NOVELLETTO, ANDREA
NOVELLETTO, ANDREA
Dipartimento di Biologia
A comprehensive mitochondrial DNA mixed-stock analysis clarifies the composition of loggerhead turtle aggregates in the Adriatic Sea
2018-01-01 Tolve, L; Casale, P; Formia, A; Garofalo, L; Lazar, B; Natali, C; Novelletto, A; Vallini, C; Buzan, E; Chelazzi, G; Gaspari, S; Fortuna, C; Kocijan, I; Marchiori, E; Novarini, N; Poppi, L; Salvemini, P; Ciofi, C
A finely resolved phylogeny of y chromosome Hg J illuminates the processes of Phoenician and Greek colonizations in the Mediterranean
2018-01-01 Finocchio, A; Trombetta, B; Messina, F; D'Atanasio, E; Akar, N; Loutradis, A; Michalodimitrakis, Ei; Cruciani, F; Novelletto, A
A genetic portrait of the South-Eastern Carpathians based on autosomal short tandem repeats loci used in forensics
2018-08-12 Benvisto, A; Messina, F; Finocchio, A; Popa, L; Stefan, M; Stefanescu, G; Mironeanu, C; Novelletto, A; Rapone, C; Berti, A
A Genome Scan for Modifiers of Age at onset in Huntington's disease: The HD MAPS Study
2003-01-01 Li, Jl; Hayden, M; Almqvist, E; Brinkman, R; Durr, A; Dodé, C; Morrison, P; Suchowersky, O; Ross, C; Margolis, R; Rosenblatt, A; Gómez, T; E, M; Cabrero, D; Novelletto, A; Frontali, M; Nance, M; Trent, R; Mccusker, E; Jones, R; Paulsen, J; Harrison, M; Zanko, A; Abramson, R; Russ, A; Knowlton, B; Djoussé, L; Mysore, J; Tariot, S; Gusella, M; Wheeler, V; Atwood, L; Cupples, L; Saint Hilaire, M; Cha, Jh; Hersch, S; Koroshetz, W; Gusella, J; Macdonald, M; Myers, R
A human derived SSADH coding variant is replacing the ancestral allele shared with primates.
2006-01-01 Leone, O; Blasi, P; Palmerio, F; Kozlov, A; Malaspina, P; Novelletto, A
A multistep process for the dispersal of a Y chromosomal lineage in the Mediterranean area
2001-01-01 Malaspina, P; Tsopanomichalou, M; Duman, T; Stefan, M; Silvestri, A; Rinaldi, B; Garcia, O; Giparaki, M; Plata, E; Kozlov, A; Barbujani, G; Vernesi, C; Papola, F; Ciavarella, G; Kovatchev, D; Kerimova, M; Anagnou, N; Gavrila, L; Veneziano, L; Akar, N; Loutradis, A; Michalodimitrakis, E; Terrenato, L; Novelletto, A
A multivariate statistical approach for the estimation of the ethnic origin of unknown genetic profiles in forensic genetics
2020-01-01 Alladio, E; Della Rocca, C; Barni, F; Dugoujon, J-; Garofano, P; Semino, O; Berti, A; Novelletto, A; Vincenti, M; Cruciani, F
A new model for prediction of the age of onset and penetrance for Huntington’s disease based on CAG length.
2004-01-01 Langbehn, D; Brinkman, R; Falush, D; Paulsen, J; Hayden, M; Huntington’s Disease Collaborative, G; Novelletto, A
A novel sampling design to explore gene-longevity associations: the ECHA study.
