Author

Anita Villani

Observed names: A. Villani, A., Villani, Villani, A, Villani, Anita

Observed institutions: BC Cancer Agency, University of Alberta, University of Toronto, York University, Children's Hospital of Eastern Ontario, Montreal Children's Hospital, Great Ormond Street Hospital, Izaak Walton Killam Health Centre, Alberta Hospital Edmonton, Hospital for Sick Children, Alberta Children's Hospital, University of Alberta Hospital, BC Children's Hospital

ORCID: 0000-0003-3283-2197

Observed ORCID: 0000-0003-3283-2197

OpenAlex ID: A5001213402

Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: 11 year follow-up of a prospective observational study

2016 · Anita Villani, Ari Shore, et al. · The Lancet Oncology · 544

Cancer Screening Recommendations for Individuals with Li-Fraumeni Syndrome

2017 · Christian P. Kratz, Maria Isabel Achatz, et al. · Clinical Cancer Research · 531

Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study

2011 · Anita Villani, Uri Tabori, et al. · The Lancet Oncology · 423

Von Hippel–Lindau and Hereditary Pheochromocytoma/Paraganglioma Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood

2017 · Surya P. Rednam, Ayelet Erez, et al. · Clinical Cancer Research · 281

Baseline Surveillance in Li-Fraumeni Syndrome Using Whole-Body Magnetic Resonance Imaging

2017 · Mandy L. Ballinger, Ana Best, et al. · JAMA Oncology · 197

Recommendations for Cancer Surveillance in Individuals with RASopathies and Other Rare Genetic Conditions with Increased Cancer Risk

2017 · Anita Villani, Mary-Louise C. Greer, et al. · Clinical Cancer Research · 163

Genomic predictors of response to PD-1 inhibition in children with germline DNA replication repair deficiency

2022 · Anirban Das, Sumedha Sudhaman, et al. · Nature Medicine · 155

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The clinical utility of integrative genomics in childhood cancer extends beyond targetable mutations

2022 · Anita Villani, Scott Davidson, et al. · Nature Cancer · 124

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Molecular Characterization of Choroid Plexus Tumors Reveals Novel Clinically Relevant Subgroups

2014 · Diana M. Merino, Adam Shlien, et al. · Clinical Cancer Research · 121

Survival Benefit for Individuals With Constitutional Mismatch Repair Deficiency Undergoing Surveillance

2021 · Carol Durno, Ayse Bahar Ercan, et al. · Journal of Clinical Oncology · 107

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DNA Polymerase and Mismatch Repair Exert Distinct Microsatellite Instability Signatures in Normal and Malignant Human Cells

2020 · Jiil Chung, Yosef E. Maruvka, et al. · Cancer Discovery · 87

Multiple Endocrine Neoplasia and Hyperparathyroid-Jaw Tumor Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood

2017 · Jonathan D. Wasserman, Gail E. Tomlinson, et al. · Clinical Cancer Research · 79

Clinical and biological landscape of constitutional mismatch-repair deficiency syndrome: an International Replication Repair Deficiency Consortium cohort study

2024 · Ayse Bahar Ercan, Melyssa Aronson, et al. · The Lancet Oncology · 75

Performance of the McGill Interactive Pediatric OncoGenetic Guidelines for Identifying Cancer Predisposition Syndromes

2021 · Catherine Goudie, Leora Witkowski, et al. · JAMA Oncology · 63

Combined Immunotherapy Improves Outcome for Replication-Repair-Deficient (RRD) High-Grade Glioma Failing Anti–PD-1 Monotherapy: A Report from the International RRD Consortium

2023 · Anirban Das, Nicholas R. Fernandez, et al. · Cancer Discovery · 50

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DICER1 syndrome: Approach to testing and management at a large pediatric tertiary care center

2017 · Kalene van Engelen, Anita Villani, et al. · Pediatric Blood & Cancer · 50

Update on Cancer Screening Recommendations for Individuals with Li–Fraumeni Syndrome

2025 · Maria Isabel Achatz, Anita Villani, et al. · Clinical Cancer Research · 48

Germline TP53 mutations undergo copy number gain years prior to tumor diagnosis

2023 · Nicholas Light, Mehdi Layeghifard, et al. · Nature Communications · 44

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Diagnostic classification of childhood cancer using multiscale transcriptomics

2023 · Federico Comitani, Joshua O. Nash, et al. · Nature Medicine · 43

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Update on Surveillance for Wilms Tumor and Hepatoblastoma in Beckwith–Wiedemann Syndrome and Other Predisposition Syndromes

2024 · Jennifer M. Kalish, Kerri D. Becktell, et al. · Clinical Cancer Research · 41

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Genomic Microsatellite Signatures Identify Germline Mismatch Repair Deficiency and Risk of Cancer Onset

2022 · Jiil Chung, Logine Negm, et al. · Journal of Clinical Oncology · 41

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The landscape of primary mismatch repair deficient gliomas in children, adolescents, and young adults: a multi-cohort study

2024 · Logine Negm, Jiil Chung, et al. · The Lancet Oncology · 37

Pediatric imaging in DICER1 syndrome

2017 · Marta Tijerin Bueno, Claudia Martínez-Ríos, et al. · Pediatric Radiology · 37

Cost‐effectiveness of early cancer surveillance for patients with Li–Fraumeni syndrome

2019 · Casey R. Tak, Eman Biltaji, et al. · Pediatric Blood & Cancer · 35

Management of familial cancer: sequencing, surveillance and society

2014 · Nardin Samuel, Anita Villani, et al. · Nature Reviews Clinical Oncology · 34

Works count: 238

Citation count: 3,900

H-index: 28

I10-index: 44