Author

Nesrine Kerkeni

Institutions: Tunis University, Hôpital Charles-Nicolle, Hôpital Charles-Nicolle, Faculté de médecine de Tunis, Tunis El Manar University

Observed institutions: Tunis University, Hôpital Charles-Nicolle, Hôpital Charles-Nicolle, Faculté de médecine de Tunis, Tunis El Manar University

ORCID: 0000-0002-8074-3052

Observed ORCID: 0000-0002-8074-3052

OpenAlex ID: A5067597375

Genome Tunisia Project: paving the way for precision medicine in North Africa

2024 · Yosr Hamdi, Mediha Trabelsi, et al. · Genome Medicine · 16

JNK Inhibition Overcomes Resistance of Metastatic Tetraploid Cancer Cells to Irradiation-Induced Apoptosis

2025 · Mohamed Jemaà, Nouha Setti Boubaker, et al. · International Journal of Molecular Sciences · 8

Novel RAB3GAP1 Mutation in the First Tunisian Family With Warburg Micro Syndrome

2022 · Nesrine Kerkeni, Maher Kharrat, et al. · Journal of Clinical Neurology · 6

First Detection of 1p36 Deletion by Whole‐Exome Sequencing in a Tunisian Patient

2026 · Nesrine Kerkeni, Maher Kharrat, et al. · Birth Defects Research · 2

Genetic characterization of Glanzmann thrombasthenia: insights from novel igta2b mutations in a Tunisian patient cohort

2026 · Hajer Elmahmoudi, Nesrine Kerkeni, et al. · Blood Coagulation & Fibrinolysis

P20- Une seule mutation ... plusieurs phenotypes ...

2016 · Nesrine Kerkeni, Faouzi Mâazoul, et al.

Works count: 6

Citation count: 32

H-index: 3

I10-index: 1