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L. Zuurbier · SciRah

Researcher profile · Semantic Scholar

L. Zuurbier

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L. Zuurbier — researcher profile on SciRah

h-index: 14
Works: 26
Citations: 1,530

Most-cited papers

Oncogenic IL7R gain-of-function mutations in childhood T-cell acute lymphoblastic leukemia
P. Zenatti, Daniel Ribeiro, Wenqing Li, L. Zuurbier +18 more
2011Nature Genetics408 citations Open access
Semantic Scholar
PHF6 mutations in T-cell acute lymphoblastic leukemia
P. Van Vlierberghe, Teresa Palomero, Hossein Khiabanian, J. Van der Meulen +29 more
2010Nature Genetics301 citations Open access
Semantic Scholar
NOTCH1 and/or FBXW7 mutations predict for initial good prednisone response but not for improved outcome in pediatric T-cell acute lymphoblastic leukemia patients treated on DCOG or COALL protocols
L. Zuurbier, I. Homminga, V. Calvert, Mlt Winkel +10 more
2010Leukemia146 citations
Semantic Scholar
NOTCH1 extracellular juxtamembrane expansion mutations in T-ALL.
M. Sulis, O. Williams, Teresa Palomero, V. Tosello +6 more
2008Blood141 citations Open access
Semantic Scholar
The significance of PTEN and AKT aberrations in pediatric T-cell acute lymphoblastic leukemia
L. Zuurbier, E. Petricoin, Maartje J Vuerhard, V. Calvert +9 more
2012Haematologica121 citations Open access
Semantic Scholar
Immature MEF2C-dysregulated T-cell leukemia patients have an early T-cell precursor acute lymphoblastic leukemia gene signature and typically have non-rearranged T-cell receptors
L. Zuurbier, Alejandro Gutierrez, C. Mullighan, K. Canté-Barrett +10 more
2014Haematologica85 citations Open access
Semantic Scholar
PTEN microdeletions in T-cell acute lymphoblastic leukemia are caused by illegitimate RAG-mediated recombination events.
Rui D. Mendes, L. Sarmento, K. Canté-Barrett, L. Zuurbier +10 more
2014Blood76 citations Open access
Semantic Scholar
Apelin: A putative novel predictive biomarker for bevacizumab response in colorectal cancer
L. Zuurbier, A. Rahman, Martijn Cordes, Jennifer R. Scheick +22 more
2017OncoTarget48 citations Open access
Semantic Scholar
ABCG5 and ABCG8 genetic variants in familial hypercholesterolemia.
L. Reeskamp, Andrea Volta, L. Zuurbier, J. Defesche +2 more
2020Journal of Clinical Lipidology40 citations Open access
Semantic Scholar
Cooperative genetic defects in TLX3 rearranged pediatric T-ALL
P. Van Vlierberghe, I. Homminga, L. Zuurbier, J. Gladdines-Buijs +5 more
2008Leukemia39 citations Open access
Semantic Scholar
A Deep Intronic Variant in LDLR in Familial Hypercholesterolemia: Time to Widen the Scope?
L. Reeskamp, M. L. Hartgers, J. Peter, G. Dallinga-Thie +4 more
2018Circulation Genomic and Precision Medicine29 citations Open access
Semantic Scholar
Phenotypic expansion of the BPTF‐related neurodevelopmental disorder with dysmorphic facies and distal limb anomalies
Kevin E. Glinton, A. Hurst, Kevin M. Bowling, I. Cristian +44 more
2021American Journal of Medical Genetics. Part A28 citations Open access
Semantic Scholar
Next-generation sequencing to confirm clinical familial hypercholesterolemia.
L. Reeskamp, T. Tromp, J. Defesche, A. Grefhorst +3 more
2020European Journal of Preventive Cardiology27 citations Open access
Semantic Scholar
Next-generation sequencing to confirm clinical familial hypercholesterolemia.
L. Reeskamp, T. Tromp, J. Defesche, A. Grefhorst +3 more
2020European Journal of Preventive Cardiology22 citations Open access
Semantic Scholar
Intronic variant screening with targeted next-generation sequencing reveals first pseudoexon in LDLR in familial hypercholesterolemia.
L. Reeskamp, Manon Balvers, J. Peter, Laura van de Kerkhof +7 more
2021Atherosclerosis13 citations Open access
Semantic Scholar
Cellular Resistance Against Troxacitabine in Human Cell Lines and Pediatric Patient Acute Myeloid Leukemia Blast Cells
A. D. Adema, L. Zuurbier, K. Floor, I. Hubeek +3 more
2006Nucleosides, Nucleotides & Nucleic Acids3 citations
Semantic Scholar
An exploratory analysis of causes for extreme LDL-C levels in patients not carrying variants in genes causing familial hypercholesterolemia
T. Tromp, L. Reeskamp, M. L. Hartgers, A. Grefhorst +3 more
20201 citations
Semantic Scholar
A deep intronic variant in LDLR causing familial hypercholesterolemia: Time to widen the scope?
L. Reeskamp, M. L. Hartgers, J. Peter, G. Dallinga-Thie +4 more
2018Atherosclerosis1 citations
Semantic Scholar
Familial hypercholesterolemia cascade testing: Insights from the Dutch Program.
Bram M. Weijs, D. Boor, W. Corpeleijn, S. E. van den Bosch +6 more
2026Journal of Clinical Lipidology0 citations Open access
Semantic Scholar
Abcg5 And Abcg8 Variants In Familial Hypercholesterolemia
L. Reeskamp, Andrea Volta, L. Zuurbier, J. Defesche +2 more
2019Atherosclerosis0 citations
Semantic Scholar
NOTCH1 extracellular juxtamembrane expansion mutations in T-ALL Running head title: New activating mutations in NOTCH1
M. Sulis, O. Williams, Teresa Palomero, V. Tosello +7 more
20160 citations
Semantic Scholar
74 : IL-7R: Mutations in T-ALL and polymorphisms in autoimmunity
S. Durum, Wenqing Li, P. Zenatti, D. Ribeiro +18 more
20130 citations
Semantic Scholar
O023 Oncogenic IL-7R gain-of-function mutations in childhood T-ALL
S. Durum, Wenqing Li, P. Zenatti, D. Ribeiro +18 more
20110 citations Open access
Semantic Scholar
Antioxidant and fatty acid augmentation strategies in schizophrenia: A systematic review and meta-analysis
L. Zuurbier
20110 citations
Semantic Scholar
PTEN/AKT Pathway Mutations Are Reciprocal to NOTCH-Activating Mutations In Pediatric T-Cell Acute Lymphoblastic Lymphoma (T-ALL)
L. Zuurbier, Maartje J Vuerhard, C. Kooi, W. Smits +5 more
20100 citations
Semantic Scholar
Clinical Relevance of NOTCH1 and FBXW7 Mutations in DCOG and COALL T-ALL Patient Cohorts.
L. Zuurbier, I. Homminga, J. Buijs-Gladdines, V. de Haas +3 more
20090 citations
Semantic Scholar

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