Watfa AL-Moamari

Dr.

  • 40 Citations
  • 4 h-Index
20142018
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Fingerprint Dive into the research topics where Watfa AL-Moamari is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 12 Similar Profiles
Oman Medicine & Life Sciences
Learning Disorders Medicine & Life Sciences
Exome Medicine & Life Sciences
Intellectual Disability Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Autistic Disorder Medicine & Life Sciences
Consanguinity Medicine & Life Sciences
Inborn Errors Metabolism Medicine & Life Sciences

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Research Output 2014 2018

  • 40 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

Lipoma
Hearing Loss
Mutation
Oman
Genes
7 Citations (Scopus)
Exome
Intellectual Disability
Computational Biology
Genetic Databases
Phenotype
2 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

Oman
Autistic Disorder
Pediatrics
2 Citations (Scopus)
Tuberous Sclerosis
Oman
Neurocutaneous Syndromes
Brain Neoplasms
Autism Spectrum Disorder
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

Intellectual Disability
Mutation
ritrosulfan
Exome
Microcephaly