Martijn T. Ernst

Rotterdam, ZH, Netherlands

Last Updated: 09/26/2026

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Found 9 publications

Disease characteristics and outcomes of acute myeloid leukemia in germline RUNX1 deficiency (Familial Platelet Disorder with associated Myeloid Malignancy).

Disease characteristics and outcomes of acute myeloid leukemia in germline RUNX1 deficiency (Familial Platelet Disorder with associated Myeloid Malignancy).

Journal: HemaSphere
Published: March 25, 2024

Correction to: Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies.

Correction to: Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies.

Journal: Leukemia
Published: October 18, 2022

A congenital CSF3R mutation in chronic neutropenia reveals a vital role for a cytokine receptor extracellular hinge motif in the response to granulocyte colony-stimulating factor.

A congenital CSF3R mutation in chronic neutropenia reveals a vital role for a cytokine receptor extracellular hinge motif in the response to granulocyte colony-stimulating factor.

Journal: Pediatric blood & cancer
Published: July 18, 2022

Hematopoietic Cell Autonomous Disruption of Hematopoiesis in a Germline Loss-of-function Mouse Model of RUNX1-FPD.

Hematopoietic Cell Autonomous Disruption of Hematopoiesis in a Germline Loss-of-function Mouse Model of RUNX1-FPD.

Journal: HemaSphere
Published: July 08, 2022

Validation and clinical application of transactivation assays for RUNX1 variant classification.

Validation and clinical application of transactivation assays for RUNX1 variant classification.

Journal: Blood advances
Published: September 14, 2021

Ready for Repair? Gene Editing Enters the Clinic for the Treatment of Human Disease.

Ready for Repair? Gene Editing Enters the Clinic for the Treatment of Human Disease.

Journal: Molecular therapy. Methods & clinical development
Published: August 11, 2020

Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies.

Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies.

Journal: Leukemia
Published: August 05, 2020

RUNX1 germline variants in RUNX1-mutant AML: how frequent?

RUNX1 germline variants in RUNX1-mutant AML: how frequent?

Journal: Blood
Published: July 31, 2020

Sharpening the Molecular Scissors: Advances in Gene-Editing Technology.

Sharpening the Molecular Scissors: Advances in Gene-Editing Technology.

Journal: iScience
Published: July 01, 2019
Showing 1-9 of 9

Last Updated: 09/26/2026