NOVELLI, GIUSEPPE

NOVELLI, GIUSEPPE  

Dipartimento di Biomedicina e Prevenzione  

Mostra records
Risultati 1 - 20 di 584 (tempo di esecuzione: 0.043 secondi).
Data di pubblicazione Titolo Autore(i) Tipo File
1-gen-2009 "The Linosa Study": Epidemiological and heritability data of the metabolic syndrome in a Caucasian genetic isolate Bellia, A; Giardina, E; Lauro, D; Tesauro, M; Di Fede, G; Cusumano, G; Federici, M; Rini, G; Novelli, G; Lauro, R; Sbraccia, P Articolo su rivista
1-gen-1995 22q11 deletions in isolated and syndromic patients with tetralogy of Fallot Amati, F; Mari, A; Digilio, Mc; Mingarelli, R; Marino, B; Giannotti, A; Novelli, G; Dallapiccola, B Articolo su rivista
1-gen-2002 3020insC mutation within the NOD2 gene in Crohn's disease: frequency and association with clinical pattern in an Italian population Vavassori, P; Borgiani, P; D'Apice, Mr; De Negris, F; DEL VECCHIO BLANCO, G; Monteleone, I; Biancone, L; Novelli, G; Pallone, E Articolo su rivista
1-giu-2021 A 14-Year Italian Experience in DM2 Genetic Testing: Frequency and Distribution of Normal and Premutated CNBP Alleles Botta, A; Visconti, Vv; Fontana, L; Bisceglia, P; Bengala, M; Massa, R; Bagni, I; Cardani, R; Sangiuolo, F; Meola, G; Antonini, G; Petrucci, A; Pegoraro, E; D'Apice, Mr; Novelli, G Articolo su rivista
1-gen-2019 A common polymorphism in MIR155 gene promoter region is associated with a lower risk to develop type 2 diabetes Latini, A; Spallone, V; D'Amato, C; Novelli, G; Borgiani, P; Ciccacci, C Articolo su rivista
11-set-1999 A distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13 Servidei, S; Capon, F; Spinazzola, A; Mirabella, M; Semprini, S; de Rosa, G; Gennarelli, M; Sangiuolo, Fc; Ricci, E; Mohrenweiser, H; Dallapiccola, B; Tonali, P; Novelli, G Articolo su rivista
4-lug-2024 A Dynamic and Effective Peptide-Based Strategy for Promptly Addressing Emerging SARS-CoV-2 Variants of Concern Murdocca, M; Romeo, I; Citro, G; Latini, A; Centofanti, F; Bugatti, A; Caccuri, F; Caruso, A; Ortuso, F; Alcaro, S; Sangiuolo, F; Novelli, G Articolo su rivista
1-set-2016 A European spectrum of pharmacogenomic biomarkers: Implications for clinical pharmacogenomics Mizzi, C; Dalabira, E; Kumuthini, J; Dzimiri, N; Balogh, I; Basak, N; Bohm, R; Borg, J; Borgiani, P; Bozina, N; Bruckmueller, H; Burzynska, B; Carracedo, A; Cascorbi, I; Deltas, C; Dolzan, V; Fenech, A; Grech, G; Kasiulevicius, V; Kadasi, L; Kucinskas, V; Khusnutdinova, E; Loukas, Y; Macek, M; Makukh, H; Mathijssen, R; Mitropoulos, K; Mitropoulou, C; Novelli, G; Papantoni, I; Pavlovic, S; Saglio, G; Setric, J; Stojiljkovic, M; Stubbs, A; Squassina, A; Torres, M; Turnovec, M; Van Schaik, R; Voskarides, K; Wakil, S; Werk, A; Zompo, M; Zukic, B; Katsila, T; Lee, M; Motsinger Rief, A; Leod, H; Van Der Spek, P; Patrinos, G Articolo su rivista
1-ott-2010 A fluorescence-based sequence-specific primer PCR for the screening of HLA-B(*)57:01 Giardina, E; Stocchi, L; Foti Cuzzola, V; Zampatti, S; Gambardella, S; Patrizi, M; Bramanti, P; Pirazzoli, A; Novelli, G Articolo su rivista
1-mag-2021 A focus on the spread of the delta variant of SARS-CoV-2 in India Novelli, G; Colona, V; Pandolfi, P Articolo su rivista
