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Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns: A pilot study.
Carrera P, Di Resta C, Volonteri C, Castiglioni E, Bonfiglio S, Lazarevic D, Cittaro D, Stupka E, Ferrari M, Somaschini M; BPD and Genetics Study Group. Carrera P, et al. Among authors: bonfiglio s. Clin Chim Acta. 2015 Dec 7;451(Pt A):39-45. doi: 10.1016/j.cca.2015.01.001. Epub 2015 Jan 8. Clin Chim Acta. 2015. PMID: 25578394
Whole exome sequencing of independent lung adenocarcinoma, lung squamous cell carcinoma, and malignant peritoneal mesothelioma: A case report.
Vanni I, Coco S, Bonfiglio S, Cittaro D, Genova C, Biello F, Mora M, Rossella V, Dal Bello MG, Truini A, Banelli B, Lazarevic D, Alama A, Rijavec E, Barletta G, Grossi F. Vanni I, et al. Among authors: bonfiglio s. Medicine (Baltimore). 2016 Nov;95(48):e5447. doi: 10.1097/MD.0000000000005447. Medicine (Baltimore). 2016. PMID: 27902597 Free PMC article.
Integrated Somatic and Germline Whole-Exome Sequencing Analysis in Women with Lung Cancer after a Previous Breast Cancer.
Coco S, Bonfiglio S, Cittaro D, Vanni I, Mora M, Genova C, Dal Bello MG, Boccardo S, Alama A, Rijavec E, Sini C, Rossella V, Barletta G, Biello F, Truini A, Bruzzo C, Gallo M, Lazarevic D, Ballestrero A, Grossi F. Coco S, et al. Among authors: bonfiglio s. Cancers (Basel). 2019 Mar 28;11(4):441. doi: 10.3390/cancers11040441. Cancers (Basel). 2019. PMID: 30925779 Free PMC article.
Identification of differential DNA methylation associated with multiple sclerosis: A family-based study.
Garcia-Manteiga JM, Clarelli F, Bonfiglio S, Mascia E, Giannese F, Barbiera G, Guaschino C, Sorosina M, Santoro S, Protti A, Martinelli V, Cittaro D, Lazarevic D, Stupka E, Filippi M, Esposito F, Martinelli-Boneschi F. Garcia-Manteiga JM, et al. Among authors: bonfiglio s. J Neuroimmunol. 2021 Jul 15;356:577600. doi: 10.1016/j.jneuroim.2021.577600. Epub 2021 Apr 30. J Neuroimmunol. 2021. PMID: 33991750
Characterisation and validation of insertions and deletions in 173 patient exomes.
Lescai F, Bonfiglio S, Bacchelli C, Chanudet E, Waters A, Sisodiya SM, Kasperavičiūtė D, Williams J, Harold D, Hardy J, Kleta R, Cirak S, Williams R, Achermann JC, Anderson J, Kelsell D, Vulliamy T, Houlden H, Wood N, Sheerin U, Tonini GP, Mackay D, Hussain K, Sowden J, Kinsler V, Osinska J, Brooks T, Hubank M, Beales P, Stupka E. Lescai F, et al. Among authors: bonfiglio s. PLoS One. 2012;7(12):e51292. doi: 10.1371/journal.pone.0051292. Epub 2012 Dec 14. PLoS One. 2012. PMID: 23251486 Free PMC article.
A CD8α- Subset of CD4+SLAMF7+ Cytotoxic T Cells Is Expanded in Patients With IgG4-Related Disease and Decreases Following Glucocorticoid Treatment.
Della-Torre E, Bozzalla-Cassione E, Sciorati C, Ruggiero E, Lanzillotta M, Bonfiglio S, Mattoo H, Perugino CA, Bozzolo E, Rovati L, Arcidiacono PG, Balzano G, Lazarevic D, Bonini C, Falconi M, Stone JH, Dagna L, Pillai S, Manfredi AA. Della-Torre E, et al. Among authors: bonfiglio s. Arthritis Rheumatol. 2018 Jul;70(7):1133-1143. doi: 10.1002/art.40469. Epub 2018 May 20. Arthritis Rheumatol. 2018. PMID: 29499100 Free PMC article.
Burden of rare coding variants in an Italian cohort of familial multiple sclerosis.
Mascia E, Clarelli F, Zauli A, Guaschino C, Sorosina M, Barizzone N, Basagni C, Santoro S, Ferrè L, Bonfiglio S, Biancolini D, Pozzato M, Guerini FR, Protti A, Liguori M, Moiola L, Vecchio D, Bresolin N, Comi G, Filippi M, Esposito F, D'Alfonso S, Martinelli-Boneschi F. Mascia E, et al. Among authors: bonfiglio s. J Neuroimmunol. 2022 Jan 15;362:577760. doi: 10.1016/j.jneuroim.2021.577760. Epub 2021 Nov 5. J Neuroimmunol. 2022. PMID: 34922125
79 results