Sonia Abdelhak

6.1k total citations · 1 hit paper
206 papers, 3.3k citations indexed

About

Sonia Abdelhak is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Sonia Abdelhak has authored 206 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 107 papers in Molecular Biology, 79 papers in Genetics and 22 papers in Cancer Research. Recurrent topics in Sonia Abdelhak's work include DNA Repair Mechanisms (28 papers), Genomics and Rare Diseases (16 papers) and Carcinogens and Genotoxicity Assessment (14 papers). Sonia Abdelhak is often cited by papers focused on DNA Repair Mechanisms (28 papers), Genomics and Rare Diseases (16 papers) and Carcinogens and Genotoxicity Assessment (14 papers). Sonia Abdelhak collaborates with scholars based in Tunisia, France and Morocco. Sonia Abdelhak's co-authors include Rym Kéfi, Christine Petit, Lilia Romdhane, C. Vincent, Vasiliki Kalatzis, Sylvie Compain, Koussay Dellagi, Yosr Hamdi, P Burlet and Judith Melki and has published in prestigious journals such as The Lancet, Nucleic Acids Research and Nature Genetics.

In The Last Decade

Sonia Abdelhak

204 papers receiving 3.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family

1997 467 citations Sonia Abdelhak et al. profile →

Peers

Countries citing papers authored by Sonia Abdelhak

Since Specialization

Citations

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

Fields of papers citing papers by Sonia Abdelhak

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sonia Abdelhak

This figure shows the co-authorship network connecting the top 25 collaborators of Sonia Abdelhak. A scholar is included among the top collaborators of Sonia Abdelhak 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 Sonia Abdelhak. Sonia Abdelhak 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	Identification of two variants in AGRN and RPL3L genes in a patient with catecholaminergic polymorphic ventricular tachycardia suggesting new candidate disease genes and digenic inheritance 2022 ·SHILAP Revista de lepidopterología ·(unknown), (unknown), (unknown), Sonia Abdelhak, Stéphane Zaffran	9
3	Inflammatory landscape in Xeroderma pigmentosum patients with cutaneous melanoma 2022 ·Scientific Reports ·(unknown), M. Jones, Tadeja Režen, Mèlika Ben Ahmed, (unknown), Radovan Komel, Mohamed Khalgui, Samir Boubaker, Sonia Abdelhak, Houda Yacoub‐Youssef	1
4	Women in Systems Science and Gender Parity: Why and How to Democratize the “Technology, Innovation, and Society Nexus” 2022 ·OMICS A Journal of Integrative Biology ·Yosr Hamdi, Nicola Mulder, Sonia Abdelhak	2
5	Identification of a CDH12 potential candidate genetic variant for an autosomal dominant form of transgrediens and progrediens palmoplantar keratoderma in a Tunisian family 2020 ·Journal of Human Genetics ·(unknown), (unknown), (unknown), Kaïs Ghedira, Yosr Hamdi, Sahar Elouej, Zied Landoulsi, Valérie Delague, Arnaud Lagarde, Nicolas Lévy, A. Amraoui, (unknown), Sonia Abdelhak, M. Mokni	3
6	High-quality genome sequence assembly of R.A73 Enterococcus faecium isolated from freshwater fish mucus 2020 ·BMC Microbiology ·(unknown), Kaïs Ghedira, Monia El Bour, Sonia Abdelhak, Alia Benkahla, Balkiss Bouhaouala‐Zahar	6
7	A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide withRAF1S259Y neomutation 2019 ·Genetics Research ·(unknown), Amel Ben Chehida, Lilia Kraoua, Heather Etchevers, Laurent Argiro, (unknown), (unknown), Valérie Delague, Nicolas Lévy, Néji Tebib, Ridha Mrad, Sonia Abdelhak, (unknown), Stéphane Zaffran	3
