Eric Soler

Lab Head

France

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Eric Soler is a Lab Head at the Institute of Molecular Genetics of Montpellier (IGMM) in France. His research focuses on molecular genetics, particularly in the areas of erythroid differentiation and genome editing technologies. Recent publications include studies on MYB regulation in β-thalassemia and the development of high-throughput methods for analyzing transcription factors. His work contributes significantly to understanding acute leukemia and the role of transcriptional cofactors in cell lineage specification.

Articles (12)

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2025

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2024

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2024

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2023

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2023

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2023

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2022

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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

Collaborators (9)

sandrina kinet

CNRS Délégation Languedoc-Roussillon

FRANCE

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Virginie Deleuze-Marquès

Institute of Molecular Genetics

FRANCE

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frédérique verdier

Institut Cochin

FRANCE

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Connor Sweeney

Haematology Consultant and Honorary Senior Clinical Lecturer

Oxford University Hospitals NHS Foundation Trust

UNITED KINGDOM

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Isabelle Hatin

Université Paris-Saclay

FRANCE

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Francoise Pflumio

INSERM

FRANCE

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Jerome Moreaux

Professor

University of Montpellier

FRANCE

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Frederik Otzen Bagger

Head of Bioinformatics

Rigshospitalet

DENMARK

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Sebastien Malinge

University of Western Australia

AUSTRALIA

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Eric Soler

Research Interests

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Articles (12)

In vivo deletion of a GWAS-identified Myb distal enhancer acts on Myb expression, globin switching, and clinical erythroid parameters in β-thalassemia.

Protocol for efficient CRISPR-Cas9-mediated fluorescent tag knockin in hard-to-transfect erythroid cell lines

The ETO2 transcriptional cofactor maintains acute leukemia by driving a MYB/EP300-dependent stemness program.

Efficient genome editing in erythroid cells unveils novel MYB target genes and regulatory functions

Var∣Decrypt: a novel and user-friendly tool to explore and prioritize variants in whole-exome sequencing data.

High-throughput methods for the analysis of transcription factors and chromatin modifications: Low input, single cell and spatial genomic technologies.

Erythroid Cell Research: 3D Chromatin, Transcription Factors and Beyond

p53 activation during ribosome biogenesis regulates normal erythroid differentiation

PPARγ agonists promote the resolution of myelofibrosis in preclinical models.

PPARγ agonists promote the resolution of myelofibrosis in preclinical models

Human erythroleukemia genetics and transcriptomes identify master transcription factors as functional disease drivers.

When basic science reaches into rational therapeutic design: From historical to novel leads for the treatment of β-globinopathies

Collaborators (9)

sandrina kinet

Virginie Deleuze-Marquès

frédérique verdier

Connor Sweeney

Isabelle Hatin

Francoise Pflumio

Jerome Moreaux

Frederik Otzen Bagger

Sebastien Malinge

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