Ichraf Kraoua

693 total citations
64 papers, 270 citations indexed

About

Ichraf Kraoua is a scholar working on Molecular Biology, Neurology and Epidemiology. According to data from OpenAlex, Ichraf Kraoua has authored 64 papers receiving a total of 270 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 17 papers in Neurology and 11 papers in Epidemiology. Recurrent topics in Ichraf Kraoua's work include Metabolism and Genetic Disorders (11 papers), Autoimmune Neurological Disorders and Treatments (8 papers) and Mitochondrial Function and Pathology (6 papers). Ichraf Kraoua is often cited by papers focused on Metabolism and Genetic Disorders (11 papers), Autoimmune Neurological Disorders and Treatments (8 papers) and Mitochondrial Function and Pathology (6 papers). Ichraf Kraoua collaborates with scholars based in Tunisia, France and Morocco. Ichraf Kraoua's co-authors include Hanène Benrhouma, N. Gouider‐Khouja, Ilhem Turki, N. Ben Achour, Mèlika Ben Ahmed, C. Drissi, Saloua Mrabet, Stefano Castellana, Sonia Abdelhak and Alessia Micalizzi and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and International Journal of Biological Macromolecules.

In The Last Decade

Ichraf Kraoua

48 papers receiving 269 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ichraf Kraoua Tunisia	9	112	111	54	50	45	64	270
Shakti Agrawal United Kingdom	11	73 0.7×	143 1.3×	67 1.2×	23 0.5×	29 0.6×	16	305
Karthik Muthusamy India	10	118 1.1×	50 0.5×	42 0.8×	17 0.3×	29 0.6×	43	268
Alessandro Iodice Italy	8	61 0.5×	61 0.5×	54 1.0×	44 0.9×	18 0.4×	24	212
Esther Ganelin‐Cohen Israel	10	106 0.9×	71 0.6×	49 0.9×	38 0.8×	23 0.5×	26	274
Anaita Hegde India	10	58 0.5×	84 0.8×	24 0.4×	31 0.6×	18 0.4×	32	240
Celeste Panteghini Italy	13	133 1.2×	118 1.1×	42 0.8×	79 1.6×	65 1.4×	25	329
Qi‐Lun Lai China	11	62 0.6×	162 1.5×	41 0.8×	21 0.4×	9 0.2×	37	295
Paola Costa Italy	8	41 0.4×	33 0.3×	50 0.9×	79 1.6×	36 0.8×	22	426
Heather Cahan United States	7	119 1.1×	27 0.2×	76 1.4×	36 0.7×	39 0.9×	16	418
Ching-Shiang Chi Taiwan	9	173 1.5×	100 0.9×	31 0.6×	126 2.5×	30 0.7×	12	487

Countries citing papers authored by Ichraf Kraoua

Since Specialization

Citations

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

Fields of papers citing papers by Ichraf Kraoua

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ichraf Kraoua

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

Labalme, Audrey, Go Hun Seo, Amel Ben Chehida, et al.. (2025). Transcript Long‐Read Sequencing Unveils the Molecular Complexity of a Novel ROGDI Splicing Variant in a Tunisian Family With Kohlschütter‐Tönz Syndrome. Clinical Genetics. 107(6). 705–707.

Benrhouma, Hanène, et al.. (2025). Post-mumps encephalitis mimicking metabolic disease on brain magnetic resonance imaging: a case report. Pediatric Radiology. 55(6). 1326–1330.

Charif, Majida, Saïd Galaï, Lilia Kraoua, et al.. (2024). Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencing. Frontiers in Genetics. 14. 1259826–1259826.

Kraoua, Ichraf, Nadège Calmels, Cathy Obringer, et al.. (2022). Heterogeneous clinical features in Cockayne syndrome patients and siblings carrying the same CSA mutations. Orphanet Journal of Rare Diseases. 17(1). 121–121. 7 indexed citations

Kraoua, Ichraf, Dimitri Schlemmer, Catherine Caillaud, et al.. (2022). Plasma GM2 ganglioside potential biomarker for diagnosis, prognosis and disease monitoring of GM2-Gangliosidosis. Molecular Genetics and Metabolism. 138(2). 106983–106983. 5 indexed citations

Benrhouma, Hanène, et al.. (2021). Autoimmune Encephalitis in Tunisia: Report of a Pediatric Cohort. Journal of Immunology Research. 2021. 1–7. 7 indexed citations

Benrhouma, Hanène, et al.. (2020). Rasmussen’s Encephalitis: A Report of a Tunisian Pediatric Case and Literature Review. SHILAP Revista de lepidopterología. 2020. 1–5. 2 indexed citations

Kraoua, Ichraf, et al.. (2020). Farber disease: A Fatal Childhood Disorder with Nervous System Involvement. 5(3). 1–4. 1 indexed citations

Chehida, Amel Ben, Ichraf Kraoua, Haïfa Sanhaji, et al.. (2020). Non-ketotic hyperglycinaemia: a frequent, but poorly diagnosed and managed genetic disorder in Tunisia. Archives of Disease in Childhood. 106(3). 311–311. 1 indexed citations

10.

Achour, N. Ben, et al.. (2018). Severe dysautonomia as a main feature of anti-GAD encephalitis: Report of a paediatric case and literature review. European Journal of Paediatric Neurology. 22(3). 548–551. 30 indexed citations

11.

Leblond, Claire S., Béatrice Regnault, Alexandre Mathieu, et al.. (2018). Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology. Journal of Applied Genetics. 60(1). 49–56. 10 indexed citations

12.

Kraoua, Ichraf, et al.. (2017). Pyridoxine-dependent epilepsy: A novel mutation in a Tunisian child. Archives de Pédiatrie. 24(3). 241–243. 5 indexed citations

13.

Achour, N. Ben, et al.. (2017). Childhood opsoclonus–myoclonus syndrome: A case series from Tunisia. Brain and Development. 39(9). 751–755. 6 indexed citations

14.

Mrabet, Saloua, N. Ben Achour, Ichraf Kraoua, et al.. (2015). Anti-Ma2-encephalitis in a 2 year-old child: A newly diagnosed case and literature review. European Journal of Paediatric Neurology. 19(6). 737–742. 15 indexed citations

15.

Achour, N. Ben, et al.. (2015). Encéphalomyélite aiguë disséminée en Tunisie : étude d’une cohorte pédiatrique. Revue Neurologique. 171(12). 882–890. 1 indexed citations

16.

Kraoua, Ichraf, et al.. (2015). Status dystonicus in childhood.. PubMed. 93(12). 756–9. 19 indexed citations

17.

Kraoua, Ichraf, et al.. (2014). Lesch Nyhan syndrome: A novel complex mutation in a Tunisian child. Brain and Development. 36(10). 921–923. 2 indexed citations

18.

Achour, N. Ben, et al.. (2013). Une sténose congénitale des foramens interventriculaires révélée par une hypertension intracrânienne à rechute. Neurochirurgie. 59(2). 93–96. 2 indexed citations

19.

Benrhouma, Hanène, et al.. (2011). Methylmalonic acidemia and hyperglycemia: An unusual association. Brain and Development. 34(2). 113–114. 11 indexed citations

20.

Kraoua, Ichraf, et al.. (2008). Tuberculose cérébromédiastinale chez un enfant atteint de syndrome de Say-Barber-Miller probable : un lien de causalité ?. Revue Neurologique. 165(12). 1111–1116. 1 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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