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Broadening of cohesinopathies: exome sequencing identifies mutations in ANKRD11 in two patients with Cornelia de Lange-overlapping phenotype.
Parenti I, Gervasini C, Pozojevic J, Graul-Neumann L, Azzollini J, Braunholz D, Watrin E, Wendt KS, Cereda A, Cittaro D, Gillessen-Kaesbach G, Lazarevic D, Mariani M, Russo S, Werner R, Krawitz P, Larizza L, Selicorni A, Kaiser FJ. Parenti I, et al. Among authors: lazarevic d. Clin Genet. 2016 Jan;89(1):74-81. doi: 10.1111/cge.12564. Epub 2015 Feb 25. Clin Genet. 2016. PMID: 25652421 Free article.
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: lazarevic d. 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
Chromas from chromatin: sonification of the epigenome.
Cittaro D, Lazarevic D, Provero P. Cittaro D, et al. Among authors: lazarevic d. F1000Res. 2016 Mar 3;5:274. doi: 10.12688/f1000research.8001.1. eCollection 2016. F1000Res. 2016. PMID: 27019695 Free PMC article.
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: lazarevic d. Medicine (Baltimore). 2016 Nov;95(48):e5447. doi: 10.1097/MD.0000000000005447. Medicine (Baltimore). 2016. PMID: 27902597 Free PMC article.
141 results