Olfa Messaoud

706 total citations
39 papers, 384 citations indexed

About

Olfa Messaoud is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Olfa Messaoud has authored 39 papers receiving a total of 384 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 13 papers in Cancer Research and 12 papers in Genetics. Recurrent topics in Olfa Messaoud's work include DNA Repair Mechanisms (17 papers), Carcinogens and Genotoxicity Assessment (11 papers) and Genomics and Rare Diseases (4 papers). Olfa Messaoud is often cited by papers focused on DNA Repair Mechanisms (17 papers), Carcinogens and Genotoxicity Assessment (11 papers) and Genomics and Rare Diseases (4 papers). Olfa Messaoud collaborates with scholars based in Tunisia, France and Italy. Olfa Messaoud's co-authors include Sonia Abdelhak, Mariem Ben Rekaya, M. Mokni, Ahlem Amouri, Mohamed Khalgui, Rym Kéfi, Hamouda Boussen, Yosra Bouyacoub, Lilia Romdhane and Ahmed Rebaï and has published in prestigious journals such as Molecules, Gene and British Journal of Dermatology.

In The Last Decade

Olfa Messaoud

39 papers receiving 382 citations

Peers

Countries citing papers authored by Olfa Messaoud

Since Specialization

Citations

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

Fields of papers citing papers by Olfa Messaoud

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Olfa Messaoud

This figure shows the co-authorship network connecting the top 25 collaborators of Olfa Messaoud. A scholar is included among the top collaborators of Olfa Messaoud 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 Olfa Messaoud. Olfa Messaoud 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	First genetic characterization of Xeroderma pigmentosum in Libya: High frequency of XP‐C founder mutation 2023 ·Molecular Genetics & Genomic Medicine ·(unknown), Olfa Messaoud, Mariem Ben Rekaya, (unknown), Mohamed Khalgui, (unknown), (unknown), M. Mokni, Sonia Abdelhak, (unknown)	2
2	The first exome wide association study in Tunisia: identification of candidate loci and pathways with biological relevance for type 2 diabetes 2023 ·Frontiers in Endocrinology ·(unknown), (unknown), (unknown), (unknown), Haifa Jmel, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Hajer Trabelsi, Afef Bahlous, H. Jamoussi, Olfa Messaoud, Abdelmajid Abid, Rym Kéfi	3
3	CVD Graphene Electrode for Direct Electrochemical Detection of Double-Stranded DNA 2023 ·Inorganics ·Afrah Bardaoui, (unknown), (unknown), (unknown), (unknown), Olfa Messaoud, Diogo M.F. Santos, R. Chtourou	1
4	A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North Africa 2021 ·npj Genomic Medicine ·Lilia Romdhane, (unknown), (unknown), Olfa Messaoud, Jingxuan Shan, Khalid A. Fakhro, Rym Kéfi, Lotfi Chouchane, Sonia Abdelhak	6
5	Case Report: Identification of Novel Variants in ERCC4 and DDB2 Genes in Two Tunisian Patients With Atypical Xeroderma Pigmentosum Phenotype 2021 ·Frontiers in Genetics ·(unknown), (unknown), Houcemeddine Othman, Sahar Elouej, M. Jones, Arnaud Lagarde, Mariem Ben Rekaya, Olfa Messaoud, Mohamed Khalgui, Valérie Delague, Nicolas Lévy, Annachiara De Sandre‐Giovannoli, Sonia Abdelhak, Houda Yacoub‐Youssef	3
6	Oligogenic Inheritance Underlying Incomplete Penetrance of PROKR2 Mutations in Hypogonadotropic Hypogonadism 2021 ·Frontiers in Genetics ·(unknown), (unknown), (unknown), (unknown), Z. Turki, Sahar Elouej, Yosra Bouyacoub, (unknown), Kenneth McElreavey, Anu Bashamboo, Sonia Abdelhak, Olfa Messaoud	3
7	Identification of a ERCC5 c.2333T>C (L778P) Variant in Two Tunisian Siblings With Mild Xeroderma Pigmentosum Phenotype 2019 ·Frontiers in Genetics ·(unknown), Sahar Elouej, (unknown), M. Jones, Arnaud Lagarde, Mariem Ben Rekaya, Olfa Messaoud, Yosr Hamdi, Mohamed Khalgui, Valérie Delague, Nicolas Lévy, Annachiara De Sandre‐Giovannoli, Sonia Abdelhak, Houda Yacoub‐Youssef	11
