Marry M. van den Heuvel‐Eibrink

Author

Erasmus MC - Sophia Children’s Hospital ORCID

Also Known As

Christian Vokuhl, Division of Oncology, Children’s National Health System, Washington, District of Columbia, USA, Dr. MH. van den Berg, Frederik J. Hes, Helena J. van der Pal, Heuvel-Eibrink, M.M. van den, Heuvel-Eibrink, Marry M van den, Kathy Pritchard-Jones, M M Van Den Heuvel-Eibrink, M M Van den Heuvel-Eibrink

843

Publications

28.3K

Citations

H-Index

206

Concepts

All Affiliations

Erasmus MC - Sophia Children’s Hospital Princess Máxima Center Erasmus MC University Medical Center Utrecht Stichting Kinderoncologie Nederland

About

Marry M. van den Heuvel‐Eibrink is an author at Erasmus MC - Sophia Children’s Hospital specializing in medicine, pathology, and oncology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	47	94	7K
2	Health Sciences	17	21	1.3K
3	Arts	2	2	105
4	Education	1	1	18
5	Engineering	1	1	24

Marry M. van den Heuvel‐Eibrink

319

Publications

20.3K

Citations

H-Index

Page 1

	Year	Citations
The MLL recombinome of acute leukemias in 2017 Claus Meyer, Thomas Burmeister, Daniela Gröger, Leukemia	2017	670
The MLL recombinome of acute leukemias in 2013 Claus Meyer, Jörg Hofmann, Thomas Burmeister, Leukemia	2013	506
Novel prognostic subgroups in childhood 11q23/MLL-rearranged acute myeloid leukemia: results of an international retrospective study Brian V. Balgobind, Susana C. Raimondi, Jochen Harbott, Blood	2009	444
Tubuloids derived from human adult kidney and urine for personalized disease modeling Frans Schutgens, Maarten B. Rookmaaker, Thanasis Margaritis, Nature Biotechnology Translational MedicineUrologyRenal DiseasePersonalized Disease ModelingRenal Function	2019	431
New insights to the MLL recombinome of acute leukemias Claus Meyer, Eric Kowarz, Jörg Hofmann, Leukemia Hematological MalignancyMixed-phenotype Acute LeukemiaHematologyNew InsightsMedicine	2009	410
Germline CBL mutations cause developmental abnormalities and predispose to juvenile myelomonocytic leukemia Charlotte M. Niemeyer, Michelle Kang, Danielle H. Shin, Nature Genetics Hematological MalignancyChromatinDevelopmental BiologyGeneticsHematology	2010	365
NUP98/NSD1 characterizes a novel poor prognostic group in acute myeloid leukemia with a distinct HOX gene expression pattern Iris H.I.M. Hollink, Marry M. van den Heuvel‐Eibrink, Susan T.C.J.M. Arentsen-Peters, Blood	2011	327
An organoid biobank for childhood kidney cancers that captures disease and tissue heterogeneity Camilla Calandrini, Frans Schutgens, Rurika Oka, Nature Communications	2020	301
Mutations in the SIX1/2 Pathway and the DROSHA/DGCR8 miRNA Microprocessor Complex Underlie High-Risk Blastemal Type Wilms Tumors Jenny Wegert, Naveed Ishaque, Romina Vardapour, Cancer Cell GeneticsMolecular GeneticsSmall RnaCancer GeneticsMicrorna Detection	2015	300
Mutations in CBL occur frequently in juvenile myelomonocytic leukemia Mignon L. Loh, Debbie S. Sakai, Christian Flotho, Blood	2009	285

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