Yosra Bouyacoub

771 total citations
27 papers, 381 citations indexed

About

Yosra Bouyacoub is a scholar working on Molecular Biology, Sensory Systems and Genetics. According to data from OpenAlex, Yosra Bouyacoub has authored 27 papers receiving a total of 381 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 6 papers in Sensory Systems and 6 papers in Genetics. Recurrent topics in Yosra Bouyacoub's work include Hearing, Cochlea, Tinnitus, Genetics (6 papers), DNA Repair Mechanisms (4 papers) and Connexins and lens biology (4 papers). Yosra Bouyacoub is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (6 papers), DNA Repair Mechanisms (4 papers) and Connexins and lens biology (4 papers). Yosra Bouyacoub collaborates with scholars based in Tunisia, France and Italy. Yosra Bouyacoub's co-authors include Sonia Abdelhak, Rym Kéfi, Olfa Messaoud, Crystel Bonnet, Christine Petit, Lilia Romdhane, Jean‐Pierre Hardelin, G. Besbes, Majdi Nagara and Imen Dorboz and has published in prestigious journals such as PLoS ONE, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Yosra Bouyacoub

27 papers receiving 381 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Yosra Bouyacoub Tunisia	12	222	103	85	40	35	27	381
Paola Primignani Italy	14	223 1.0×	82 0.8×	104 1.2×	30 0.8×	12 0.3×	32	526
Carina Frykholm Sweden	10	100 0.5×	56 0.5×	94 1.1×	102 2.5×	38 1.1×	15	276
Caroline Abadie France	8	265 1.2×	94 0.9×	101 1.2×	33 0.8×	5 0.1×	21	358
Dinah Clark United States	15	495 2.2×	250 2.4×	97 1.1×	48 1.2×	24 0.7×	21	711
Angus Dobbie United Kingdom	12	402 1.8×	284 2.8×	13 0.2×	9 0.2×	24 0.7×	20	675
Majida Charif France	17	417 1.9×	114 1.1×	167 2.0×	105 2.6×	4 0.1×	51	617
Polona Le Quesne Stabej United Kingdom	14	348 1.6×	167 1.6×	123 1.4×	44 1.1×	2 0.1×	18	535
Martin Krenn Austria	13	135 0.6×	60 0.6×	54 0.6×	16 0.4×	5 0.1×	36	394
Flavia Palombo Italy	10	226 1.0×	155 1.5×	18 0.2×	25 0.6×	3 0.1×	27	416
Saïda Ben Arab Tunisia	12	248 1.1×	75 0.7×	252 3.0×	86 2.1×	2 0.1×	19	555

Countries citing papers authored by Yosra Bouyacoub

Since Specialization

Citations

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

Fields of papers citing papers by Yosra Bouyacoub

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yosra Bouyacoub

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

Turki, Z., Sahar Elouej, Yosra Bouyacoub, et al.. (2021). Oligogenic Inheritance Underlying Incomplete Penetrance of PROKR2 Mutations in Hypogonadotropic Hypogonadism. Frontiers in Genetics. 12. 665174–665174. 3 indexed citations

Sahbatou, Mourad, Antoine Daunay, Laura G. Baudrin, et al.. (2020). Improvements and inter-laboratory implementation and optimization of blood-based single-locus age prediction models using DNA methylation of the ELOVL2 promoter. Scientific Reports. 10(1). 15652–15652. 15 indexed citations

Bouyacoub, Yosra, Lilia Kraoua, Amira Zaroui, et al.. (2020). Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young. Herz. 46(S1). 94–102. 8 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

Nagara, Majdi, Gregory Papagregoriou, Zied Landoulsi, et al.. (2017). Distal renal tubular acidosis in a Libyan patient: Evidence for digenic inheritance. European Journal of Medical Genetics. 61(1). 1–7. 7 indexed citations

Rekaya, Mariem Ben, Olfa Messaoud, M. Jones, et al.. (2017). Whole Exome Sequencing allows the identification of two novel groups of Xeroderma pigmentosum in Tunisia, XP-D and XP-E: Impact on molecular diagnosis. Journal of Dermatological Science. 89(2). 172–180. 15 indexed citations

Delmaghani, Sedigheh, Asadollah Aghaie, Yosra Bouyacoub, et al.. (2016). Mutations in CDC14A , Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness. The American Journal of Human Genetics. 98(6). 1266–1270. 29 indexed citations

Bonnet, Crystel, Yosra Bouyacoub, Jean‐Pierre Hardelin, et al.. (2015). Whole Exome Sequencing Identifies Mutations in Usher Syndrome Genes in Profoundly Deaf Tunisian Patients. PLoS ONE. 10(3). e0120584–e0120584. 18 indexed citations

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

10.

Romdhane, Lilia, Nizar Ben Halim, Rym Kéfi, et al.. (2014). Specific Aspects of Consanguinity: Some Examples from the Tunisian Population. Human Heredity. 77(1-4). 167–174. 17 indexed citations

11.

Nagara, Majdi, Sahar Elouej, Olfa Messaoud, et al.. (2014). A Tunisian Patient with Two Rare Syndromes: Triple A Syndrome and Congenital Hypogonadotropic Hypogonadism. Hormone Research in Paediatrics. 82(5). 338–343. 7 indexed citations

12.

Rekaya, Mariem Ben, Olfa Messaoud, M. Jones, et al.. (2014). A Founder Large Deletion Mutation in Xeroderma Pigmentosum-Variant Form in Tunisia: Implication for Molecular Diagnosis and Therapy. BioMed Research International. 2014. 1–8. 10 indexed citations

13.

Bouyacoub, Yosra, Hatem Azzouz, Mariem Ben Rekaya, et al.. (2013). Novel and recurrent mutations in the TAT gene in Tunisian families affected with Richner–Hanhart Syndrome. Gene. 529(1). 45–49. 8 indexed citations

14.

Bouyacoub, Yosra, N. Beltaïef, Rym Kéfi, et al.. (2013). Compound heterozygosity for dominant and recessive GJB2 mutations in a Tunisian family and association with successful cochlear implant outcome. International Journal of Pediatric Otorhinolaryngology. 77(9). 1481–1484. 10 indexed citations

15.

Bouyacoub, Yosra, Lilia Romdhane, Rym Kéfi, et al.. (2013). Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss. Gene. 525(1). 1–4. 27 indexed citations

16.

Jaafoura, H., Olfa Messaoud, Majdi Nagara, et al.. (2013). A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian families. International Journal of Pediatric Otorhinolaryngology. 77(9). 1485–1488. 3 indexed citations

17.

Messaoud, Olfa, Mariem Ben Rekaya, Inès Ouertani, et al.. (2013). The Experience of a Tunisian Referral Centre in Prenatal Diagnosis of <b><i>Xeroderma pigmentosum</i></b>. Public Health Genomics. 16(5). 251–254. 6 indexed citations

18.

Azzouz, Hatem, François Petit, Mariem Ben Khelifa, et al.. (2013). Molecular and biochemical characterization of a novel intronic single point mutation in a Tunisian family with glycogen storage disease type III. Molecular Biology Reports. 40(7). 4197–4202. 7 indexed citations

19.

Bouyacoub, Yosra, Leila Tiab, Ahmed Rebaï, et al.. (2010). Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 gene. Journal of Human Genetics. 56(1). 22–28. 13 indexed citations

20.

Gribaa, Moez, M. Younès, Yosra Bouyacoub, et al.. (2009). An autosomal dominant hypophosphatemic rickets phenotype in a Tunisian family caused by a new FGF23 missense mutation. Journal of Bone and Mineral Metabolism. 28(1). 111–115. 40 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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