8	A genome wide SNP genotyping study in the Tunisian population: specific reporting on a subset of common breast cancer risk loci 2018 ·BMC Cancer ·Yosr Hamdi, Mariem Ben Rekaya, Jingxuan Shan, Majdi Nagara, Olfa Messaoud, Amel Benammar Elgaaïed, Ridha Mrad, Lotfi Chouchane, (unknown), Sonia Abdelhak, Hamouda Boussen, Lilia Romdhane	11
9	Whole Exome Sequencing allows the identification of two novel groups of Xeroderma pigmentosum in Tunisia, XP-D and XP-E: Impact on molecular diagnosis 2017 ·Journal of Dermatological Science ·Mariem Ben Rekaya, (unknown), Olfa Messaoud, M. Jones, Yosra Bouyacoub, Majdi Nagara, Tommaso Pippucci, Haifa Jmel, (unknown), (unknown), (unknown), (unknown), Anu Bashamboo, Kenneth McElreavey, G. Cara Romeo, Abdelhamid Barakat, Mohamed Khalgui, Houda Yacoub‐Youssef, Sonia Abdelhak	15
10	Specific Aspects of Consanguinity: Some Examples from the Tunisian Population 2014 ·Human Heredity ·Lilia Romdhane, Nizar Ben Halim, (unknown), Rym Kéfi, Yosra Bouyacoub, Mariem Ben Rekaya, (unknown), Olfa Messaoud, (unknown), Crystel Bonnet, (unknown), Majdi Nagara, Christine Petit, Ken McElreavey, Giovanni Romeo, Sonia Abdelhak	17
11	A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian families 2013 ·International Journal of Pediatric Otorhinolaryngology ·(unknown), (unknown), H. Jaafoura, (unknown), Olfa Messaoud, (unknown), Majdi Nagara, (unknown), (unknown), Yosra Bouyacoub, Rym Kéfi, Crystel Bonnet, G. Besbes, Sonia Abdelhak	3
12	The Experience of a Tunisian Referral Centre in Prenatal Diagnosis of <b><i>Xeroderma pigmentosum</i></b> 2013 ·Public Health Genomics ·Olfa Messaoud, Mariem Ben Rekaya, (unknown), Inès Ouertani, Rym Kéfi, (unknown), Yosra Bouyacoub, (unknown), Houda Yacoub‐Youssef, S Boubaker, (unknown), Ridha Mrad, Ahlem Amouri, Sonia Abdelhak	6
13	Mutational spectrum of Xeroderma pigmentosum group A in Egyptian patients 2013 ·Gene ·Khalda Amr, Olfa Messaoud, (unknown), Sonia Abdelhak, Ghada El‐Kamah	12
14	Novel and recurrent mutations in the TAT gene in Tunisian families affected with Richner–Hanhart Syndrome 2013 ·Gene ·Yosra Bouyacoub, (unknown), Hatem Azzouz, (unknown), (unknown), (unknown), Mariem Ben Rekaya, Olfa Messaoud, Lilia Romdhane, (unknown), (unknown), (unknown), Néji Tebib, M. Mokni, Naziha Kaabachi, Samir Boubaker, Sonia Abdelhak	8
15	c.1643_1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosum 2012 ·Archives of Dermatological Research ·(unknown), Omar Abidi, Sellama Nadifi, H. Benchikhi, K. Khadir, Mariem Ben Rekaya, (unknown), Olfa Messaoud, Sonia Abdelhak, Abdelhamid Barakat	14
16	A novel POLH gene mutation in a xeroderma pigmentosum-V Tunisian patient: phenotype–genotype correlation 2011 ·Journal of Genetics ·Mariem Ben Rekaya, Olfa Messaoud, Amel Mebazâa, (unknown), Héla Azaiez, (unknown), Mohamed Khalgui, Samir Boubaker, Ahlem Amouri, (unknown), Sonia Abdelhak, M. Mokni	11
17	Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity 2011 ·Archives of Dermatological Research ·Olfa Messaoud, Mariem Ben Rekaya, (unknown), (unknown), Héla Azaiez, Rym Kéfi, N. Gouider‐Khouja, I Mokhtar, Ahlem Amouri, (unknown), (unknown), Sonia Abdelhak	18
18	Identification of a primarily neurological phenotypic expression of xeroderma pigmentosum complementation group A in a Tunisian family 2010 ·British Journal of Dermatology ·Olfa Messaoud, Mariem Ben Rekaya, Rym Kéfi, (unknown), (unknown), (unknown), N. Gouider‐Khouja, (unknown), (unknown), I Mokhtar, Sonia Abdelhak, (unknown)	15
19	Genetic homogeneity of mutational spectrum of group‐A xeroderma pigmentosum in Tunisian patients 2010 ·International Journal of Dermatology ·Olfa Messaoud, Mariem Ben Rekaya, (unknown), (unknown), Hammouda Boussen, I Mokhtar, Samir Boubaker, Ahlem Amouri, Sonia Abdelhak, Mohamed Khalgui	21
20	High frequency of the V548A fs X572 XPC mutation in Tunisia: implication for molecular diagnosis 2009 ·Journal of Human Genetics ·Mariem Ben Rekaya, Olfa Messaoud, (unknown), (unknown), (unknown), Ahlem Amouri, Hamouda Boussen, S Boubaker, M. Mokni, (unknown), Sonia Abdelhak, (unknown)	38

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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