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Nadia Al Wardy


  • 142 Citations
  • 7 h-Index

Research output per year

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Research Output

  • 142 Citations
  • 7 h-Index
  • 13 Article
  • 2 Review article
  • 1 Letter

LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss

Al-Amri, A. H., Al Saegh, A., AL-Moamari, W., El-Asrag, M. E., Al-Kindi, M. N., Al Khabouri, M., Al Wardy, N., Al Lamki, K., Gabr, A., Idris, A., Inglehearn, C. F., Clapcote, S. J. & Ali, M., Jan 1 2018, (Accepted/In press) In : European Journal of Medical Genetics.

Research output: Contribution to journalArticle

  • A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman

    Palombo, F., Al-Wardy, N., Ruscone, G. A. G., Oppo, M., Kindi, M. N. A., Angius, A., Al Lamki, K., Girotto, G., Giangregorio, T., Benelli, M., Magi, A., Seri, M., Gasparini, P., Cucca, F., Sazzini, M., Al Khabori, M., Pippucci, T. & Romeo, G., Feb 1 2017, In : Journal of Human Genetics. 62, 2, p. 259-264 6 p.

    Research output: Contribution to journalArticle

  • 11 Citations (Scopus)

    A novel missense mutation in the C2C domain of otoferlin causes profound hearing impairment in an Omani family with auditory neuropathy

    Al-Wardy, N. M., Al-Kindi, M. N., Al-Khabouri, M. J., Tamimi, Y. & Van Camp, G., 2016, In : Saudi Medical Journal. 37, 10, p. 1068-1075 8 p.

    Research output: Contribution to journalArticle

  • 5 Citations (Scopus)

    Acylation stimulating protein: A female lipogenic factor?

    Saleh, J., Al-Wardy, N., Farhan, H., Al-Khanbashi, M. & Cianflone, K., Jun 2011, In : Obesity Reviews. 12, 6, p. 440-448 9 p.

    Research output: Contribution to journalArticle

  • 13 Citations (Scopus)

    Assessment methods in undergraduate medical education

    Al-Wardy, N. M., Aug 1 2010, In : Sultan Qaboos University Medical Journal. 10, 2, p. 203-209 7 p.

    Research output: Contribution to journalReview article

  • 19 Citations (Scopus)