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Marcin W Wlodarski

St. Jude Children's Research Hospital

United States

Research Interests

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Professors in United States

Articles (20)

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2026

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2023

Collaborators (18)

Sharon Savage

Clinical Director

National Cancer Institute

UNITED STATES

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Alessandra Giorgetti

Universitat Autònoma de Barcelona Facultat de Medicina

SPAIN

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Kirsi Jahnukainen

University of Helsinki

FINLAND

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Hana Willner

Life Science Research Profesisonal II

Stanford University

UNITED STATES

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Luca Vinci

University Medical Center Freiburg

GERMANY

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Agnieszka Mizia-Malarz

Medical University of Silesia

POLAND

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Moon Ley Tung

UNITED STATES

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Amedeo Azizi

Assoc. Prof

Medical University of Vienna

AUSTRIA

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Sushree Sahoo

Assistant Professor

Virginia Tech

UNITED STATES

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Wojciech Mlynarski

Head/Professor

Medical University of Lodz

POLAND

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Guolian Kang

Member

St. Jude Children's Research Hospital

UNITED STATES

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Tracy M. Bryan

University of Sydney

AUSTRALIA

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Hoong-Wei Gan

Honorary Lecturer

University College London Great Ormond Street Institute of Child Health

UNITED KINGDOM

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Lorenzo Pasquali

Associate Professor and group leader

Universitat Pompeu Fabra

SPAIN

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Heather Conklin

Chief, Division of Neuropsychology

St. Jude Children's Research Hospital

UNITED STATES

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Mireya Plass

Associate Professor

University of Barcelona

SPAIN

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Alice Bertaina

Stanford University School of Medicine

UNITED STATES

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Stephane Pelletier

Associate Professor

Indiana University School of Medicine

UNITED STATES

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Marcin W Wlodarski

Research Interests

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Articles (20)

Generation of iPSC and isogenic gene-corrected lines from a patient with RPS7 (c.277_279delGTC)-mutated Diamond-Blackfan anemia syndrome.

Age-dependent phenotypic and molecular evolution of pediatric MDS arising from GATA2 deficiency.

Multiple phenotypes and epigenetic profiles in a three-generation family history with GATA2 deficiency.

Evacuating Patients With Pediatric Cancer From Ukraine: Impact on Medical Care Capacity in Poland

CRISPR-engineered human GATA2 deficiency model uncovers mitotic dysfunction and premature aging in HSPCs, impairing hematopoietic fitness.

Distinct developmental outcomes in DNA repair-deficient FANCC c.67delG mutant and FANCC−/− Mice

Inducible pluripotent stem cell models to study bone marrow failure and MDS predisposition syndromes

Genetic and clinical spectrum of SAMD9 and SAMD9L syndromes: from variant interpretation to patient management

Human iPSCs-based modeling unveils SETBP1 as a driver of chromatin rewiring in GATA2 deficiency

Irradiation- and busulfan-free stem cell transplantation in Fanconi anemia using an anti-CD117 antibody: a phase 1b trial.

DBA syndrome 2.0: Rpl11 mouse model revisited

Erratum: Evacuating Patients With Pediatric Cancer From Ukraine: Impact on Medical Care Capacity in Poland

Germline and somatic genetic landscape of pediatric myelodysplastic syndromes

Hematological phenotypes in GATA2 deficiency syndrome arise from aging, maladaptation to proliferation, and somatic events

LNKing genotype to phenotype: the expanding clinical spectrum of SH2B3 disorders

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

Seq2Karyotype (S2K): A Method for in-silico Karyotyping Using Single-Sample Whole-Genome Sequencing Data

Different phenotypes with different endings-Telomere biology disorders and cancer predisposition with long telomeres.

Author Correction: A joint international consensus statement for measuring quality of survival for patients with childhood cancer.

Biallelic inactivation of the NF1 tumour suppressor gene in juvenile myelomonocytic leukaemia: Genetic evidence of driver function and implications for diagnostic workup

Collaborators (18)

Sharon Savage

Alessandra Giorgetti

Kirsi Jahnukainen

Hana Willner

Luca Vinci

Agnieszka Mizia-Malarz

Moon Ley Tung

Amedeo Azizi

Sushree Sahoo

Wojciech Mlynarski

Guolian Kang

Tracy M. Bryan

Hoong-Wei Gan

Lorenzo Pasquali

Heather Conklin

Mireya Plass

Alice Bertaina

Stephane Pelletier

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