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  • Maternal serum screening and triploidy
     https://pubmed.ncbi.nlm.nih.gov/7521965
Prenatal Diagnosis 1994,14
  • Culture of fetal erythroid progenitor cells from maternal blood for non invasive prenatal diagnosis
​https://pubmed.ncbi.nlm.nih.gov/8994241
Prenatal Diagnosis 1996;16;1073-1082
  • Maternal serum screening of fetal chromosomal abnormalities by AFP, UE3, HCG and free BHCG:
Prospective and retrospective results
https://pubmed.ncbi.nlm.nih.gov/8783867
Minerva Ginecologica 1996; 48,5;169-173
  • Caratterizzazione citogenetica di cromosomi markers individuati all'amniocentesi:
Implicazioni per correlazioni cario tipo - fetale
https://pubmed.ncbi.nlm.nih.gov/8999384
Minerva Ginecologica 1996; 48,9;365-369
  • Isolation of fetal erythroid cells from maternal blood based on expression of erythropoietin receptors
      https://pubmed.ncbi.nlm.nih.gov/9239731
Molecular Human Reproduction ;1997. 3,451-455
  • Characterization of fetal hematopoietic progenitors circulating in maternal blood of seven aneuploid pregnancies
https://pubmed.ncbi.nlm.nih.gov/9467814
Prenatal Diagnosis 1997;.17;1159-1169
                                                                              
  • Detection of fetal trisomy 18 by short term culture of maternal peripheral blood
https://pubmed.ncbi.nlm.nih.gov/10920335             
Am J. Obstet Gynecol 2000;183:222-225
  • Prenatal diagnosis of congenital diseases:
5 years experience of Prenatal Diagnosis Center at the "Second University of Naples" 
Gazzetta Medica Italiana Arch Sci Med 2004;163;249-256
  • Prenatal diagnosis of partial trisomy 6q: a case report
​https://pubmed.ncbi.nlm.nih.gov/16845680
Prenatal Diagnosis 2006; 26;917-919
Abstract 7 th International Congress of Fetal Medicine Foundation at Sorrento Conference 2008
  1. First trimester combined screening in a low risk population
  2. Prenatal detection of partial fetal chromosomal deletionsby first trimester combined screening
Dissezione cito - molecolare di anomalie cromosomiche sbilanciate alla diagnosi prenatale: 
Valutazione prognostica dell'outcome fenotipico postnatale
  • Cohesin SA1 and SA2 proteins and NAD + deacetylase protein modulate telomere homeostasis in cumulus cells and are eligible biomarkers of oocyte ontogeny and ovarian ageing​
  • Gene expression and apoptosis in cumulus cells of patients with polymorphisms of FSHR and LHB undergoing in vitro fertilization program
https://pubmed.ncbi.nlm.nih.gov/29481647
Paper in collaboration submitted for publication in a peer review journal, 2017