10 Jan 2026
Identification of Novel and Known Variants in Epigenetic Genes Associated with Syndromic 46,XY Differences of Sex Development among Moroccan PatientsPublisher siteSexual Development, Sexual Differentiation and Disorders
Active, last published 2026
In hearing, cochlea, tinnitus, genetics
Redouane
Boulouiz
Scholar“Research focused on Hearing, Cochlea, Tinnitus, Genetics and adjacent fields.”
Mohamed I University
Morocco
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723
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01 · About the work
What I study
edouane Boulouiz is a researcher working on Hearing, Cochlea, Tinnitus, Genetics. A fuller summary will appear once they update their profile.
02 · Reach
Publication output and reach
Redouane's work has been cited 723 times across 4 active years. Bars show publications per year; the line shows cumulative citation totals across publications first appearing in each year.
03 · Research focus
Topics
Hearing, Cochlea, Tinnitus, Genetics×16Vestibular and auditory disorders×7Connexins and lens biology×6Genomics and Rare Diseases×6Global Cancer Incidence and Screening×5
04 · Where I am
Affiliations
Affiliation on published researchMohamed I University, MoroccoDrawn from the institution listed on this researcher’s published work.
Research themes (UN SDGs)
05 · Selected work
Recent publications
10 works1 Dec 2025Open access
Utility of liquid biopsy for EGFR mutation testing in lung adenocarcinoma in a resource-limited settingPublisher siteLabMed discovery., Lung Cancer Treatments and Mutations
12 Jun 2025Open access
Identification of the Genetic Causes of Inherited Diseases in a North African Biobank: Implications for Genetic DiagnosisPublisher siteMolecular Syndromology, Genomics and Rare Diseases
8 Feb 20252cites
Clinical and Molecular Spectrum of Wilson Disease in the Arab World: A Systematic ReviewPublisher siteBiochemical Genetics, Trace Elements in Health
6 Nov 20241cites
Carrier frequency and molecular basis of hemoglobinopathies among blood donors in eastern Morocco: Implications for blood donation and genetic diagnosisPublisher siteClinical Biochemistry, Hemoglobinopathies and Related Disorders
6 Oct 2024Open access
JAK2 mutational status and the contribution of TERT and JAK2 polymorphisms to the occurrence of myeloproliferative neoplasms in Eastern MoroccoPublisher siteAfrican Health Sciences, Myeloproliferative Neoplasms: Diagnosis and Treatment
22 Jan 2024Open access3cites
First report on chromosomal abnormalities in Eastern Morocco: Identification of a new case of a de novo partial trisomy 13q using single-nucleotide polymorphism arrayPublisher siteArchives de Pédiatrie, Genomic variations and chromosomal abnormalities
29 Sept 2023Open access6cites
Triple-A Syndrome in Morocco: Founder Effect, Age Estimation of the <i>AAAS</i> c.1331+1G&gt;A Variant, and Implications for Genetic DiagnosisPublisher siteMolecular Syndromology, Complement system in diseases
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