Elenco Pubblicazioni

Elenco prinicipali pubblicazioni:

1. Giachini C, Nuti F, Turner DJ, Laface I, Xue Y, Daguin F, Forti G, Tyler-SmithC, Krausz C. TSPY1 copy number variation influences spermatogenesis and shows differences among Y lineages. J Clin Endocrinol Metab. 2009 94:4016-22. (I.F. 6,32)
2. Nuti F, Luciani P, Marinari E, Erdei E, Bak M, Deledda C, Rosati F, Mazzinghi B, Danza G, Stoop H, Looijenga LH, Peri A, Serio M, Krausz C. Seladin-1 and testicular germ cell tumours: new insights into cisplatin responsiveness. J Pathol. 2009 219:491-500. (I.F. 5,12)
3. Tyler-Smith C, Krausz C. The will-o'-the-wisp of genetics--hunting for the azoospermia factor gene. N Engl J Med. 2009 26;360:925-7. (I.F. 50,02)
4. Krausz C, Giachini C, Xue Y, O'Bryan MK, Gromoll J, Rajpert-de Meyts E, Oliva R, Aknin-Seifer I, Erdei E, Jorgensen N, Simoni M, Ballescà JL, Levy R, Balercia G, Piomboni P, Nieschlag E, Forti G, McLachlan R, Tyler-Smith C. Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal background. J Med Genet. 2009 46:21-31. (I.F. 5,71)
5. Krausz C, Sassone-Corsi P. Florence-Utah Symposium corner: from genetics to epigenetics of male infertility. Int J Androl. 2008 31:535-6. (I.F. 4,02)
6. Krausz C, Looijenga LH. Genetic aspects of testicular germ cell tumors. Cell Cycle. 2008 7:3519-24. Review. (I.F. 4,12)
7. Giachini C, Laface I, Guarducci E, Balercia G, Forti G, Krausz C. Partial AZFc deletions and duplications: clinical correlates in the Italian population. Hum Genet. 2008 124:399-410. (I.F. 4,04)
8. Nuti F, Krausz C. Gene polymorphisms/mutations relevant to abnormal spermatogenesis. Reprod Biomed Online. 2008 16:504-13. Review. (I.F. 2,.95)
9. Nuti F, Marinari E, Erdei E, El-Hamshari M, Echavarria MG, Ars E, Balercia G,Merksz M, Giachini C, Shaeer KZ, Forti G, Ruiz-Castané E, Krausz C. The leucine-rich repeat-containing G protein-coupled receptor 8 gene T222P mutation does not cause cryptorchidism. J Clin Endocrinol Metab. 2008 93:1072-6. (I.F. 6,32)
10. Giachini C, Nuti F, Marinari E, Forti G, Krausz C. Partial AZFc deletions in infertile men with cryptorchidism. Hum Reprod. 2007 22:2398-403. (I.F. 3,77)
11. Galan JJ, Guarducci E, Nuti F, Gonzalez A, Ruiz M, Ruiz A, Krausz C. Molecular analysis of estrogen receptor alpha gene AGATA haplotype and SNP12 in European populations: potential protective effect for cryptorchidism and lack of association with male infertility. Hum Reprod. 2007 22:444-9. (I.F. 3,77)
12. Krausz C, Degl'Innocenti S, Nuti F, Morelli A, Felici F, Sansone M, Varriale G, Forti G. Natural transmission of USP9Y gene mutations: a new perspective on the role of AZFa genes in male fertility. Hum Mol Genet. 2006 15:2673-81. (I.F. 7,25)
13. Krausz C, Degl'Innocenti S. Y chromosome and male infertility: update, 2006. Front Biosci. 2006 11:3049-61. Review. (I.F. 3,31)
14. Guarducci E, Nuti F, Becherini L, Rotondi M, Balercia G, Forti G, Krausz C. Estrogen receptor alpha promoter polymorphism: stronger estrogen action is coupled with lower sperm count. Hum Reprod. 2006 21:994-1001. (I.F. 3,77)
15. Krausz C. Y chromosome and male infertility. Andrologia. 2005 37:219-23. (I.F. 1,.30; CI: 4)
