Houda Kanoun

865 total citations
6 papers, 44 citations indexed

About

Houda Kanoun is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Pathology and Forensic Medicine. According to data from OpenAlex, Houda Kanoun has authored 6 papers receiving a total of 44 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Pulmonary and Respiratory Medicine and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Houda Kanoun's work include Porphyrin Metabolism and Disorders (2 papers), Kidney Stones and Urolithiasis Treatments (2 papers) and Autoimmune Bullous Skin Diseases (1 paper). Houda Kanoun is often cited by papers focused on Porphyrin Metabolism and Disorders (2 papers), Kidney Stones and Urolithiasis Treatments (2 papers) and Autoimmune Bullous Skin Diseases (1 paper). Houda Kanoun collaborates with scholars based in Tunisia and Spain. Houda Kanoun's co-authors include Faiza Fakhfakh, Moez Elloumi, J. Hachicha, F. Makni, Emna Mkaouar‐Rebai, F. Jarraya, Hassen Kamoun, Patricia Ruíz, Tahya Sellami Boudawara and H. Makni and has published in prestigious journals such as Gene, Clinical Rheumatology and Annals of Hematology.

In The Last Decade

Houda Kanoun

5 papers receiving 44 citations

Peers

Houda Kanoun

PRM

MB

HEMAT

PFM

NEPHR

Nadica Ristoska-Bojkovska Austria

Fabrício Augusto Martinelli de Oliveira Brazil

Sunil Narula United States

Antonio d'Avanzo Italy

Rebecca Hudson Australia

Charlotte Gaskell United Kingdom

Leena Mukherjee United Kingdom

I Hassan Pakistan

Miriam Gutiérrez-Jimeno Spain

Rajesh Rawal Germany

Nadica Ristoska-Bojkovska Austria

Houda Kanoun

16 ×0.6

PRM

23 ×1.4

MB

2 ×0.1

HEMAT

18 ×1.6

PFM

12 ×2.4

NEPHR

Citations per year, relative to Houda Kanoun Houda Kanoun (= 1×) peers Nadica Ristoska-Bojkovska

Countries citing papers authored by Houda Kanoun

Since Specialization

Citations

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

Fields of papers citing papers by Houda Kanoun

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Houda Kanoun

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

All Works

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6 of 6 papers shown

1.

Kanoun, Houda, et al.. (2023). Dorfman–Chanarin Syndrome with Renal Involvement: A Rare Case Report and Literature Review. Indian Journal of Nephrology. 33(6). 472–475.

2.

Abida, Olfa, Nésrine Elloumi, Houda Kanoun, et al.. (2022). Annexin A1 and its receptor gene polymorphisms in systemic lupus erythematosus in the Tunisian population. Clinical Rheumatology. 41(5). 1359–1369. 4 indexed citations

3.

Kanoun, Houda, Patricia Ruíz, Marc Pybus, et al.. (2021). Next-generation sequencing in patients with familial FSGS: first report of collagen gene mutations in Tunisian patients. Journal of Human Genetics. 66(8). 795–803. 6 indexed citations

4.

Kanoun, Houda, et al.. (2017). Identification of compound heterozygous patients with primary hyperoxaluria type 1: clinical evaluations and in silico investigations. BMC Nephrology. 18(1). 303–303. 7 indexed citations

5.

Kanoun, Houda, et al.. (2013). A double mutation in AGXT gene in families with primary hyperoxaluria type 1. Gene. 531(2). 451–456. 6 indexed citations

6.

Mkaouar‐Rebai, Emna, et al.. (2009). Congenital factor XIII deficiency caused by two mutations in eight Tunisian families: molecular confirmation of a founder effect. Annals of Hematology. 89(5). 499–504. 21 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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