Marie Engvall - Department of Immunology, Genetics, and Pathology, Uppsala University

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论文共 19 篇作者统计合作学者相似作者

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Supplementary Table 1 from Somatic Exonic Deletions in RUNX1 Constitutes a Novel Recurrent Genomic Abnormality in Acute Myeloid Leukemia

Anna Eriksson,Marie Engvall,Lucy Mathot,Albin Österroos,Martin Rippin,Lucia Cavelier,Claes Ladenvall, Panagiotis Baliakas

crossref（2023）

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Supplementary Table 2 from Somatic Exonic Deletions in RUNX1 Constitutes a Novel Recurrent Genomic Abnormality in Acute Myeloid Leukemia

Anna Eriksson,Marie Engvall,Lucy Mathot,Albin Österroos,Martin Rippin,Lucia Cavelier,Claes Ladenvall, Panagiotis Baliakas

crossref（2023）

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Somatic Exonic Deletions in RUNX1 Constitutes a Novel Recurrent Genomic Abnormality in Acute Myeloid Leukemia

Anna Eriksson,Marie Engvall,Lucy Mathot,Albin Osterroos,Martin Rippin,Lucia Cavelier,Claes Ladenvall,Panagiotis Baliakas

Clinical Cancer Researchno. 15 (2023): 2826-2834

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Supplementary Table1 from Somatic Exonic Deletions in RUNX1 Constitutes a Novel Recurrent Genomic Abnormality in Acute Myeloid Leukemia

Anna Eriksson,Marie Engvall,Lucy Mathot,Albin Österroos,Martin Rippin,Lucia Cavelier,Claes Ladenvall,Panagiotis Baliakas

crossref（2023）

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Five Percent Variant Allele Frequency is a Reliable Reporting Threshold for TP53 Variants Detected by Next Generation Sequencing in Chronic Lymphocytic Leukemia in the Clinical Setting

Tatjana Pandzic,Claes Ladenvall,Marie Engvall,Mattias Mattsson,Monica Hermanson,Lucia Cavelier,Viktor Ljungstrom,Panagiotis Baliakas

HemaSphere（2022）

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Standardization of Molecular Monitoring of CML: Results and Recommendations from the European Treatment and Outcome Study

Helen E. White,Matthew Salmon,Francesco Albano,Christina Søs Auður Andersen,Stefan Balabanov,Gueorgui Balatzenko,Gisela Barbany,Jean-Michel Cayuela,Nuno Cerveira, Pascale Cochaux,Dolors Colomer,Daniel Coriu,Joana Diamond,Christian Dietz,Stéphanie Dulucq,Marie Engvall,Georg N. Franke, Egle Gineikiene-Valentine,Michal Gniot,María Teresa Gómez-Casares,Enrico Gottardi,Chloe Hayden,Sandrine Hayette, Andreas Hedblom,Anca Ilea,Barbara Izzo,Antonio Jiménez-Velasco,Tomas Jurcek,Veli Kairisto,Stephen E. Langabeer,Thomas Lion,Nora Meggyesi,Semir Mešanović,Luboslav Mihok,Gerlinde Mitterbauer-Hohendanner, Sylvia Moeckel,Nicole Naumann,Olivier Nibourel,Elisabeth Oppliger Leibundgut,Panayiotis Panayiotidis,Helena Podgornik,Christiane Pott,Inmaculada Rapado,Susan J. Rose,Vivien Schäfer,Tasoula Touloumenidou,Christopher Veigaard,Bianca Venniker-Punt,Claudia Venturi,Paolo Vigneri, Ingvild Vorkinn, Elizabeth Wilkinson,Renata Zadro,Magdalena Zawada,Hana Zizkova,Martin C. Müller,Susanne Saussele,Thomas Ernst,Katerina Machova Polakova,Andreas Hochhaus,Nicholas C. P. Cross

Leukemia（2022）

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Familial Platelet Disorder Due to Germline Exonic Deletions Inrunx1: a Diagnostic Challenge with Distinct Alterations of the Transcript Isoform Equilibrium

Marie Engvall, Ylva Karlsson,Ekaterina Kuchinskaya, Asa Jornegren,Lucy Mathot,Tatjana Pandzic,Josefine Palle,Viktor Ljungstrom,Lucia Cavelier,Eva Hellstrom Lindberg,Jorg Cammenga,Panagiotis Baliakas

Leukemia & lymphoma/Leukemia and lymphoma（2022）

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Prognostic Scoring Systems And Comorbidities In Chronic Myelomonocytic Leukaemia: A Nationwide Population-Based Study

Daniel Moreno Berggren,Matilda Kjellander, Ellen Backlund,Marie Engvall,Hege Garelius,Fryderyk Lorenz,Lars Nilsson,Bengt Rasmussen,Sören Lehmann,Eva Hellström-Lindberg,Martin Jädersten,Johanna Ungerstedt,Elisabeth Ejerblad

BRITISH JOURNAL OF HAEMATOLOGY（2021）

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