Associated Papers
Leveraging genomic diagnostics for prognostics and therapeutics in pediatric acute leukemia.
Newman H et al.
Hemasphere, 2025
41306327 (PubMed )
Supplement: HEM3-9-e70269-s013.xlsx › Supplemental_Table_5_-_SSVs
Specification of frequency criteria for secondary findings genes to improve variant classification concordance.
Johnston JJ et al.
Biorxiv : the Preprint Server for Biology, 2025
Clinical Characterization of a National Cohort of Patients With Germline WT1 Variants Including Late-Onset Phenotypes.
van Peer SE et al.
Kidney International Reports, 2024
Long-term kidney function in children with Wilms tumour and constitutional WT1 pathogenic variant.
Falcone MP et al.
Pediatric Nephrology (berlin, Germany), 2022
Comprehensive germline genomic profiles of children, adolescents and young adults with solid tumors.
Akhavanfard S et al.
Nature Communications, 2020
32371905 (PubMed )
Supplement: 41467_2020_16067_MOESM12_ESM.xlsx › Supplementary_Data_6
Identifying the role of Wilms tumor 1 associated protein in cancer prediction using integrative genomic analyses.
Wu LS et al.
Molecular Medicine Reports, 2016
Bilateral Wilms tumor and early presentation in pediatric patients is associated with the truncation of the Wilms tumor 1 protein.
Hu M et al.
The Journal of Pediatrics, 2013
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