Imen Dorboz

1.6k citations

30 papers · 650 indexed · h-index 14

Co-authors: Odile Boespflug‐Tanguy Diana Rodriguez Martin Teichmann Adeline Vanderver Monique Elmaleh Geneviève Bernard Éliane Chouery Joelle Abou Ghoch
Topics: RNA regulation and disease (14 papers)RNA Research and Splicing (9 papers)RNA and protein synthesis mechanisms (5 papers)
Cited by: Neurology Clinical Biochemistry Molecular Biology
Journals: PLoS ONE Brain Neurology
Partner nations: France Tunisia United States

In The Last Decade

Imen Dorboz

30 papers receiving 647 citations

Peers

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

#	Work	Indexed citations
1	A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability 2022 ·BMC Medical Genomics ·Mutaz Amin,(unknown),(unknown),(unknown),Ahlam A. Hamed,(unknown),(unknown),(unknown),(unknown),(unknown),Mohamed Mustafa,Séverine Drunat,Liena E. O. Elsayed,Ammar Ahmed,Odile Boespflug‐Tanguy,Imen Dorboz	4
2	SLC13A3 variants cause acute reversible leukoencephalopathy and α‐ketoglutarate accumulation 2019 ·Annals of Neurology ·Joseph P. Dewulf,Elsa Wiame,Imen Dorboz,Monique Elmaleh,Apolline Imbard,Dana Dumitriu,Malgorzata Rak,Agnès Bourillon,Raphaël Helaers,(unknown),Florence Renaldo,Odile Boespflug‐Tanguy,Marie‐Françoise Vincent,Jean‐François Benoist,Ron A. Wevers,Avner Schlessinger,Emile Van Schaftingen,Marie‐Cécile Nassogne,Manuel Schiff	19
3	Deleterious mutations in ALDH1L2 suggest a novel cause for neuro-ichthyotic syndrome 2019 ·npj Genomic Medicine ·Catherine Sarret,Zahra Ashkavand,(unknown),Imen Dorboz,Peter Pediaditakis,Susan Sumner,Éléonore Eymard-Pierre,Christine Francannet,Natalia I. Krupenko,Odile Boespflug‐Tanguy,Sergey A. Krupenko	15
4	Mutation in POLR3K causes hypomyelinating leukodystrophy and abnormal ribosomal RNA regulation 2018 ·Neurology Genetics ·Imen Dorboz,Hélène Dumay‐Odelot,(unknown),Yosra Bouyacoub,(unknown),Simon Samaan,Haifa Jmel,Éléonore Eymard-Pierre,Claude Cancès,(unknown),Anne‐Lise Poulat,Christophe Rousselle,Florence Renaldo,(unknown),Martin Teichmann,Odile Boespflug‐Tanguy	55
5	KARS-related diseases: progressive leukoencephalopathy with brainstem and spinal cord calcifications as new phenotype and a review of literature 2018 ·Orphanet Journal of Rare Diseases ·Anna Ardissone,Davide Tonduti,Andrea Legati,Eleonora Lamantea,Rita Barone,Imen Dorboz,Odile Boespflug‐Tanguy,Gabriella Nebbia,Marco Maggioni,Barbara Garavaglia,Isabella Moroni,Laura Farina,Anna Pichiecchio,Simona Orcesi,Luisa Chiapparini,Daniele Ghezzi	28
6	Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases 2018 ·American Journal of Neuroradiology ·(unknown),Xavier Ayrignac,Fanny Mochel,Kévin Mouzat,Clarisse Carra‐Dallière,Giovanni Castelnovo,Emmanuel Ellie,Frédérique Etcharry‐Bouyx,Christophe Verny,Serge Belliard,Didier Hannequin,Cécilia Marelli,Yann Nadjar,Isabelle Le Ber,Imen Dorboz,Simon Samaan,Odile Boespflug‐Tanguy,Serge Lumbroso,Pierre Labauge	30
7	Mutation in the AGK gene in two siblings with unusual Sengers syndrome 2017 ·Metabolic Brain Disease ·(unknown),Imen Dorboz,Simon Samaan,Abdelhamid Slama,(unknown),Odile Boespflug‐Tanguy,Catherine Sarret	12
8	Biallelic mutations in the homeodomain of NKX6-2 underlie a severe hypomyelinating leukodystrophy 2017 ·Brain ·Imen Dorboz,Chiara Aiello,Cas Simons,Robert Thompson Stone,Marcello Niceta,Monique Elmaleh,(unknown),Diane Doummar,Alessandro Bruselles,Nicole I. Wolf,Lorena Travaglini,Odile Boespflug‐Tanguy,Marco Tartaglia,Adeline Vanderver,Diana Rodriguez,Enrico Bertini	15
9	Clinical, radiological and possible pathological overlap of cystic leukoencephalopathy without megalencephaly and Aicardi-Goutières syndrome 2016 ·European Journal of Paediatric Neurology ·Davide Tonduti,Simona Orcesi,Emma M. Jenkinson,Imen Dorboz,Florence Renaldo,Celeste Panteghini,Gillian Rice,Marco Henneke,John H. Livingston,Monique Elmaleh,Lydie Bürglen,Michèl A.A.P. Willemsen,Luisa Chiapparini,Barbara Garavaglia,Diana Rodriguez,Odile Boespflug‐Tanguy,Isabella Moroni,Yanick J. Crow	24
10	Transient neonatal renal failure and massive polyuria in MEGDEL syndrome 2016 ·Molecular Genetics and Metabolism Reports ·(unknown),(unknown),Imen Dorboz,Samia Pichard,Agnès Bourillon,Jean‐François Benoist,Claude Jardel,Hélène Ogier de Baulny,Odile Boespflug‐Tanguy,Manuel Schiff	4
