Imen Dorboz

1.6k total citations
30 papers, 650 citations indexed

About

Imen Dorboz is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Imen Dorboz has authored 30 papers receiving a total of 650 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Clinical Biochemistry. Recurrent topics in Imen Dorboz's work include RNA regulation and disease (14 papers), RNA Research and Splicing (9 papers) and RNA and protein synthesis mechanisms (5 papers). Imen Dorboz is often cited by papers focused on RNA regulation and disease (14 papers), RNA Research and Splicing (9 papers) and RNA and protein synthesis mechanisms (5 papers). Imen Dorboz collaborates with scholars based in France, Tunisia and United States. Imen Dorboz's co-authors include Odile Boespflug‐Tanguy, Diana Rodriguez, Martin Teichmann, Adeline Vanderver, Monique Elmaleh, Geneviève Bernard, Éliane Chouery, Joelle Abou Ghoch, Giovanni A. Carosso and Valérie Delague and has published in prestigious journals such as PLoS ONE, Brain and Neurology.

In The Last Decade

Imen Dorboz

30 papers receiving 647 citations

Peers

Imen Dorboz

GENET

NEURO

CMN

Alessia Indrieri Italy

Sarah S. Subaran United States

Morad Khayat Israel

Amrita Mandal United States

Lauren Brady Canada

Majida Charif Morocco

Juliana Maria Ferraz Sallum Brazil

Cinzia Cancellieri Italy

Nisha Patel Saudi Arabia

Martina Cesani Italy

Alessia Indrieri Italy

Imen Dorboz

429 ×0.9

69 ×0.7

GENET

31 ×0.4

NEURO

36 ×0.5

43 ×0.7

CMN

Citations per year, relative to Imen Dorboz Imen Dorboz (= 1×) peers Alessia Indrieri

Countries citing papers authored by Imen Dorboz

Since Specialization

Citations

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

Fields of papers citing papers by Imen Dorboz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Imen Dorboz

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

Amin, Mutaz, Ahlam A. Hamed, Mohamed Mustafa, et al.. (2022). A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability. BMC Medical Genomics. 15(1). 236–236. 4 indexed citations

Dewulf, Joseph P., Elsa Wiame, Imen Dorboz, et al.. (2019). SLC13A3 variants cause acute reversible leukoencephalopathy and α‐ketoglutarate accumulation. Annals of Neurology. 85(3). 385–395. 19 indexed citations

Sarret, Catherine, Zahra Ashkavand, Imen Dorboz, et al.. (2019). Deleterious mutations in ALDH1L2 suggest a novel cause for neuro-ichthyotic syndrome. npj Genomic Medicine. 4(1). 17–17. 15 indexed citations

Dorboz, Imen, Hélène Dumay‐Odelot, Yosra Bouyacoub, et al.. (2018). Mutation in POLR3K causes hypomyelinating leukodystrophy and abnormal ribosomal RNA regulation. Neurology Genetics. 4(6). e289–e289. 55 indexed citations

Ardissone, Anna, Davide Tonduti, Andrea Legati, et al.. (2018). KARS-related diseases: progressive leukoencephalopathy with brainstem and spinal cord calcifications as new phenotype and a review of literature. Orphanet Journal of Rare Diseases. 13(1). 45–45. 28 indexed citations

Ayrignac, Xavier, Fanny Mochel, Kévin Mouzat, et al.. (2018). Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases. American Journal of Neuroradiology. 39(9). 1657–1661. 30 indexed citations

Dorboz, Imen, et al.. (2017). Mutation in the AGK gene in two siblings with unusual Sengers syndrome. Metabolic Brain Disease. 32(6). 2149–2154. 12 indexed citations

Dorboz, Imen, Chiara Aiello, Cas Simons, et al.. (2017). Biallelic mutations in the homeodomain of NKX6-2 underlie a severe hypomyelinating leukodystrophy. Brain. 140(10). 2550–2556. 15 indexed citations

Tonduti, Davide, Simona Orcesi, Emma M. Jenkinson, et al.. (2016). Clinical, radiological and possible pathological overlap of cystic leukoencephalopathy without megalencephaly and Aicardi-Goutières syndrome. European Journal of Paediatric Neurology. 20(4). 604–610. 24 indexed citations

10.

Dorboz, Imen, Samia Pichard, Agnès Bourillon, et al.. (2016). Transient neonatal renal failure and massive polyuria in MEGDEL syndrome. Molecular Genetics and Metabolism Reports. 7. 8–10. 4 indexed citations

11.

Dorboz, Imen, et al.. (2015). Screening for GFAP rearrangements in a cohort of Alexander disease and undetermined leukoencephalopathy patients. European Journal of Medical Genetics. 58(9). 466–470. 6 indexed citations

12.

Barakat, Abdelhamid, et al.. (2015). A novel mutation in the ABCD1 gene of a Moroccan patient with X-linked adrenoleukodystrophy: case report. BMC Neurology. 15(1). 244–244. 4 indexed citations

13.

Dorboz, Imen, et al.. (2015). Efficient detection of frequent eIF2B mutations for the rapid molecular diagnosis of CACH/VWM syndrome. Clinical Biochemistry. 48(18). 1317–1323. 2 indexed citations

14.

Halim, Nizar Ben, Imen Dorboz, Rym Kéfi, et al.. (2015). Determination of arylsulfatase A pseudodeficiency allele and haplotype frequency in the Tunisian population. Neurological Sciences. 37(3). 403–409. 9 indexed citations

15.

Bonnet, Crystel, Malek Louha, Yosra Bouyacoub, et al.. (2014). Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness. PLoS ONE. 9(6). e99797–e99797. 21 indexed citations

16.

Dorboz, Imen, Marie Coutelier, A. Bertrand, et al.. (2014). Severe dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1. Orphanet Journal of Rare Diseases. 9(1). 174–174. 39 indexed citations

17.

Cacciagli, Pierre, Jean‐Christophe Roux, Imen Dorboz, et al.. (2013). Mutations in BCAP31 Cause a Severe X-Linked Phenotype with Deafness, Dystonia, and Central Hypomyelination and Disorganize the Golgi Apparatus. The American Journal of Human Genetics. 93(3). 579–586. 48 indexed citations

18.

Bernard, Geneviève, Éliane Chouery, Martine Tétreault, et al.. (2012). Mutations of POLR3A Encoding a Catalytic Subunit of RNA Polymerase Pol III Cause a Recessive Hypomyelinating Leukodystrophy p415. The American Journal of Human Genetics. 91(5). 972–972. 1 indexed citations

19.

Bernard, Geneviève, Éliane Chouery, Martine Tétreault, et al.. (2011). Mutations of POLR3A Encoding a Catalytic Subunit of RNA Polymerase Pol III Cause a Recessive Hypomyelinating Leukodystrophy. The American Journal of Human Genetics. 89(3). 415–423. 181 indexed citations

20.

Sarret, Catherine, Catherine Vaurs‐Barrière, Imen Dorboz, et al.. (2011). Sjögren–Larsson syndrome: Novel mutations in the ALDH3A2 gene in a French cohort. Journal of the Neurological Sciences. 312(1-2). 123–126. 8 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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