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United Arab Emirates University: Al Ain, AE

2020 to present | Research Associate (Department of Genetics and Genomics)
Employment
Source: Self-asserted source
Mohammed Tabouni

Works (6)

A Novel Nonsense Homozygous Mutation in <I>SMARCD2</I> Gene Causing Specific Granulocyte Deficiency Type 2: Case Report

International Journal of Immunology
2024-12-31 | Journal article
DOI: 10.11648/j.iji.20241204.11
Contributors: Amna Kuwaiti; Haifa Awadi; Praseetha Kizhakkedath; Ibrahim Baydoun; Mohammed Tabouni; Hiba Alblooshi; Fatma Al-Jasmi; Aisha Shamsi; Hiba Shendi
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Profiling genetic variants in cardiovascular disease genes among a Heterogeneous cohort of Mendelian conditions patients and electronic health records

Frontiers in Molecular Biosciences
2024-10-01 | Journal article
DOI: 10.3389/fmolb.2024.1451457
Part of ISSN: 2296-889X
Contributors: Nadia Akawi; Ghadeera Al Mansoori; Anwar Al Zaabi; Andrea Badics; Noura Al Dhaheri; Aisha Al Shamsi; Amal Al Tenaiji; Bashar Alzohily; Fatmah S. A. Almesmari; Hamad Al Hammadi et al.
Source: Self-asserted source
Mohammed Tabouni

Spectrum of genetic variants in bilateral sensorineural hearing loss

Frontiers in Genetics
2024-02-12 | Journal article
DOI: 10.3389/fgene.2024.1314535
Part of ISSN: 1664-8021
Contributors: Amanat Ali; Mohammed Tabouni; Praseetha Kizhakkedath; Ibrahim Baydoun; Mushal Allam; Anne John; Faiza Busafared; Ayesha Alnuaimi; Fatma Al-Jasmi; Hiba Alblooshi
Source: Self-asserted source
Mohammed Tabouni

Case report: Birk–Landau–Perez syndrome linked to the SLC30A9 gene—identification of additional cases and expansion of the phenotypic spectrum

Frontiers in Genetics
2023-07-27 | Journal article
DOI: 10.3389/fgene.2023.1219514
Part of ISSN: 1664-8021
Contributors: Praseetha Kizhakkedath; Watfa AlDhaheri; Ibrahim Baydoun; Mohammed Tabouni; Anne John; Taleb M. Almansoori; Saeed Al-Turki; Fatma Al-Jasmi; Hiba Alblooshi
Source: Self-asserted source
Mohammed Tabouni

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
2023-07-12 | Journal article
DOI: 10.3389/fped.2023.1183574
Part of ISSN: 2296-2360
Contributors: Feda E. Mohamed; Mohammad A. Ghattas; Taleb M. Almansoori; Mohammed Tabouni; Ibrahim Baydoun; Praseetha Kizhakkedath; Anne John; Hiba Alblooshi; Qudsia Shaukat; Fatma Al-Jasmi
Source: Self-asserted source
Mohammed Tabouni

Lupus nephritis: A focus on the United Arab Emirates and the potential role of genetics

Lupus
2022-10 | Journal article
DOI: 10.1177/09612033221122982
Part of ISSN: 0961-2033
Part of ISSN: 1477-0962
Contributors: Mohammed Tabouni; Amanat Ali; Najla Aljaberi; Hiba Alblooshi
Source: Self-asserted source
Mohammed Tabouni
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