Salem Abbès

1.9k total citations
69 papers, 1.4k citations indexed

About

Salem Abbès is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Salem Abbès has authored 69 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Genetics, 29 papers in Hematology and 23 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Salem Abbès's work include Hemoglobinopathies and Related Disorders (32 papers), Neonatal Health and Biochemistry (20 papers) and Erythrocyte Function and Pathophysiology (20 papers). Salem Abbès is often cited by papers focused on Hemoglobinopathies and Related Disorders (32 papers), Neonatal Health and Biochemistry (20 papers) and Erythrocyte Function and Pathophysiology (20 papers). Salem Abbès collaborates with scholars based in Tunisia, France and Germany. Salem Abbès's co-authors include Ghada Bouguerra, Florian Läng, Rosi Bissinger, Anthi Drousiotou, Anna Piro, Andrew G. Clark, Mark Stoneking, Jacques Loiselet, Scott M. Williams and Sarah A. Tishkoff and has published in prestigious journals such as Science, Oncotarget and Journal of Medical Genetics.

In The Last Decade

Salem Abbès

67 papers receiving 1.4k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Salem Abbès Tunisia	20	492	401	386	350	326	69	1.4k
G. Modiano Italy	20	176 0.4×	120 0.3×	324 0.8×	337 1.0×	179 0.5×	69	1.4k
P. Sistonen Finland	25	351 0.7×	88 0.2×	643 1.7×	144 0.4×	111 0.3×	52	2.2k
Corinne D. Boehm United States	22	295 0.6×	101 0.3×	1.4k 3.6×	1.6k 4.6×	470 1.4×	38	3.3k
Anthi Drousiotou Cyprus	14	188 0.4×	76 0.2×	465 1.2×	159 0.5×	150 0.5×	47	1.1k
Sabine Kupzig United Kingdom	16	286 0.6×	84 0.2×	735 1.9×	83 0.2×	45 0.1×	24	1.4k
D S Anson Australia	23	698 1.4×	59 0.1×	875 2.3×	189 0.5×	28 0.1×	35	1.8k
Michał Witt Poland	25	66 0.1×	607 1.5×	690 1.8×	81 0.2×	158 0.5×	87	1.7k
P. Meera Khan Netherlands	23	138 0.3×	66 0.2×	950 2.5×	163 0.5×	93 0.3×	66	1.9k
Luı́sa Romão Portugal	24	82 0.2×	72 0.2×	1.4k 3.6×	344 1.0×	93 0.3×	56	1.9k
Emilie H. Mules United States	19	337 0.7×	57 0.1×	825 2.1×	57 0.2×	63 0.2×	29	1.6k

Countries citing papers authored by Salem Abbès

Since Specialization

Citations

This map shows the geographic impact of Salem Abbès's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Salem Abbès with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Salem Abbès more than expected).

Fields of papers citing papers by Salem Abbès

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Salem Abbès. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Salem Abbès. The network helps show where Salem Abbès may publish in the future.

Co-authorship network of co-authors of Salem Abbès

This figure shows the co-authorship network connecting the top 25 collaborators of Salem Abbès. A scholar is included among the top collaborators of Salem Abbès based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Salem Abbès. Salem Abbès is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Halim, Nizar Ben, et al.. (2025). Cord Blood-Based Neonatal Screening for Hemoglobinopathies in Northern Tunisia. International Journal of Neonatal Screening. 11(4). 107–107.

