H. Ben Hamouda

408 total citations
27 papers, 121 citations indexed

About

H. Ben Hamouda is a scholar working on Pediatrics, Perinatology and Child Health, Surgery and Genetics. According to data from OpenAlex, H. Ben Hamouda has authored 27 papers receiving a total of 121 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pediatrics, Perinatology and Child Health, 8 papers in Surgery and 8 papers in Genetics. Recurrent topics in H. Ben Hamouda's work include Prenatal Screening and Diagnostics (5 papers), Congenital Anomalies and Fetal Surgery (3 papers) and Urological Disorders and Treatments (3 papers). H. Ben Hamouda is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Congenital Anomalies and Fetal Surgery (3 papers) and Urological Disorders and Treatments (3 papers). H. Ben Hamouda collaborates with scholars based in Tunisia, Switzerland and Italy. H. Ben Hamouda's co-authors include Mohamed Tahar Sfar, Ibtissem Ghédira, M. Jeddi, Amani Mankaï, F. Amri, A.S. Essoussi, R. Braham, Anis Ben Haj Khalifa, Ilhem Ben Charfeddine and Filomena De Luca and has published in prestigious journals such as Gene, Pediatric Research and Diagnostic and Interventional Imaging.

In The Last Decade

H. Ben Hamouda

24 papers receiving 120 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
H. Ben Hamouda Tunisia 6 34 30 25 23 23 27 121
Irma D Fleming United States 6 6 0.2× 50 1.7× 16 0.6× 56 2.4× 6 0.3× 11 183
Pierluigi Puca Italy 8 62 1.8× 66 2.2× 46 1.8× 30 1.3× 28 1.2× 21 165
Guillermina Calo Argentina 12 22 0.6× 27 0.9× 51 2.0× 22 1.0× 13 0.6× 25 318
Monica M. Schmitt United States 7 38 1.1× 25 0.8× 8 0.3× 24 1.0× 5 0.2× 19 164
Chhavi Goel India 7 9 0.3× 91 3.0× 32 1.3× 35 1.5× 13 0.6× 8 210
Kellie Fakes Australia 6 20 0.6× 23 0.8× 38 1.5× 23 1.0× 3 0.1× 9 444
Ivana V. Yang United States 9 29 0.9× 94 3.1× 13 0.5× 24 1.0× 3 0.1× 13 289
Madeleine Birgersson Sweden 7 58 1.7× 80 2.7× 19 0.8× 18 0.8× 5 0.2× 17 281
William D. Rawlinson Australia 8 84 2.5× 32 1.1× 66 2.6× 61 2.7× 10 0.4× 9 203
HE Drummond United Kingdom 3 83 2.4× 24 0.8× 61 2.4× 23 1.0× 15 0.7× 5 114

Countries citing papers authored by H. Ben Hamouda

Since Specialization
Citations

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

Fields of papers citing papers by H. Ben Hamouda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by H. Ben Hamouda. 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 H. Ben Hamouda. The network helps show where H. Ben Hamouda may publish in the future.

