Stratified analyses of genome wide association study data reveal haplotypes for a candidate gene on chromosome 2 (KIAA1211L) is associated with opioid use in patients of Arabian de...

por Alblooshi, Hiba, Al Safar, Habiba, El Kashef, Ahmed, Al Ghaferi, Hamad, Shawky, Mansour, Hulse, Gary K., Tay, Guan K.
Publicado 2020

The frequency of DRD2 rs1076560 and OPRM1 rs1799971 in substance use disorder patients from the United Arab Emirates

por Alblooshi, Hiba, Hulse, Gary, Osman, Wael, El Kashef, Ahmed, Shawky, Mansour, Al Ghaferi, Hamad, Al Safar, Habiba, Tay, Guan K.
Publicado 2018

Case report: Birk–Landau–Perez syndrome linked to the SLC30A9 gene—identification of additional cases and expansion of the phenotypic spectrum

por Kizhakkedath, Praseetha, AlDhaheri, Watfa, Baydoun, Ibrahim, Tabouni, Mohammed, John, Anne, Almansoori, Taleb M., Al-Turki, Saeed, Al-Jasmi, Fatma, Alblooshi, Hiba
Publicado 2023

The pattern of substance use disorder in the United Arab Emirates in 2015: results of a National Rehabilitation Centre cohort study

por Alblooshi, Hiba, Hulse, Gary K., El Kashef, Ahmed, Al Hashmi, Hanan, Shawky, Mansour, Al Ghaferi, Hamad, Al Safar, Habiba, Tay, Guan K.
Publicado 2016

Novel compound heterozygous variants (c.971delA/c.542C > T) in SLC1A4 causes spastic tetraplegia, thin corpus callosum, and progressive microcephaly: a case report and mutational a...

por Mohamed, Feda E., Ghattas, Mohammad A., Almansoori, Taleb M., Tabouni, Mohammed, Baydoun, Ibrahim, Kizhakkedath, Praseetha, John, Anne, Alblooshi, Hiba, Shaukat, Qudsia, Al-Jasmi, Fatma
Publicado 2023