Abbès, Salem, et al.. (2019). EZH2, new diagnosis and prognosis marker in acute myeloid leukemia patients. Advances in Medical Sciences. 64(2). 395–401. 18 indexed citations

Youssef, Yosra Ben, et al.. (2017). Molecular study of ABCB1 gene and its correlation with imatinib response in chronic myeloid leukemia. Cancer Chemotherapy and Pharmacology. 80(4). 829–839. 14 indexed citations

Ammar, Slim Ben, et al.. (2016). Genetic link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1.. PubMed. 21(2). 121–5. 2 indexed citations

Bouguerra, Ghada, et al.. (2016). Regulatory network analysis of microRNAs and genes in imatinib-resistant chronic myeloid leukemia. Functional & Integrative Genomics. 17(2-3). 263–277. 7 indexed citations

Ouerhani, Slah, et al.. (2016). Association of genetic variation inIKZF1, ARID5B, CDKN2A, andCEBPEwith the risk of acute lymphoblastic leukemia in Tunisian children and their contribution to racial differences in leukemia incidence. Pediatric Hematology and Oncology. 33(3). 157–167. 20 indexed citations

Talhaoui, Ibtissam, Xénia Cabagnols, Véronique Della Valle, et al.. (2016). TET2-mediated 5-hydroxymethylcytosine induces genetic instability and mutagenesis. DNA repair. 43. 78–88. 23 indexed citations

Abbès, Salem, et al.. (2015). rs11886868 and rs4671393 ofBCL11Aassociated with HbF level variation and modulate clinical events among sickle cell anemia patients. Hematology. 430666719–430666719. 1 indexed citations

Abbès, Salem, et al.. (2015). Gilbert syndrome acts as a risk factor of developing gallstone among β hemoglobinopathy Tunisian patients.. PubMed. 93(4). 237–41. 3 indexed citations

10.

Bissinger, Rosi, et al.. (2015). Triggering of Suicidal Erythrocyte Death by Topotecan. Cellular Physiology and Biochemistry. 37(4). 1607–1618. 50 indexed citations

11.

Bouguerra, Ghada, Rosi Bissinger, Salem Abbès, & Florian Läng. (2015). Zopolrestat Induced Suicidal Death of Human Erythrocytes. Cellular Physiology and Biochemistry. 37(4). 1537–1546. 38 indexed citations

12.

Bissinger, Rosi, et al.. (2015). Saquinavir Induced Suicidal Death of Human Erythrocytes. Cellular Physiology and Biochemistry. 37(5). 1973–1982. 47 indexed citations

13.

Mellouli, Fethi, et al.. (2015). Fetal Hemoglobin in Tunisian Sickle Cell Disease Patient: Relationship with Polymorphic Sequences Cis to the β-Globin Gene. Indian Journal of Hematology and Blood Transfusion. 32(1). 114–119. 4 indexed citations

14.

Ouerhani, Slah, et al.. (2014). Polymorphisms in XPC, XPD and XPG DNA repair genes and leukemia risk in a Tunisian population. Leukemia & lymphoma. 56(6). 1856–1862. 17 indexed citations

15.

Ouerhani, Slah, et al.. (2013). The prevalence and prognostic significance of KRAS mutation in bladder cancer, chronic myeloid leukemia and colorectal cancer. Molecular Biology Reports. 40(6). 4109–4114. 29 indexed citations

16.

Ouerhani, Slah, et al.. (2012). KIT mutation detection in Tunisian patients with newly diagnosed myelogenous leukemia: prevalence and prognostic significance. Cancer Genetics. 205(9). 436–441. 3 indexed citations

17.

Abbès, Salem, et al.. (2011). Molecular characterization of a discrete hemoglobinopathy upon investigation for a lung hydatic cyst in an old Tunisian patient. Annales de biologie clinique. 69(3). 353–356. 1 indexed citations

18.

Préhu, Claude, et al.. (2008). Molecular characterization of erythrocyte glucose-6-phosphate dehydrogenase deficiency in Tunisia. Pathologie Biologie. 56(5). 260–267. 19 indexed citations

19.

Harteveld, Cornelis L., et al.. (2003). Frequency and spectrum of hemochromatosis mutations in Tunisia. The Hematology Journal. 4(6). 433–435. 13 indexed citations

20.

Abbès, Salem, J. Louvel, M Lamarche, & R. Pumain. (1991). Laminar analysis of the origin of the various components of evoked potentials in slices of rat sensorimotor cortex. Electroencephalography and Clinical Neurophysiology/Evoked Potentials Section. 80(4). 310–320. 13 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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