CHIANESE, CHIARA
CHIANESE, CHIARA
Scienze Biomediche, Sperimentali e Cliniche 'Mario Serio'
Aspetti Genetici ed Epigenetici dell'Infertilità Maschile
2015 Chianese, Chiara
Comprehensive investigation in patients affected by sperm macrocephaly and globozoospermia
2015 Chianese, C; Fino, M G; Riera Escamilla, A; López Rodrigo, O; Vinci, S; Guarducci, E; Daguin, F; Muratori, M; Tamburrino, L; Lo Giacco, D; Ars, E; Bassas, L; Costa, M; Pisatauro, V; Noci, I; Coccia, E; Provenzano, A; Ruiz-Castañé, E; Giglio, S; Piomboni, P; Krausz, C
Corrigendum. Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest.
2020 Riera-Escamilla A, Enguita-Marruedo A, Moreno-Mendoza D, Chianese C, Sleddens-Linkels E, Contini E, Benelli M, Natali A, Colpi GM, Ruiz-Castañé E, Maggi M, Baarends WM, Krausz C.
From exome analysis in idiopathic azoospermia to the identification of a high-risk subgroup for occult Fanconi anemia
2019 Krausz, Csilla; Riera-Escamilla, Antoni; Chianese, Chiara; Moreno-Mendoza, Daniel; Ars, Elisabet; Rajmil, Osvaldo; Pujol, Roser; Bogliolo, Massimo; Blanco, Ignacio; Rodríguez, Ines; Badell, Isabel; Ruiz-Castañé, Eduard; Surrallés, Jordi
Genetics of male infertility: from research to clinic
2015 Krausz, Csilla; Escamilla, Antoni Riera; Chianese, Chiara
Genomic changes in spermatozoa of the aging male.
2014 C. Chianese;S. Brilli;C. Krausz
gr/gr deletion predisposes to testicular germ cell tumour independently from altered spermatogenesis: results from the largest European study
2019 Moreno-Mendoza D.; Casamonti E.; Paoli D.; Chianese C.; Riera-Escamilla A.; Giachini C.; Fino M.G.; Cioppi F.; Lotti F.; Vinci S.; Magini A.; Ars E.; Sanchez-Curbelo J.; Ruiz-Castane E.; Lenzi A.; Lombardo F.; Krausz C.
High resolution X chromosome-specific array-CGH detects new CNVs in infertile males.
2012 C. Krausz; C. Giachini; D.L. Giacco; F. Daguin; C. Chianese; E. Ars; E. Ruiz-Castane; G. Forti; E. Rossi
Novel insights into DNA methylation features in spermatozoa: stability and peculiarities.
2012 C. Krausz;J. Sandoval;S. Sayols;C. Chianese;C. Giachini;H. Heyn;M. Esteller
Recurrent X chromosome-linked deletions: discovery of new genetic factors in male infertility
2014 Lo Giacco, D; Chianese, C; Ars, E; Ruiz-Castañé, E; Forti, G; Krausz, C
Reply: Y-chromosome microdeletions are not associated with SHOX haploinsufficiency
2014 C. Krausz;C. Chianese;D. Lo Giacco;F. Tuttelmann;A. Ferlin;P. Ntostis;S. Vinci;G. Balercia;E. Ars;E. Ruiz-Castane;S. Giglio;S. Kliesch;G. Forti
Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest.
2019 Riera-Escamilla A, Enguita-Marruedo A, Moreno-Mendoza D, Chianese C, Sleddens-Linkels E, Contini E, Benelli M, Natali A, Colpi GM, Ruiz-Castañé E, Maggi M, Baarends WM, Krausz C.
The Y chromosome-linked copy number variations and male fertility.
2011 C. Krausz ;C. Chianese ; C. Giachini ;E. Guarducci ;I. Laface ; G.Forti
X chromosome-linked CNVs in male infertility: discovery of overall duplication load and recurrent, patient-specific gains with potential clinical relevance.
2014 C. Chianese;A. C. Gunning;C. Giachini;F. Daguin;G. Balercia;E. Ars;D. L. Giacco;E. Ruiz-Castañé;G. Forti;C. Krausz
Y-chromosome microdeletions are not associated with SHOX haploinsufficiency.
