Esme Waanders
Utrecht, UT, Netherlands
Last Updated: 09/26/2026
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Found 40 publications
In-depth analysis of osmotic gradient ektacytometry parameters across different genotypes in hereditary spherocytosis.
Journal: British journal of haematology
Published: November 12, 2025
Corrigendum to "Implementation of paediatric precision oncology into clinical practice: The individualized therapies for children with cancer program 'iTHER'" [Eur J Cancer 175 (2022) 311-325].
Journal: European journal of cancer (Oxford, England : 1990)
Published: April 13, 2025
Challenging Conventional Diagnostic Methods by Comprehensive Molecular Diagnostics: A Nationwide Prospective Comparison in Children With ALL.
Journal: JCO precision oncology
Published: February 28, 2025
Wilms tumor characteristics in children with heterozygous germline DIS3L2 variants.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 22, 2024
A novel germline PAX5 single exon deletion in a pediatric patient with precursor B-cell leukemia.
Journal: Leukemia
Published: February 14, 2023
Implementation of paediatric precision oncology into clinical practice: The Individualized Therapies for Children with cancer program 'iTHER'.
Journal: European journal of cancer (Oxford, England : 1990)
Published: July 18, 2022
Heterozygosity for bisphosphoglycerate mutase deficiency expressing clinically as congenital erythrocytosis: A case series and literature review.
Journal: British journal of haematology
Published: May 24, 2022
European standard clinical practice - Key issues for the medical care of individuals with familial leukemia.
Journal: European journal of medical genetics
Published: March 22, 2022
Prevalence of (Epi)genetic Predisposing Factors in a 5-Year Unselected National Wilms Tumor Cohort: A Comprehensive Clinical and Genomic Characterization.
Journal: Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Published: March 01, 2022
Characteristics of white blood cell count in acute lymphoblastic leukemia: A COST LEGEND phenotype-genotype study.
Journal: Pediatric blood & cancer
Published: September 13, 2021
Optical genome mapping identifies a germline retrotransposon insertion in SMARCB1 in two siblings with atypical teratoid rhabdoid tumors.
Journal: The Journal of pathology
Published: May 26, 2021
Last Updated: 09/26/2026