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Georges Nemer

  • PhD
  • Professor
  • American University of Beirut
  • 19h-indexImpact measure calculated using publication and citation counts. Updated daily.
  • 2105CitationsNumber of citations received by Georges's publications. Updated daily.

Research interests

Congenital Heart Disease

Co-authors (275)

Publications (5)

  • SLURP-1 is mutated in Mal de Meleda, a potential molecular signature for melanoma and a putative squamous lineage tumor suppressor gene

    • Bergqvist C
    • Kadara H
    • Hamie L
    • et al.
    N/AReaders
    0Citations
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  • A novel role for CSRP1 in a lebanese family with congenital cardiac defects

    • Kamar A
    • Fahed A
    • Shibbani K
    • et al.
    N/AReaders
    0Citations
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  • Mutations in the ABCG8 gene are associated with sitosterolaemia in the homozygous form and xanthelasmas in the heterozygous form

    • Bardawil T
    • Rebeiz A
    • Chaabouni M
    • et al.
    N/AReaders
    0Citations
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  • Retinoids: a journey from the molecular structures and mechanisms of action to clinical uses in dermatology and adverse effects

    • Khalil S
    • Bardawil T
    • Stephan C
    • et al.
    N/AReaders
    0Citations
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  • Mutations in SDR9C7 gene encoding an enzyme for vitamin A metabolism underlie autosomal recessive congenital ichthyosis

    • Shigehara Y
    • Okuda S
    • Nemer G
    • et al.
    N/AReaders
    11Citations

Professional experience

Professor

American University of Beirut

October 2015 - Present

Education history

PhD

Universite de Montreal

January 1996 - January 2002(6 years)