Peter Vandenberghe - Concepedia

Author

Peter Vandenberghe

Also Known As

Benavente Cuesta, E Legius, M Delforge, O Gheysens, P Vandenberghe, P. VANDENBERGHE, P. Vandenberghe, PETER VANDENBERGHE, Peter A. Vandenberghe, Peter Vandenberghe

632

Publications

25.3K

Citations

H-Index

170

Concepts

All Affiliations

KU Leuven Universitair Ziekenhuis Leuven Munich Leukemia Laboratory (Germany)VIB-KU Leuven Center for Cancer Biology Center for Human Genetics

About

Peter Vandenberghe is an author at KU Leuven specializing in medicine, immunology, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	48	92	12.9K
2	Health Sciences	15	17	1.7K
3	Engineering	4	4	400
4	Public Health	3	3	136
5	Allergy	1	1	13

Peter Vandenberghe

182

Publications

22.5K

Citations

H-Index

Page 1

	Year	Citations
Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis Ross L. Levine, Martha Wadleigh, Jan Cools, Cancer Cell Hematological MalignancyPolycythemia VeraEssential ThrombocythemiaReceptor Tyrosine KinaseMalignant Blood Disorder	2005	3K
A Tyrosine Kinase Created by Fusion of the <i>PDGFRA</i> and <i>FIP1L1</i> Genes as a Therapeutic Target of Imatinib in Idiopathic Hypereosinophilic Syndrome Jan Cools, Daniel J. DeAngelo, Jason Gotlib, New England Journal of Medicine	2003	1.7K
Axicabtagene Ciloleucel as Second-Line Therapy for Large B-Cell Lymphoma Frederick L. Locke, David B. Miklos, Caron A. Jacobson, New England Journal of Medicine	2021	1.4K
Contemporary consensus proposal on criteria and classification of eosinophilic disorders and related syndromes Peter Valent, Amy D. Klion, Hans‐Peter Horny, Journal of Allergy and Clinical Immunology Eosinophilic DisordersPsychiatryClinical EpidemiologyPediatricsEosinophilic Disorder	2012	747
Somatic mutations of the histone methyltransferase gene EZH2 in myelodysplastic syndromes Gorica Nikoloski, Saskia Langemeijer, Roland P. Kuiper, Nature Genetics Histone ModificationsChromatinDevelopmental BiologySomatic MutationsChromatin Remodeling	2010	745
Acquired mutations in TET2 are common in myelodysplastic syndromes Saskia Langemeijer, Roland P. Kuiper, M Berends, Nature Genetics Hematological MalignancyGenetic DisorderMedicineGeneticsHematology	2009	740
Prognostic Value of Positron Emission Tomography (PET) With Fluorine-18 Fluorodeoxyglucose ([<sup>18</sup>F]FDG) After First-Line Chemotherapy in Non-Hodgkin’s Lymphoma: Is [<sup>18</sup>F]FDG-PET a Valid Alternative to Conventional Diagnostic Methods? Karoline Spaepen, Sigrid Stroobants, Patrick Dupont, Journal of Clinical Oncology	2001	466
Constitutively activating mutation in WASP causes X-linked severe congenital neutropenia Koenraad Devriendt, Annette S. Kim, Gert Mathijs, Nature Genetics Genetic DisorderGeneticsPathologyMolecular GeneticsMedicine	2001	432
Fusion of NUP214 to ABL1 on amplified episomes in T-cell acute lymphoblastic leukemia Carlos Graux, Jan Cools, Cindy Melotte, Nature Genetics Hematological MalignancyTumor BiologyMedicineMixed-phenotype Acute LeukemiaMolecular Biology	2004	421
Exome sequencing identifies mutation in CNOT3 and ribosomal genes RPL5 and RPL10 in T-cell acute lymphoblastic leukemia Kim De Keersmaecker, Zeynep Kalender Atak, Ning Li, Nature Genetics Hematological MalignancyMedicineGeneticsMolecular GeneticsIdentifies Mutation	2012	420

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