8	Novel MED12 variant in a multiplex Fragile X syndrome family: dual molecular etiology of two X-linked intellectual disabilities with autism in the same family 2019 ·Molecular Biology Reports ·(unknown), (unknown), (unknown), (unknown), (unknown), Rym Kéfi, Ridha Mrad, Sonia Abdelhak, Naoufel Gaddour	4
9	Identification of novel pathogenic MSH2 mutation and new DNA repair genes variants: investigation of a Tunisian Lynch syndrome family with discordant twins 2019 ·Journal of Translational Medicine ·(unknown), H. Tounsi, (unknown), Yosr Hamdi, Sahar Elouej, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Najla Mezghani, Sonia Abdelhak, (unknown), (unknown), Samir Boubaker	7
10	Novel ALPK3 mutation in a Tunisian patient with pediatric cardiomyopathy and facio-thoraco-skeletal features 2018 ·Journal of Human Genetics ·(unknown), Lilia Kraoua, (unknown), Alexandre Atkinson, Valérie Delague, Nicolas Lévy, (unknown), Ridha Mrad, Sonia Abdelhak, Stéphane Zaffran	16
11	<b><i>TOP3B</i></b>: A Novel Candidate Gene in Juvenile Myoclonic Epilepsy? 2018 ·Cytogenetic and Genome Research ·(unknown), (unknown), Mohamed Kacem Ben Fradj, (unknown), (unknown), Lilia Kraoua, (unknown), Faouzi Mâazoul, (unknown), Nadia Ali, Sonia Abdelhak, Ridha Mrad	16
12	Genetic Analysis of <b><i>TREM2</i></b> Variants in Tunisian Patients with Alzheimer's Disease 2018 ·Medical Principles and Practice ·Zied Landoulsi, Mouna Ben Djebara, Imen Kacem, Youssef Sidhom, Rym Kéfi, Sonia Abdelhak, Amina Gargouri, Riadh Gouider	5
13	Bathing suit ichthyosis caused by a TGM1 mutation in a Tunisian child 2014 ·International Journal of Dermatology ·(unknown), (unknown), Ridha Mrad, (unknown), Sonia Abdelhak, Alain Hovnanian, I. Mokhtar	5
14	Retinal dystrophy and congenital glaucoma as major causes of vision loss in students attending two institutions for the visually disabled in Tunis city, Tunisia 2014 ·Journal Français d Ophtalmologie ·(unknown), (unknown), Nizar Ben Halim, (unknown), (unknown), Sonia Abdelhak, L. El Matri	3
15	Clinical Polymorphism of Stargardt Disease in a Large Consanguineous Tunisian Family; Implications for Nosology 2013 ·SHILAP Revista de lepidopterología ·L. El Matri, (unknown), A. Chebil, (unknown), Sonia Abdelhak	1
16	Association study of mitochondrial DNA polymorphisms with type 2 diabetes in Tunisian population 2013 ·Mitochondrial DNA ·(unknown), Nizar Ben Halim, Khaled Lasram, (unknown), H. Jamoussi, (unknown), Slim Ben Ammar, (unknown), H. Abid, Sonia Abdelhak, Rym Kéfi	11
17	Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 gene 2010 ·Journal of Human Genetics ·(unknown), (unknown), Yosra Bouyacoub, (unknown), (unknown), (unknown), (unknown), Leila Tiab, (unknown), Ahmed Rebaï, Daniel F. Schorderet, Francis L. Munier, Léonidas Zografos, Sonia Abdelhak, L. El Matri	13
18	[Mutation spectrum of Gaucher disease in Tunisia: high frequency of N370S/Rec NciI compound heterozygous]. 2007 ·PubMed ·(unknown), Hadhami Ben Turkia, Néji Tebib, Olga Amaral, (unknown), (unknown), (unknown), Catherine Caillaud, Clara Sá-Miranda, Sonia Abdelhak, (unknown)	5
19	Hyperoxalurie primitive chez l'enfant au centre Tunisien 2007 ·Jalel Chemli, (unknown), (unknown), Sonia Abdelhak, Naoufel Nabli, Saoussen Abroug, Mohamed Tahar Sfar, (unknown), F. Amri, (unknown)	3
20	Phenotypic Variation in a Family With Stargardt Like Retinal Dystrophy and ABCA4 Mutation 2006 ·Investigative Ophthalmology & Visual Science ·L. El Matri, (unknown), F. Mghaieth, (unknown), (unknown), (unknown), (unknown), Sonia Abdelhak	2

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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