Can a genetic test improve the treatment of complex depression?

The Utility of CYP2D6 and CYP2C19 Variants to Guide Pharmacological Treatment in Complex Unipolar Major Depression: A Pilot Longitudinal Study, Psychiatric Quarterly, July 2023
By: Reshma Ramaraj · Zeina N. Al-Mahayri · Reema Saleous · Karim Abdel Aziz Fadwa Al-Mugaddam · Mouza Al-Sabousi· Aysha Alhassani· Noura Ali Al Ahbabi Emmanuel Stip · George P. Patrinos · Bassam R. Ali · Danilo Arnone

Exploring the feasibility of pharmacogenomic testing in the UAE clinics for the first time!

Pharmacogenomics Implementation in Cardiovascular Disease in a Highly Diverse Population: Initial Findings and Lessons Learned from a Pilot Study in United Arab Emirates. Human Genomics, 2022 Sep 25;16(1):42
Al-Mahayri Z, Khasawneh L, Alqasrawi M, Sahar Altoum, Gohar Jamil, Sally Badawi, Dana Hamza, Lizy George, Anwar AlZaabi, Husam Ouda, Fatima Al-Maskari, Juma AlKaabi, George P. Patrinos, Bassam R. Ali

Pharmacogenomics in Southeast Asia: an Explorative Study

Pharmacogenetic variants of 100 genes among Southeast Asian populations under the collaboration of SEAPharm network. Human Genome Variation, 2021.
By: Runcharoen C, Fukunaga K, Sensorn I, Iemwimangsa N, Klumsathian S, Tong H, Sy Vo N, Le L, Hlaing T M, Thant M, Zain S M, Mohamed Z, Capule F, Nevado Jr. J, Silao C L, Al-Mahayri Z, Ali B R, et al.

Genetics of a rare disorder “Cutis Laxa”

Genotype-phenotype spectrum of PYCR1-related autosomal recessive cutis laxa. Molecular Genetics and Metabolism. November 2013
By: Dimpopoulou A, Fischer B, Gardeitchik T, Schröter P, Kayserili H, Schlack C, Li Y, Brum J, Barisic I, Castori M, Spaich C, Fletcher E, Mahayri Z, et al.

Genetics of Azoospermia

High prevalence of genetic abnormalities in Middle Eastern patients with idiopathic non-obstructive azoospermia. Journal of Assisted Reproduction and Genetics. 2013, 30(6)799
By: Halabi M., Kenj M., Monem F., Mahayri Z., Abou AlChamat G. & Madania A.

Congenital Deafness in Syria

Study of GJB2 Gene Mutations in Syrians with Hearing Loss: High frequency of consanguinity and limited concern of genetic tests. SCLA, 2013, 6(8) [Arabic]
By: Mahayri Z. & Monem F.

Cytogenetic tests in Syria

A Review of 1125 cases referred for cytogenetic analysis in Syria. Middle East Journal of Human Genetics. January 2012, 1 (1):35-43 https://oce.ovid.com/article/01607934-201201000-00006/HTML
By: Mahayri Z. & Monem F.