Sahar Elouej

410 total citations
19 papers, 173 citations indexed

About

Sahar Elouej is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Sahar Elouej has authored 19 papers receiving a total of 173 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Genetics and 5 papers in Cancer Research. Recurrent topics in Sahar Elouej's work include DNA Repair Mechanisms (3 papers), Genetic Associations and Epidemiology (2 papers) and Carcinogens and Genotoxicity Assessment (2 papers). Sahar Elouej is often cited by papers focused on DNA Repair Mechanisms (3 papers), Genetic Associations and Epidemiology (2 papers) and Carcinogens and Genotoxicity Assessment (2 papers). Sahar Elouej collaborates with scholars based in Tunisia, France and Italy. Sahar Elouej's co-authors include Sonia Abdelhak, Nicolas Lévy, Rym Kéfi, Majdi Nagara, Annachiara De Sandre‐Giovannoli, Shehla Mohammed, Ana Beleza‐Meireles, Richard Caswell, H. Jamoussi and Kevin Colclough and has published in prestigious journals such as Metabolism, Journal of Translational Medicine and Frontiers in Genetics.

In The Last Decade

Sahar Elouej

19 papers receiving 173 citations

Peers

Countries citing papers authored by Sahar Elouej

Since Specialization

Citations

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

Fields of papers citing papers by Sahar Elouej

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sahar Elouej

This figure shows the co-authorship network connecting the top 25 collaborators of Sahar Elouej. A scholar is included among the top collaborators of Sahar Elouej 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 Sahar Elouej. Sahar Elouej is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Association of HNF1A gene variants and haplotypes with metabolic syndrome: a case–control study in the Tunisian population and a meta-analysis 2022 ·Diabetology & Metabolic Syndrome ·(unknown), (unknown), (unknown), Sahar Elouej, Haifa Jmel, (unknown), Abdelmajid Abid, Afef Bahlous, Abdelhamid Barakat, H. Jamoussi, Sonia Abdelhak, Rym Kéfi	5
2	A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrome II Screening in Tunisia: A Case of Diffuse Gastric Carcinoma 2022 ·Genes ·(unknown), (unknown), Houcemeddine Othman, (unknown), (unknown), Sahar Elouej, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Hassen Touinsi, (unknown), Emna Chelbi, Sonia Abdelhak, (unknown), (unknown)	3
3	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
4	The Potential of Induced Pluripotent Stem Cells to Test Gene Therapy Approaches for Neuromuscular and Motor Neuron Disorders 2021 ·Frontiers in Cell and Developmental Biology ·(unknown), Sahar Elouej, Maria Grazia Biferi	6
5	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
6	FANCA Gene Mutations in North African Fanconi Anemia Patients 2021 ·Frontiers in Genetics ·(unknown), Olfa Messaoud, Sahar Elouej, (unknown), (unknown), Fethi Mellouli, Monia Ouederni, (unknown), Annachiara De Sandre‐Giovannoli, Valérie Delague, Nicolas Lévy, Massimo Bogliolo, Jordi Surrallés, Sonia Abdelhak, Ahlem Amouri	2
7	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
8	Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young 2020 ·Herz ·(unknown), Yosra Bouyacoub, (unknown), Lilia Kraoua, Amira Zaroui, Sahar Elouej, Majdi Nagara, (unknown), Valérie Delague, Nicolas Lévy, (unknown), Rachid Mechmèche, Stéphane Zaffran, Sonia Abdelhak	8
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	Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing 2019 ·Acta Diabetologica ·(unknown), (unknown), (unknown), (unknown), Sahar Elouej, Haifa Jmel, (unknown), (unknown), (unknown), Luana Mercuri, (unknown), Tommaso Mazza, (unknown), Mèlika Ben Ahmed, H. Jamoussi, Abdelmajid Abid, Vincenzo Trischitta, Sonia Abdelhak, Sabrina Prudente, Rym Kéfi	17
11	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
12	Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome 2018 ·BMC Pediatrics ·(unknown), Arnaud Lagarde, (unknown), Sahar Elouej, (unknown), Emna Kerkeni, (unknown), Sylviane Olschwang, Jean‐Pierre Desvignes, Sonia Abdelhak, Valérie Delague, Nicolas Lévy, Kamel Monastiri, Annachiara De Sandre‐Giovannoli	3
13	Distal renal tubular acidosis in a Libyan patient: Evidence for digenic inheritance 2017 ·European Journal of Medical Genetics ·Majdi Nagara, Gregory Papagregoriou, (unknown), Zied Landoulsi, Yosra Bouyacoub, Sahar Elouej, Rym Kéfi, Tommaso Pippucci, Konstantinos Voskarides, Anu Bashamboo, Kenneth McElreavey, M. Hachicha, G. Cara Romeo, Marco Seri, Constantinos Deltas, Sonia Abdelhak	7
14	Lactase persistence in Tunisia as a result of admixture with other Mediterranean populations 2017 ·Genes & Nutrition ·(unknown), Rym Kéfi, Marco Sazzini, Cristina Giuliani, Sara De Fanti, (unknown), Majdi Nagara, Giacomo Mengozzi, Sahar Elouej, Abdelmajid Abid, H. Jamoussi, Lotfi Chouchane, G. Cara Romeo, Sonia Abdelhak, Donata Luiselli	8
15	Exome sequencing reveals a de novo POLD1 mutation causing phenotypic variability in mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome (MDPL) 2017 ·Metabolism ·Sahar Elouej, Ana Beleza‐Meireles, Richard Caswell, Kevin Colclough, Sian Ellard, Jean‐Pierre Desvignes, Christophe Béroud, Nicolas Lévy, Shehla Mohammed, Annachiara De Sandre‐Giovannoli	37
16	Association of rs9939609 Polymorphism with Metabolic Parameters and FTO Risk Haplotype Among Tunisian Metabolic Syndrome 2016 ·Metabolic Syndrome and Related Disorders ·Sahar Elouej, (unknown), Majdi Nagara, Khaled Lasram, Redha Attaoua, (unknown), (unknown), (unknown), Lilia Romdhane, H. Jamoussi, Z. Turki, Abdelmajid Abid, C. Ben Slama, (unknown), Sonia Abdelhak, Florin Grigorescu, Habiba Ben Romdhane, Rym Kéfi	25
17	Gender-specific associations of genetic variants with metabolic syndrome components in the Tunisian population 2016 ·Endocrine Research ·Sahar Elouej, (unknown), Redha Attaoua, Majdi Nagara, (unknown), (unknown), (unknown), H. Jamoussi, Z. Turki, H. Abid, C. Ben Slama, (unknown), Habiba Ben Romdhane, Sonia Abdelhak, Rym Kéfi, Florin Grigorescu	15
18	A Tunisian Patient with Two Rare Syndromes: Triple A Syndrome and Congenital Hypogonadotropic Hypogonadism 2014 ·Hormone Research in Paediatrics ·(unknown), (unknown), Majdi Nagara, (unknown), Sahar Elouej, Olfa Messaoud, Yosra Bouyacoub, Lilia Romdhane, Z. Turki, Sonia Abdelhak, (unknown)	7
19	A novel splice-site mutation in ATP6V0A4 gene in two brothers with distal renal tubular acidosis from a consanguineous Tunisian family 2014 ·Journal of Genetics ·Majdi Nagara, Konstantinos Voskarides, Sahar Elouej, Apostolos Zaravinos, (unknown), Gregory Papagregoriou, Rym Kéfi, Khadija Boussetta, Constantinos Deltas, Sonia Abdelhak, Faten Tinsa	3

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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