16. Giachini C, Guarducci E, Longepied G, Degl'Innocenti S, Becherini L, Forti G,Mitchell MJ, Krausz C. The gr/gr deletion(s): a new genetic test in male infertility? J Med Genet. 2005 42:497-502. (I.F. 5,71)
17. Krausz C, Sassone-Corsi P. Genetic control of spermiogenesis: insights from the CREM gene and implications for human infertility. Reprod Biomed Online. 2005 10:64-71. Review. (I.F. 2,95)
18. Becherini L, Guarducci E, Degl'Innocenti S, Rotondi M, Forti G, Krausz C.DAZL polymorphisms and susceptibility to spermatogenic failure: an example of remarkable ethnic differences. Int J Androl. 2004 27:375-81. (I.F. 4,02)
19. Krausz C, Guarducci E, Becherini L, Degl'Innocenti S, Gerace L, Balercia G,Forti G. The clinical significance of the POLG gene polymorphism in male infertility. J Clin Endocrinol Metab. 2004 89:4292-7. (I.F. 6,32)
20. Simoni M, Bakker E, Krausz C. EAA/EMQN best practice guidelines for molecular diagnosis of y-chromosomal microdeletions. State of the art 2004. Int J Androl.2004 27:240-9. (I.F. 4,02; CI:88)
21. Krausz C, Quintana-Murci L, Forti G. Y chromosome polymorphisms in medicine. Ann Med. 2004 36:573-83. Review. (I.F. 5,43)
22. Aitken RJ, Krausz C. Oxidative stress, DNA damage and the Y chromosome. Reproduction. 2001 122:497-506. Review. (I.F. 3,07)
23. Krausz C, Forti G, McElreavey K. The Y chromosome and male fertility and infertility. Int J Androl. 2003 26:70-5. Review. (I.F. 4,02)
24. Krausz C, Quintana-Murci L, Rajpert-De Meyts E, Jørgensen N, Jobling MA,Rosser ZH, Skakkebaek NE, McElreavey K. Identification of a Y chromosome haplogroup associated with reduced sperm counts. Hum Mol Genet. 2001 10:1873-7. (I.F. 7,25)
25. Krausz C, McElreavey K. Y chromosome microdeletions in 'fertile' males. Hum Reprod. 2001 16:1306-7. (I.F. 3,77)
26. Krausz C, Rajpert-De Meyts E, Frydelund-Larsen L, Quintana-Murci L,McElreavey K, Skakkebaek NE. Double-blind Y chromosome microdeletion analysis in men with known sperm parameters and reproductive hormone profiles: microdeletions are specific for spermatogenic failure. J Clin Endocrinol Metab. 2001 86:2638-42. (I.F. 6,32)
27. Tóth A, Tardy EP, Gombos S, Hajdu K, Bátorfi J, Krausz C. AZFc deletion detected in a newborn with prenatally diagnosed Yq deletion. Prenat Diagn. 2001 21:253-5. (I.F. 1,60)
28. Krausz C, Quintana-Murci L, McElreavey K. Prognostic value of Y deletion analysis: what is the clinical prognostic value of Y chromosome microdeletion analysis? Hum Reprod. 2000 15:1431-4. Review. (I.F. 3,77)
29. Krausz C, Quintana-Murci L, Fellous M, Siffroi JP, McElreavey K. Absence of mutations involving the INSL3 gene in human idiopathic cryptorchidism. Mol Hum Reprod. 2000 6:298-302. (I.F. 2,54)
30. Krausz C, Quintana-Murci L, Barbaux S, Siffroi JP, Rouba H, Delafontaine D,Souleyreau-Therville N, Arvis G, Antoine JM, Erdei E, Taar JP, Tar A, Jeandidier E, Plessis G, Bourgeron T, Dadoune JP, Fellous M, McElreavey K. A high frequency of Y chromosome deletions in males with non idiopathic infertility. J Clin Endocrinol Metab. 1999 84:3606-12. (I.F. 5,49)