Forti G - Search Results

1

Partial AZFc deletions and duplications: clinical correlates in the Italian population.

Giachini C, Laface I, Guarducci E, Balercia G, Forti G, Krausz C. Giachini C, et al. Among authors: forti g. Hum Genet. 2008 Nov;124(4):399-410. doi: 10.1007/s00439-008-0561-1. Epub 2008 Sep 21. Hum Genet. 2008. PMID: 18807255

2

Natural transmission of USP9Y gene mutations: a new perspective on the role of AZFa genes in male fertility.

Krausz C, Degl'Innocenti S, Nuti F, Morelli A, Felici F, Sansone M, Varriale G, Forti G. Krausz C, et al. Among authors: forti g. Hum Mol Genet. 2006 Sep 15;15(18):2673-81. doi: 10.1093/hmg/ddl198. Epub 2006 Aug 7. Hum Mol Genet. 2006. PMID: 16893908

3

TSPY1 copy number variation influences spermatogenesis and shows differences among Y lineages.

Giachini C, Nuti F, Turner DJ, Laface I, Xue Y, Daguin F, Forti G, Tyler-Smith C, Krausz C. Giachini C, et al. Among authors: forti g. J Clin Endocrinol Metab. 2009 Oct;94(10):4016-22. doi: 10.1210/jc.2009-1029. Epub 2009 Sep 22. J Clin Endocrinol Metab. 2009. PMID: 19773397 Free PMC article.

4

Estrogen receptor alpha promoter polymorphism: stronger estrogen action is coupled with lower sperm count.

Guarducci E, Nuti F, Becherini L, Rotondi M, Balercia G, Forti G, Krausz C. Guarducci E, et al. Among authors: forti g. Hum Reprod. 2006 Apr;21(4):994-1001. doi: 10.1093/humrep/dei439. Epub 2006 Jan 5. Hum Reprod. 2006. PMID: 16396937

5

Sperm cryopreservation in male infertility due to genetic disorders.

Krausz C, Forti G. Krausz C, et al. Among authors: forti g. Cell Tissue Bank. 2006;7(2):105-12. doi: 10.1007/s10561-005-1967-9. Cell Tissue Bank. 2006. PMID: 16732413 Review.

6

The leucine-rich repeat-containing G protein-coupled receptor 8 gene T222P mutation does not cause cryptorchidism.

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. Nuti F, et al. Among authors: forti g. J Clin Endocrinol Metab. 2008 Mar;93(3):1072-6. doi: 10.1210/jc.2007-1993. Epub 2007 Dec 11. J Clin Endocrinol Metab. 2008. PMID: 18073304

7

High resolution X chromosome-specific array-CGH detects new CNVs in infertile males.

Krausz C, Giachini C, Lo Giacco D, Daguin F, Chianese C, Ars E, Ruiz-Castane E, Forti G, Rossi E. Krausz C, et al. Among authors: forti g. PLoS One. 2012;7(10):e44887. doi: 10.1371/journal.pone.0044887. Epub 2012 Oct 9. PLoS One. 2012. PMID: 23056185 Free PMC article.

8

TSPY and Male Fertility.

Krausz C, Giachini C, Forti G. Krausz C, et al. Among authors: forti g. Genes (Basel). 2010 Sep 21;1(2):308-16. doi: 10.3390/genes1020308. Genes (Basel). 2010. PMID: 24710048 Free PMC article.

9

X chromosome-linked CNVs in male infertility: discovery of overall duplication load and recurrent, patient-specific gains with potential clinical relevance.

Chianese C, Gunning AC, Giachini C, Daguin F, Balercia G, Ars E, Lo Giacco D, Ruiz-Castañé E, Forti G, Krausz C. Chianese C, et al. Among authors: forti g. PLoS One. 2014 Jun 10;9(6):e97746. doi: 10.1371/journal.pone.0097746. eCollection 2014. PLoS One. 2014. PMID: 24914684 Free PMC article.

10

Y chromosome polymorphisms in medicine.

Krausz C, Quintana-Murci L, Forti G. Krausz C, et al. Among authors: forti g. Ann Med. 2004;36(8):573-83. doi: 10.1080/07853890410018853. Ann Med. 2004. PMID: 15768829 Free article. Review.

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