TRAVERSA, ALICE
TRAVERSA, ALICE
DIPARTIMENTO DI MEDICINA SPERIMENTALE
Absence of 6’Sialyllactose during lactation impairs cognitive capabilities and modulates gene expression
2020 Pisa, Edoardo; Traversa, Alice; Caputo, Viviana; Martire, Alberto; Chiodi, Valentina; Hauser, Jonas; Macrì, Simone
Additional lesions identified by genomic microarrays are associated with an inferior outcome in low-risk chronic lymphocytic leukaemia patients
2023 Rigolin, Gian Matteo; Traversa, Alice; Caputo, Viviana; Del Giudice, Ilaria; Bardi, Antonella; Saccenti, Elena; Raponi, Sara; Ilari, Caterina; Cafforio, Luciana; Giovannetti, Agnese; Pizzuti, Antonio; Guarini, Anna; Foà, Robin; Cuneo, Antonio
Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration
2018 Muto, Valentina; Flex, Elisabetta; Kupchinsky, Zachary; Primiano, Guido; Galehdari, Hamid; Dehghani, Mohammadreza; Cecchetti, Serena; Carpentieri, Giovanna; Rizza, Teresa; Mazaheri, Neda; Sedaghat, Alireza; Vahidi Mehrjardi, Mohammad Yahya; Traversa, Alice; Di Nottia, Michela; Kousi, Maria M; Jamshidi, Yalda; Ciolfi, Andrea; Caputo, Viviana; Malamiri, Reza Azizi; Pantaleoni, Francesca; Martinelli, Simone; Jeffries, Aaron R; Zeighami, Jawaher; Sherafat, Amir; Di Giuda, Daniela; Shariati, Gholam Reza; Carrozzo, Rosalba; Katsanis, Nicholas; Maroofian, Reza; Servidei, Serenella; Tartaglia, Marco
Characterization of molecular bases of Myhre syndrome
2016 Traversa, Alice
Co-occurring WARS2 and CHRNA6 mutations in a child with a severe form of infantile parkinsonism
2020 Martinelli, Simone; Cordeddu, Viviana; Galosi, Serena; Lanzo, Ambra; Palma, Eleonora; Pannone, Luca; Ciolfi, Andrea; Di Nottia, Michela; Rizza, Teresa; Bocchinfuso, Gianfranco; Traversa, Alice; Caputo, Viviana; Farrotti, Andrea; Carducci, Claudia; Bernardini, Laura; Cogo, Susanna; Paglione, Maria; Venditti, Martina; Bentivoglio, Annarita; Ng, Joanne; Kurian, Manju A; Civiero, Laura; Greggio, Elisa; Stella, Lorenzo; Trettel, Flavia; Sciaccaluga, Miriam; Roseti, Cristina; Carrozzo, Rosalba; Fucile, Sergio; Limatola, Cristina; Di Schiavi, Elia; Tartaglia, Marco; Leuzzi, Vincenzo
Exploring non-coding genetic variability in ACE2: Functional annotation and in vitro validation of regulatory variants
2024 Giovannetti, Agnese; Lazzari, Sara; Mangoni, Manuel; Traversa, Alice; Mazza, Tommaso; Parisi, Chiara; Caputo, Viviana
Exposure to 3′sialyllactose‐poor milk during lactation impairs cognitive capabilities in adulthood
2021 Pisa, E.; Martire, A.; Chiodi, V.; Traversa, A.; Caputo, V.; Hauser, J.; Macri, S.
GDF5 mutation case report and a systematic review of molecular and clinical spectrum: Expanding current knowledge on genotype-phenotype correlations
2021 Genovesi, M. L.; Guadagnolo, D.; Marchionni, E.; Giovannetti, A.; Traversa, A.; Panzironi, N.; Bernardo, S.; Palumbo, P.; Petrizzelli, F.; Carella, M.; Mazza, T.; Pizzuti, A.; Caputo, V.
