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Identification and characterization of functional risk variants for colorectal cancer mapping to chromosome 11q23.1.
Biancolella M, Fortini BK, Tring S, Plummer SJ, Mendoza-Fandino GA, Hartiala J, Hitchler MJ, Yan C, Schumacher FR, Conti DV, Edlund CK, Noushmehr H, Coetzee SG, Bresalier RS, Ahnen DJ, Barry EL, Berman BP, Rice JC, Coetzee GA, Casey G. Biancolella M, et al. Hum Mol Genet. 2014 Apr 15;23(8):2198-209. doi: 10.1093/hmg/ddt584. Epub 2013 Nov 20. Hum Mol Genet. 2014. PMID: 24256810 Free PMC article.
COVID-19 and Molecular Genetics.
Novelli G, Biancolella M. Novelli G, et al. Among authors: biancolella m. Genes (Basel). 2022 Apr 12;13(4):676. doi: 10.3390/genes13040676. Genes (Basel). 2022. PMID: 35456482 Free PMC article.
Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: a novel recognizable microdeletion syndrome?
D'Apice MR, Novelli A, di Masi A, Biancolella M, Antoccia A, Gullotta F, Licata N, Minella D, Testa B, Nardone AM, Palmieri G, Calabrese E, Biancone L, Tanzarella C, Frontali M, Sangiuolo F, Novelli G, Pallone F. D'Apice MR, et al. Among authors: biancolella m. BMC Med Genet. 2015 Apr 2;16:20. doi: 10.1186/s12881-015-0164-3. BMC Med Genet. 2015. PMID: 25927938 Free PMC article.
Analysis of ACE2 genetic variants in 131 Italian SARS-CoV-2-positive patients.
Novelli A, Biancolella M, Borgiani P, Cocciadiferro D, Colona VL, D'Apice MR, Rogliani P, Zaffina S, Leonardis F, Campana A, Raponi M, Andreoni M, Grelli S, Novelli G. Novelli A, et al. Among authors: biancolella m. Hum Genomics. 2020 Sep 11;14(1):29. doi: 10.1186/s40246-020-00279-z. Hum Genomics. 2020. PMID: 32917283 Free PMC article.
41 results