19 Apr 2026
Clinical and molecular spectrum of primary hyperoxaluria type 1 in Tunisia: pediatric presentation and minimum observed prevalencePublisher sitePediatric Nephrology, Kidney Stones and Urolithiasis Treatments
UniversitiesAhlem Achour
Active, last published 2026
Ahlem
Achour
Scholar“Research profile drawn from open scholarly records.”
Hôpital Charles-Nicolle
Claim Your Profile2
H-index
17
Citations
Ahlem has not officially claimed their profile. If you are Ahlem, claim it free.
Claim Your Profile
Pioneer
LOCKED
Pathfinder
LOCKED
Scholar
EARNED
Innovator
LOCKED
Inventor
LOCKED
Catalyst
LOCKED
Expert
UPGRADE
01 · About the work
What I study
research summary for Ahlem Achour will appear here once their profile is updated.
02 · Reach
Publication output and reach
Ahlem's work has been cited 17 times across 4 active years. Bars show publications per year; the line shows cumulative citation totals across publications first appearing in each year.
04 · Where I am
Affiliations
Affiliation on published researchHôpital Charles-NicolleDrawn from the institution listed on this researcher’s published work.
Research themes (UN SDGs)
05 · Selected work
Recent publications
9 works1 Jan 2026Open access
First Detection of 1p36 Deletion by Whole‐Exome Sequencing in a Tunisian PatientPublisher siteBirth Defects Research, Genomic variations and chromosomal abnormalities
4 Mar 2025Open access2cites
Unusual Causes of β Thalassemia Trait: Discovery of another Three Novel <i>SUPT5H</i> VariantsPublisher siteHemoglobin, Hemoglobinopathies and Related Disorders
23 Oct 20241cites
Automated Recognition of Cattle's Breed Through Computer Vision: A Case Study on the Oulmes-Zaer BreedPublisher site26 Aug 2024Open access10cites
Genome Tunisia Project: paving the way for precision medicine in North AfricaPublisher siteGenome Medicine, Genomics and Rare Diseases
14 Aug 2024
Genetic study of Alport syndrome in TunisiaPublisher sitePediatric Nephrology, Cell Adhesion Molecules Research
30 May 2024Open access2cites
Moderate–severe beta‐thalassemia intermedia phenotype caused by sextuplicated alpha‐globin gene allele in two beta‐thalassemia carriersPublisher siteAmerican Journal of Hematology, Hemoglobinopathies and Related Disorders
28 Nov 2023Open access
Inversion of the Frequencies of Autosomal Recessive and X-Linked Dominant Forms of Alport Syndrome in the Tunisian PopulationPublisher siteResearch Square, Cell Adhesion Molecules Research
Expert Academic Profiles go further
Citation trend analytics, exportable publication records, and direct enquiry routing from industry and funders.
Are you Ahlem?
Claim it to verify your details, connect with industry partners, and explore Fractional Domain Expert opportunities through MARATTO™.
African researchers are full of potential that too often goes unrecognised. Your MARATTO™ profile gives your work the commercial pathway it deserves.
Claim Your Profile
Free to claim · takes a minute to verify it’s you