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Rob Pieters

Utrecht University · NL
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Area of research
Public Health, Environmental and Occupational Health · Hematology
Research interest
Research interests include Acute Lymphoblastic Leukemia research, Acute Myeloid Leukemia Research, Childhood Cancer Survivors' Quality of Life, and Chronic Myeloid Leukemia Treatments.
h-index
105
citations
39,997
works
911
NIH funding
primary concept
email

Recent publications

Sustained Benefit of Blinatumomab in Infants With <i>KMT2A</i>-Rearranged ALL: Long-Term Outcomes, Toxicity, and Pharmacokinetics.
2026cited by 1position: contributordoi
Challenging Conventional Diagnostic Methods by Comprehensive Molecular Diagnostics: A Nationwide Prospective Comparison in Children With ALL.
2025cited by 7position: contributordoi
The genomic landscape of relapsed infant and childhood KMT2A-rearranged acute leukemia.
2025cited by 1position: contributordoi
BEHAV3D: a 3D live imaging platform for comprehensive analysis of engineered T cell behavior and tumor response
Nature Protocols 2024cited by 30position: middledoi
Biologic and Clinical Analysis of Childhood Gamma Delta T-ALL Identifies LMO2/STAG2 Rearrangements as Extremely High Risk.
2024cited by 13position: contributordoi
Biologic and Clinical Analysis of Childhood Gamma Delta T-ALL Identifies <i>LMO2/STAG2</i> Rearrangements as Extremely High Risk
Cancer Discovery 2024cited by 13position: middledoi
ETV6::RUNX1 Acute Lymphoblastic Leukemia: how much therapy is needed for cure?
2024cited by 11position: contributordoi
Increased risk of subsequent neoplasm after hematopoietic stem cell transplantation in 5-year survivors of childhood acute lymphoblastic leukemia
Blood Cancer Journal 2024cited by 7position: middledoi
Increased risk of subsequent neoplasm after hematopoietic stem cell transplantation in 5-year survivors of childhood acute lymphoblastic leukemia.
2024cited by 5position: contributordoi
Continuous PEGasparaginase Dosing Reduces Hypersensitivity Reactions in Pediatric ALL: A Dutch Childhood Oncology Group ALL11 Randomized Trial.
2024cited by 5position: contributordoi
Integration of genetics and MRD to define low risk patients with B-cell precursor acute lymphoblastic leukaemia with intermediate MRD levels at the end of induction.
2024cited by 5position: contributordoi
Are measurable residual disease results after consolidation therapy useful in children with acute lymphoblastic leukemia?
2024cited by 3position: contributordoi
Author Correction: A joint international consensus statement for measuring quality of survival for patients with childhood cancer.
2024cited by 1position: contributordoi
Author Correction: A joint international consensus statement for measuring quality of survival for patients with childhood cancer.
2024cited by 0position: contributordoi
Author Correction: A joint international consensus statement for measuring quality of survival for patients with childhood cancer.
2024cited by 0position: contributordoi
Supplementary Table S2 from Biologic and Clinical Analysis of Childhood Gamma Delta T-ALL Identifies &lt;i&gt;LMO2/STAG2&lt;/i&gt; Rearrangements as Extremely High Risk
2024cited by 0position: contributordoi
Supplementary Table S22 from Biologic and Clinical Analysis of Childhood Gamma Delta T-ALL Identifies &lt;i&gt;LMO2/STAG2&lt;/i&gt; Rearrangements as Extremely High Risk
2024cited by 0position: contributordoi
Supplementary Figure S1 from Biologic and Clinical Analysis of Childhood Gamma Delta T-ALL Identifies &lt;i&gt;LMO2/STAG2&lt;/i&gt; Rearrangements as Extremely High Risk
2024cited by 0position: contributordoi
Supplementary Figure S3 from Biologic and Clinical Analysis of Childhood Gamma Delta T-ALL Identifies &lt;i&gt;LMO2/STAG2&lt;/i&gt; Rearrangements as Extremely High Risk
2024cited by 0position: contributordoi
Supplementary Figure S4 from Biologic and Clinical Analysis of Childhood Gamma Delta T-ALL Identifies &lt;i&gt;LMO2/STAG2&lt;/i&gt; Rearrangements as Extremely High Risk
2024cited by 0position: contributordoi
Supplementary Table S14 from Biologic and Clinical Analysis of Childhood Gamma Delta T-ALL Identifies &lt;i&gt;LMO2/STAG2&lt;/i&gt; Rearrangements as Extremely High Risk
2024cited by 0position: contributordoi
Supplementary Table S10 from Biologic and Clinical Analysis of Childhood Gamma Delta T-ALL Identifies &lt;i&gt;LMO2/STAG2&lt;/i&gt; Rearrangements as Extremely High Risk
2024cited by 0position: contributordoi
Supplementary Table S15 from Biologic and Clinical Analysis of Childhood Gamma Delta T-ALL Identifies &lt;i&gt;LMO2/STAG2&lt;/i&gt; Rearrangements as Extremely High Risk
2024cited by 0position: contributordoi
Supplementary Figure S9 from Biologic and Clinical Analysis of Childhood Gamma Delta T-ALL Identifies &lt;i&gt;LMO2/STAG2&lt;/i&gt; Rearrangements as Extremely High Risk
2024cited by 0position: contributordoi
Supplementary Table S21 from Biologic and Clinical Analysis of Childhood Gamma Delta T-ALL Identifies &lt;i&gt;LMO2/STAG2&lt;/i&gt; Rearrangements as Extremely High Risk
2024cited by 0position: contributordoi
Supplementary Table S25 from Biologic and Clinical Analysis of Childhood Gamma Delta T-ALL Identifies &lt;i&gt;LMO2/STAG2&lt;/i&gt; Rearrangements as Extremely High Risk
2024cited by 0position: contributordoi
Supplementary Table S5 from Biologic and Clinical Analysis of Childhood Gamma Delta T-ALL Identifies &lt;i&gt;LMO2/STAG2&lt;/i&gt; Rearrangements as Extremely High Risk
2024cited by 0position: contributordoi
Supplementary Table S9 from Biologic and Clinical Analysis of Childhood Gamma Delta T-ALL Identifies &lt;i&gt;LMO2/STAG2&lt;/i&gt; Rearrangements as Extremely High Risk
2024cited by 0position: contributordoi
Supplementary Table S4 from Biologic and Clinical Analysis of Childhood Gamma Delta T-ALL Identifies &lt;i&gt;LMO2/STAG2&lt;/i&gt; Rearrangements as Extremely High Risk
2024cited by 0position: contributordoi
Supplementary Figure S8 from Biologic and Clinical Analysis of Childhood Gamma Delta T-ALL Identifies &lt;i&gt;LMO2/STAG2&lt;/i&gt; Rearrangements as Extremely High Risk
2024cited by 0position: contributordoi

