Marcin W Wlodarski
Overview
Explore the profile of Marcin W Wlodarski including associated specialties, affiliations and a list of published articles.
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89
Citations
2104
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Recent Articles
1.
Beesetti S, Guy C, Sirasanagandla S, Yang M, Sumpter R, Sheppard H, et al.
Cell Death Differ
. 2025 Feb;
PMID: 39962244
Fanconi Anemia (FA) is an autosomal recessive disorder characterized by diverse clinical manifestations such as aplastic anemia, cancer predisposition, and developmental defects including hypogonadism, microcephaly, organ dysfunction, infertility, hyperpigmentation, microphthalmia,...
2.
Oszer A, Kliuchkivska K, Kolodrubiec J, Sopilnyak A, Salek M, Wlodarski M, et al.
JCO Glob Oncol
. 2025 Feb;
11:e2400046.
PMID: 39946670
Purpose: Soon after the Russian invasion of Ukraine in February 2022, an initiative was organized to evacuate Ukrainian children with cancer, most initially to Poland. This study assessed the impact...
3.
Tometten M, Beier F, Kirschner M, Schumacher Y, Walter J, Vieri M, et al.
Blood Adv
. 2025 Feb;
PMID: 39938003
Pathogenic germline variants affecting proper telomere maintenance result in premature telomere shortening and cause telomere biology disorders (TBDs). While classical dyskeratosis congenita in children is rather well defined, late-onset ("cryptic")...
4.
Romero-Moya D, Pera J, Marin-Bejar O, Torralba-Sales E, Murillo-Sanjuan L, Diaz-de-Heredia C, et al.
Leukemia
. 2025 Jan;
PMID: 39890964
No abstract available.
5.
Inducible pluripotent stem cell models to study bone marrow failure and MDS predisposition syndromes
Sahoo S, Khiami M, Wlodarski M
Exp Hematol
. 2024 Nov;
143:104669.
PMID: 39491640
Induced pluripotent stem cells (iPSCs) have emerged as powerful tools for in vitro modeling of bone marrow failure (BMF) syndromes and hereditary conditions predisposing to myelodysplastic syndrome (MDS) and acute...
6.
Sahoo S, Erlacher M, Wlodarski M
Blood
. 2024 Oct;
145(5):475-485.
PMID: 39475954
Sterile alpha motif domain-containing protein 9 (SAMD9) and SAMD9-like (SAMD9L) are paralogous genes encoding antiviral proteins that negatively regulate cell proliferation. Heterozygous germ line gain-of-function (GoF) SAMD9/9L variants cause multisystem...
7.
Granger S, Sharma R, Kaushik V, Razzaghi M, Honda M, Gaur P, et al.
Nucleic Acids Res
. 2024 Sep;
52(20):12422-12437.
PMID: 39329264
Human replication protein A (RPA) is a heterotrimeric ssDNA binding protein responsible for many aspects of cellular DNA metabolism. Dynamic interactions of the four RPA DNA binding domains (DBDs) with...
8.
Khiami M, Ju Y, Han L, Klein J, Han M, Pruett-Miller S, et al.
Stem Cell Res
. 2024 Sep;
81:103532.
PMID: 39276527
Induced pluripotent stem cells (iPSCs) harboring patient derived SAMD9 mutation offer a unique platform to study the multi-organ involvement observed in this rare disease, referred to as myelodysplasia, infections, restriction...
9.
Gray N, Sims K, Lewis S, Lei S, Bhatt N, Gheorghe G, et al.
Pediatr Blood Cancer
. 2024 Aug;
71(11):e31252.
PMID: 39129170
No abstract available.
10.
Maese L, Wlodarski M, Kim S, Bertuch A, Bougeard G, Chang V, et al.
Clin Cancer Res
. 2024 Jul;
30(19):4286-4295.
PMID: 39078402
Children harboring certain germline gene variants have an increased risk of developing myelodysplastic syndrome (MDS) and other hematopoietic malignancies (HM), such as leukemias and lymphomas. Recent studies have identified an...