Genomic and physiological resilience in extreme environments are associated with a secure attachment style
2020 Caputo, Viviana; Pacilli, Maria Giuseppina; Arisi, Ivan; Mazza, Tommaso; Brandi, Rossella; Traversa, Alice; Casasanta, Giampietro; Pisa, Edoardo; Sonnessa, Michele; Healey, Beth; Moggio, Lorenzo; D’Onofrio, Mara; Alleva, Enrico; Macrì, Simone
Heterozygous nonsense ARX mutation in a family highlights the complexity of clinical and molecular diagnosis in case of chromosomal and single gene disorder co-inheritance
2020 Traversa, Alice; Marchionni, Enrica; Giovannetti, Agnese; Genovesi, Maria L; Panzironi, Noemi; Margiotti, Katia; Napoli, Giulia; Piceci Sparascio, Francesca; De Luca, Alessandro; Petrizzelli, Francesco; Carella, Massimo; Cardona, Francesco; Bernardo, Silvia; Manganaro, Lucia; Mazza, Tommaso; Pizzuti, Antonio; Caputo, Viviana
Increased availability of the human milk oligosaccharide sialyl(alpha2,3)lactose during lactation promotes the development of executive functions
2019 Pisa, Edoardo; Tomasi, Flavio; Traversa, Alice; Caputo, Viviana; Macrì, Simone; Hauser, Jonas
Long-term consequences of reduced availability and compensatory supplementation of sialylated HMOs on cognitive capabilities
2023 Pisa, Edoardo; Traversa, Alice; Caputo, Viviana; Ottomana, Angela Maria; Hauser, Jonas; Macrì, Simone
MiRLog and dbmiR: Prioritization and functional annotation tools to study human microRNA sequence variants
2022 Giovannetti, Agnese; Bianco, SALVATORE DANIELE; Traversa, Alice; Panzironi, Noemi; Bruselles, Alessandro; Lazzari, Sara; Liorni, Niccolò; Tartaglia, Marco; Carella, Massimo; Pizzuti, Antonio; Mazza, Tommaso; Caputo, Viviana
Molecular Approaches in Fetal Malformations, Dynamic Anomalies and Soft Markers: Diagnostic Rates and Challenges—Systematic Review of the Literature and Meta-Analysis
2022 Mastromoro, Gioia; Guadagnolo, Daniele; KHALEGHI HASHEMIAN, Nader; Marchionni, Enrica; Traversa, Alice; Pizzuti, Antonio
Mutations impairing GSK3-mediated MAF phosphorylation cause cataract, deafness, intellectual disability, seizures, and a down syndrome-like facies
2015 E. Stellacci, M. Niceta; Gripp, K. W.; Zampino, G.; Kousi, M.; Manselmi, M. Anselmi; Traversa, A.; Ciolfi, A.; Stabley, D.; Bruselles, A.; Caputo, V.; Scecchetti, S. Cecchetti; Prudente, S.; Fiorenza, M. T.; Boitani, C.; Philip, N.; Dniyazov, D. Niyazov; Leoni, C.; Nakane, T.; Keppler-Noreuil, K.; Braddock, S. R.; Gillessen-Kaesbach, G.; Palleschi, A.; Campeau, P. M.; Lee, B. H. L.; Pouponnot, C.; Stella, L.; Gbocchinfuso, G. Bocchinfuso; Nkatsanis, N. Katsanis; KSol-Church, K. Sol-Church
Novel SMAD4 mutation causing Myhre syndrome
2014 Caputo, Viviana; Gianfranco, Bocchinfuso; Marco, Castori; Traversa, Alice; Pizzuti, Antonio; Lorenzo, Stella; Grammatico, Paola; Marco, Tartaglia
Potassium Channel {KCNH}1 Activating Variants Cause Altered Functional and Morphological Ciliogenesis
2022 Napoli, Giulia; Panzironi, Noemi; Traversa, Alice; Catalanotto, Caterina; Pace, Valentina; Petrizzelli, Francesco; Giovannetti, Agnese; Lazzari, Sara; Cogoni, Carlo; Tartaglia, Marco; Carella, Massimo; Mazza, Tommaso; Pizzuti, Antonio; Parisi, Chiara; Caputo, Viviana
Prenatal whole exome sequencing detects a new homozygous fukutin (FKTN) mutation in a fetus with an ultrasound suspicion of familial Dandy-Walker malformation.
