Research & Literature
Explore the leading researchers and institutions driving advances in this area, and dive into the full body of literature that informs this resource.
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St. Jude Children's Research Hospital
Memphis, United States
Princess Máxima Center
Utrecht, The Netherlands
Broad Institute
Cambridge, United States
Fundación para la Investigación, Docencia y Prevención del Cáncer
Buenos Aires, Argentina
German Cancer Research Center
Heidelberg, Germany
Baylor College of Medicine
Houston, United States
Memorial Sloan Kettering Cancer Center
New York, United States
Institute of Cancer Research
London, United Kingdom
Children's Hospital of Philadelphia
Philadelphia, United States
National Cancer Institute
Bethesda, United States
References
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International journal of cancer 2019; (145(4)):941-951 doi:10.1002/ijc.32167.
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Agreement between clinicoradiological signs at diagnosis and radiohistological analysis after neoadjuvant chemotherapy of suspected Wilms tumor rupture: Consequences on therapeutic choices.
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Pediatric blood & cancer 2019; (66(6)):e27674 doi:10.1002/pbc.27674.
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A rare case of a Wilms tumor: case report.
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Augmentation of Therapy for Combined Loss of Heterozygosity 1p and 16q in Favorable Histology Wilms Tumor: A Children's Oncology Group AREN0532 and AREN0533 Study Report.
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Copy Number Variations in Wilms Tumor: A Pilot Study From India.
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Molecular genetics & genomic medicine 2020; (8(4)):e1183 doi:10.1002/mgg3.1183.
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From Wilms to kidney tumors: which ones require a biopsy?
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Pediatric radiology 2020; (50(8)):1049-1051 doi:10.1007/s00247-020-04660-x.
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Evaluation of the nephron-sparing surgery formula in Wilms tumors.
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Immune-complex glomerulonephritis with a membranoproliferative pattern in Frasier syndrome: a case report and review of the literature.
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Effectiveness of Nephron Sparing Surgery and Radical Nephrectomy in the Management of Unilateral Wilms Tumor: A Meta-Analysis.
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Frontiers in oncology 2020; (10()):1248 doi:10.3389/fonc.2020.01248.
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Syndromic Wilms tumor: a review of predisposing conditions, surveillance and treatment.
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Translational andrology and urology 2020; (9(5)):2370-2381 doi:10.21037/tau.2020.03.27.
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Preoperative Wilms tumor rupture in children.
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Case Report: Denys-Drash Syndrome With WT1 Causative Variant Presenting as Atypical Hemolytic Uremic Syndrome.
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Frontiers in pediatrics 2020; (8()):605889 doi:10.3389/fped.2020.605889.
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New approaches to risk stratification for Wilms tumor.
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Current opinion in pediatrics 2021; (33(1)):40-48 doi:10.1097/MOP.0000000000000988.
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Do children with solitary or hypofunctioning kidney have the same prevalence for masked hypertension?
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Outcome of Stage IV Completely Necrotic Wilms Tumour and Local Stage III Treated According to the SIOP 2001 Protocol.
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Cancers 2021; (13(5)) doi:10.3390/cancers13050976.
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Many faces of Wilms Tumor: Recent advances and future directions.
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Annals of medicine and surgery (2012) 2021; (64()):102202 doi:10.1016/j.amsu.2021.102202.
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Improving the prenatal diagnosis of Beckwith-Wiedemann syndrome.
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Prenatal diagnosis 2021; (41(7)):795-797 doi:10.1002/pd.5971.
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New mutation in WT1 gene in a boy with an incomplete form of Denys-Drash syndrome: A CARE-compliant case report.
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Impact of the First Generation of Children's Oncology Group Clinical Trials on Clinical Practice for Wilms Tumor.
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Wilms Tumor (Nephroblastoma), Version 2.2021, NCCN Clinical Practice Guidelines in Oncology.
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Long-term Follow-up Care for Childhood, Adolescent, and Young Adult Cancer Survivors.
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Pediatrics 2021; (148(3)) doi:10.1542/peds.2021-053127.
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Bromodomain 4 inhibition leads to MYCN downregulation in Wilms tumor.
Woods AD, Berlow NE, Ortiz MV, et al.
Pediatric blood & cancer 2022; (69(2)):e29401 doi:10.1002/pbc.29401.
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Osteopathia striata with cranial sclerosis: a new case supporting the link with bilateral Wilms tumor.
Sinibaldi L, Micalizzi A, Serra A, et al.