2008-01-01 De Rango, F; Dato, S; Bellizzi, D; Rose, G; Marzi, E; Cavallone, L; Franceschi, C; Skytthe, A; Jeune, B; Cournil, A; Robine, J; Gampe, J; Vaupel, J; Mari, V; Feraco, E; Passarino, G; Novelletto, A; De Benedictis, G
A predominantly Neolithic origin for Y-chromosomal DNA variation in North Africa
2004-01-01 Arredi, B; Poloni, E; Paracchini, S; Zerjal, T; Fathallah, D; Makrelouf, M; Pascali, V; Novelletto, A; Tyler Smith, C
A shared haplotype for dentatorubropallidoluysian atrophy (DRPLA) in Italian families testifies of the recent introduction of the mutation
2014-01-09 Veneziano, L; Mantuano, E; Catalli, C; Gellera, C; Durr, A; Romano, S; Spadaro, M; Frontali, M; Novelletto, A
A signal, from human mtDNA, of postglacial recolonization in Europe
2001-01-01 Torroni, A; Bandelt, H; Macaulay, V; Richards, M; Cruciani, F; Rengo, C; Martinez Cabrera, V; Villems, R; Kivisild, T; Metspalu, E; Parik, J; Tolk, H; Tambets, K; Forster, P; Karger, B; Francalacci, P; Rudan, P; Janicijevic, B; Rickards, O; Savontaus, M; Huoponen, K; Laitinen, V; Koivumaki, S; Sykes, B; Hickey, E; Novelletto, A; Moral, P; Sellitto, D; Coppa, A; Al Zaheri, N; Santachiara Benerecetti, A; Semino, O; Scozzari, R
An additional HindIII polymorphism at the coagulation factor XIIIA locus
1990-01-01 Iodice, C; Novelletto, A; Malaspina, P; Persichetti, F
An unbiased resource of novel SNP markers provides a new chronology for the human y chromosome and reveals a deep phylogenetic structure in Africa
2014-01-01 Scozzari, R; Massaia, A; Trombetta, B; Bellusci, G; Myres, N; Novelletto, A; Cruciani, F
Analysis of three RFLPs of the COL1A2 (Type I Collagen) in the Amhara and the Oromo of Ethiopia
2002-01-01 De Stefano, G; MARTINEZ-LABARGA, Mc; Casalotti, R; Tartaglia, M; Novelletto, A; Pepe, G; Rickards, O
CAG repeat expansion in Huntington’s disease determines age at onset in a fully dominant fashion
2012-01-01 Lee, J; Ramos, E; Lee, J; Gillis, T; Mysore, J; Hayden, M; Warby, S; Morrison, P; Nance, M; Ross, C; Margolis, R; Squitieri, F; Orobello, S; Di Donato, S; Gomez Tortosa, E; Ayuso, C; Suchowersky, O; Trent, R; Mccusker, E; Novelletto, A; Frontali, M; Jones, R; Ashizawa, T; Frank, S; Saint Hilaire, M; Hersch, S; Rosas, H; Lucente, D; Harrison, M; Zanko, A; Abramson, R; Marder, K; Sequeiros, J; Paulsen, J; PREDICT HD study of the Huntington Study, G; Landwehrmeyer, G; REGISTRY study of the European Huntington's Disease, N; Myers, R; HD MAPS Study, G; Macdonald, M; Gusella, J; COHORT study of the, H
CAG repeat instability, cryptic sequence variation and pathogeneticity: evidence from different loci
1999-01-01 Frontali, M; Novelletto, A; Annesi, G; Iodice, C
CAGn repeat instability, cryptic sequence variation and pathogenicity: evidence from different loci
2001-01-01 Frontali, M; Novelletto, A; Annesi, G; Iodice, C
Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset
2013-01-01 Ramos, Em; Latourelle, Jc; Gillis, T; Mysore, Js; Squitieri, F; Di Pardo, A; Di Donato, S; Gellera, C; Hayden, Mr; Morrison, Pj; Nance, M; Ross, Ca; Margolis, Rl; Gomez-Tortosa, E; Ayuso, C; Suchowersky, O; Trent, Rj; Mccusker, E; Novelletto, A; Frontali, M; Jones, R; Ashizawa, T; Frank, S; Saint-Hilaire, M-; Hersch, Sm; Rosas, Hd; Lucente, D; Harrison, Mb; Zanko, A; Abramson, Rk; Marder, K; Gusella, Jf; Lee, J-; Alonso, I; Sequeiros, J; Myers, Rh; Macdonald, Me
Characterization of a small family (CAIII) of microsatellite-containing sequences with X-Y homology
