Author

Lihadh Al‐Gazali

United Arab Emirates UniversityORCID 0000-0003-2029-2218Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Approach:benchmark study· 1 Research Focus:database / resource· 1 Research Focus:deconvolution· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1

Frequent Co-Authors

Agness GidnaiD· 1 shared Aisha Mohamed Saeed Mohamed Al Shamsi· 1 shared Alexandria T.M. BlackburniD· 1 shared Amandus Kwekason· 1 shared Angela E. ScheuerleiD· 1 shared Angela KabiruiD· 1 shared Ann Marie LawsoniD· 1 shared Asha Deepthi· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

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1 shared paperGenetics

Agness GidnaORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicineFrontiers in GeneticsPeer-reviewedMay 4, 2023

Spectrum of Genetic Disorders and Gene Variants in the United Arab Emirates National Population: Insights from the CTGA Database

Sami Bizzari, Pratibha Nair, Sayeeda Hana…·Stephany El‐Hayek

The paper analyzes genetic disorders and variants in Emiratis using the CTGA database, highlighting high prevalence of rare, Mendelian conditions and discrepancies in variant classification.

19 citations

humanGWAS summary statistics

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GeneticsbioRxivPreprintJul 10, 2022

The Entwined African and Asian Genetic Roots of the Medieval Peoples of the Swahili Coast

Esther S. Brielle, Jeffrey Fleisher, Stephanie Wynne‐Jones…·Chapurukha M. Kusimba

This study analyzes ancient DNA from the Swahili coast to trace genetic admixture between African and Asian populations over time.

42 citations

humanDNA methylation

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GeneticsGenetics in MedicinePeer-reviewedJul 1, 2019

DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract

Alexandria T.M. Blackburn, Nasim Bekheirnia, Vanessa C. Uma…·Mir Reza Bekheirnia

The paper investigates congenital kidney and urinary tract anomalies and genital defects in DYRK1A mutation carriers, showing DYRK1A's role in genitourinary development through Xenopus studies.

34 citationstop 4%

mousewhole-exome sequencing

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