European journal of human genetics : EJHG 2022; (30(3)):262-264 doi:10.1038/s41431-021-01035-0.
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Characteristics and outcomes of preoperatively treated patients with anaplastic Wilms tumors registered in the UK SIOP-WT-2001 and IMPORT study cohorts (2002-2020).
Vujanić GM, Mifsud W, Chowdhury T, et al.
Cancer 2022; (128(8)):1666-1675 doi:10.1002/cncr.34107.
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Cardiovascular Health Status And Genetic Risk In Survivors of Childhood Neuroblastoma and Nephroblastoma Treated With Doxorubicin: Protocol of the Pharmacogenetic Part of the LESS-Anthra Cross-Sectional Cohort Study.
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Mindfulness Stress Management for Female Cancer Survivors Facing the Uncertainty of Disease Progression: A Randomized Controlled Study.
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International journal of environmental research and public health 2022; (19(8)) doi:10.3390/ijerph19084497.
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Breast Cancer Secondary to Radiation Therapy in a Patient With Wilms Tumor.
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Cureus 2022; (14(3)):e23597 doi:10.7759/cureus.23597.
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How we approach paediatric renal tumour core needle biopsy in the setting of preoperative chemotherapy: A Review from the SIOP Renal Tumour Study Group.
Jackson TJ, Brisse HJ, Pritchard-Jones K, et al.
Pediatric blood & cancer 2022; (69(9)):e29702 doi:10.1002/pbc.29702.
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Molecular Basis of Beckwith-Wiedemann Syndrome Spectrum with Associated Tumors and Consequences for Clinical Practice.
Eggermann T, Maher ER, Kratz CP, Prawitt D
Cancers 2022; (14(13)) doi:10.3390/cancers14133083.
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Evidence-based surgical guidelines for treating children with Wilms tumor in low-resource settings.
Abdelhafeez AH, Reljic T, Kumar A, et al.
Pediatric blood & cancer 2022; (69(12)):e29906 doi:10.1002/pbc.29906.
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Nephron-sparing surgery for Wilms tumor.
Murphy AJ, Davidoff AM
Frontiers in pediatrics 2023; (11()):1122390 doi:10.3389/fped.2023.1122390.
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Radical Nephrectomy After Immune Checkpoint Inhibitors for Metastatic Renal Cell Carcinoma.
Yanagisawa T, Schmidinger M, Kawada T, et al.
European urology focus 2023; (9(2)):275-277 doi:10.1016/j.euf.2023.01.022.
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Scanxiety among Adults with Cancer: A Scoping Review to Guide Research and Interventions.
Derry-Vick HM, Heathcote LC, Glesby N, et al.
Cancers 2023; (15(5)) doi:10.3390/cancers15051381.
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Novel concept of Wilms' tumor development: involvement of pluripotential cells of ureteric bud.
Sarkany B, Kuthi L, Kovacs G
Human pathology 2023; (138()):34-40 doi:10.1016/j.humpath.2023.05.004.
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Children's Oncology Group's 2023 blueprint for research: Renal tumors.
Geller JI, Hong AL, Vallance KL, et al.
Pediatric blood & cancer 2023; (70 Suppl 6()):e30586 doi:10.1002/pbc.30586.
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Bilateral Nephroblastomatosis With a Unilateral Wilms Tumor: A Case Report Highlighting Imaging Characteristics.
Naggar A, Assila S, Laasri K, et al.
Global pediatric health 2024; (11()):2333794X231224566 doi:10.1177/2333794X231224566.
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Wilms tumour resulting from paternal transmission of a TRIM28 pathogenic variant-A first report.
Whitworth J, Armstrong R, Maher ER
European journal of human genetics : EJHG 2024; (32(3)):361-364 doi:10.1038/s41431-024-01545-7.
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Case Report: Autosomal dominant polycystic kidney disease and Wilms' tumor in infancy and childhood.
Zina D, Rosita K, Kristina Z, et al.
Frontiers in pediatrics 2024; (12()):1322142 doi:10.3389/fped.2024.1322142.
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Anaplasia in Wilms tumor: A critical review.
Vujanić GM, Mifsud W
Pediatric blood & cancer 2024; (71(7)):e31000 doi:10.1002/pbc.31000.
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Cognitive-behavioural therapy effectiveness for fear of cancer recurrence: systematic review and meta-analysis.
Wei F, He R, Yang X, et al.
BMJ supportive & palliative care 2024; (15(1)):1-11 doi:10.1136/spcare-2023-004639.