1-nov-2010 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1 Strange, A; Capon, F; Spencer, C; Knight, J; Weale, M; Allen, M; Barton, A; Band, G; Bellenguez, C; Bergboer, J; Blackwell, J; Bramon, E; Bumpstead, S; Casas, J; Cork, M; Corvin, A; Deloukas, P; Dilthey, A; Duncanson, A; Edkins, S; Estivill, X; Fitzgerald, O; Freeman, C; Giardina, E; Gray, E; Hofer, A; Hüffmeier, U; Hunt, S; Irvine, A; Jankowski, J; Kirby, B; Langford, C; Lascorz, J; Leman, J; Leslie, S; Mallbris, L; Markus, H; Mathew, C; Mclean, W; Mcmanus, R; Mössner, R; Moutsianas, L; Naluai, A; Nestle, F; Novelli, G; Onoufriadis, A; Palmer, C; Perricone, C; Pirinen, M; Plomin, R; Potter, S; Pujol, R; Rautanen, A; Riveira Munoz, E; Ryan, A; Salmhofer, W; Samuelsson, L; Sawcer, S; Schalkwijk, J; Smith, C; Ståhle, M; Su, Z; Tazi Ahnini, R; Traupe, H; Viswanathan, A; Warren, R; Weger, W; Wolk, K; Wood, N; Worthington, J; Young, H; Zeeuwen, P; Hayday, A; Burden, A; Griffiths, C; Kere, J; Reis, A; Mcvean, G; Evans, D; Brown, M; Barker, J; Peltonen, L; Donnelly, P; Trembath, R Articolo su rivista
1-gen-2022 A global effort to dissect the human genetic basis of resistance to SARS-CoV-2 infection Andreakos, E; Abel, L; Vinh, D; Kaja, E; Drolet, B; Zhang, Q; O'Farrelly, C; Novelli, G; Rodriguez-Gallego, C; Haerynck, F; Prando, C; Pujol, A; Su, H; Casanova, J; Spaan, A; Bastard, P; Biggs, C; Bigio, B; Boisson, B; Bolze, A; Bondarenko, A; Brodin, P; Chakravorty, S; Christodoulou, J; Cobat, A; Condino-Neto, A; Constantinescu, S; Feldman, H; Fellay, J; Halwani, R; Jouanguy, E; Lau, Y; Meyts, I; Mogensen, T; Okada, S; Okamoto, K; Ozcelik, T; Pan-Hammarstrom, Q; Planas, A; Puel, A; Quintana-Murci, L; Renia, L; Resnick, I; Sediva, A; Shcherbina, A; Slaby, O; Tancevski, I; Turvey, S; Uddin, K; van de Beek, D; Zatz, M; Zawadzki, P; Zhang, S Articolo su rivista
1-gen-1998 A highly polymorphic CA/GT repeat (LIMK1GT) within the Williams syndrome critical region Mari, A; Amati, F; Conti, E; Bengala, M; Novelli, G; Dallapiccola, B Articolo su rivista
1-giu-2023 A likely pathogenic ACTG1 variant in a child showing partial phenotypic overlap with Baraitser-Winter syndrome Graziani, L; Cinnirella, G; Ferradini, V; Conte, C; Bascio, Fl; Bengala, M; Sangiuolo, F; Novelli, G Articolo su rivista
1-gen-2004 A long PCR-based molecular protocol for detecting normal and expanded ZNF9 alleles in myotonic dystrophy type 2 Bonifazi, E; Vallo, L; Giardina, E; Botta, A; Novelli, G Articolo su rivista
1-gen-2014 A multilocus genetic study in a cohort of Italian SLE patients confirms the association with STAT4 gene and describes a new association with HCP5 gene Ciccacci, C; Perricone, C; Ceccarelli, F; Rufini, S; Di Fusco, D; Alessandri, C; Spinelli, F; Cipriano, E; Novelli, G; Valesini, G; Borgiani, P; Conti, F Articolo su rivista
1-gen-2006 A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries, in mice Cipollone, D; Amati, F; Carsetti, R; Placidi, S; Biancolella, M; D'Amati, G; Novelli, G; Siracusa, G; Marino, B Articolo su rivista
1-dic-2008 A multiplex molecular assay for the detection of uniparental disomy for human chromosome 15 Giardina, E; Peconi, C; Cascella, R; Sinibaldi, C; Nardone, A; Novelli, G Articolo su rivista
1-giu-2009 A multiplex molecular assay for the detection of uniparental disomy for human chromosome 7 Giardina, E; Peconi, C; Cascella, R; Sinibaldi, C; Foti Cuzzola, V; Nardone, A; Bramanti, P; Novelli, G Articolo su rivista
1-gen-2018 A multivariate genetic analysis confirms rs5010528 in the human leucocyte antigen-C locus as a significant contributor to Stevens-Johnson syndrome/toxic epidermal necrolysis susceptibility in a Mozambique HIV population treated with nevirapine Ciccacci, C; Politi, C; Mancinelli, S; Ciccacci, F; Lucaroni, F; Novelli, G; Marazzi, Mc; Palombi, L; Borgiani, P Articolo su rivista