Home › Researcher directory › Hela Sassi
Hela Sassi
Affiliation : Habib hospital Thameur · Tunis El Manar University
- 15Publications (affiliation in Tunisia)
- 28Total publications
- 109Citations
- 6h-index
Research profile
Hela Sassi has 15 indexed publications (2019–2023). Their work appears mainly in “Acta Ophthalmologica”, “Clinical Rheumatology” and “Journal of Pediatric Endocrinology and Metabolism”. Their most cited article, “Quantitative Analysis of Microvascular Network with Optical Coherence Tomography Angiography and Its Correlation with Visual Acuity in Retin” (2021), has been cited 20 times. 13 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers.
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Create my free profile Add my publicationsResearch areas
- BRCA gene mutations in cancer
- Retinal Diseases and Treatments
- Genomics and Rare Diseases
- Cancer Genomics and Diagnostics
- Ocular Diseases and Behçet’s Syndrome
Publications (15)
- Turner Syndrome: results of the first Tunisian study group on Turner Syndrome (TuSGOT)
- Li–Fraumeni syndrome in Tunisian carriers with different and rare tumor phenotype: genotype–phenotype correlation
- Choroidal vascularity index: An emerging useful metric for choroidal structure assessment in pachychoroid spectrum disease
- Central serous chorioretinopathy complicated by neovascularization following panretinal photocoagulation for diabetic retinopathy
- Uveal effusion after trabeculectomy: Management challenges
- Multimodal imaging features in chorioretinitis sclopetaria
- Swept source optical coherence tomography and optical coherence tomography angiography for diagnosis and follow‐up of type 2 macular telangiectasia
- Optical coherence tomography angiography findings in patients with essential hypertension
- Quantitative Analysis of Microvascular Network with Optical Coherence Tomography Angiography and Its Correlation with Visual Acuity in Retinal Vein Occlusion
- Beckwith–Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature
- JAK2 p.(V617F) mutation in Tunisian myeloproliferative neoplasms and its genotype-phenotype correlation.
- Multinodular scleritis in a patient with rheumatoid arthritis
- Identification of Novel BRCA1 Germline Deleterious Variant Among a Tunisian Family
- Skeletal phenotype/genotype in progressive pseudorheumatoid chondrodysplasia
- Granular type I corneal dystrophy in a large consanguineous Tunisian family with homozygous p.R124S mutation in theTGFBIgene
Publication venues
- Acta Ophthalmologica × 6
- Clinical Rheumatology × 2
- Journal of Pediatric Endocrinology and Metabolism × 1
- BMC Medical Genomics × 1
- Journal of Current Ophthalmology × 1
- Molecular Genetics & Genomic Medicine × 1
Publications per year
- 20231
- 20227
- 20215
- 20192
Collaborations
Partner institutions : Faculté de médecine de Tunis · Tunis University · Hôpital Mongi Slim · Institut Pasteur de Tunis · Hôpital Charles-Nicolle
Co-authors
- Monia Cheour
- M. Ouederni
- Slim Nouri
- Ridha Mrad
- Samia Hannachi
- Yosra Abid
- Rym Meddeb
- Syrine Hizem
- Yasmina Elaribi
- Lamia Ben Jemâa
- Neïla Belguith
- Safa Ben Aoun
Bibliographic data from OpenAlex (open database).
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