BLASI, FRANCESCA
BLASI, FRANCESCA
DIP. DI BIOLOGIA EVOLUZIONISTICA SPERIMENTALE
BLASI F.
Circadian rhythm of COPD symptoms in clinically based phenotypes. Results from the STORICO Italian observational study
2019 Scichilone N.; Antonelli Incalzi R.; Blasi F.; Schino P.; Cuttitta G.; Zullo A.; Ori A.; Canonica G.; Schino P.; Titta X.; Foschino M.P.; Prediletto R.; Tranfa C.M.E.; Zappa M.C.; Patriciello P.; Labate L.; Mariotta S.; Nava S.; Vatrella A.; Mastroberardino M.; Sarzani R.; Iuliano A.; Maggi L.; Zedda A.; Pesci A.; Sera G.; Nicolini A.; Salvatore Walter D.D.; Forte S.; Mario D.D.; Rivolta F.; Ferliga M.; Raco A.F.; Luigi D.R.; Cabibbo G.; Maselli R.; Gulotta C.; Nardini S.; Guffanti E.E.; Castellani W.; Triolo L.; Passalacqua G.; Beghe B.; Salvatore L.C.; Faccini E.; Atzeni E.; Tazza R.; Giamesio P.
Individualizing duration of antibiotic therapy in community-acquired pneumonia
2017 Aliberti S.; Ramirez J.; Giuliani F.; Wiemken T.; Sotgiu G.; Tedeschi S.; Carugati M.; Valenti V.; Marchioni M.; Camera M.; Piro R.; Del Forno M.; Milani G.; Faverio P.; Richeldi L.; Deotto M.; Villani M.; Voza A.; Tobaldini E.; Bernardi M.; Bellone A.; Bassetti M.; Blasi F.
How to choose the duration of antibiotic therapy in patients with pneumonia
2015 Aliberti S.; Giuliani F.; Ramirez J.; Blasi F.; Giulia B.; Paola F.; Manuela C.; Giulia S.; Riccardo F.; Sara T.; Giuseppe M.; Massimiliano V.; Manuela D.F.; Roberto P.; Martina D.; Lisa P.; Antonio V.
Analysis of X chromosome inactivation in autism spectrum disorders.
2008 Gong X; Bacchelli E; Blasi F; Toma C; Betancur C; Chaste P; Delorme R; Durand CM; Fauchereau F; Botros HG; Leboyer M; Mouren-Simeoni MC; Nygren G; Anckarsäter H; Rastam M; Gillberg IC; Gillberg C; Moreno-De-Luca D; Carone S; Nummela I; Rossi M; Battaglia A; International Molecular Genetic Study of Autism Consortium (IMGSAC); Jarvela I; Maestrini E; Bourgeron T.
Is ASMT a susceptibility gene for autism spectrum disorders? A replication study in European populations.
2007 Toma C; Rossi M; Sousa I; Blasi F; Bacchelli E; Alen R; Vanhala R; Monaco AP; Järvelä I; Maestrini E
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
2007 Autism Genome Project Consortium; Szatmari P; Paterson AD; Zwaigenbaum L; Roberts W; Brian J; Liu XQ; Vincent JB; Skaug JL; Thompson AP; Senman L; Feuk L; Qian C; Bryson SE; Jones MB; Marshall CR; Scherer SW; Vieland VJ; Bartlett C; Mangin LV; Goedken R; Segre A; Pericak-Vance MA; Cuccaro ML; Gilbert JR; Wright HH; Abramson RK; Betancur C; Bourgeron T; Gillberg C; Leboyer M; Buxbaum JD; Davis KL; Hollander E; Silverman JM; Hallmayer J; Lotspeich L; Sutcliffe JS; Haines JL; Folstein SE; Piven J; Wassink TH; Sheffield V; Geschwind DH; Bucan M; Brown WT; Cantor RM; Constantino JN; Gilliam TC; Herbert M; Lajonchere C; Ledbetter DH; Lese-Martin C; Miller J; Nelson S; Samango-Sprouse CA; Spence S; State M; Tanzi RE; Coon H; Dawson G; Devlin B; Estes A; Flodman P; Klei L; McMahon WM; Minshew N; Munson J; Korvatska E; Rodier PM; Schellenberg GD; Smith M; Spence MA; Stodgell C; Tepper PG; Wijsman EM; Yu CE; Roge B; Mantoulan C; Wittemeyer K; Poustka A; Felder B; Klauck SM; Schuster C; Poustka F; Bolte S; Feineis-Matthews S; Herbrecht E; Schmotzer G; Tsiantis J; Papanikolaou K; Maestrini E; Bacchelli E; Blasi F; Carone S; Toma C; Van Engeland H; de Jonge M; Kemner C; Koop F; Langemeijer M; Hijimans C; Staal WG; Baird G; Bolton PF; Rutter ML; Weisblatt E; Green J; Aldred C; Wilkinson JA; Pickles A; Le Couteur A; Berney T; McConachie H; Bailey AJ; Francis K; Honeyman G; Hutchinson A; Parr JR; Wallace S; Monaco AP; Barnby G; Kobayashi K; Lamb JA; Sousa I; Sykes N; Cook EH; Guter SJ; Leventhal BL; Salt J; Lord C; Corsello C; Hus V; Weeks DE; Volkmar F; Tauber M; Fombonne E; Shih A.
