The Role of Recent Admixture in Forming the Contemporary West Eurasian Genomic Landscape
2015-01-01 Georgebj, Busby; Garrett, Hellenthal; Francesco, Montinaro; Sergio, Tofanelli; Kazima, Bulayeva; Igor, Rudan; Tatijana, Zemunik; Caroline, Hayward; Draga, Toncheva; Sena, Karachanak-Yankova; Desislava, Nesheva; Paolo, Anagnostou; Cali', Francesco; Francesca, Brisighelli; Valentino, Romano; Gerard, Lefranc; Catherine, Buresi; Ben , ; Jemni, Chibani; Amel, Haj-Khelil; Sabri, Denden; Rafal, Ploski; Pawel, Krajewski; Tor, Hervig; Torolf, Moen; Rene , Herrera; James , Wilson; Simon, Myers; Cristian, Capelli
Novel compound heterozygous mutation in NPC1 gene cause Niemann–Pick disease type C with juvenile onset
2020-01-01 Costanzo, Maria Cristina; Nicotera, Antonio Gennaro; Vinci, Mirella; Vitello, Aurelio; Fiumara, Agata; Cali, Francesco; Musumeci, Sebastiano Antonino
Novel c.C2254T (p.Q752*) mutation in ZFYVE26 (SPG15) gene in a patient with hereditary spastic paraparesis
2018-01-01 Vinci, Mirella; Fichera, Marco; Musumeci, Sebastiano Antonino; Cali, Francesco; Vitello, Girolamo Aurelio
Genetic diversity within the R408W phenylketonuria mutation lineages in Europe
2003-01-01 Tighe, Orna; Dunican, Donncha; O'Neill, Charles; Bertorelle, Giorgio; Beattie, Diane; Graham, Colin; Zschocke, Johannes; Cali, Francesco; Romano, Valentino; Hrabincova, Eva; Kozak, Libor; Nechyporenko, Marina; Livshits, Ludmilla; Guldberg, Per; Jurkowska, Monika; Zekanowski, Cezary; Perez, Belen; Desviat, Lourdes Ruiz; Ugarte, Magdalena; Ku?inskas, Vaidutis; Knappskog, Per; Treacy, Eileen; Naughten, Eileen; Tyfield, Linda; Byck, Susan; Scriver, Charles R.; Mayne, Philip D.; Croke, David T.
A methodological strategy for PAH genotyping in populations with a marked molecular heterogeneity of hyperphenylalaninemia
2001-01-01 Romano, V.; Lio, D.; Cali', Francesco; Scola, L.; Leggio, L.; D»anna, C.; De Leo, G.; Salerno, A.
PAH Gene Mutations in the Sicilian Population: Association with Minihaplotypes and Expression Analysis
2001-01-01 Mirisola, Mario G.; Cali, Francesco; Gloria, Angelo; Schinocca, Pietro; D'Amato, Monica; Cassara, Georgia; Leo, Giacomo De; Palillo, Letizia; Meli, Concetta; Romano, Valentino
PAH deficiency in Italy: correlation of genotype with phenotype in the Sicilian population
1996-01-01 Romano, V.; Guldberg, P.; Güttler, F.; Meli, C.; Mollica, F.; Pavone, L.; Giovannini, M.; Riva, E.; Biasucci, G.; Luotti, D.; Palillo, L.; Cali, F.; Ceratto, N.; Anello, G.; Bosco, P.
MtDNA control region and RFLP data for Sicily and France
2001-01-01 Cali, Francesco; Le Roux, M. G.; D'Anna, R.; Flugy, A.; De Leo, G.; Chiavetta, V.; Ayala, G. F.; Romano, V.
