Luigi Picci

University of Padua

Papers

1

Total Citations

49

H-Index

1

About

Luigi Picci is a geneticist whose research has significantly advanced the understanding of cystic fibrosis (CF) genetics, particularly in Southern Italy. His major contributions center on identifying rare and population-specific CF mutations, which are critical for accurate diagnosis and genetic screening. In his highly cited 1999 study, Picci and his team detected five rare CF mutations peculiar to Southern Italy, demonstrating that standard mutation panels—which typically cover only the most common alleles like DeltaF508—are insufficient for this genetically distinct population. This work, which has garnered 49 citations, not only improved screening protocols but also enabled better phenotype characterization for patients with homozygous mutations. By highlighting the importance of regional genetic variation, Picci's research has had a lasting impact on clinical genetics, ensuring that patients in Southern Italy receive more precise diagnoses and tailored care. His findings underscore the necessity of population-specific approaches in medical genetics, making his work essential reading for researchers and clinicians focused on CF and genetic screening.

Research Focus

Key Achievements

1
H-Index
1
Papers
49
Total Citations
49
Avg Citations/Paper
🏆 Most Cited Paper
Detection of Five Rare Cystic Fibrosis Mutations Peculiar to Southern Italy: Implications in Screening for the Disease and Phenotype Characterization for Patients with Homozygote Mutations
49 citations · 1999
📈 Most Prolific Year: 1999 (1 Papers)
🤝 Key Collaborators: 8
🏛 Institutions: University of Padua

Top Papers

  1. 1

Key Collaborators

Contact & Links

Available for collaboration
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