Get started
Author

Houyem Ouragini

Observed names: H Ouragini, H. Ouragini, Ouragini Houyem
ORCID: 0000-0003-2427-2804
Observed ORCID: 0000-0003-2427-2804
OpenAlex ID: A5018246144
High frequency of the V548A fs X572 XPC mutation in Tunisia: implication for molecular diagnosis
2009 · M Ben Rekaya, O Messaoud, et al. · Journal of Human Genetics · 55
Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss
2013 · Zied Riahi, Hassen Hammami, et al. · Gene · 36
Abstracts from the 3rd International Genomic Medicine Conference (3rd IGMC 2015): Jeddah, Kingdom of Saudi Arabia. 30 November - 3 December 2015
2016 · Jerry W. Shay, Noriko Homma, et al. · BMC Genomics · 34
PDF
Differential impact of consanguineous marriages on autosomal recessive diseases in T unisia
2015 · Nizar Ben Halim, Sana Hsouna, et al. · American Journal of Human Biology · 33
rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients
2015 · Leila Chaouch, Imen Moumni, et al. · Hematology · 24
PDF
Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity
2011 · O. Messaoud, M. Ben Rekaya, et al. · Archives of Dermatological Research · 24
Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 gene
2010 · Farah Ouechtati, Ahlem Merdassi, et al. · Journal of Human Genetics · 20
PDF
Dystrophic epidermolysis bullosa phenotypes in a large consanguineous Tunisian family
2009 · Houyem Ouragini, Faïka Cherif, et al. · Journal of Dermatological Science · 12
The role of rs1984112_G atCD36gene in increasing reticulocyte level among sickle cell disease patients
2016 · Miniar Kalai, Marwa Dridi, et al. · Hematology · 10
PDF
Clinical and Genetic Investigation of Atrial Septal Defect with Atrioventricular Conduction Defect in a Large Consanguineous Tunisian Family
2008 · Sonia Nouira, Ikram Kamoun, et al. · Archives of Medical Research · 8
Haplotypic classification of dystrophic epidermolysis bullosa in Tunisian consanguineous families: implication for diagnosis
2008 · Houyem Ouragini, Faïka Cherif, et al. · Archives of Dermatological Research · 7
Genetic analysis of hereditary multiple exostoses in Tunisian families: a novel frame-shift mutation in the EXT1 gene
2008 · Sana Sfar, Abderrazak Abid, et al. · Molecular Biology Reports · 7
Mutational founder effect in recessive dystrophic epidermolysis bullosa families from Southern Tunisia
2013 · Ahlem Sabrine Ben Brick, Nadia Laroussi, et al. · Archives of Dermatological Research · 6
Mutational survey of recessive dystrophic epidermolysis bullosa in Tunisian families unveils a spectrum of private, ethnic specific and world wide recurrent mutations
2010 · Houyem Ouragini, Faïka Cherif, et al. · Journal of Dermatological Science · 6
Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert’s Syndrome
2017 · Faten Haddad, Nawel Trabelsi, et al. · Hemoglobin · 5
Cord Blood-Based Neonatal Screening for Hemoglobinopathies in Northern Tunisia
2025 · Houyem Ouragini, Nizar Ben Halim, et al. · International Journal of Neonatal Screening · 4
PDF
Coinheritance of HbO Arab/β0-thalassemia with Severe Manifestation in Newborn
2022 · Miniar Kalai, Imen Moumni, et al. · American Journal of Perinatology · 4
Identification of two novel variants in PRKAG2 gene in Tunisian type 2 diabetic patients with family history of cardiovascular disease
2009 · S. Nouira, I. Arfa, et al. · Diabetes Research and Clinical Practice · 4
Genetic basis of dominant dystrophic epidermolysis bullosa in tunisian families and co‐occurrence of dominant and recessive mutations
2014 · A.S. Ben Brick, N. Laroussi, et al. · Journal of the European Academy of Dermatology and Venereology · 3
Rapid and inexpensive detection of common HBB gene mutations in Tunisian population by high-resolution melting analysis: Implication for molecular diagnosis
2013 · Houyem Ouragini, Faten Haddad, et al. · Hematology · 3
PDF
PHINDaccess Hackathons for COVID‐19 and Host‐Pathogen Interaction: Lessons Learned and Recommendations for Low‐ and Middle‐Income Countries
2023 · Kais Ghedira, Hamza Dallali, et al. · BioMed Research International · 2
PDF
Tunisian Newborn's Cord Blood: Reference Values of Complete Blood Count and Hemoglobin Fractions
2020 · Sana Zitouni, Emna Bouatrous, et al. · American Journal of Perinatology · 2
The Role of Precision Medicine in Sickle Cell Disease
2025 · Kais Ghedira, Houyem Ouragini, et al. · Springer eBooks · 1
PDF
First Observation of HbM-Saskatoon at the Origin of Neonatal Cyanosis in a Tunisian Baby
2021 · Emna Bouatrous, Sonia Nouira, et al. · Journal of Pediatric Hematology/Oncology · 1
Clinical and genetic investigation of catecholaminergic polymorphic ventricular tachycardia in a consanguineous Tunisian family
2019 · Sonia Nouira, Sonia Chabrak, et al. · Acta cardiologica. Supplementum · 1
Works count: 40
Citation count: 314
H-index: 9
I10-index: 9
Year
Topic
Type