Continental and subcontinental distributions of mtDNA control region types
2002-01-01 Forster, Peter; Cali, Francesco; Röhl, Arne; Metspalu, Ene; D'Anna, Rosalba; Mirisola, Mario; De Leo, Giacomo; Flugy, Anna; Salerno, Alfredo; Ayala, Giovanni; Kouvatsi, Anastasia; Villems, Richard; Romano, Valentino
DXYS156: a multi-purpose short tandem repeat locus for determination of sex, paternal and maternal geographic origins and DNA fingerprinting
2002-01-01 Cali, Francesco; Forster, P.; Kersting, Christian; Mirisola, Mario G.; D'Anna, Rosalba; De Leo, Giacomo; Romano, Valentino
Maternal phenylketonuria in two Sicilian families identified by maternal blood phenylalanine level screening and identification of a new phenylalanine hydroxylase gene mutation (P407L)
1999-01-01 Corsello, G.; Bosco, P.; Cali, Francesco; Greco, Donatella; Cammarata, M.; Ciaccio, M.; Piccione, M.; Romano, V.
Preliminary studies on the molecular basis of hyperphenylalaninemia in Egypt
1996-01-01 Hashem, Nemat; Bosco, Paolo; Chiavetta, Valeria; Cali, Francesco; Ceratto, Nadia; Romano, V.
Two novel PAH gene mutations detected in Italian phenylketonuric patients
1997-01-01 Argiolas, Alessandra; Bosco, Paolo; Cali', Francesco; Ceratto, Nadia; Anello, Guido; Riva, Enrica; Biasucci, Giacomo; Carducci, Carla; Romano, V.
New Insights Into TRMT10A Syndrome: Case Report and Literature Review
2025-01-01 Ceraolo, Graziana; Spoto, Giulia; Butera, Ambra; Spanò, Maria; Vinci, Mirella; Vitello, Girolamo Aurelio; Musumeci, Antonino; Cali, Francesco; Nicotera, Antonio Gennaro; Di Rosa, Gabriella
The STR252 - IVS10nt546 - VNTR7 phenylalanine hydroxylase minihaplotype in five Mediterranean samples
1997-01-01 Calì, Francesco; Dianzani, Irma; Desviat, Lourdes R.; Perez, Belen; Ugarte, Magdalena; Ozguc, Meral; Seyrantepe, Volkan; Shiloh, Yossi; Giannattasio, Sergio; Carducci, Carla; Bosco, Paolo; Leo, Giacomo De; Piazza, Alberto; Romano, V.
GRIN2A: involvement in movement disorders and intellectual disability without seizures
2019-01-01 Nicotera, Antonio Gennaro; Cali', Francesco; Vinci, Mirella; Musumeci, Sebastiano Antonino
Autosomal recessive spino-cerebellar ataxia type 10 (SCAR10): clinical presentation associated with c.289delA ANO10 gene variant
2024-01-01 Norata, Davide; Alonge, Paolo; Grillo, Lucia; Calì, Francesco; Sturnio, Maurizio; Lupica, Antonino; Costa, Vanessa; Brighina, Filippo; Di Stefano, Vincenzo
Autologous platelet gel as adjunctive therapy for severe corneal ulcers: a pilot study
2025-01-01 Harouch, Merieme; Jihad, Safaa; Allou, Younes; D'Oria, Francesco; Ferrise, Marco; Borroni Marco Zagari, Davide; Mazzotta, Cosimo
Medullary thyroid cancer in MEN2 pediatric/adolescent carriers of RET mutation: genotype/phenotype correlation and outcome in a retrospective series of 23 patients
2024-01-01 Di Benedetto, G; Barca, I; De Gregorio, L; Scollo, C; Giani', Fiorenza; Martorana, F; Russo, M; Frasca, F; Pellegriti, G; Sapuppo, G
PARP-1 as a novel target in endocrine-resistant breast cancer