1997-01-01 Malaspina, P; Ciminelli, Bm; Viggiano, L; Iodice, C; Cruciani, F; Santolamazza, P; Sellitto, D; Scozzari, R; Terrenato, L; Rocchi, M; Novelletto, A
| Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
|---|---|---|---|---|
| 1-gen-2018 | A comprehensive mitochondrial DNA mixed-stock analysis clarifies the composition of loggerhead turtle aggregates in the Adriatic Sea | Tolve, L; Casale, P; Formia, A; Garofalo, L; Lazar, B; Natali, C; Novelletto, A; Vallini, C; Buzan, E; Chelazzi, G; Gaspari, S; Fortuna, C; Kocijan, I; Marchiori, E; Novarini, N; Poppi, L; Salvemini, P; Ciofi, C | Articolo su rivista | |
| 1-gen-2018 | A finely resolved phylogeny of y chromosome Hg J illuminates the processes of Phoenician and Greek colonizations in the Mediterranean | Finocchio, A; Trombetta, B; Messina, F; D'Atanasio, E; Akar, N; Loutradis, A; Michalodimitrakis, Ei; Cruciani, F; Novelletto, A | Articolo su rivista | |
| 12-ago-2018 | A genetic portrait of the South-Eastern Carpathians based on autosomal short tandem repeats loci used in forensics | Benvisto, A; Messina, F; Finocchio, A; Popa, L; Stefan, M; Stefanescu, G; Mironeanu, C; Novelletto, A; Rapone, C; Berti, A | Articolo su rivista | |
| 1-gen-2003 | A Genome Scan for Modifiers of Age at onset in Huntington's disease: The HD MAPS Study | Li, Jl; Hayden, M; Almqvist, E; Brinkman, R; Durr, A; Dodé, C; Morrison, P; Suchowersky, O; Ross, C; Margolis, R; Rosenblatt, A; Gómez, T; E, M; Cabrero, D; Novelletto, A; Frontali, M; Nance, M; Trent, R; Mccusker, E; Jones, R; Paulsen, J; Harrison, M; Zanko, A; Abramson, R; Russ, A; Knowlton, B; Djoussé, L; Mysore, J; Tariot, S; Gusella, M; Wheeler, V; Atwood, L; Cupples, L; Saint Hilaire, M; Cha, Jh; Hersch, S; Koroshetz, W; Gusella, J; Macdonald, M; Myers, R | Articolo su rivista | |
| 1-gen-2006 | A human derived SSADH coding variant is replacing the ancestral allele shared with primates. | Leone, O; Blasi, P; Palmerio, F; Kozlov, A; Malaspina, P; Novelletto, A | Articolo su rivista | |
| 1-gen-2001 | A multistep process for the dispersal of a Y chromosomal lineage in the Mediterranean area | Malaspina, P; Tsopanomichalou, M; Duman, T; Stefan, M; Silvestri, A; Rinaldi, B; Garcia, O; Giparaki, M; Plata, E; Kozlov, A; Barbujani, G; Vernesi, C; Papola, F; Ciavarella, G; Kovatchev, D; Kerimova, M; Anagnou, N; Gavrila, L; Veneziano, L; Akar, N; Loutradis, A; Michalodimitrakis, E; Terrenato, L; Novelletto, A | Articolo su rivista | |
| 1-gen-2020 | A multivariate statistical approach for the estimation of the ethnic origin of unknown genetic profiles in forensic genetics | Alladio, E; Della Rocca, C; Barni, F; Dugoujon, J-; Garofano, P; Semino, O; Berti, A; Novelletto, A; Vincenti, M; Cruciani, F | Articolo su rivista | |
| 1-gen-2004 | A new model for prediction of the age of onset and penetrance for Huntington’s disease based on CAG length. | Langbehn, D; Brinkman, R; Falush, D; Paulsen, J; Hayden, M; Huntington’s Disease Collaborative, G; Novelletto, A | Articolo su rivista | |
| 1-gen-2008 | A novel sampling design to explore gene-longevity associations: the ECHA study. | De Rango, F; Dato, S; Bellizzi, D; Rose, G; Marzi, E; Cavallone, L; Franceschi, C; Skytthe, A; Jeune, B; Cournil, A; Robine, J; Gampe, J; Vaupel, J; Mari, V; Feraco, E; Passarino, G; Novelletto, A; De Benedictis, G | Articolo su rivista | |
| 1-gen-2004 | A predominantly Neolithic origin for Y-chromosomal DNA variation in North Africa | Arredi, B; Poloni, E; Paracchini, S; Zerjal, T; Fathallah, D; Makrelouf, M; Pascali, V; Novelletto, A; Tyler Smith, C | Articolo su rivista | |
