Irith Baumann

Kaufbeuren, BY, Germany

Last Updated: 09/26/2026

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Found 22 publications

Parvovirus B19 infection preceding the diagnosis of childhood myelodysplastic syndrome with low blasts: a case report.

Parvovirus B19 infection preceding the diagnosis of childhood myelodysplastic syndrome with low blasts: a case report.

Journal: Frontiers in oncology

Published: February 26, 2026

Unique hematological presentation of patients with biallelic inactivation of FANCD1/BRCA2.

Unique hematological presentation of patients with biallelic inactivation of FANCD1/BRCA2.

Journal: Blood advances

Published: June 23, 2025

Long-term outcomes of patients with refractory cytopenia of childhood under observation only.

Long-term outcomes of patients with refractory cytopenia of childhood under observation only.

Journal: Blood advances

Published: February 11, 2025

Publisher Correction: Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes.

Publisher Correction: Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes.

Journal: Nature medicine

Published: November 20, 2021

A novel classification of hematologic conditions in patients with Fanconi anemia.

A novel classification of hematologic conditions in patients with Fanconi anemia.

Journal: Haematologica

Published: May 28, 2021

Response to upfront azacitidine in juvenile myelomonocytic leukemia in the AZA-JMML-001 trial.

Response to upfront azacitidine in juvenile myelomonocytic leukemia in the AZA-JMML-001 trial.

Journal: Blood advances

Published: December 30, 2020

Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes.

Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes.

Journal: Nature medicine

Published: September 24, 2020

Loss of the Fanconi anemia-associated protein NIPA causes bone marrow failure.

Loss of the Fanconi anemia-associated protein NIPA causes bone marrow failure.

Journal: The Journal of clinical investigation

Published: November 26, 2018

Molecular profile of inflammatory and megakaryocytic factors in pediatric myelodysplastic syndrome with acute myelofibrosis.

Molecular profile of inflammatory and megakaryocytic factors in pediatric myelodysplastic syndrome with acute myelofibrosis.

Journal: Pediatric blood & cancer

Published: November 01, 2017

Constitutional SAMD9L mutations cause familial myelodysplastic syndrome and transient monosomy 7.

Constitutional SAMD9L mutations cause familial myelodysplastic syndrome and transient monosomy 7.

Journal: Haematologica

Published: September 12, 2017

A common ancestral DNMT3A-mutated preleukemic clone giving rise to AML and MDS in an adolescent girl.

A common ancestral DNMT3A-mutated preleukemic clone giving rise to AML and MDS in an adolescent girl.

Journal: Leukemia & lymphoma

Published: November 29, 2016

Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents.

Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents.

Journal: Blood

Published: September 21, 2015

Showing 1-12 of 22

Last Updated: 09/26/2026