11	Screening for GFAP rearrangements in a cohort of Alexander disease and undetermined leukoencephalopathy patients 2015 ·European Journal of Medical Genetics ·(unknown),Imen Dorboz,Diana Rodriguez,Odile Boespflug‐Tanguy	6
12	A novel mutation in the ABCD1 gene of a Moroccan patient with X-linked adrenoleukodystrophy: case report 2015 ·BMC Neurology ·(unknown),Abdelhamid Barakat,(unknown),(unknown),I. Slassi,Imen Dorboz,Odile Boespflug‐Tanguy,Sellama Nadifi	4
13	Efficient detection of frequent eIF2B mutations for the rapid molecular diagnosis of CACH/VWM syndrome 2015 ·Clinical Biochemistry ·(unknown),Imen Dorboz,Odile Boespflug‐Tanguy	2
14	Determination of arylsulfatase A pseudodeficiency allele and haplotype frequency in the Tunisian population 2015 ·Neurological Sciences ·Nizar Ben Halim,Imen Dorboz,Rym Kéfi,Najla Kharrat,Éléonore Eymard-Pierre,Majdi Nagara,Lilia Romdhane,Nissaf Ben Alaya,Ahmed Rebaï,(unknown),Odile Boespflug‐Tanguy,Sonia Abdelhak	9
15	Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness 2014 ·PLoS ONE ·(unknown),Crystel Bonnet,(unknown),Malek Louha,Yosra Bouyacoub,(unknown),(unknown),Rym Kéfi,Laurence Jonard,Imen Dorboz,Jean‐Pierre Hardelin,(unknown),Jacqueline Levilliers,Dominique Weil,Kenneth McElreavey,Odile Boespflug‐Tanguy,G. Besbes,Sonia Abdelhak,Christine Petit	21
16	Severe dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1 2014 ·Orphanet Journal of Rare Diseases ·Imen Dorboz,Marie Coutelier,A. Bertrand,Jean‐Hubert Caberg,Monique Elmaleh,Jeanne Lainé,Giovanni Stévanin,Gisèle Bonne,Odile Boespflug‐Tanguy,Laurent Servais	39
17	Mutations in BCAP31 Cause a Severe X-Linked Phenotype with Deafness, Dystonia, and Central Hypomyelination and Disorganize the Golgi Apparatus 2013 ·The American Journal of Human Genetics ·Pierre Cacciagli,(unknown),(unknown),Jean‐Christophe Roux,Imen Dorboz,Jean‐Pierre Desvignes,Catherine Badens,Marc Délepine,Mark Lathrop,Pierre Cau,Nicolas Lévy,Nadine Girard,Pierre Sarda,Odile Boespflug‐Tanguy,Laurent Villard	48
18	Mutations of POLR3A Encoding a Catalytic Subunit of RNA Polymerase Pol III Cause a Recessive Hypomyelinating Leukodystrophy p415 2012 ·The American Journal of Human Genetics ·Geneviève Bernard,Éliane Chouery,(unknown),Martine Tétreault,Asako Takanohashi,Giovanni A. Carosso,I Clément,Odile Boespflug‐Tanguy,Diana Rodriguez,Valérie Delague,Joelle Abou Ghoch,Nadine Jalkh,Imen Dorboz,Sébastien Fribourg,Martin Teichmann,André Mégarbané,Raphael Schiffmann,Adeline Vanderver,Bernard Brais	1
19	Mutations of POLR3A Encoding a Catalytic Subunit of RNA Polymerase Pol III Cause a Recessive Hypomyelinating Leukodystrophy 2011 ·The American Journal of Human Genetics ·Geneviève Bernard,Éliane Chouery,(unknown),Martine Tétreault,Asako Takanohashi,Giovanni A. Carosso,I Clément,Odile Boespflug‐Tanguy,Diana Rodriguez,Valérie Delague,Joelle Abou Ghoch,Nadine Jalkh,Imen Dorboz,Sébastien Fribourg,Martin Teichmann,André Mégarbané,Raphael Schiffmann,Adeline Vanderver,Bernard Brais	181
20	Sjögren–Larsson syndrome: Novel mutations in the ALDH3A2 gene in a French cohort 2011 ·Journal of the Neurological Sciences ·Catherine Sarret,(unknown),Catherine Vaurs‐Barrière,Imen Dorboz,Éléonore Eymard-Pierre,Patricia Combes,G Giraud,Ronald J. A. Wanders,Alexandra Afenjar,Christine Francannet,Odile Boespflug‐Tanguy	8

About Imen Dorboz

Imen Dorboz is a scholar working on Clinical Biochemistry, Biochemistry and Neurology, having authored 30 papers that have together received 650 indexed citations. Recurring topics across this work include RNA regulation and disease (14 papers), RNA Research and Splicing (9 papers) and RNA and protein synthesis mechanisms (5 papers). The work is most often cited by research in Neurology (74 citations), Clinical Biochemistry (50 citations) and Molecular Biology (492 citations). Imen Dorboz has collaborated with scholars based in France, Tunisia and United States. Frequent 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. Their work appears in journals such as PLoS ONE, Brain and Neurology.

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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