Grants

No grants ingested yet.

Frequent collaborators

· 20 papers (2021–2026)Marry M. van den Heuvel‐Eibrink · Nationwide Children's Hospital8 papers (2013–2024)Monique L. den Boer · Princess Máxima Center6 papers (2012–2024)Andrea Biondi · Associazione Italiana Ematologia Oncologia Pediatrica6 papers (2013–2024)Valerie Haas · Emma Kinderziekenhuis6 papers (2023–2025)Marta Fiocco · University of Applied Sciences Leiden6 papers (2020–2024)Martin Schrappe · University Hospital and Clinics6 papers (2013–2026)Stephen P. Hunger · University College London6 papers (2013–2023)Jan Starý · University Hospital in Motol5 papers (2013–2026)Ajay Vora · Great Ormond Street Hospital5 papers (2019–2024)Dirk Reinhardt · Charité - Universitätsmedizin Berlin5 papers (2012–2016) · 5 papers (2021–2024)André Baruchel · HIPI - Immunologie humaine, physiopathologie et immunithérapie5 papers (2013–2023)Inge M. van der Sluis · Princess Máxima Center5 papers (2019–2026)Hanneke M. van Santen · University Medical Center Utrecht4 papers (2023–2024)Christine J. Harrison · Newcastle University4 papers (2013–2022)Válerie de Haas · Medizinische Hochschule Hannover4 papers (2012–2013)Rachel T. Webster · St. Jude Children's Research Hospital4 papers (2023–2024)Antoinette Schouten-van Meeteren · Princess Máxima Center4 papers (2023–2024) · 4 papers (2023–2024)
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