Conserved genes regulating human sex differentiation, gametogenesis and fertilization by Khalid A. Fakhro (3158862)

Copy number variations in the genome of the Qatari population by Khalid A. Fakhro (3158862)

Clinical, Genetic and Functional Characterization of a Novel AVPR2 Missense Mutation in a Woman with X-Linked Recessive Nephrogenic Diabetes Insipidus by Senthil Selvaraj (314873)

Other Authors:

Reading between the (Genetic) Lines: How Epigenetics is Unlocking Novel Therapies for Type 1 Diabetes by Ammira-Sarah AL-Shabeeb Akil (18949477)

Other Authors:

Diagnosis and treatment of type 1 diabetes at the dawn of the personalized medicine era by Ammira Al-Shabeeb Akil (15143925)

Other Authors:

Ethnic-specific association of amylase gene copy number with adiposity traits in a large Middle Eastern biobank by Niccolo’ Rossi (14152692)

Other Authors:

PGAP3 Associated with Hyperphosphatasia with Mental Retardation Plays a Novel Role in Brain Morphogenesis and Neuronal Wiring at Early Development by Sahar I. Da’as (9631717)

Other Authors:

Deciphering the complex interplay of obesity, epithelial barrier dysfunction, and tight junction remodeling: Unraveling potential therapeutic avenues by Sara K. AlMarzooqi (18767743)

Other Authors:

Validation of plasma protein glycation and oxidation biomarkers for the diagnosis of autism by Aisha Nasser J. M. Al-Saei (17885957)

Other Authors:

Patterns and distribution of de novo mutations in multiplex Middle Eastern families by Muhammad Kohailan (748774)

Other Authors:

A Complex Intrachromosomal Rearrangement Disrupting <i>IRF6 </i>in a Family with Popliteal Pterygium and Van der Woude Syndromes by Alya A. Al-Kurbi (18324927)

Other Authors:

A loss-of-function AGTR1 variant in a critically-ill infant with renal tubular dysgenesis: case presentation and literature review by Aljazi Al-Maraghi (14056975)

Other Authors:

The link between glycemic control measures and eye microvascular complications in a clinical cohort of type 2 diabetes with microRNA-223-3p signature by Sahar I. Da’as (9631717)

Other Authors:

A GHRHR founder mutation causes isolated growth hormone deficiency type IV in a consanguineous Pakistani family by Safeer Ahmad (9079257)

Other Authors:

Transcriptome Profile Identifies Actin as an Essential Regulator of Cardiac Myosin Binding Protein C3 Hypertrophic Cardiomyopathy in a Zebrafish Model by Sahar Isa Da’as (18288880)

Other Authors:

The immune landscape of solid pediatric tumors by Shimaa Sherif (12862990)

Other Authors:

Assessing the genetic burden of familial hypercholesterolemia in a large middle eastern biobank by Geethanjali Devadoss Gandhi (14056966)

Other Authors:

Willingness to participate in genome testing: a survey of public attitudes from Qatar by Hanan F. Abdul Rahim (9330201)

Other Authors:

Integrating Genome Sequencing and Untargeted Metabolomics in Monozygotic Twins with a Rare Complex Neurological Disorder by Rulan Shaath (17112852)

Other Authors:

Genomic architecture of autism spectrum disorder in Qatar: The BARAKA-Qatar Study by Mona Abdi (10196665)

Other Authors: