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emilia vitale

  • doctorate in biological science
  • 16h-indexImpact measure calculated using publication and citation counts. Updated daily.
  • 1773CitationsNumber of citations received by emilia's publications. Updated daily.

Co-authors (206)

  • Yunita Syawal

Publications (5)

  • GRN deletion in familial frontotemporal dementia showing association with clinical variability in 3 familial cases

    • Milan G
    • Napoletano S
    • Pappatà S
    • et al.
    N/AReaders
    0Citations
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  • A second Middle Eastern kindred with autosomal recessive non-syndromic hearing loss segregates DFNB9

    • Leal S
    • Apaydin F
    • Barnwell C
    • et al.
    N/AReaders
    7Citations
  • Mapping, cloning and genetic characterization of the region containing the wilson disease gene

    • Petrukhin K
    • Fischer S
    • Pirastu M
    • et al.
    N/AReaders
    398Citations
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  • Genetic linkage of the Marfan syndrome, ectopia lentis, and congenital contractural arachnodactyly to the fibrillin genes on chromosomes 15 and 5

    • Tsipouras P
    • Del Mastro R
    • Sarfarazi M
    • et al.
    N/AReaders
    205Citations
  • Linkage disequilibrium between cystic fibrosis and linked DNA polymorphisms in Italian families: a collaborative study

    • Estivill X
    • Farrall M
    • Williamson R
    • et al.
    N/AReaders
    56Citations