| 9-gen-2014 | A shared haplotype for dentatorubropallidoluysian atrophy (DRPLA) in Italian families testifies of the recent introduction of the mutation | Veneziano, L; Mantuano, E; Catalli, C; Gellera, C; Durr, A; Romano, S; Spadaro, M; Frontali, M; Novelletto, A | Articolo su rivista | |
| 1-gen-2001 | A signal, from human mtDNA, of postglacial recolonization in Europe | Torroni, A; Bandelt, H; Macaulay, V; Richards, M; Cruciani, F; Rengo, C; Martinez Cabrera, V; Villems, R; Kivisild, T; Metspalu, E; Parik, J; Tolk, H; Tambets, K; Forster, P; Karger, B; Francalacci, P; Rudan, P; Janicijevic, B; Rickards, O; Savontaus, M; Huoponen, K; Laitinen, V; Koivumaki, S; Sykes, B; Hickey, E; Novelletto, A; Moral, P; Sellitto, D; Coppa, A; Al Zaheri, N; Santachiara Benerecetti, A; Semino, O; Scozzari, R | Articolo su rivista | |
| 1-gen-1990 | An additional HindIII polymorphism at the coagulation factor XIIIA locus | Iodice, C; Novelletto, A; Malaspina, P; Persichetti, F | Articolo su rivista | |
| 1-gen-2014 | An unbiased resource of novel SNP markers provides a new chronology for the human y chromosome and reveals a deep phylogenetic structure in Africa | Scozzari, R; Massaia, A; Trombetta, B; Bellusci, G; Myres, N; Novelletto, A; Cruciani, F | Articolo su rivista | |
| 1-gen-2002 | Analysis of three RFLPs of the COL1A2 (Type I Collagen) in the Amhara and the Oromo of Ethiopia | De Stefano, G; MARTINEZ-LABARGA, Mc; Casalotti, R; Tartaglia, M; Novelletto, A; Pepe, G; Rickards, O | Articolo su rivista | |
| 1-gen-2012 | CAG repeat expansion in Huntington’s disease determines age at onset in a fully dominant fashion | Lee, J; Ramos, E; Lee, J; Gillis, T; Mysore, J; Hayden, M; Warby, S; Morrison, P; Nance, M; Ross, C; Margolis, R; Squitieri, F; Orobello, S; Di Donato, S; Gomez Tortosa, E; Ayuso, C; Suchowersky, O; Trent, R; Mccusker, E; Novelletto, A; Frontali, M; Jones, R; Ashizawa, T; Frank, S; Saint Hilaire, M; Hersch, S; Rosas, H; Lucente, D; Harrison, M; Zanko, A; Abramson, R; Marder, K; Sequeiros, J; Paulsen, J; PREDICT HD study of the Huntington Study, G; Landwehrmeyer, G; REGISTRY study of the European Huntington's Disease, N; Myers, R; HD MAPS Study, G; Macdonald, M; Gusella, J; COHORT study of the, H | Articolo su rivista | |
| 1-gen-1999 | CAG repeat instability, cryptic sequence variation and pathogeneticity: evidence from different loci | Frontali, M; Novelletto, A; Annesi, G; Iodice, C | Articolo su rivista | |
| 1-gen-2001 | CAGn repeat instability, cryptic sequence variation and pathogenicity: evidence from different loci | Frontali, M; Novelletto, A; Annesi, G; Iodice, C | Contributo in libro | |
| 1-gen-2013 | Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset | Ramos, Em; Latourelle, Jc; Gillis, T; Mysore, Js; Squitieri, F; Di Pardo, A; Di Donato, S; Gellera, C; Hayden, Mr; Morrison, Pj; Nance, M; Ross, Ca; Margolis, Rl; Gomez-Tortosa, E; Ayuso, C; Suchowersky, O; Trent, Rj; Mccusker, E; Novelletto, A; Frontali, M; Jones, R; Ashizawa, T; Frank, S; Saint-Hilaire, M-; Hersch, Sm; Rosas, Hd; Lucente, D; Harrison, Mb; Zanko, A; Abramson, Rk; Marder, K; Gusella, Jf; Lee, J-; Alonso, I; Sequeiros, J; Myers, Rh; Macdonald, Me | Articolo su rivista | |
| 1-gen-1997 | Characterization of a small family (CAIII) of microsatellite-containing sequences with X-Y homology | Malaspina, P; Ciminelli, Bm; Viggiano, L; Iodice, C; Cruciani, F; Santolamazza, P; Sellitto, D; Scozzari, R; Terrenato, L; Rocchi, M; Novelletto, A | Articolo su rivista |