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 global cancer incidence and screening
Manal Elidrissi
Errahhali
Scholar“Research focused on Global Cancer Incidence and Screening and adjacent fields.”
Mohamed I University
Morocco
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187
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01 · About the work
What I study
anal Elidrissi Errahhali is a researcher working on Global Cancer Incidence and Screening. A fuller summary will appear once they update their profile.
02 · Reach
Publication output and reach
Manal's work has been cited 187 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
Global Cancer Incidence and Screening×5Genomics and Rare Diseases×3Multiple and Secondary Primary Cancers×3Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities×2Blood groups and transfusion×2
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
6 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
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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