Anita Villani
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Explore the profile of Anita Villani including associated specialties, affiliations and a list of published articles.
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61
Citations
1228
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Recent Articles
1.
Achatz M, Villani A, Bertuch A, Bougeard G, Chang V, Doria A, et al.
Clin Cancer Res
. 2025 Mar;
PMID: 40072304
Li-Fraumeni syndrome (LFS) is an autosomal dominant cancer predisposition condition characterized by a high lifetime risk for a wide spectrum of malignancies associated with germline pathogenic/likely pathogenic (P/LP) variants in...
2.
Negm L, Chung J, Nobre L, Bennett J, Fernandez N, Nunes N, et al.
Lancet Oncol
. 2024 Dec;
26(1):123-135.
PMID: 39701117
Background: Gliomas are a major cause of cancer-related death among children, adolescents, and young adults (age 0-40 years). Primary mismatch repair deficiency (MMRD) is a pan-cancer mechanism with unique biology...
3.
Tambasco D, Zlotnik M, Joshi S, Moineddin R, Harris S, Villani A, et al.
J Clin Med
. 2024 Nov;
13(22).
PMID: 39597804
: To determine the diagnostic accuracy of quantitative diffusion-weighted (DW) MRI apparent diffusion coefficient (ADC) and tumour volumes to differentiate between malignant (neuroblastoma (NB)) and benign types of neuroblastic tumours...
4.
Brzezinski J, Becktell K, Bougeard G, Brodeur G, Diller L, Doria A, et al.
Clin Cancer Res
. 2024 Oct;
31(1):18-24.
PMID: 39466169
Wilms tumors are commonly associated with predisposition syndromes. Many of these syndromes are associated with specific phenotypic features and are discussed in the related article from the AACR Pediatric Cancer...
5.
Kalish J, Becktell K, Bougeard G, Brodeur G, Diller L, Doria A, et al.
Clin Cancer Res
. 2024 Sep;
30(23):5260-5269.
PMID: 39320341
Wilms tumors are commonly associated with predisposition syndromes, many but not all of which include overgrowth. Several of these syndromes also include a risk of other embryonal malignancies-particularly hepatoblastoma. Guidelines...
6.
Wong D, Tageldein M, Luo P, Ensminger E, Bruce J, Oldfield L, et al.
Nat Commun
. 2024 Aug;
15(1):7386.
PMID: 39191772
Germline pathogenic TP53 variants predispose individuals to a high lifetime risk of developing multiple cancers and are the hallmark feature of Li-Fraumeni syndrome (LFS). Our group has previously shown that...
7.
Azma R, Arenos-Abril J, Junhasavasdiku T, Tewattanarat N, Nourmohammad A, Abadeh A, et al.
J Pediatr Hematol Oncol
. 2024 Aug;
46(7):335-348.
PMID: 39185882
Although tumors of Li-Fraumeni syndrome (LFS) have a premalignant or dormant phase that could be exploited by early imaging detection, this has been underevaluated in the literature. We present a...
8.
Nakano Y, Acker M, Druker H, van Engelen K, Meyn M, Wasserman J, et al.
Eur J Hum Genet
. 2024 Aug;
32(11):1474-1482.
PMID: 39117932
Rhabdoid tumor predisposition syndrome type-1 (RTPS1) is characterized by germline pathogenic variants in SMARCB1 and development of INI1-deficient rhabdoid tumors in early childhood. Due to its poor prognosis, the risk...
9.
Ercan A, Aronson M, Fernandez N, Chang Y, Levine A, Liu Z, et al.
Lancet Oncol
. 2024 Mar;
25(5):668-682.
PMID: 38552658
Background: Constitutional mismatch repair deficiency (CMMRD) syndrome is a rare and aggressive cancer predisposition syndrome. Because a scarcity of data on this condition contributes to management challenges and poor outcomes,...
10.
Two congenital cases of pigmented epithelioid melanocytoma with unique clinical and genetic features
Zaaroura H, Cyrenne B, Somers G, Wong K, Davidge K, Propst E, et al.
Dermatol Online J
. 2024 Mar;
29(5).
PMID: 38478639
Pigmented epithelioid melanocytomas (PEM) are intermediate-grade melanocytic lesions with frequent lymph node involvement and rare metastases that tend to follow an indolent course with a favorable outcome. We report two...