2025-01-01 Zicarelli, A.; Talia, M.; Laine, M.; Lappano, R.; Maggiolini, M.; Greene, G. L.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| The Role of Recent Admixture in Forming the Contemporary West Eurasian Genomic Landscape | 1-gen-2015 | Georgebj, Busby; Garrett, Hellenthal; Francesco, Montinaro; Sergio, Tofanelli; Kazima, Bulayeva; Igor, Rudan; Tatijana, Zemunik; Caroline, Hayward; Draga, Toncheva; Sena, Karachanak-Yankova; Desislava, Nesheva; Paolo, Anagnostou; Cali', Francesco; Francesca, Brisighelli; Valentino, Romano; Gerard, Lefranc; Catherine, Buresi; Ben , ; Jemni, Chibani; Amel, Haj-Khelil; Sabri, Denden; Rafal, Ploski; Pawel, Krajewski; Tor, Hervig; Torolf, Moen; Rene , Herrera; James , Wilson; Simon, Myers; Cristian, Capelli | |
| Novel compound heterozygous mutation in NPC1 gene cause Niemann–Pick disease type C with juvenile onset | 1-gen-2020 | Costanzo, Maria Cristina; Nicotera, Antonio Gennaro; Vinci, Mirella; Vitello, Aurelio; Fiumara, Agata; Cali, Francesco; Musumeci, Sebastiano Antonino | |
| Novel c.C2254T (p.Q752*) mutation in ZFYVE26 (SPG15) gene in a patient with hereditary spastic paraparesis | 1-gen-2018 | Vinci, Mirella; Fichera, Marco; Musumeci, Sebastiano Antonino; Cali, Francesco; Vitello, Girolamo Aurelio | |
| Genetic diversity within the R408W phenylketonuria mutation lineages in Europe | 1-gen-2003 | Tighe, Orna; Dunican, Donncha; O'Neill, Charles; Bertorelle, Giorgio; Beattie, Diane; Graham, Colin; Zschocke, Johannes; Cali, Francesco; Romano, Valentino; Hrabincova, Eva; Kozak, Libor; Nechyporenko, Marina; Livshits, Ludmilla; Guldberg, Per; Jurkowska, Monika; Zekanowski, Cezary; Perez, Belen; Desviat, Lourdes Ruiz; Ugarte, Magdalena; Ku?inskas, Vaidutis; Knappskog, Per; Treacy, Eileen; Naughten, Eileen; Tyfield, Linda; Byck, Susan; Scriver, Charles R.; Mayne, Philip D.; Croke, David T. | |
| A methodological strategy for PAH genotyping in populations with a marked molecular heterogeneity of hyperphenylalaninemia | 1-gen-2001 | Romano, V.; Lio, D.; Cali', Francesco; Scola, L.; Leggio, L.; D»anna, C.; De Leo, G.; Salerno, A. | |
| PAH Gene Mutations in the Sicilian Population: Association with Minihaplotypes and Expression Analysis | 1-gen-2001 | Mirisola, Mario G.; Cali, Francesco; Gloria, Angelo; Schinocca, Pietro; D'Amato, Monica; Cassara, Georgia; Leo, Giacomo De; Palillo, Letizia; Meli, Concetta; Romano, Valentino | |
| PAH deficiency in Italy: correlation of genotype with phenotype in the Sicilian population | 1-gen-1996 | Romano, V.; Guldberg, P.; Güttler, F.; Meli, C.; Mollica, F.; Pavone, L.; Giovannini, M.; Riva, E.; Biasucci, G.; Luotti, D.; Palillo, L.; Cali, F.; Ceratto, N.; Anello, G.; Bosco, P. | |
| MtDNA control region and RFLP data for Sicily and France | 1-gen-2001 | Cali, Francesco; Le Roux, M. G.; D'Anna, R.; Flugy, A.; De Leo, G.; Chiavetta, V.; Ayala, G. F.; Romano, V. | |
| Continental and subcontinental distributions of mtDNA control region types | 1-gen-2002 | Forster, Peter; Cali, Francesco; Röhl, Arne; Metspalu, Ene; D'Anna, Rosalba; Mirisola, Mario; De Leo, Giacomo; Flugy, Anna; Salerno, Alfredo; Ayala, Giovanni; Kouvatsi, Anastasia; Villems, Richard; Romano, Valentino | |
