Hiba Alblooshi

United Arab Emirates University — AE

Medicine · Health Sciences

6h-index130citations26works1.92yr avg
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Research Topics

Substance Abuse Treatment and Outcomes(4), Genomics and Rare Diseases(3), Neurotransmitter Receptor Influence on Behavior(2), Genetic Associations and Epidemiology(2), Systemic Lupus Erythematosus Research(2)

Publications26 total

Response to Letter to the Editor
Human Genomics·2026Open Access
Correction: A novel LACC1 variant c.658G > A (p.Asp220Asn) in familial juvenile arthritis: identification and functional analysis
Human Genomics·2025Open Access
The impact of familial autoimmunity and familial lupus on the clinical presentations and disease outcomes of SLE patients in the United Arab Emirates
BMC Rheumatology·2025Open Access
Comparison of machine learning models for mucopolysaccharidosis early diagnosis using UAE medical records
Scientific Reports·2025Open Access
A novel LACC1 variant c.658G>A (p. Asp220Asn) in familial juvenile arthritis: identification and functional analysis
Human Genomics·2025· 4 citedOpen Access
Emerging Trends and Research Hotspots in Inborn Error of Immunity: A Bibliometric Perspective
Journal of Human Immunity·2025Open Access
Clinical Features of Families with a Novel Pathogenic Mutation in Sepiapterin Reductase
International Journal of Molecular Sciences·2025Open Access
Identification and functional characterisation of a novel DNASE1L3 variant (c.572A>G, p.Asn191Ser) in three Emirati families with systemic lupus erythematosus and hypocomplementaemic urticarial vasculitis
Lupus Science & Medicine·2025· 1 citedOpen Access
A Novel Nonsense Homozygous Mutation in <I>SMARCD2</I> Gene Causing Specific Granulocyte Deficiency Type 2: Case Report
International Journal of Immunology·2024Open Access
Profiling genetic variants in cardiovascular disease genes among a Heterogeneous cohort of Mendelian conditions patients and electronic health records
Frontiers in Molecular Biosciences·2024· 3 citedOpen Access
A Comparison of Machine Learning Models for Mucopolysaccharidosis Early Diagnosis: A Retrospective Cohort Study using UAE SEHA Electronic Medical Records
2024Open Access
OP0055 LACC1 MUTATION IN MULTIPLE CONSANGUINEOUS FAMILIES CAUSING REFRACTORY JUVENILE IDIOPATHIC ARTHRITIS
Annals of the Rheumatic Diseases·2024· 1 cited
Spectrum of genetic variants in bilateral sensorineural hearing loss
Frontiers in Genetics·2024· 6 citedOpen Access
Utilizing Pharmacogenomic Data for a Safer Use of Statins among theEmirati Population
Current Vascular Pharmacology·2024· 6 cited
Utilizing machine learning for survival analysis to identify risk factors for COVID-19 intensive care unit admission: A retrospective cohort study from the United Arab Emirates
PLoS ONE·2024· 3 citedOpen Access
The diversity and clinical implications of genetic variants influencing clopidogrel bioactivation and response in the Emirati population
Human Genomics·2024· 7 citedOpen Access
Case report: Birk–Landau–Perez syndrome linked to the SLC30A9 gene—identification of additional cases and expansion of the phenotypic spectrum
Frontiers in Genetics·2023· 3 citedOpen Access
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 analysis
Frontiers in Pediatrics·2023· 2 citedOpen Access
OP0292 MUTATIONS IN DNASE1L3 CAUSING FAMILIAL HYPOCOMPLEMENTEMIC URTICARIAL VASCULITIS AND EARLY ONSET SYSTEMIC LUPUS ERYTHEMATOSUS
Annals of the Rheumatic Diseases·2023· 2 citedOpen Access
Lupus nephritis: A focus on the United Arab Emirates and the potential role of genetics
Lupus·2022· 4 cited
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Frequent Co-authors

Mohammed Tabouni(9), Ibrahim Baydoun(9), Najla Aljaberi(8), Praseetha Kizhakkedath(7), Mushal Allam(6), Gary Kenneth Hulse(4), Ahmed El Kashef(4), Mansour Shawky(4), Hamad Al Ghaferi(4), Habiba Al Safar(4), Guan K. Tay(4), Fatma Al‐Jasmi(4), Anand Bharathan(4), Fatma Al‐Jasmi(4), Bassam R. Ali(3), Anne John(3), Noor Mustafa(3), E A Mohammed(3), Aamna AlShehhi(3), Taleb M. Almansoori(3)