Ahlem Amouri

633 total citations
27 papers, 257 citations indexed

About

Ahlem Amouri is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Ahlem Amouri has authored 27 papers receiving a total of 257 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 10 papers in Genetics and 8 papers in Cancer Research. Recurrent topics in Ahlem Amouri's work include DNA Repair Mechanisms (11 papers), Carcinogens and Genotoxicity Assessment (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers). Ahlem Amouri is often cited by papers focused on DNA Repair Mechanisms (11 papers), Carcinogens and Genotoxicity Assessment (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers). Ahlem Amouri collaborates with scholars based in Tunisia, France and United States. Ahlem Amouri's co-authors include Sonia Abdelhak, N. Bouayed Abdelmoula, Olfa Messaoud, Mariem Ben Rekaya, Saad Hasan Mohammed Ali, Tarek Rebaï, Fethi Zhioua, I Mokhtar, M. Mokni and S Boubaker and has published in prestigious journals such as Blood, Frontiers in Genetics and Archives of Dermatological Research.

In The Last Decade

Ahlem Amouri

27 papers receiving 249 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ahlem Amouri Tunisia 9 169 127 51 35 31 27 257
Maren Mönnich Germany 9 280 1.7× 106 0.8× 23 0.5× 30 0.9× 13 0.4× 10 357
Jane M. vanWert United States 11 370 2.2× 158 1.2× 40 0.8× 77 2.2× 17 0.5× 12 446
Mónica Román-Trufero United Kingdom 9 502 3.0× 124 1.0× 33 0.6× 24 0.7× 26 0.8× 14 560
Mariko Yamane Japan 10 308 1.8× 86 0.7× 21 0.4× 34 1.0× 29 0.9× 17 388
Hila Fridman Israel 7 104 0.6× 130 1.0× 18 0.4× 36 1.0× 33 1.1× 8 219
Jennifer McDaid United Kingdom 8 271 1.6× 99 0.8× 29 0.6× 9 0.3× 21 0.7× 8 325
Roser Pujol Spain 7 154 0.9× 73 0.6× 36 0.7× 26 0.7× 10 0.3× 9 188
Nour Ewida Saudi Arabia 9 255 1.5× 138 1.1× 33 0.6× 26 0.7× 21 0.7× 9 328
Rachel Kalifa Israel 8 224 1.3× 80 0.6× 47 0.9× 35 1.0× 17 0.5× 12 343
Sabine Merker Germany 7 221 1.3× 189 1.5× 24 0.5× 15 0.4× 14 0.5× 10 345

Countries citing papers authored by Ahlem Amouri

Since Specialization
Citations

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

Fields of papers citing papers by Ahlem Amouri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ahlem Amouri

