| Genetics of male infertility: from research to clinic C Krausz, AR Escamilla, C Chianese Reproduction 150 (5), R159-R174, 2015 | 283 | 2015 |
| High resolution X chromosome-specific array-CGH detects new CNVs in infertile males C Krausz, C Giachini, D Lo Giacco, F Daguin, C Chianese, E Ars, ... Public Library of Science 7 (10), e44887, 2012 | 111 | 2012 |
| Clinical relevance of Y-linked CNV screening in male infertility: new insights based on the 8-year experience of a diagnostic genetic laboratory D Lo Giacco, C Chianese, J Sánchez-Curbelo, L Bassas, P Ruiz, O Rajmil, ... European Journal of Human Genetics 22 (6), 754-761, 2014 | 106 | 2014 |
| Novel insights into DNA methylation features in spermatozoa: stability and peculiarities C Krausz, J Sandoval, S Sayols, C Chianese, C Giachini, H Heyn, ... Public Library of Science 7 (10), e44479, 2012 | 87 | 2012 |
| Sequencing of a ‘mouse azoospermia’ gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest A Riera-Escamilla, A Enguita-Marruedo, D Moreno-Mendoza, C Chianese, ... Human Reproduction 34 (6), 978-988, 2019 | 76 | 2019 |
| The Y chromosome-linked copy number variations and male fertility C Krausz, C Chianese, C Giachini, E Guarducci, I Laface, G Forti Journal of endocrinological investigation 34, 376-382, 2011 | 66 | 2011 |
| Genetic testing and counselling for male infertility C Krausz, C Chianese Current Opinion in Endocrinology, Diabetes and Obesity 21 (3), 244-250, 2014 | 64 | 2014 |
| From exome analysis in idiopathic azoospermia to the identification of a high-risk subgroup for occult Fanconi anemia C Krausz, A Riera-Escamilla, C Chianese, D Moreno-Mendoza, E Ars, ... Genetics in Medicine 21 (1), 189-194, 2019 | 54 | 2019 |
| Recurrent X chromosome-linked deletions: discovery of new genetic factors in male infertility DL Giacco, C Chianese, E Ars, E Ruiz-Castane, G Forti, C Krausz Journal of medical genetics 51 (5), 340-344, 2014 | 54 | 2014 |
| Impact of circulating tumor DNA mutant allele fraction on prognosis in RAS‐mutant metastatic colorectal cancer E Elez, C Chianese, E Sanz‐García, E Martinelli, A Noguerido, ... Molecular Oncology 13 (9), 1827-1835, 2019 | 51 | 2019 |
| Comprehensive investigation in patients affected by sperm macrocephaly and globozoospermia C Chianese, MG Fino, A Riera Escamilla, O López Rodrigo, S Vinci, ... Andrology 3 (2), 203-212, 2015 | 42 | 2015 |
| X chromosome-linked CNVs in male infertility: discovery of overall duplication load and recurrent, patient-specific gains with potential clinical relevance C Chianese, AC Gunning, C Giachini, F Daguin, G Balercia, E Ars, ... PLoS One 9 (6), e97746, 2014 | 41 | 2014 |
| Genomic changes in spermatozoa of the aging male C Chianese, S Brilli, C Krausz Genetic damage in human spermatozoa, 13-26, 2014 | 34 | 2014 |
| gr/gr deletion predisposes to testicular germ cell tumour independently from altered spermatogenesis: results from the largest European study D Moreno-Mendoza, E Casamonti, D Paoli, C Chianese, ... European Journal of Human Genetics 27 (10), 1578-1588, 2019 | 16 | 2019 |
| Y-chromosome microdeletions are not associated with SHOX haploinsufficiency C Chianese, D Lo Giacco, F Tüttelmann, A Ferlin, P Ntostis, S Vinci, ... Human Reproduction 28 (11), 3155-3160, 2013 | 14 | 2013 |
| Corrigendum. Sequencing of a ‘mouse azoospermia’gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest A Riera-Escamilla, A Enguita-Marruedo, D Moreno-Mendoza, C Chianese, ... Human Reproduction 35 (8), 1945-1946, 2020 | 3 | 2020 |
| The role of aging on fecundity in the male C Krausz, C Chianese Paternal Influences on Human Reproductive Success, 70-81, 2013 | 3 | 2013 |
| Correction: gr/gr deletion predisposes to testicular germ cell tumour independently from altered spermatogenesis: results from the largest European study D Moreno-Mendoza, E Casamonti, D Paoli, C Chianese, ... European Journal of Human Genetics 28 (10), 1476, 2020 | 1 | 2020 |
| Whole exome sequencing in non-obstructive azoospermia allows the identification of a high-risk subgroup of infertile men for undiagnosed Fanconi Anemia, a cancer-prone disease C Krausz, A Riera-Escamilla, C Chianese, D Moreno-Mendoza, O Rajmil, ... Endocrine Abstracts 56, 2018 | 1 | 2018 |
| Reply: Y-chromosome microdeletions are not associated with SHOX haploinsufficiency C Krausz, C Chianese, D Lo Giacco, F Tüttelmann, A Ferlin, P Ntostis, ... Human Reproduction 29 (5), 1114-1115, 2014 | 1 | 2014 |
