Author

Salem Abbes

Observed name: Abbes Salem

Institutions: Tunis University, Institut Pasteur de Tunis, Tunis El Manar University

Observed institutions: Tunis University, Hôpital La Rabta, Institut Pasteur de Tunis, Faculté de médecine de Tunis, Tunis El Manar University, University of Gezira

OpenAlex ID: A5103754417

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

Restriction mapping of βS locus among tunisian sickle‐cell patients

2011 · Moumni Imen, Ben Mansour Mosbehi Ikbel, et al. · American Journal of Human Biology · 14

Hb S [β6(A3)Glu→Val, GAG>GTG] and β-Globin Gene Cluster Haplotype Distribution in Mauritania

2012 · Fatimetou M. Veten, Isselmou O. Abdelhamid, et al. · Hemoglobin · 13

Hb H Disease Among Tunisians: Molecular Characterization of α‐Thalassemia Determinants and Hematological Findings

2003 · Amine Zorai, Salem Abbes, et al. · Hemoglobin · 11

The role of rs1984112_G atCD36gene in increasing reticulocyte level among sickle cell disease patients

2016 · Miniar Kalai, Marwa Dridi, et al. · Hematology · 10

Two new β+‐thalassemia mutation [β ‐56 (G → C); HBBc. −106 G → C] and [β −83 (G → A); HBBc. −133 G → A] described among the Tunisian population

2015 · Kais Douzi, Imen Moumni, et al. · American Journal of Human Biology · 6

Hb A2-Pasteur-Tunis [δ59(E3)Lys→Asn, AAG→AAC]: A New δ Chain Variant Detected by DNA Sequencing in a Tunisian Carrier of the Codon 39 (C→T) β0-Thalassemia Mutation

2007 · Imen Moumni, Amine Zorai, et al. · Hemoglobin · 6

New Deletion at Promoter of HBG1 Gene in Sickle Cell Disease Patients With High HbF Level

2019 · Leila Chaouch, Houssem Sellami, et al. · Journal of Pediatric Hematology/Oncology · 5

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

A New δ Chain Variant, Hb A2-Tunis [δ46(CD5)Gly → Glu;HBD: c.140G>A], Observed in a Tunisian Family in Association with a Compound Heterozygosity for Hb C [β6(A3)Glu → Lys;HBB: c.19G>A] β0-Thalassemia [IVS-I-1 (β143, G>A);HBB: c.92+1G>A]

2014 · Imen Moumni, Amine Zorai, et al. · Hemoglobin · 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

Phenotypic and molecular genetic analysis of Pyruvate Kinase deficiency in a Tunisian family

2015 · Jaouani Mouna, Hamdi Nadia, et al. · Egyptian Journal of Medical Human Genetics · 2

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

Novel mutations in Uridyl-diphosphate-glucuronosyl-transferase 1A1 (UGT1A1) gene in Tunisian patients with unconjugated hyperbilirubinemia

2021 · Nawel Trabelsi, Leila Chaouch, et al. · European Journal of Medical Genetics · 1

Works count: 14

Citation count: 114

H-index: 6

I10-index: 5