This figure shows the co-authorship network connecting the top 25 collaborators of Ahlem Amouri. A scholar is included among the top collaborators of Ahlem Amouri 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 Ahlem Amouri. Ahlem Amouri is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Messaoud, Olfa, Sahar Elouej, Fethi Mellouli, et al.. (2021). FANCA Gene Mutations in North African Fanconi Anemia Patients. Frontiers in Genetics. 12. 610050–610050. 2 indexed citations
2.
Amouri, Ahlem, Saloua Makni, Lilia Romdhane, et al.. (2019). Cytogenetic and molecular diagnosis of Fanconi anemia revealed two hidden phenotypes: Disorder of sex development and cerebro‐oculo‐facio‐skeletal syndrome. Molecular Genetics & Genomic Medicine. 7(7). e00694–e00694. 3 indexed citations
3.
Amouri, Ahlem, et al.. (2017). Chromosomal abnormalities in 163 Tunisian couples with recurrent miscarriages. Pan African Medical Journal. 28. 99–99. 8 indexed citations
4.
Amouri, Ahlem, et al.. (2015). Leukemia in Patients with Klinefelter Syndrome: A Report of Two Cases. Indian Journal of Hematology and Blood Transfusion. 32(S1). 66–68. 3 indexed citations
5.
Khelifa, Mariem Ben, et al.. (2014). Prevalence of Y chromosome microdeletions in infertile Tunisian men. Annales de biologie clinique. 72(3). 331–336. 8 indexed citations
6.
Amouri, Ahlem, et al.. (2014). Cytogenetic abnormalities in Tunisian women with premature ovarian failure. Comptes Rendus Biologies. 337(12). 691–694. 11 indexed citations
7.
Messaoud, Olfa, Mariem Ben Rekaya, Inès Ouertani, et al.. (2013). The Experience of a Tunisian Referral Centre in Prenatal Diagnosis of <b><i>Xeroderma pigmentosum</i></b>. Public Health Genomics. 16(5). 251–254. 6 indexed citations
8.
Ouederni, Monia, Amel Lakhal, Fethi Mellouli, et al.. (2013). Cytogenetic Assessment of Fanconi Anemia in Children With Aplastic Anemia in Tunisia. Journal of Pediatric Hematology/Oncology. 35(7). 547–550. 4 indexed citations
9.
Halim, Nizar Ben, Fethi Mellouli, Yosra Ben Youssef, et al.. (2013). Differentiation of Fanconi anemia and aplastic anemia using mitomycin C test in Tunisia. Comptes Rendus Biologies. 336(1). 29–33. 4 indexed citations
10.
Youssef, Yosra Ben, Ahlem Amouri, Hatem Elghezal, et al.. (2012). Création et rapport du registre tunisien de l’anémie de Fanconi (TFAR). Archives de Pédiatrie. 19(5). 467–475. 5 indexed citations
11.
Gouas, Laëtitia, et al.. (2012). Trisomie 21 et cancers. Morphologie. 96(314-315). 57–66. 8 indexed citations
12.
Rekaya, Mariem Ben, Olfa Messaoud, Amel Mebazâa, et al.. (2011). A novel POLH gene mutation in a xeroderma pigmentosum-V Tunisian patient: phenotype–genotype correlation. Journal of Genetics. 90(3). 483–487. 11 indexed citations
13.
Messaoud, Olfa, Mariem Ben Rekaya, Héla Azaiez, et al.. (2011). Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity. Archives of Dermatological Research. 304(2). 171–176. 18 indexed citations
14.
Messaoud, Olfa, Mariem Ben Rekaya, Hammouda Boussen, et al.. (2010). Genetic homogeneity of mutational spectrum of group‐A xeroderma pigmentosum in Tunisian patients. International Journal of Dermatology. 49(5). 544–548. 21 indexed citations
15.
Rekaya, Mariem Ben, Olfa Messaoud, Ahlem Amouri, et al.. (2009). High frequency of the V548A fs X572 XPC mutation in Tunisia: implication for molecular diagnosis. Journal of Human Genetics. 54(7). 426–429. 38 indexed citations
16.
Abdelmoula, N. Bouayed, et al.. (2006). EVALUATION OF DAZ MICRODELETIONS IN 34 INFERTILE MEN. Archives of Andrology. 52(3). 175–178. 2 indexed citations
17.
Abdelkefi, Abderrahman, Saloua Ladeb, Tarek Ben Othman, et al.. (2006). Timing of Second Autologous Transplantations in Multiple Myeloma: Results of a Multicenter Sequential Randomized Clinical Trial.. Blood. 108(11). 59–59. 6 indexed citations
18.
Abdelmoula, N. Bouayed, Ahlem Amouri, M. Chakroun, et al.. (2004). Turner syndrome female with a small ring X chromosome lacking the XIST, an unexpectedly mild phenotype and an atypical association with alopecia universalis. Annales de Génétique. 47(3). 305–313. 8 indexed citations
19.
Abdelmoula, N. Bouayed, Ahlem Amouri, Marie‐France Portnoï, et al.. (2003). Cytogenetics and fluorescence in situ hybridization assessment of sex-chromosome mosaicism in Klinefelter’s syndrome. Annales de Génétique. 47(2). 163–175. 26 indexed citations
20.
Abdelhak, Sonia, Ahlem Amouri, H. Abid, et al.. (2003). Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations. Journal of Human Genetics. 48(7). 352–361. 31 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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