World's Best Scientists 2026 revealed!
Peter Marynen

Peter Marynen

Award Badge
Genetics
Belgium
2026

D-Index & Metrics

Genetics

D-Index
98
Citations
31869
World Ranking
811
National Ranking
9

Medicine

D-Index
101
Citations
34460
World Ranking
8039
National Ranking
94

Research.com Recognitions

  • 2026 - Research.com Genetics in Belgium Leader Award
  • 2025 - Research.com Genetics in Belgium Leader Award

Overview

Peter Marynen is affiliated with KU Leuven in Belgium. Their academic career is primarily situated within this institution, indicating a stable research environment and connection to one of Europe's prominent universities.

The available data does not list any recent papers published by Peter Marynen, nor does it specify any frequent co-authors or publication venues connected to their work. Similarly, there is no detailed information on main or subfields of study, topics, or specific research areas they focus on.

There are also no records of book publications or academic awards mentioned for Peter Marynen. This lack of detailed publication and award data suggests either limited public indexing of their research output or specialization outside widely tracked publication formats.

Due to the absence of citations, co-author networks, and documented topics, it is not possible to outline a detailed thematic profile or expertise domain based on the current data.

Despite these gaps, Peter Marynen's role at KU Leuven places them within a university known for diverse research disciplines, potentially contributing to various academic efforts not captured here.

Best Publications

  • Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis.

    Ross L. Levine;Ross L. Levine;Martha Wadleigh;Jan Cools;Benjamin L. Ebert;Benjamin L. Ebert

  • A Tyrosine Kinase Created by Fusion of the PDGFRA and FIP1L1 Genes as a Therapeutic Target of Imatinib in Idiopathic Hypereosinophilic Syndrome

    Jan Cools;Jan Cools;Daniel J. DeAngelo;Jason Gotlib;Elizabeth H. Stover

  • Allele-specific copy number analysis of tumors

    Peter Van Loo;Silje H. Nordgard;Silje H. Nordgard;Ole Christian Lingjærde;Hege G. Russnes

  • Gene prioritization through genomic data fusion.

    Stein Aerts;Diether Lambrechts;Sunit Maity;Peter Van Loo

  • The Apoptosis Inhibitor Gene API2 and a Novel 18q Gene,MLT, Are Recurrently Rearranged in the t(11;18)(q21;q21) Associated With Mucosa-Associated Lymphoid Tissue Lymphomas

    Judith Dierlamm;Mathijs Baens;Iwona Wlodarska;Margarita Stefanova-Ouzounova

  • Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males.

    Hilde Van Esch;Marijke Bauters;Jaakko Ignatius;Mieke Jansen

  • Fusion of TEL, the ETS-Variant Gene 6 (ETV6), to the Receptor-Associated Kinase JAK2 as a Result of t(9; 12) in a Lymphoid and t(9; 15; 12) in a Myeloid Leukemia

    Pieter Peeters;Sophie D. Raynaud;Jan Cools;Iwona Wlodarska

  • Mechanisms of resistance to imatinib mesylate in gastrointestinal stromal tumors and activity of the PKC412 inhibitor against imatinib-resistant mutants

    Maria Debiec-Rychter;Jan Cools;Herlinde Dumez;Raf Sciot

  • Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype.

    Hilde Brems;Magdalena Chmara;Magdalena Chmara;Mourad Sahbatou;Ellen Denayer

  • Fusion of NUP214 to ABL1 on amplified episomes in T-cell acute lymphoblastic leukemia

    C Graux;Jan Cools;C Melotte;H Quentmeier

  • A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation

    A. Carrie;L. Jun;T. Bienvenu;M.C. Vinet

  • Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports

    B. Menten;N. Maas;B. Thienpont;K. Buysse

  • Molecular cloning of a phosphatidylinositol-anchored membrane heparan sulfate proteoglycan from human lung fibroblasts.

    G David;V Lories;B Decock;P Marynen

  • Genomic imbalances including amplification of the tyrosine kinase gene JAK2 in CD30+ Hodgkin cells

    Stefan Joos;M Küpper;S Ohl;F von Bonin

  • Myeloid cell differentiation arrest by miR-125b-1 in myelodysplasic syndrome and acute myeloid leukemia with the t(2;11)(p21;q23) translocation

    Marina Bousquet;Cathy Quelen;Roberto Rosati;Véronique Mansat-De Mas;Véronique Mansat-De Mas

  • Efficacy of the kinase inhibitor SU11248 against gastrointestinal stromal tumor mutants refractory to imatinib mesylate.

    Hans Prenen;Jan Cools;Nicole Mentens;Cedric Folens

  • Identification of novel fusion partners of ALK, the anaplastic lymphoma kinase, in anaplastic large-cell lymphoma and inflammatory myofibroblastic tumor.

    Jan Cools;Iwona Wlodarska;Riet Somers;Nicole Mentens

  • The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemia.

    S Raynaud;H Cave;M Baens;C Bastard

  • Duplication of the MYB oncogene in T cell acute lymphoblastic leukemia

    Idoya Lahortiga;Kim De Keersmaecker;Kim De Keersmaecker;Pieter Van Vlierberghe;Carlos Graux;Carlos Graux;Carlos Graux

  • Transformation of hematopoietic cell lines to growth‐factor independence and induction of a fatal myelo‐ and lymphoproliferative disease in mice by retrovirally transduced TEL/JAK2 fusion genes

    J Schwaller;J Frantsve;J Aster;I R Williams

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