NOVELLI, GIUSEPPE
NOVELLI, GIUSEPPE
Dipartimento di Biomedicina e Prevenzione
"The Linosa Study": Epidemiological and heritability data of the metabolic syndrome in a Caucasian genetic isolate
2009-01-01 Bellia, A; Giardina, E; Lauro, D; Tesauro, M; Di Fede, G; Cusumano, G; Federici, M; Rini, G; Novelli, G; Lauro, R; Sbraccia, P
22q11 deletions in isolated and syndromic patients with tetralogy of Fallot
1995-01-01 Amati, F; Mari, A; Digilio, Mc; Mingarelli, R; Marino, B; Giannotti, A; Novelli, G; Dallapiccola, B
3020insC mutation within the NOD2 gene in Crohn's disease: frequency and association with clinical pattern in an Italian population
2002-01-01 Vavassori, P; Borgiani, P; D'Apice, Mr; De Negris, F; DEL VECCHIO BLANCO, G; Monteleone, I; Biancone, L; Novelli, G; Pallone, E
A 14-Year Italian Experience in DM2 Genetic Testing: Frequency and Distribution of Normal and Premutated CNBP Alleles
2021-06-01 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
A common polymorphism in MIR155 gene promoter region is associated with a lower risk to develop type 2 diabetes
2019-01-01 Latini, A; Spallone, V; D'Amato, C; Novelli, G; Borgiani, P; Ciccacci, C
A distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13
1999-09-11 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
A Dynamic and Effective Peptide-Based Strategy for Promptly Addressing Emerging SARS-CoV-2 Variants of Concern
2024-07-04 Murdocca, M; Romeo, I; Citro, G; Latini, A; Centofanti, F; Bugatti, A; Caccuri, F; Caruso, A; Ortuso, F; Alcaro, S; Sangiuolo, F; Novelli, G
A European spectrum of pharmacogenomic biomarkers: Implications for clinical pharmacogenomics
2016-09-01 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
A fluorescence-based sequence-specific primer PCR for the screening of HLA-B(*)57:01
2010-10-01 Giardina, E; Stocchi, L; Foti Cuzzola, V; Zampatti, S; Gambardella, S; Patrizi, M; Bramanti, P; Pirazzoli, A; Novelli, G
A focus on the spread of the delta variant of SARS-CoV-2 in India
2021-05-01 Novelli, G; Colona, V; Pandolfi, P
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1
2010-11-01 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
A global effort to dissect the human genetic basis of resistance to SARS-CoV-2 infection
2022-01-01 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
A highly polymorphic CA/GT repeat (LIMK1GT) within the Williams syndrome critical region
1998-01-01 Mari, A; Amati, F; Conti, E; Bengala, M; Novelli, G; Dallapiccola, B
A likely pathogenic ACTG1 variant in a child showing partial phenotypic overlap with Baraitser-Winter syndrome
2023-06-01 Graziani, L; Cinnirella, G; Ferradini, V; Conte, C; Bascio, Fl; Bengala, M; Sangiuolo, F; Novelli, G
A long PCR-based molecular protocol for detecting normal and expanded ZNF9 alleles in myotonic dystrophy type 2
2004-01-01 Bonifazi, E; Vallo, L; Giardina, E; Botta, A; Novelli, G
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
2014-01-01 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
A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries, in mice
2006-01-01 Cipollone, D; Amati, F; Carsetti, R; Placidi, S; Biancolella, M; D'Amati, G; Novelli, G; Siracusa, G; Marino, B
A multiplex molecular assay for the detection of uniparental disomy for human chromosome 15
2008-12-01 Giardina, E; Peconi, C; Cascella, R; Sinibaldi, C; Nardone, A; Novelli, G
A multiplex molecular assay for the detection of uniparental disomy for human chromosome 7
2009-06-01 Giardina, E; Peconi, C; Cascella, R; Sinibaldi, C; Foti Cuzzola, V; Nardone, A; Bramanti, P; Novelli, G
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
2018-01-01 Ciccacci, C; Politi, C; Mancinelli, S; Ciccacci, F; Lucaroni, F; Novelli, G; Marazzi, Mc; Palombi, L; Borgiani, P
| 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 |