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"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 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
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 | |
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 |
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Opzioni
Scopri
Tipologia
- Pubblicazioni 521
- Pubblicazioni::01 - Articolo su r... 521
Data di pubblicazione
- 2020 - 2024 113
- 2010 - 2019 199
- 2000 - 2009 139
- 1990 - 1999 57
- 1983 - 1989 13
Editore
- Elsevier Science Limited 14
- Nature Publishing Group 13
- Wiley-Blackwell 11
- MDPI 10
- Elsevier 9
- BioMed Central 8
- Public Library of Science 7
- WILEY 7
- BMC 6
- Future Medicine Ltd 5
Rivista
- HUMAN GENOMICS 14
- PLOS ONE 12
- GENES 11
- PHARMACOGENOMICS 10
- HUMAN GENETICS 9
- JOURNAL OF INVESTIGATIVE DERMATOLOGY 8
- CLINICAL GENETICS 7
- BMC MEDICAL GENETICS 6
- CELL DEATH & DISEASE 6
- EUROPEAN JOURNAL OF HUMAN GENETICS 6
Serie
- MOLECULAR MEDICINE 1
Settore disciplinare
- Settore MED/03 447
- Settore MED/26 15
- Settore MED/09 12
- Settore BIO/11 11
- Settore MED/03 - GENETICA MEDICA 10
- Settore MED/11 10
- Settore MED/13 8
- Settore MED/04 6
- Settore MED/08 6
- Settore MED/49 6
Keyword
- Humans 168
- Male 68
- Female 66
- Polymorphism 48
- Adult 40
- DNA 39
- Italy 37
- Mutation 37
- Animals 32
- Genetic Predisposition to Disease 30
Lingua
- eng 511
- ita 11
Accesso al fulltext
- no fulltext 371
- restricted 81
- open 69
Settori ISICRUI
- Biologia Molecolare e Genetica 263
- 06 - Scienze mediche 172
- Ricerca Medica, Generale 36
- 05 - Scienze biologiche 15
- Medicina Generale e Interna 13
- Neurologia 11
- Biologia Molecolare e Genetica ::... 10
- Ricerca Cardiovascolare ed Ematol... 9
- Endocrinologia, Metabolismo e Nut... 8
- Ricerca/Medicina di Laboratorio e... 6
Appartenenza
- Dipartimento di Biologia 95
- Dipartimento di Biomedicina e Pre... 398
- Dipartimento di Biomedicina e pre... 123
- Dipartimento di Economia e Finanza 5
- Dipartimento di Giurisprudenza 1
- Dipartimento di Ingegneria dell'I... 1
- Dipartimento di Ingegneria Elettr... 7
- Dipartimento di Medicina dei sistemi 128
- Dipartimento di Medicina Sperimen... 61
- Dipartimento di Medicina sperimen... 1