M. Benabadji

571 total citations
46 papers, 496 citations indexed

About

M. Benabadji is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, M. Benabadji has authored 46 papers receiving a total of 496 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 17 papers in Hematology and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in M. Benabadji's work include Hemoglobinopathies and Related Disorders (20 papers), Iron Metabolism and Disorders (10 papers) and Neonatal Health and Biochemistry (8 papers). M. Benabadji is often cited by papers focused on Hemoglobinopathies and Related Disorders (20 papers), Iron Metabolism and Disorders (10 papers) and Neonatal Health and Biochemistry (8 papers). M. Benabadji collaborates with scholars based in Algeria, France and United States. M. Benabadji's co-authors include Dominique Labie, Narla Mohandas, Yuichi Takakuwa, Gil Tchernia, M Rossi, G Trabuchet, C. Beldjord, Abderrezak Reghis, C. Sternberg and Alain Fischer and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Investigation and Blood.

In The Last Decade

M. Benabadji

45 papers receiving 457 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. Benabadji Algeria	12	213	194	118	117	100	46	496
DL Rucknagel United States	11	214 1.0×	124 0.6×	109 0.9×	169 1.4×	38 0.4×	16	376
J. Ganesan Malaysia	9	349 1.6×	227 1.2×	110 0.9×	96 0.8×	20 0.2×	26	511
V. Bony France	7	135 0.6×	251 1.3×	63 0.5×	210 1.8×	49 0.5×	10	360
Joel Weinthal United States	11	58 0.3×	166 0.9×	125 1.1×	60 0.5×	59 0.6×	16	496
Meira Zoldan Israel	8	116 0.5×	154 0.8×	53 0.4×	96 0.8×	80 0.8×	9	306
Guy H. Grayson United States	5	78 0.4×	115 0.6×	89 0.8×	193 1.6×	19 0.2×	7	393
Maria Franca Marongiu Italy	12	571 2.7×	496 2.6×	142 1.2×	209 1.8×	32 0.3×	18	774
Samaneh Farashi Iran	9	244 1.1×	200 1.0×	149 1.3×	49 0.4×	42 0.4×	31	452
K Schaefer-Rego United States	7	528 2.5×	487 2.5×	93 0.8×	79 0.7×	16 0.2×	8	670
C.P. Brizard France	10	97 0.5×	79 0.4×	38 0.3×	36 0.3×	39 0.4×	27	244

Countries citing papers authored by M. Benabadji

Since Specialization

Citations

This map shows the geographic impact of M. Benabadji'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 M. Benabadji with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Benabadji more than expected).

Fields of papers citing papers by M. Benabadji

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. Benabadji. 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 M. Benabadji. The network helps show where M. Benabadji may publish in the future.

Co-authorship network of co-authors of M. Benabadji

This figure shows the co-authorship network connecting the top 25 collaborators of M. Benabadji. A scholar is included among the top collaborators of M. Benabadji 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 M. Benabadji. M. Benabadji 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

Benabadji, M., et al.. (2023). Renal involvement in familial Mediterranean fever in an Algerian population. Clinical Nephrology. 99(4). 172–179. 2 indexed citations

Djerdjouri, Bahia, et al.. (2016). The M694I/M694I genotype: A genetic risk factor of AA-amyloidosis in a group of Algerian patients with familial Mediterranean fever. European Journal of Medical Genetics. 60(3). 149–153. 16 indexed citations

Benabadji, M., et al.. (1995). Kell and Xg gene frequencies in Algeria.. PubMed. 9(3). 177–84. 1 indexed citations

Nafa, Khédoudja, et al.. (1993). G6PD Aures: a new mutation (48 lle → Thr) causing mild G6PD deficiency is associated with favism. Human Molecular Genetics. 2(1). 81–82. 27 indexed citations

Tamouza, Ryad, F. Rouabhi, M. Benabadji, et al.. (1993). The spectrum of β‐thalassaemia in Algeria: possible origins of the molecular heterogeneity and a tentative diagnostic strategy. British Journal of Haematology. 84(2). 335–337. 18 indexed citations

Benabadji, M., et al.. (1990). Kidd and MNS gene frequencies in Algeria.. PubMed. 4(1). 1–7. 4 indexed citations

Nafa, Khédoudja, Abderrezak Reghis, M. Benabadji, et al.. (1990). Investigation of factor VIII:C gene restriction fragment length polymorphisms and search for deletions in hemophiliac subjects in Algeria. Human Genetics. 84(5). 401–5. 8 indexed citations

Rouabhi, F., et al.. (1989). [Treatment of homozygote beta thalassemia in Algiers. A 5-year follow-up of 66 patients].. PubMed. 18(20). 1010–13. 1 indexed citations

Fischer, Alain, et al.. (1989). A new case of ‘type II’ inherited protein S deficiency. British Journal of Haematology. 73(4). 501–505. 9 indexed citations

10.

Beldjord, Chérif, et al.. (1988). A novelβthalassemia gene with a single base mutation in the conserved polypyrimidine sequence at the 3′ end of IVS 2. Nucleic Acids Research. 16(11). 4927–4935. 29 indexed citations

11.

Blouquit, Y., N. Arous, J. Bardakdjian, et al.. (1987). [Hemoglobin Boumerdès alpha 2(37) (C2) Pro----Arg beta 2: a new variant of the alpha chain associated with hemoglobin S in an Algerian family].. PubMed. 29(5). 317–20. 4 indexed citations

12.

Rouabhi, F., M. Benabadji, Y. Blouquit, et al.. (1985). Hemoglobin M Saskatoon (α₂β²63(E7) His→Tyr) in an Algerian Family. Hemoglobin. 9(5). 509–511. 6 indexed citations

13.

Beldjord, C., Michael L. Baird, Robert Girot, et al.. (1983). Four new haplotypes observed in Algerian ?-thalassemia patients. Human Genetics. 65(2). 204–206. 19 indexed citations

14.

Vergnes, Hugues, et al.. (1979). Genetic Variants of Human Glucose-6-Phosphate Dehydrogenase in a Saharian and Pygmy Family. Human Heredity. 29(1). 50–56. 2 indexed citations

15.

Trabuchet, G, M. Benabadji, & Dominique Labie. (1978). Genetic and biosynthetic studies of families carrying hemoglobin J ? Mexico: Association of ?-thalassemia with Hb J. Human Genetics. 42(2). 189–199. 6 indexed citations

16.

Trabuchet, G, et al.. (1977). Hémoglobines anormales en Algérie.. 53(16). 4 indexed citations

17.

Trabuchet, G, J. Pagnier, M. Benabadji, & Dominique Labie. (1976). Hozygous Cases for Hemoglobin J Mexico (α⁵⁰ (E3)Gln→Glu) Evidence for a Duplicated α Gene with Unequal Expression. Hemoglobin. 1(1). 13–25. 11 indexed citations

18.

Trabuchet, G, et al.. (1976). Hb j mexico in algeria: Arguments for an heterogenous distribution of α genes. FEBS Letters. 61(2). 156–158. 10 indexed citations

19.

Krulik, M, M. Benabadji, G Trabuchet, et al.. (1974). Hémoglobine Sétif (alpha94 (G1) Asp yields Tyr). Etude génétique, biochimique et hématologique. 14(5). 1 indexed citations

20.

Benabadji, M., et al.. (1965). Étude hémotypologique des populations du massif du Hoggar et du plateau de l'Aïr ; II. Les groupes sériques.. Bulletins et Mémoires de la Société d anthropologie de Paris. 7(2). 181–184. 3 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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