| DXYS156: a multi-purpose short tandem repeat locus for determination of sex, paternal and maternal geographic origins and DNA fingerprinting | 1-gen-2002 | Cali, Francesco; Forster, P.; Kersting, Christian; Mirisola, Mario G.; D'Anna, Rosalba; De Leo, Giacomo; Romano, Valentino | |
| Maternal phenylketonuria in two Sicilian families identified by maternal blood phenylalanine level screening and identification of a new phenylalanine hydroxylase gene mutation (P407L) | 1-gen-1999 | Corsello, G.; Bosco, P.; Cali, Francesco; Greco, Donatella; Cammarata, M.; Ciaccio, M.; Piccione, M.; Romano, V. | |
| Preliminary studies on the molecular basis of hyperphenylalaninemia in Egypt | 1-gen-1996 | Hashem, Nemat; Bosco, Paolo; Chiavetta, Valeria; Cali, Francesco; Ceratto, Nadia; Romano, V. | |
| Two novel PAH gene mutations detected in Italian phenylketonuric patients | 1-gen-1997 | Argiolas, Alessandra; Bosco, Paolo; Cali', Francesco; Ceratto, Nadia; Anello, Guido; Riva, Enrica; Biasucci, Giacomo; Carducci, Carla; Romano, V. | |
| New Insights Into TRMT10A Syndrome: Case Report and Literature Review | 1-gen-2025 | Ceraolo, Graziana; Spoto, Giulia; Butera, Ambra; Spanò, Maria; Vinci, Mirella; Vitello, Girolamo Aurelio; Musumeci, Antonino; Cali, Francesco; Nicotera, Antonio Gennaro; Di Rosa, Gabriella | |
| The STR252 - IVS10nt546 - VNTR7 phenylalanine hydroxylase minihaplotype in five Mediterranean samples | 1-gen-1997 | Calì, Francesco; Dianzani, Irma; Desviat, Lourdes R.; Perez, Belen; Ugarte, Magdalena; Ozguc, Meral; Seyrantepe, Volkan; Shiloh, Yossi; Giannattasio, Sergio; Carducci, Carla; Bosco, Paolo; Leo, Giacomo De; Piazza, Alberto; Romano, V. | |
| GRIN2A: involvement in movement disorders and intellectual disability without seizures | 1-gen-2019 | Nicotera, Antonio Gennaro; Cali', Francesco; Vinci, Mirella; Musumeci, Sebastiano Antonino | |
| Autosomal recessive spino-cerebellar ataxia type 10 (SCAR10): clinical presentation associated with c.289delA ANO10 gene variant | 1-gen-2024 | Norata, Davide; Alonge, Paolo; Grillo, Lucia; Calì, Francesco; Sturnio, Maurizio; Lupica, Antonino; Costa, Vanessa; Brighina, Filippo; Di Stefano, Vincenzo | |
| Autologous platelet gel as adjunctive therapy for severe corneal ulcers: a pilot study | 1-gen-2025 | Harouch, Merieme; Jihad, Safaa; Allou, Younes; D'Oria, Francesco; Ferrise, Marco; Borroni Marco Zagari, Davide; Mazzotta, Cosimo | |
| Medullary thyroid cancer in MEN2 pediatric/adolescent carriers of RET mutation: genotype/phenotype correlation and outcome in a retrospective series of 23 patients | 1-gen-2024 | Di Benedetto, G; Barca, I; De Gregorio, L; Scollo, C; Giani', Fiorenza; Martorana, F; Russo, M; Frasca, F; Pellegriti, G; Sapuppo, G | |
| PARP-1 as a novel target in endocrine-resistant breast cancer | 1-gen-2025 | Zicarelli, A.; Talia, M.; Laine, M.; Lappano, R.; Maggiolini, M.; Greene, G. L. |
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