2019 Traversa, A; Bernardo, S; Paiardini, A; Giovannetti, A; Marchionni, E; Genovesi, Ml; Guadagnolo, D; Torres, B; Paolacci, S; Bernardini, L; Mazza, T; Carella, M; Caputo, V; Pizzuti, A
Reduced availability of a selective human milk oligosaccharide during lactation impairs post-weaning executive functions
2019 Pisa, Edoardo; Tomasi, Flavio; Traversa, Alice; Caputo, Viviana; Hauser, Jonas; Macrì, Simone
Sialylated human milk oligosaccharides program cognitive development through a non-genomic transmission mode
2021 Hauser, Jonas; Pisa, Edoardo; Arias Vásquez, Alejandro; Tomasi, Flavio; Traversa, Alice; Chiodi, Valentina; Martin, Francois-Pierre; Sprenger, Norbert; Lukjancenko, Oksana; Zollinger, Alix; Metairon, Sylviane; Schneider, Nora; Steiner, Pascal; Martire, Alberto; Caputo, Viviana; Macrì, Simone
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Absence of 6’Sialyllactose during lactation impairs cognitive capabilities and modulates gene expression | 2020 | Pisa, Edoardo; Traversa, Alice; Caputo, Viviana; Martire, Alberto; Chiodi, Valentina; Hauser, Jonas; Macrì, Simone | |
| Additional lesions identified by genomic microarrays are associated with an inferior outcome in low-risk chronic lymphocytic leukaemia patients | 2023 | Rigolin, Gian Matteo; Traversa, Alice; Caputo, Viviana; Del Giudice, Ilaria; Bardi, Antonella; Saccenti, Elena; Raponi, Sara; Ilari, Caterina; Cafforio, Luciana; Giovannetti, Agnese; Pizzuti, Antonio; Guarini, Anna; Foà, Robin; Cuneo, Antonio | |
| Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration | 2018 | Muto, Valentina; Flex, Elisabetta; Kupchinsky, Zachary; Primiano, Guido; Galehdari, Hamid; Dehghani, Mohammadreza; Cecchetti, Serena; Carpentieri, Giovanna; Rizza, Teresa; Mazaheri, Neda; Sedaghat, Alireza; Vahidi Mehrjardi, Mohammad Yahya; Traversa, Alice; Di Nottia, Michela; Kousi, Maria M; Jamshidi, Yalda; Ciolfi, Andrea; Caputo, Viviana; Malamiri, Reza Azizi; Pantaleoni, Francesca; Martinelli, Simone; Jeffries, Aaron R; Zeighami, Jawaher; Sherafat, Amir; Di Giuda, Daniela; Shariati, Gholam Reza; Carrozzo, Rosalba; Katsanis, Nicholas; Maroofian, Reza; Servidei, Serenella; Tartaglia, Marco | |
| Characterization of molecular bases of Myhre syndrome | 2016 | Traversa, Alice | |
| Co-occurring WARS2 and CHRNA6 mutations in a child with a severe form of infantile parkinsonism | 2020 | Martinelli, Simone; Cordeddu, Viviana; Galosi, Serena; Lanzo, Ambra; Palma, Eleonora; Pannone, Luca; Ciolfi, Andrea; Di Nottia, Michela; Rizza, Teresa; Bocchinfuso, Gianfranco; Traversa, Alice; Caputo, Viviana; Farrotti, Andrea; Carducci, Claudia; Bernardini, Laura; Cogo, Susanna; Paglione, Maria; Venditti, Martina; Bentivoglio, Annarita; Ng, Joanne; Kurian, Manju A; Civiero, Laura; Greggio, Elisa; Stella, Lorenzo; Trettel, Flavia; Sciaccaluga, Miriam; Roseti, Cristina; Carrozzo, Rosalba; Fucile, Sergio; Limatola, Cristina; Di Schiavi, Elia; Tartaglia, Marco; Leuzzi, Vincenzo | |
| Exploring non-coding genetic variability in ACE2: Functional annotation and in vitro validation of regulatory variants | 2024 | Giovannetti, Agnese; Lazzari, Sara; Mangoni, Manuel; Traversa, Alice; Mazza, Tommaso; Parisi, Chiara; Caputo, Viviana | |
| Exposure to 3′sialyllactose‐poor milk during lactation impairs cognitive capabilities in adulthood | 2021 | Pisa, E.; Martire, A.; Chiodi, V.; Traversa, A.; Caputo, V.; Hauser, J.; Macri, S. | |
| GDF5 mutation case report and a systematic review of molecular and clinical spectrum: Expanding current knowledge on genotype-phenotype correlations | 2021 | Genovesi, M. L.; Guadagnolo, D.; Marchionni, E.; Giovannetti, A.; Traversa, A.; Panzironi, N.; Bernardo, S.; Palumbo, P.; Petrizzelli, F.; Carella, M.; Mazza, T.; Pizzuti, A.; Caputo, V. | |
| Genomic and physiological resilience in extreme environments are associated with a secure attachment style | 2020 | Caputo, Viviana; Pacilli, Maria Giuseppina; Arisi, Ivan; Mazza, Tommaso; Brandi, Rossella; Traversa, Alice; Casasanta, Giampietro; Pisa, Edoardo; Sonnessa, Michele; Healey, Beth; Moggio, Lorenzo; D’Onofrio, Mara; Alleva, Enrico; Macrì, Simone | |