Absence of coding mutations in the X-linked genes Neuroligin 3 and Neuroligin 4 in individuals with autism from the IMGSAC collection
2006 Blasi F.; Bacchelli E.; Pesaresi G.; Carone S.; Bailey A.J.; Maestrini E.
SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample.
2006 Blasi F.; Bacchelli E.; Carone S.; Toma C.; Monaco AP.; Bailey AJ.; Maestrini E.
Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.
2005 Lamb J.A.; Barnby G.; Bonora E.; Sykes N.; Bacchelli E.; Blasi F.; Maestrini E.; Broxholme J.; Tzenova J.; Weeks D.; Bailey A.J.; Monaco A.P.; International Molecular Genetic Study of Autism Consortium (IMGSAC).
Mutation screening and association analysis of six candidate genes for autism on chromosome 7q.
2005 Bonora E.; Lamb J.A.; Barnby G.; Sykes N.; Moberly T.; Beyer K.S.; Klauck S.M.; Poustka F.; Bacchelli E.; Blasi F.; Maestrini E.; Battaglia A.; Haracopos D.; Pedersen L.; Isager T.; Eriksen G.; Viskum B.; Sorensen E.U.; Brondum-Nielsen K.; Cotterill R.; Engeland H.; Jonge M.; Kemner C.; Steggehuis K.; Scherpenisse M.; Rutter M.; Bolton P.F.; Parr J.R.; Poustka A.; Bailey A.J.; Monaco A.P.; International Molecular Genetic Study of Austism Consortium.
DNA variants in the human RAB3A gene are not associated with autism.
2004 D'Adamo P.; Bacchelli E.; Blasi F.; Lipp H.P.; Toniolo D.; Maestrini E.
Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene
2003 Bacchelli E.; Blasi F.; Biondolillo M.; Lamb J.A.; Bonora E.; Barnby G.; Parr J.; Beyer K.S.; Klauck S.M.; Poustka A.; Bailey A.J.; Monaco A.P.; Maestrini E.
Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region
2002 Bonora E.; Bacchelli E.; Levy E.R.; Blasi F.; Marlow A.; Monaco A.P.; Maestrini E.
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| Circadian rhythm of COPD symptoms in clinically based phenotypes. Results from the STORICO Italian observational study | Scichilone N.; Antonelli Incalzi R.; Blasi F.; Schino P.; Cuttitta G.; Zullo A.; Ori A.; Canonica... G.; Schino P.; Titta X.; Foschino M.P.; Prediletto R.; Tranfa C.M.E.; Zappa M.C.; Patriciello P.; Labate L.; Mariotta S.; Nava S.; Vatrella A.; Mastroberardino M.; Sarzani R.; Iuliano A.; Maggi L.; Zedda A.; Pesci A.; Sera G.; Nicolini A.; Salvatore Walter D.D.; Forte S.; Mario D.D.; Rivolta F.; Ferliga M.; Raco A.F.; Luigi D.R.; Cabibbo G.; Maselli R.; Gulotta C.; Nardini S.; Guffanti E.E.; Castellani W.; Triolo L.; Passalacqua G.; Beghe B.; Salvatore L.C.; Faccini E.; Atzeni E.; Tazza R.; Giamesio P. | 2019-01-01 | BMC PULMONARY MEDICINE | - | 1.01 Articolo in rivista | - |
| Individualizing duration of antibiotic therapy in community-acquired pneumonia | Aliberti S.; Ramirez J.; Giuliani F.; Wiemken T.; Sotgiu G.; Tedeschi S.; Carugati M.; Valenti V....; Marchioni M.; Camera M.; Piro R.; Del Forno M.; Milani G.; Faverio P.; Richeldi L.; Deotto M.; Villani M.; Voza A.; Tobaldini E.; Bernardi M.; Bellone A.; Bassetti M.; Blasi F. | 2017-01-01 | PULMONARY PHARMACOLOGY & THERAPEUTICS | - | 1.01 Articolo in rivista | - |
| How to choose the duration of antibiotic therapy in patients with pneumonia | Aliberti S.; Giuliani F.; Ramirez J.; Blasi F.; Giulia B.; Paola F.; Manuela C.; Giulia S.; Ricca...rdo F.; Sara T.; Giuseppe M.; Massimiliano V.; Manuela D.F.; Roberto P.; Martina D.; Lisa P.; Antonio V. | 2015-01-01 | CURRENT OPINION IN INFECTIOUS DISEASES | - | 1.01 Articolo in rivista | - |
| Analysis of X chromosome inactivation in autism spectrum disorders. | Gong X; Bacchelli E; Blasi F; Toma C; Betancur C; Chaste P; Delorme R; Durand CM; Fauchereau F; B...otros HG; Leboyer M; Mouren-Simeoni MC; Nygren G; Anckarsäter H; Rastam M; Gillberg IC; Gillberg C; Moreno-De-Luca D; Carone S; Nummela I; Rossi M; Battaglia A; International Molecular Genetic Study of Autism Consortium (IMGSAC); Jarvela I; Maestrini E; Bourgeron T. | 2008-01-01 | AMERICAN JOURNAL OF MEDICAL GENETICS. PART B, NEUROPSYCHIATRIC GENETICS | - | 1.01 Articolo in rivista | - |
| Is ASMT a susceptibility gene for autism spectrum disorders? A replication study in European populations. | Toma C; Rossi M; Sousa I; Blasi F; Bacchelli E; Alen R; Vanhala R; Monaco AP; Järvelä I; Maestrini E | 2007-01-01 | MOLECULAR PSYCHIATRY | - | 1.01 Articolo in rivista | - |
| Mapping autism risk loci using genetic linkage and chromosomal rearrangements | Autism Genome Project Consortium; Szatmari P; Paterson AD; Zwaigenbaum L; Roberts W; Brian J; Liu... XQ; Vincent JB; Skaug JL; Thompson AP; Senman L; Feuk L; Qian C; Bryson SE; Jones MB; Marshall CR; Scherer SW; Vieland VJ; Bartlett C; Mangin LV; Goedken R; Segre A; Pericak-Vance MA; Cuccaro ML; Gilbert JR; Wright HH; Abramson RK; Betancur C; Bourgeron T; Gillberg C; Leboyer M; Buxbaum JD; Davis KL; Hollander E; Silverman JM; Hallmayer J; Lotspeich L; Sutcliffe JS; Haines JL; Folstein SE; Piven J; Wassink TH; Sheffield V; Geschwind DH; Bucan M; Brown WT; Cantor RM; Constantino JN; Gilliam TC; Herbert