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Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics|October 15, 2015
Scattering mean free path in continuous complex media: beyond the Helmholtz equationIbrahim Baydoun, Diego Baresch, Romain Pierrat, et al.
Physical Review. E|December 15, 2016
Radiative transfer of acoustic waves in continuous complex media: Beyond the Helmholtz equationIbrahim Baydoun, Diego Baresch, Romain Pierrat, et al.
Iscience|May 25, 2026
Gestational dysbiosis is associated with altered early-life microbial seeding and favors pathobiont expansion in offspringMohammed M Nakhal, Faheema Nafees, Ayishal B Mydeen, et al.
Human Genomics|July 27, 2025
A novel LACC1 variant c.658G>A (p. Asp220Asn) in familial juvenile arthritis: identification and functional analysisHiba Alblooshi, Noor Mustafa, Azeem Abdul Khalam, et al.
Frontiers in Genetics|August 14, 2023
Case report: Birk-Landau-Perez syndrome linked to the gene-identification of additional cases and expansion of the phenotypic spectrumPraseetha Kizhakkedath, Watfa AlDhaheri, Ibrahim Baydoun, et al.
Frontiers in Genetics|February 27, 2024
Spectrum of genetic variants in bilateral sensorineural hearing lossAmanat Ali, Mohammed Tabouni, Praseetha Kizhakkedath, et al.
Frontiers in Pediatrics|July 28, 2023
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 analysisFeda E Mohamed, Mohammad A Ghattas, Taleb M Almansoori, et al.
Lupus Science & Medicine|February 13, 2025
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 vasculitisNajla Aljaberi, Anjali Bharathan, Remya Prajesh Gopal, et al.
International Journal of Molecular Sciences|April 17, 2025
Clinical Features of Families with a Novel Pathogenic Mutation in Sepiapterin ReductaseFeda E Mohamed, Lara Alzyoud, Mohammad A Ghattas, et al.
Frontiers in Molecular Biosciences|October 16, 2024
Profiling genetic variants in cardiovascular disease genes among a Heterogeneous cohort of Mendelian conditions patients and electronic health recordsNadia Akawi, Ghadeera Al Mansoori, Anwar Al Zaabi, et al.
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