Co-authorship network of co-authors of H. Ben Hamouda

This figure shows the co-authorship network connecting the top 25 collaborators of H. Ben Hamouda. A scholar is included among the top collaborators of H. Ben Hamouda 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 H. Ben Hamouda. H. Ben Hamouda 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.
Hamouda, H. Ben, et al.. (2017). Diagnostic prénatal et prise en charge de deux cas d’urétérocèles bilatéraux sur uretères simplex. Archives de Pédiatrie. 24(9). 860–864.
2.
Hamouda, H. Ben, et al.. (2017). Prenatal diagnosis of caudal regression syndrome and omphalocele in a fetus of a diabetic mother. Pan African Medical Journal. 27. 128–128. 3 indexed citations
3.
Hamouda, H. Ben, et al.. (2017). Neonatal duodenal obstruction due to a preduodenal portal vein associated with intestinal malrotation: A case report. Pediatria Polska. 92(5). 623–626. 1 indexed citations
4.
Hamouda, H. Ben, et al.. (2016). Rupture spontanée de l’imperforation de l’hymen chez deux nouveau-nés. Archives de Pédiatrie. 23(3). 275–278. 3 indexed citations
5.
Hamouda, H. Ben, et al.. (2016). Expression néonatale d’un trait bêta-thalassémique associé à une sphérocytose héréditaire chez deux jumelles monozygotes. Archives de Pédiatrie. 24(2). 126–130. 1 indexed citations
6.
Charfeddine, Ilhem Ben, Jihène Bouguila, H. Ben Hamouda, et al.. (2015). Multiplex Minisequencing of theHBBGene: A Rapid Strategy to Confirm the Most Frequentβ-Thalassemia Mutations in the Tunisian Population. Hemoglobin. 39(4). 251–255. 1 indexed citations
7.
Luca, Filomena De, et al.. (2014). Occurrence of conjugative IncF-type plasmids harboring the blaCTX-M-15 gene in Enterobacteriaceae isolates from newborns in Tunisia. Pediatric Research. 77(1). 107–110. 12 indexed citations
8.
Hamouda, H. Ben, et al.. (2014). Diagnostic anténatal d’un lymphangiome kystique géant de la paroi thoraco-axillaire. Archives de Pédiatrie. 21(9). 1011–1015. 2 indexed citations
9.
Hamouda, H. Ben, et al.. (2013). Aspects cliniques et évolutifs des méningites bactériennes néonatales. Archives de Pédiatrie. 20(9). 938–944. 15 indexed citations
10.
Hamouda, H. Ben, et al.. (2012). Pfeiffer syndrome type II discovered perinatally: Report of an observation and review of the literature. Diagnostic and Interventional Imaging. 93(10). 785–789. 4 indexed citations
11.
Charfeddine, Ilhem Ben, Felix G. Riepe, Éric Clauser, et al.. (2012). Steroid 21-hydroxylase gene mutational spectrum in 50 Tunisian patients: Characterization of three novel polymorphisms. Gene. 507(1). 20–26. 8 indexed citations
12.
Braham, H, et al.. (2012). Thrombose néonatale de la veine rénale et double hétérozygotie pour la mutation du facteur V de Leiden et du gène de la MTHFR. Archives de Pédiatrie. 19(4). 419–421. 3 indexed citations
13.
Hamouda, H. Ben, et al.. (2011). Prise en charge et évolution des méga-uretères primitifs de découverte anténatale. Progrès en Urologie. 21(7). 486–491. 1 indexed citations
14.
Hamouda, H. Ben, et al.. (2010). Obstructive congenital epulis. European Annals of Otorhinolaryngology Head and Neck Diseases. 127(2). 86–89. 4 indexed citations
15.
Hamouda, H. Ben, et al.. (2010). Bacteriological and Pathological Studies on Some Aerobic and Anaerobic Bacteria Causing Diarrhoea in Camel Calves.. Veterinary Medical Journal Giza. 58(2). 177–197. 1 indexed citations
16.
Hamouda, H. Ben, et al.. (2010). Diagnostic postnatal et pronostic de 2 cas de triploïdie. Archives de Pédiatrie. 17(7). 1078–1082. 1 indexed citations
17.
Hamouda, H. Ben, et al.. (2009). Prenatal diagnosis and prognosis of triple X syndrome: 47, XXX. Journal de gynécologie, obstétrique et biologie de la reproduction. Supplément. 38(7). 599–603. 4 indexed citations
18.
Mankaï, Amani, H. Ben Hamouda, F. Amri, et al.. (2007). Screening by anti-endomysium antibodies for celiac disease in Tunisian children with type 1 diabetes mellitus. Gastroentérologie Clinique et Biologique. 31(5). 462–466. 25 indexed citations
19.
Hsaïri, M., et al.. (2006). Déshydratation hypernatrémique et allaitement maternel. Journal de Pédiatrie et de Puériculture. 19(7). 265–267. 1 indexed citations
20.
Hamouda, H. Ben, et al.. (2001). Association of severe autosomal recessive osteopetrosis and Dandy-Walker syndrome with agenesis of the corpus callosum.. PubMed. 67(5). 528–32. 19 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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