2013 Chianese C; Lo Giacco D; Tüttelmann F; Ferlin A; Ntostis P; Vinci S; Balercia G; Ars E; Ruiz-Castañé E; Giglio S; Forti G; Kliesch S; Krausz C.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Aspetti Genetici ed Epigenetici dell'Infertilità Maschile | 2015 | Chianese, Chiara | |
| Comprehensive investigation in patients affected by sperm macrocephaly and globozoospermia | 2015 | Chianese, C; Fino, M G; Riera Escamilla, A; López Rodrigo, O; Vinci, S; Guarducci, E; Daguin, F; Muratori, M; Tamburrino, L; Lo Giacco, D; Ars, E; Bassas, L; Costa, M; Pisatauro, V; Noci, I; Coccia, E; Provenzano, A; Ruiz-Castañé, E; Giglio, S; Piomboni, P; Krausz, C | |
| Corrigendum. Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest. | 2020 | Riera-Escamilla A, Enguita-Marruedo A, Moreno-Mendoza D, Chianese C, Sleddens-Linkels E, Contini E, Benelli M, Natali A, Colpi GM, Ruiz-Castañé E, Maggi M, Baarends WM, Krausz C. | |
| From exome analysis in idiopathic azoospermia to the identification of a high-risk subgroup for occult Fanconi anemia | 2019 | Krausz, Csilla; Riera-Escamilla, Antoni; Chianese, Chiara; Moreno-Mendoza, Daniel; Ars, Elisabet; Rajmil, Osvaldo; Pujol, Roser; Bogliolo, Massimo; Blanco, Ignacio; Rodríguez, Ines; Badell, Isabel; Ruiz-Castañé, Eduard; Surrallés, Jordi | |
| Genetics of male infertility: from research to clinic | 2015 | Krausz, Csilla; Escamilla, Antoni Riera; Chianese, Chiara | |
| Genomic changes in spermatozoa of the aging male. | 2014 | C. Chianese;S. Brilli;C. Krausz | |
| gr/gr deletion predisposes to testicular germ cell tumour independently from altered spermatogenesis: results from the largest European study | 2019 | Moreno-Mendoza D.; Casamonti E.; Paoli D.; Chianese C.; Riera-Escamilla A.; Giachini C.; Fino M.G.; Cioppi F.; Lotti F.; Vinci S.; Magini A.; Ars E.; Sanchez-Curbelo J.; Ruiz-Castane E.; Lenzi A.; Lombardo F.; Krausz C. | |
| High resolution X chromosome-specific array-CGH detects new CNVs in infertile males. | 2012 | C. Krausz; C. Giachini; D.L. Giacco; F. Daguin; C. Chianese; E. Ars; E. Ruiz-Castane; G. Forti; E. Rossi | |
| Novel insights into DNA methylation features in spermatozoa: stability and peculiarities. | 2012 | C. Krausz;J. Sandoval;S. Sayols;C. Chianese;C. Giachini;H. Heyn;M. Esteller | |
| Recurrent X chromosome-linked deletions: discovery of new genetic factors in male infertility | 2014 | Lo Giacco, D; Chianese, C; Ars, E; Ruiz-Castañé, E; Forti, G; Krausz, C | |
| Reply: Y-chromosome microdeletions are not associated with SHOX haploinsufficiency | 2014 | C. Krausz;C. Chianese;D. Lo Giacco;F. Tuttelmann;A. Ferlin;P. Ntostis;S. Vinci;G. Balercia;E. Ars;E. Ruiz-Castane;S. Giglio;S. Kliesch;G. Forti | |
| Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest. | 2019 | Riera-Escamilla A, Enguita-Marruedo A, Moreno-Mendoza D, Chianese C, Sleddens-Linkels E, Contini E, Benelli M, Natali A, Colpi GM, Ruiz-Castañé E, Maggi M, Baarends WM, Krausz C. | |
| The Y chromosome-linked copy number variations and male fertility. | 2011 | C. Krausz ;C. Chianese ; C. Giachini ;E. Guarducci ;I. Laface ; G.Forti | |
| X chromosome-linked CNVs in male infertility: discovery of overall duplication load and recurrent, patient-specific gains with potential clinical relevance. | 2014 | C. Chianese;A. C. Gunning;C. Giachini;F. Daguin;G. Balercia;E. Ars;D. L. Giacco;E. Ruiz-Castañé;G. Forti;C. Krausz | |
| Y-chromosome microdeletions are not associated with SHOX haploinsufficiency. | 2013 | Chianese C; Lo Giacco D; Tüttelmann F; Ferlin A; Ntostis P; Vinci S; Balercia G; Ars E; Ruiz-Castañé E; Giglio S; Forti G; Kliesch S; Krausz C. |