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The learning curve for modified hand-assisted retroperitoneoscopic living donor nephrectomy.
Shang L, Zheng M, Wang Z, Zhu Y
BMC urology 2024; (24(1)):191 doi:10.1186/s12894-024-01581-x.
PMID: 39227858 - 67
Update on Surveillance for Wilms Tumor and Hepatoblastoma in Beckwith-Wiedemann Syndrome and Other Predisposition Syndromes.
Kalish JM, Becktell KD, Bougeard G, et al.
Clinical cancer research : an official journal of the American Association for Cancer Research 2024; (30(23)):5260-5269 doi:10.1158/1078-0432.CCR-24-2100.
PMID: 39320341 - 68
A Chromosomal Microarray Detects Microdeletion at Chromosome Locus 11p14.3-p12 Leading to Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation (WAGR) Syndrome.
Majjigudda RA, Menon P, Gupte S, et al.
Cureus 2024; (16(10)):e72479 doi:10.7759/cureus.72479.
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Wilms tumor and associated predisposing syndromes and conditions.
Meni D
JAAPA : official journal of the American Academy of Physician Assistants 2025; (38(1)):27-33 doi:10.1097/01.JAA.0000000000000165.
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Secondary ovarian germ cell tumor following Wilms tumor after eight years post-treatment: A rare case report.
Ansari-Damavandi S, Pakbaz Y, Zarei E, Shadani S
International journal of surgery case reports 2025; (128()):111107 doi:10.1016/j.ijscr.2025.111107.
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Distinct pathways for genetic and epigenetic predisposition in familial and bilateral Wilms tumor.
Wegert J, Appenzeller S, Treger TD, et al.
Genome medicine 2025; (17(1)):49 doi:10.1186/s13073-025-01482-0.
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A rare case of fetal bilateral Wilms' tumor in horseshoe kidney: A case report.
Melis A, Tadesse T, Jemal S, Ketema W
International journal of surgery case reports 2025; (133()):111619 doi:10.1016/j.ijscr.2025.111619.
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Current clinical and surgical insights in the workup and management of Wilms tumor (nephroblastoma).
Jhaveri HF, Sarantos N, Aitelli A, et al.
Current opinion in pediatrics 2025; (37(5)):488-494 doi:10.1097/MOP.0000000000001490.
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Analysis of prognostic factors and development of a predictive model following radical nephrectomy for Wilms tumor in children.
Teng H, Hou B, Shi K, et al.
Oncology letters 2025; (30(5)):506 doi:10.3892/ol.2025.15252.
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Wilms Tumor With Hepatic and Pulmonary Metastases in a Toddler: A Case Report.
Elaitari K, Boujida N, Jabour S, et al.
Cureus 2025; (17(8)):e91176 doi:10.7759/cureus.91176.
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NCYM facilitates cell proliferation and invasion in Wilms tumor by regulating SIX1/β-catenin axis.
Wang Z, Ning F, Tu L, et al.
American journal of clinical and experimental urology 2025; (13(5)):316-331 doi:10.62347/MVNT6272.
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"You Always Worry": Scan-Related Anxiety Among Patients With Metastatic Lung Cancer.
Derry-Vick H, Prigerson HG, Hahne J, et al.
Journal of the American College of Radiology : JACR 2025; (22(12)):1572-1577 doi:10.1016/j.jacr.2025.08.021.
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[Teratoid Wilms tumor in an adult: A case report].
Hernández-Marchena YN, González-Medina WE, Bolado-García PB, et al.
Revista medica del Instituto Mexicano del Seguro Social 2026; (64(1)):e6762 doi:10.5281/zenodo.17477324.
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[Paediatric kidney tumours: Update on the challenges of nephroblastoma and other kidney tumours].
L'Herminé-Coulomb A, Berrebi D
Annales de pathologie 2026; (46(3)):195-206 doi:10.1016/j.annpat.2026.02.011.
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Tumor Microenvironment and Immune Response Against Wilms Tumor: Evasion Mechanisms and Implications for Immunotherapeutic Approaches.
Cantoni C, Vellone VG, Cafferata B, et al.
Cancers 2026; (18(6)) doi:10.3390/cancers18060908.
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Gain of chromosome 1q and MYCN characterize unique subgroups of Asian Wilms tumor patients.
Wong MK, Lim KT, Thùy ĐTN, et al.
Cancer treatment and research communications 2026; (47()):101191 doi:10.1016/j.ctarc.2026.101191.
PMID: 41905202