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Filling the gap: A thorough investigation for the genetic diagnosis of unsolved polyposis patients with monoallelic MUTYH pathogenic variants.
Dell'Elice A, Cini G, Fornasarig M, Armelao F, Barana D, Bianchi F, Casalis Cavalchini GC, Maffè A, Mammi I, Pedroni M, Percesepe A, Sorrentini I, Tibiletti M, Maestro R, Quaia M, Viel A. Dell'Elice A, et al. Among authors: bianchi f. Mol Genet Genomic Med. 2021 Dec;9(12):e1831. doi: 10.1002/mgg3.1831. Epub 2021 Oct 26. Mol Genet Genomic Med. 2021. PMID: 34704405 Free PMC article.
Assessing the pathogenicity of MLH1 missense mutations in patients with suspected hereditary nonpolyposis colorectal cancer: correlation with clinical, genetic and functional features.
Belvederesi L, Bianchi F, Loretelli C, Gagliardini D, Galizia E, Bracci R, Rosati S, Bearzi I, Viel A, Cellerino R, Porfiri E. Belvederesi L, et al. Among authors: bianchi f. Eur J Hum Genet. 2006 Jul;14(7):853-9. doi: 10.1038/sj.ejhg.5201628. Epub 2006 May 17. Eur J Hum Genet. 2006. PMID: 16724012
An intronic mutation in MLH1 associated with familial colon and breast cancer.
Bianchi F, Raponi M, Piva F, Viel A, Bearzi I, Galizia E, Bracci R, Belvederesi L, Loretelli C, Brugiati C, Corradini F, Baralle D, Cellerino R. Bianchi F, et al. Fam Cancer. 2011 Mar;10(1):27-35. doi: 10.1007/s10689-010-9371-4. Fam Cancer. 2011. PMID: 20717847 Free PMC article.
CAT25 is a mononucleotide marker to identify HNPCC patients.
Bianchi F, Galizia E, Catalani R, Belvederesi L, Ferretti C, Corradini F, Cellerino R. Bianchi F, et al. J Mol Diagn. 2009 May;11(3):248-52. doi: 10.2353/jmoldx.2009.080155. Epub 2009 Mar 26. J Mol Diagn. 2009. PMID: 19324995 Free PMC article.
Expectations and psychological issues before genetic counseling: analysis of distress determinant factors.
Ballatore Z, Bracci R, Maccaroni E, Svarca L, Bianchi F, Belvederesi L, Bruciati C, Pagliaretta S, Murrone A, Bini F, Pistelli M, Ricci G, Berardi R. Ballatore Z, et al. Among authors: bianchi f. Hered Cancer Clin Pract. 2020 Apr 29;18:10. doi: 10.1186/s13053-020-00142-1. eCollection 2020. Hered Cancer Clin Pract. 2020. PMID: 32368313 Free PMC article.
Lynch syndrome-associated lung cancer: pitfalls of an immunotherapy-based treatment strategy in an unusual tumor type.
Maccaroni E, Lenci E, Agostinelli V, Cognigni V, Giampieri R, Mazzanti P, Di Pietro Paolo M, Bianchi F, Brugiati C, Belvederesi L, Pagliaretta S, Mandolesi A, Scarpelli M, Murrone A, Morgese F, Ballatore Z, Berardi R. Maccaroni E, et al. Among authors: bianchi f. Explor Target Antitumor Ther. 2021;2(3):240-248. doi: 10.37349/etat.2021.00044. Epub 2021 Jun 28. Explor Target Antitumor Ther. 2021. PMID: 36046437 Free PMC article.
Molecular Tumour Board (MTB): From Standard Therapy to Precision Medicine.
Ballatore Z, Bozzi F, Cardea S, Savino FD, Migliore A, Tarantino V, Chiodi N, Ambrosini E, Bianchi F, Goteri G, Filosa A, Barbisan F, Bartoli E, Papa R, Berardi R. Ballatore Z, et al. Among authors: bianchi f. J Clin Med. 2023 Oct 21;12(20):6666. doi: 10.3390/jcm12206666. J Clin Med. 2023. PMID: 37892804 Free PMC article.
2,147 results