Crovella S, Moura RR, Cappellani S, Celsi F, Trevisan E, Schneider M, Brollo A, Nicastro EM, Vita F, Finotto L, Zabucchi G, Borelli V. A genetic variant of NLRP1 gene is associated with asbestos body burden in patients with malignant pleural mesothelioma. J Toxicol Environ Health A 2018;81(5):98-105.

Catamo E, Zupin L, Freato N, Polesello V, Celsi F, Crocè SL, Masutti F, Pozzato G, Segat L, Crovella S. HLA-G regulatory polymorphisms are associated with susceptibility to HCV infection. HLA 2017;89(3):135-142.

Zupin L, Robino A, Navarra CO, Pirastu N, Di Lenarda R, Gasparini P, Crovella S, Bevilacqua L. LTF and DEFB1 polymorphisms are associated with susceptibility toward chronic periodontitis development. Oral Dis 2017;23(7):1001-1008.

Lima CAD, Javorski NR, Souza APO, Barbosa AD, Valença APMC, Crovella S, Souza PRE, J Silva deAzevêdo, Sandrin-Garcia P. Polymorphisms in key bone modulator cytokines genes influence bisphosphonates therapy in postmenopausal women. Inflammopharmacology 2017;25(2):191-201.

Garziera M, Catamo E, Crovella S, Montico M, Cecchin E, Lonardi S, Mini E, Nobili S, Romanato L, Toffoli G. Association of the HLA-G 3'UTR polymorphisms with colorectal cancer in Italy: a first insight. Int J Immunogenet 2016;43(1):32-9.

Zupin L, Polesello V, Alberi G, Moratelli G, Crocè SL, Masutti F, Pozzato G, Crovella S, Segat L. MBL2 Genetic Variants in HCV Infection Susceptibility, Spontaneous Viral Clearance and Pegylated Interferon Plus Ribavirin Treatment Response. Scand J Immunol 2016;84(1):61-9.

Pontillo A, Bricher P, Leal VNC, Lima S, Souza PRE, Crovella S. Role of inflammasome genetics in susceptibility to HPV infection and cervical cancer development. J Med Virol 2016;88(9):1646-51.

Catamo E, Addobbati C, Segat L, T Fragoso S, A Dantas T, H Mariz deAtaíde, L Junior Fda Rocha, PintoDuarte ALBranco, Coelho AVC, de Moura RR, Polesello V, Crovella S, P Garcia S. Comprehensive analysis of polymorphisms in the HLA-G 5' upstream regulatory and 3' untranslated regions in Brazilian patients with systemic lupus erythematosus. Tissue Antigens 2015;85(6):458-65.

Santos SM, Souza CA, Rabelo KCN, Souza PRE, Moura RR, Oliveira TC, Crovella S. Distribution of forensic marker allelic frequencies in Pernambuco, Northestern Brazil. Genet Mol Res 2015;14(2):4303-10.

Angelo HD, Silva IIFGomes, Oliveira RDR, Louzada-Júnior P, Donadi EA, Crovella S, Maia MMD, de Souza PRE, Sandrin-Garcia P. Interleukin-18, interleukin-12B and interferon-? gene polymorphisms in Brazilian patients with rheumatoid arthritis: a pilot study. Tissue Antigens 2015;86(4):276-8.

Coelho AVC, Moura RR, Cavalcanti CAJ, Guimarães RL, Sandrin-Garcia P, Crovella S, Brandão LAC. A rapid screening of ancestry for genetic association studies in an admixed population from Pernambuco, Brazil. Genet Mol Res 2015;14(1):2876-84.

Addobbati CJC, J Silva deAzevêdo, Tavares NAC, Araujo J, Guimarães RL, Brandão L, Crovella S, Sandrin-Garcia P. Short Communication FYB polymorphisms in Brazilian patients with type I diabetes mellitus and autoimmune polyglandular syndrome type III. Genet Mol Res 2015;14(1):29-33.

Rabelo KCN, Albuquerque CMR, Tavares VB, Santos SM, Souza CA, Oliveira TC, Oliveira NCL, Crovella S. Trace samples of human blood in mosquitoes as a forensic investigation tool. Genet Mol Res 2015;14(4):14847-56.

Maranhão RM de Albuq, Esteves FAMartins, Crovella S, Segat L, Souza PREleutér. Tumor necrosis factor-? and interleukin-6 gene polymorphism association with susceptibility to celiac disease in Italian patients. Genet Mol Res 2015;14(4):16343-52.

Barrani M, Massei F, Scaglione M, Paolicchi A, Vitali S, Ciancia EM, Crovella S, Caparello MC, Consolini R. Unusual onset of a case of chronic recurrent multifocal osteomyelitis. Pediatr Rheumatol Online J 2015;13(1):60.

