Abeer Al-Saegh

Dr.

  • 194 Citations
  • 5 h-Index
20082018
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Fingerprint Dive into the research topics where Abeer Al-Saegh is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 14 Similar Profiles
Mutation Medicine & Life Sciences
Exome Medicine & Life Sciences
Genes Medicine & Life Sciences
Oman Medicine & Life Sciences
Intellectual Disability Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Inborn Genetic Diseases Medicine & Life Sciences
Thyroid Hormone Receptors beta Medicine & Life Sciences

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Research Output 2008 2018

  • 194 Citations
  • 5 h-Index
  • 12 Article
6 Citations (Scopus)
Exome
Intellectual Disability
Computational Biology
Genetic Databases
Phenotype
3 Citations (Scopus)

Inborn errors of metabolism in a cohort of pregnancies with non-immune hydrops fetalis: A single center experience

Bruwer, Z., Al Riyami, N., Al Dughaishi, T., Al Murshedi, F., Al Sayegh, A., Al Kindy, A., Meftah, D., Al Kharusi, K., Al Foori, A., Al Yarubi, N., Scott, P. & Al-Thihli, K., Aug 19 2017, (Accepted/In press) In : Unknown Journal.

Research output: Contribution to journalArticle

Hydrops Fetalis
Inborn Errors Metabolism
Pregnancy
Prenatal Care
55 Citations (Scopus)

The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes

Monies, D., Abouelhoda, M., AlSayed, M., Alhassnan, Z., Alotaibi, M., Kayyali, H., Al-Owain, M., Shah, A., Rahbeeni, Z., Al-Muhaizea, M. A., Alzaidan, H. I., Cupler, E., Bohlega, S., Faqeih, E., Faden, M., Alyounes, B., Jaroudi, D., Goljan, E., Elbardisy, H., Akilan, A. & 87 others, Albar, R., Aldhalaan, H., Gulab, S., Chedrawi, A., Al Saud, B. K., Kurdi, W., Makhseed, N., Alqasim, T., El Khashab, H. Y., Al-Mousa, H., Alhashem, A., Kanaan, I., Algoufi, T., Alsaleem, K., Basha, T. A., Al-Murshedi, F., Khan, S., Al-Kindy, A., Alnemer, M., Al-Hajjar, S., Alyamani, S., Aldhekri, H., Al-Mehaidib, A., Arnaout, R., Dabbagh, O., Shagrani, M., Broering, D., Tulbah, M., Alqassmi, A., Almugbel, M., AlQuaiz, M., Alsaman, A., Al-Thihli, K., Sulaiman, R. A., Al-Dekhail, W., Alsaegh, A., Bashiri, F. A., Qari, A., Alhomadi, S., Alkuraya, H., Alsebayel, M., Hamad, M. H., Szonyi, L., Abaalkhail, F., Al-Mayouf, S. M., Almojalli, H., Alqadi, K. S., Elsiesy, H., Shuaib, T. M., Seidahmed, M. Z., Abosoudah, I., Akleh, H., AlGhonaium, A., Alkharfy, T. M., Al Mutairi, F., Eyaid, W., Alshanbary, A., Sheikh, F. R., Alsohaibani, F. I., Alsonbul, A., Al Tala, S., Balkhy, S., Bassiouni, R., Alenizi, A. S., Hussein, M. H., Hassan, S., Khalil, M., Tabarki, B., Alshahwan, S., Oshi, A., Sabr, Y., Alsaadoun, S., Salih, M. A., Mohamed, S., Sultana, H., Tamim, A., El-Haj, M., Alshahrani, S., Bubshait, D. K., Alfadhel, M., Faquih, T., El-Kalioby, M., Subhani, S., Shah, Z., Moghrabi, N., Meyer, B. F. & Alkuraya, F. S., Aug 1 2017, In : Human Genetics. 136, 8, p. 921-939 19 p.

Research output: Contribution to journalArticle

Exome
Inborn Genetic Diseases
Saudi Arabia
Mutation
Phenotype
2 Citations (Scopus)
Tuberous Sclerosis
Oman
Neurocutaneous Syndromes
Brain Neoplasms
Autism Spectrum Disorder
2 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