Watfa AL-Moamari


  • 53 Citations
  • 4 h-Index

Research output per year

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Research Output

  • 53 Citations
  • 4 h-Index
  • 10 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

  • 12 Citations (Scopus)

    A turning point for paediatric developmental services in Oman: Establishment of a national autism screening programme

    Al-Mamari, W., Idris, A. B., Al-Jabri, M., Abdelsattar, A., Al-Hinai, F., Al-Hatmi, M. & Al-Raidan, A., Feb 1 2017, In : Sultan Qaboos University Medical Journal. 17, 1, p. e125-e126

    Research output: Contribution to journalLetter

  • 3 Citations (Scopus)
  • 3 Citations (Scopus)

    Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family

    Al-Amri, A., Saegh, A. A., Al-Mamari, W., El-Asrag, M. E., Ivorra, J. L., Cardno, A. G., Inglehearn, C. F., Clapcote, S. J. & Ali, M., Jul 1 2016, In : American Journal of Medical Genetics, Part A. 170, 7, p. 1826-1831 6 p.

    Research output: Contribution to journalArticle

  • 4 Citations (Scopus)