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 coccidia and coccidiosis research
Meryem
Ouarzane
Scholar“Research focused on Coccidia and coccidiosis research and adjacent fields.”
Mohamed I University
Morocco
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01 · About the work
What I study
eryem Ouarzane is a researcher working on Coccidia and coccidiosis research. A fuller summary will appear once they update their profile.
02 · Reach
Publication output and reach
Meryem's work has been cited 312 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
Coccidia and coccidiosis research×6Global Cancer Incidence and Screening×5Multiple and Secondary Primary Cancers×4Ethics in Clinical Research×3Genomics and Rare Diseases×3
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
7 works12 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 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
29 Jul 20234cites
A novel variant in BMPR1B causes acromesomelic dysplasia Grebe type in a consanguineous Moroccan family: Expanding the phenotypic and mutational spectrum of acromesomelic dysplasiasPublisher siteBone, Connective tissue disorders research
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