

Articles (10)

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2022

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2021

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2021

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2021

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2021

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2021

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2021

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2020

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2020

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2020

Collaborators (2)

Mireya Morote Faubel

Profesora

Universidad Europea de Valencia SLU

SPAIN

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Alexander Neef

Teaching Fellow

Universidad Católica de Valencia San Vicente Mártir

SPAIN

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Mariam Ibáñez

Research Interests

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Articles (10)

Panel Sequencing for Clinically Oriented Variant Screening and Copy Number Detection in Chronic Lymphocytic Leukemia Patients

A single-run next-generation sequencing (Ngs) assay for the simultaneous detection of both gene mutations and large chromosomal abnormalities in patients with myelodysplastic syndromes (mds) and related myeloid neoplasms

A Single-Run Next-Generation Sequencing (NGS) Assay for the Simultaneous Detection of Both Gene Mutations and Large Chromosomal Abnormalities in Patients with Myelodysplastic Syndromes (MDS) and Related Myeloid Neoplasms

Case Report: Partial Uniparental Disomy Unmasks a Novel Recessive Mutation in the LYST Gene in a Patient With a Severe Phenotype of Chédiak-Higashi Syndrome

Case Report: Partial Uniparental Disomy Unmasks a Novel Recessive Mutation in the LYST Gene in a Patient With a Severe Phenotype of Chediak-Higashi Syndrome

Correction: Liquori et al. acute promyelocytic leukemia: A constellation of molecular events around a single pml-rara fusion gene. cancers 2020, 12, 624

Acute Promyelocytic Leukemia: A Constellation of Molecular Events around a Single PML-RARA Fusion Gene (vol 12, 624, 2020)

Acute promyelocytic leukemia: A constellation of molecular events around a single PML-RARA fusion gene

Acute Promyelocytic Leukemia: A Constellation of Molecular Events around a Single PML-RARA Fusion Gene

Analysis of SNP Array Abnormalities in Patients with DE NOVO Acute Myeloid Leukemia with Normal Karyotype

Collaborators (2)

Mireya Morote Faubel

Alexander Neef

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