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Caterina Congregati

Observed name: C. Congregati
OpenAlex ID: A5050444137
Interleukin-10 promoter polymorphisms influence susceptibility to ulcerative colitis in a gender-specific manner
2008 · Andrea Tedde, Anna Laura Putignano, et al. · Scandinavian Journal of Gastroenterology · 56
A PALB2 germline mutation associated with hereditary breast cancer in Italy
2009 · Laura Papi, Anna Laura Putignano, et al. · Familial Cancer · 47
Germline investigation in male breast cancer of DNA repair genes by next-generation sequencing
2019 · R. Scarpitta, I. Zanna, et al. · Breast Cancer Research and Treatment · 39
Founder mutations account for the majority of BRCA1-attributable hereditary breast/ovarian cancer cases in a population from Tuscany, Central Italy
2008 · Laura Papi, Anna Laura Putignano, et al. · Breast Cancer Research and Treatment · 37
Characterization of an Italian Founder Mutation in the RING-Finger Domain of BRCA1
2014 · Laura Caleca, Anna Laura Putignano, et al. · PLoS ONE · 24
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Functional Interaction Between BRCA1 and DNA Repair in Yeast May Uncover a Role of RAD50, RAD51, MRE11A, and MSH6 Somatic Variants in Cancer Development
2018 · Luisa Maresca, Samuele Lodovichi, et al. · Frontiers in Genetics · 23
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Germline mutations in MEN1 and BRCA1 genes in a woman with familial multiple endocrine neoplasia type 1 and inherited breast–ovarian cancer syndromes: a case report
2009 · Laura Papi, Domenico Palli, et al. · Cancer Genetics and Cytogenetics · 19
Role of 18F-DOPA PET/CT in Diagnosis and Follow-up of Adrenal and Extra-adrenal Paragangliomas
2013 · Alessandra Bacca, Serena Chiacchio, et al. · Clinical Nuclear Medicine · 15
Whole-exome analysis of a Li–Fraumeni family trio with a novel TP53 PRD mutation and anticipation profile
2017 · Sara Franceschi, Laura Spugnesi, et al. · Carcinogenesis · 14
Acro‐cardio‐facial syndrome: A microdeletion syndrome?
2012 · Benedetta Toschi, Angelo Valetto, et al. · American Journal of Medical Genetics Part A · 14
Detection of Germline Variants in 450 Breast/Ovarian Cancer Families with a Multi-Gene Panel Including Coding and Regulatory Regions
2021 · Chiara Guglielmi, Rosa Scarpitta, et al. · International Journal of Molecular Sciences · 10
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Sporadic or familial head neck paragangliomas enrolled in a single center: Clinical presentation and genotype/phenotype correlations
2012 · Alessandra Bacca, Stefano Sellari Franceschini, et al. · Head & Neck · 10
Validation and Data-Integration of Yeast-Based Assays for Functional Classification of BRCA1 Missense Variants
2022 · Francesca Bellè, Alberto Mercatanti, et al. · International Journal of Molecular Sciences · 6
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The BRCA1 c.4096+1G>A Is a Founder Variant Which Originated in Ancient Times
2023 · Paolo Aretini, Silvano Presciuttini, et al. · International Journal of Molecular Sciences · 3
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Sclerosing Paragangliomas: Correlations of Histological Features with Patients’ Genotype and Vesicular Monoamine Transporter Expression
2022 · Angela Pucci, Alessandra Bacca, et al. · Head and Neck Pathology · 3
A 17q duplication prenatally detected
2015 · Rossella Bruno, Angelo Valetto, et al. · Taiwanese Journal of Obstetrics and Gynecology · 2
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P-173 Extended molecular profiling in patients with biliary tract cancers: Impact of the BRCAness phenotype in patients management
2023 · V. Genovesi, C. Vivaldi, et al. · Annals of Oncology
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18F-DOPA PET/CT in the diagnosis of paragangliomas
2013 · Serena Chiacchio, Alessandra Bacca, et al. · Society of Nuclear Medicine Annual Meeting Abstracts
Works count: 18
Citation count: 322
H-index: 10
I10-index: 12
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