| Heterozygous nonsense ARX mutation in a family highlights the complexity of clinical and molecular diagnosis in case of chromosomal and single gene disorder co-inheritance | 2020 | Traversa, Alice; Marchionni, Enrica; Giovannetti, Agnese; Genovesi, Maria L; Panzironi, Noemi; Margiotti, Katia; Napoli, Giulia; Piceci Sparascio, Francesca; De Luca, Alessandro; Petrizzelli, Francesco; Carella, Massimo; Cardona, Francesco; Bernardo, Silvia; Manganaro, Lucia; Mazza, Tommaso; Pizzuti, Antonio; Caputo, Viviana | |
| Increased availability of the human milk oligosaccharide sialyl(alpha2,3)lactose during lactation promotes the development of executive functions | 2019 | Pisa, Edoardo; Tomasi, Flavio; Traversa, Alice; Caputo, Viviana; Macrì, Simone; Hauser, Jonas | |
| Long-term consequences of reduced availability and compensatory supplementation of sialylated HMOs on cognitive capabilities | 2023 | Pisa, Edoardo; Traversa, Alice; Caputo, Viviana; Ottomana, Angela Maria; Hauser, Jonas; Macrì, Simone | |
| MiRLog and dbmiR: Prioritization and functional annotation tools to study human microRNA sequence variants | 2022 | Giovannetti, Agnese; Bianco, SALVATORE DANIELE; Traversa, Alice; Panzironi, Noemi; Bruselles, Alessandro; Lazzari, Sara; Liorni, Niccolò; Tartaglia, Marco; Carella, Massimo; Pizzuti, Antonio; Mazza, Tommaso; Caputo, Viviana | |
| Molecular Approaches in Fetal Malformations, Dynamic Anomalies and Soft Markers: Diagnostic Rates and Challenges—Systematic Review of the Literature and Meta-Analysis | 2022 | Mastromoro, Gioia; Guadagnolo, Daniele; KHALEGHI HASHEMIAN, Nader; Marchionni, Enrica; Traversa, Alice; Pizzuti, Antonio | |
| Mutations impairing GSK3-mediated MAF phosphorylation cause cataract, deafness, intellectual disability, seizures, and a down syndrome-like facies | 2015 | E. Stellacci, M. Niceta; Gripp, K. W.; Zampino, G.; Kousi, M.; Manselmi, M. Anselmi; Traversa, A.; Ciolfi, A.; Stabley, D.; Bruselles, A.; Caputo, V.; Scecchetti, S. Cecchetti; Prudente, S.; Fiorenza, M. T.; Boitani, C.; Philip, N.; Dniyazov, D. Niyazov; Leoni, C.; Nakane, T.; Keppler-Noreuil, K.; Braddock, S. R.; Gillessen-Kaesbach, G.; Palleschi, A.; Campeau, P. M.; Lee, B. H. L.; Pouponnot, C.; Stella, L.; Gbocchinfuso, G. Bocchinfuso; Nkatsanis, N. Katsanis; KSol-Church, K. Sol-Church | |
| Novel SMAD4 mutation causing Myhre syndrome | 2014 | Caputo, Viviana; Gianfranco, Bocchinfuso; Marco, Castori; Traversa, Alice; Pizzuti, Antonio; Lorenzo, Stella; Grammatico, Paola; Marco, Tartaglia | |
| Potassium Channel {KCNH}1 Activating Variants Cause Altered Functional and Morphological Ciliogenesis | 2022 | Napoli, Giulia; Panzironi, Noemi; Traversa, Alice; Catalanotto, Caterina; Pace, Valentina; Petrizzelli, Francesco; Giovannetti, Agnese; Lazzari, Sara; Cogoni, Carlo; Tartaglia, Marco; Carella, Massimo; Mazza, Tommaso; Pizzuti, Antonio; Parisi, Chiara; Caputo, Viviana | |
| Prenatal whole exome sequencing detects a new homozygous fukutin (FKTN) mutation in a fetus with an ultrasound suspicion of familial Dandy-Walker malformation. | 2019 | Traversa, A; Bernardo, S; Paiardini, A; Giovannetti, A; Marchionni, E; Genovesi, Ml; Guadagnolo, D; Torres, B; Paolacci, S; Bernardini, L; Mazza, T; Carella, M; Caputo, V; Pizzuti, A | |
| Reduced availability of a selective human milk oligosaccharide during lactation impairs post-weaning executive functions | 2019 | Pisa, Edoardo; Tomasi, Flavio; Traversa, Alice; Caputo, Viviana; Hauser, Jonas; Macrì, Simone | |
| Sialylated human milk oligosaccharides program cognitive development through a non-genomic transmission mode | 2021 | Hauser, Jonas; Pisa, Edoardo; Arias Vásquez, Alejandro; Tomasi, Flavio; Traversa, Alice; Chiodi, Valentina; Martin, Francois-Pierre; Sprenger, Norbert; Lukjancenko, Oksana; Zollinger, Alix; Metairon, Sylviane; Schneider, Nora; Steiner, Pascal; Martire, Alberto; Caputo, Viviana; Macrì, Simone |