M; Lajonchere C; Ledbetter DH; Lese-Martin C; Miller J; Nelson S; Samango-Sprouse CA; Spence S; State M; Tanzi RE; Coon H; Dawson G; Devlin B; Estes A; Flodman P; Klei L; McMahon WM; Minshew N; Munson J; Korvatska E; Rodier PM; Schellenberg GD; Smith M; Spence MA; Stodgell C; Tepper PG; Wijsman EM; Yu CE; Roge B; Mantoulan C; Wittemeyer K; Poustka A; Felder B; Klauck SM; Schuster C; Poustka F; Bolte S; Feineis-Matthews S; Herbrecht E; Schmotzer G; Tsiantis J; Papanikolaou K; Maestrini E; Bacchelli E; Blasi F; Carone S; Toma C; Van Engeland H; de Jonge M; Kemner C; Koop F; Langemeijer M; Hijimans C; Staal WG; Baird G; Bolton PF; Rutter ML; Weisblatt E; Green J; Aldred C; Wilkinson JA; Pickles A; Le Couteur A; Berney T; McConachie H; Bailey AJ; Francis K; Honeyman G; Hutchinson A; Parr JR; Wallace S; Monaco AP; Barnby G; Kobayashi K; Lamb JA; Sousa I; Sykes N; Cook EH; Guter SJ; Leventhal BL; Salt J; Lord C; Corsello C; Hus V; Weeks DE; Volkmar F; Tauber M; Fombonne E; Shih A. | 2007-01-01 | NATURE GENETICS | - | 1.01 Articolo in rivista | - |
| Absence of coding mutations in the X-linked genes Neuroligin 3 and Neuroligin 4 in individuals with autism from the IMGSAC collection | Blasi F.; Bacchelli E.; Pesaresi G.; Carone S.; Bailey A.J.; Maestrini E. | 2006-01-01 | AMERICAN JOURNAL OF MEDICAL GENETICS. PART B, NEUROPSYCHIATRIC GENETICS | - | 1.01 Articolo in rivista | - |
| SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample. | Blasi F.; Bacchelli E.; Carone S.; Toma C.; Monaco AP.; Bailey AJ.; Maestrini E. | 2006-01-01 | EUROPEAN JOURNAL OF HUMAN GENETICS | - | 1.01 Articolo in rivista | - |
| Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects. | Lamb J.A.; Barnby G.; Bonora E.; Sykes N.; Bacchelli E.; Blasi F.; Maestrini E.; Broxholme J.; Tz...enova J.; Weeks D.; Bailey A.J.; Monaco A.P.; International Molecular Genetic Study of Autism Consortium (IMGSAC). | 2005-01-01 | JOURNAL OF MEDICAL GENETICS | - | 1.01 Articolo in rivista | - |
| Mutation screening and association analysis of six candidate genes for autism on chromosome 7q. | Bonora E.; Lamb J.A.; Barnby G.; Sykes N.; Moberly T.; Beyer K.S.; Klauck S.M.; Poustka F.; Bacch...elli E.; Blasi F.; Maestrini E.; Battaglia A.; Haracopos D.; Pedersen L.; Isager T.; Eriksen G.; Viskum B.; Sorensen E.U.; Brondum-Nielsen K.; Cotterill R.; Engeland H.; Jonge M.; Kemner C.; Steggehuis K.; Scherpenisse M.; Rutter M.; Bolton P.F.; Parr J.R.; Poustka A.; Bailey A.J.; Monaco A.P.; International Molecular Genetic Study of Austism Consortium. | 2005-01-01 | EUROPEAN JOURNAL OF HUMAN GENETICS | - | 1.01 Articolo in rivista | - |
| DNA variants in the human RAB3A gene are not associated with autism. | D'Adamo P.; Bacchelli E.; Blasi F.; Lipp H.P.; Toniolo D.; Maestrini E. | 2004-01-01 | GENES BRAIN AND BEHAVIOR | - | 1.01 Articolo in rivista | - |
| Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene | Bacchelli E.; Blasi F.; Biondolillo M.; Lamb J.A.; Bonora E.; Barnby G.; Parr J.; Beyer K.S.; Kla...uck S.M.; Poustka A.; Bailey A.J.; Monaco A.P.; Maestrini E. | 2003-01-01 | MOLECULAR PSYCHIATRY | - | 1.01 Articolo in rivista | - |
| Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region | Bonora E.; Bacchelli E.; Levy E.R.; Blasi F.; Marlow A.; Monaco A.P.; Maestrini E. | 2002-01-01 | MOLECULAR PSYCHIATRY | - | 1.01 Articolo in rivista | - |