Pellegrin MC, Matarazzo L, Neri E, Pennesi M, Crovella S. HLA-B35, a common genetic trait, in a familial case of Henoch-Schoenlein purpura and Berger's disease. Genet Mol Res 2014;13(2):2669-73.

Segat L, Zupin L, Kim H-Y, Catamo E, Thea DM, Kankasa C, Aldrovandi GM, Kuhn L, Crovella S. HLA-G 14?bp deletion/insertion polymorphism and mother-to-child transmission of HIV. Tissue Antigens 2014;83(3):161-7.

Catamo E, Addobbati C, Segat L, T Fragoso S, A Barbosa D, A Dantas T, H Mariz deAtaíde, da Rocha LF, Duarte ALBranco P, Monasta L, Sandrin-Garcia P, Crovella S. HLA-G gene polymorphisms associated with susceptibility to rheumatoid arthritis disease and its severity in Brazilian patients. Tissue Antigens 2014;84(3):308-15.

Lenarduzzi S, Morgutti M, Crovella S, Coiana A, Rosatelli MC. Short communication: novel truncating mutations in the CFTR gene causing a severe form of cystic fibrosis in Italian patients. Genet Mol Res 2014;13(4):9636-41.

Girardelli M, Bianco AM, Marcuzzi A, Crovella S. A comparative analysis of serologic parameters and oxidative stress in osteoarthritis and rheumatoid arthritis: reply to Mishra and colleagues. Rheumatol Int 2013;33(9):2445-6.

Filho CB, Rodrigues FF, Segat L, Fonseca AM, Araujo J, Arahata C, Pontes L, Vilar L, Filho JL de Lima, Crovella S. Association of MBL2 gene exon 1 variants with autoimmune thyroid disease in Brazilian patients. Int J Immunogenet 2012;39(4):357-61.

Catamo E, Segat L, Lenarduzzi S, Petix V, Morgutti M, Crovella S. CD14 polymorphisms correlate with an augmented risk for celiac disease in Italian patients. Genes Immun 2012;13(6):489-95.

da Silva MFPTBald, Guimarães V, Silva MAR, Amaral CMMedeiros, Beçak W, Stocco RC, Freitas AC, Crovella S. Frequency of human papillomavirus types 16, 18, 31, and 33 and sites of cervical lesions in gynecological patients from Recife, Brazil. Genet Mol Res 2012;11(1):462-6.

Sandrin-Garcia P, Brandão LAC, Guimarães RL, Pancoto JAT, Donadi EA, de Lima-Filho JL, Segat L, Crovella S. Functional single-nucleotide polymorphisms in the DEFB1 gene are associated with systemic lupus erythematosus in Southern Brazilians. Lupus 2012;21(6):625-31.

Segat L, Crovella S. HLA-G 14bp del/ins genetic variation: association with susceptibility to human immunodeficiency virus-1 vertical transmission but not with human immunodeficiency virus-1 infection through horizontal transmission. Tissue Antigens 2012;80(1):12-3.

Bianco AM, Vuch J, Girardelli M, Zanin V, Marcuzzi A, Crovella S. Letter: inflammatory bowel disease, complementary and alternative medicine, and genetics. Aliment Pharmacol Ther 2012;35(9):1110-1.

Ferraroni NR, Segat L, Guimarães RL, Brandão LAC, Crovella S, Constantino-Silva RN, Loja C, Duarte AJ da Silva, Grumach AS. Mannose-binding lectin and MBL-associated serine protease-2 gene polymorphisms in a Brazilian population from Rio de Janeiro. Int J Immunogenet 2012;39(1):32-8.

Pontillo A, Di Toro N, Edomi P, Shadlow A, Ammadeo A, Gattorno M, Not T, Lepore L, Crovella S. Anti-?-enolase Antibodies in Serum from Pediatric Patients Affected by Inflammatory Diseases: Diagnostic and Pathogenetic Insights. Int J Rheumatol 2011;2011:870214.

Segat L, Crovella S. MBL2 polymorphisms and the choice of controls for association studies: just another story?. Int J Immunogenet 2011;38(2):101-4; author reply 105-8.

Segat L, Morgutti M, Athanasakis E, Trevisiol C, Amaddeo A, Poli F, Crovella S. Analysis of DEFB1 regulatory SNPs in cystic fibrosis patients from North-Eastern Italy. Int J Immunogenet 2010;37(3):169-75.

Bulla R, De Seta F, Radillo O, Agostinis C, Durigutto P, Pellis V, De Santo D, Crovella S, Tedesco F. Mannose-binding lectin is produced by vaginal epithelial cells and its level in the vaginal fluid is influenced by progesterone. Mol Immunol 2010;48(1-3):281-6.