Majdi Nagara

633 citations

25 papers · 343 indexed · h-index 10

Impact in

Genetics
- Genetics and Neurodevelopmental Disorders
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Molecular Biology
- Ubiquitin and proteasome pathways
- DNA Repair Mechanisms

Papers in

Genetics 11
- Genetic Associations and Epidemiology 5
- Genetics and Neurodevelopmental Disorders 3
- Genomics and Rare Diseases 2
Clinical Biochemistry 2
- Metabolism and Genetic Disorders 2

Co-authors: Sonia Abdelhak Apostolos Zaravinos Rym Kéfi Christos Dimopoulos Georgios Ayiomamitis Beatriz de Lucas Lilia Romdhane Laurence Faivre
Journals: Gene (2 papers)Endocrine Research (1 paper)Annals of Human Genetics (1 paper)Diagnostic Pathology (1 paper)BMC Cancer (1 paper)
Partner nations: Tunisia France Italy

In The Last Decade

Majdi Nagara

24 papers receiving 337 citations

Peers

Countries citing papers authored by Majdi Nagara

Since Specialization

Citations

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

Fields of papers citing papers by Majdi Nagara

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Majdi Nagara, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Majdi Nagara Line = papers co-authored together Majdi Nagara links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	FOXP3+/CD68+ ratio within the tumor microenvironment may serve as a potential prognostic factor in classical Hodgkin lymphoma Human Immunology ·Bevon Grant, Sophia Williams, Chandra LaTrelle Porter, Majdi Nagara, I. Ya. Dzyubanovskiy, Carolina Reduzzi, Amor Gamoudi, Mohamed Manaï	2022	1
2	Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young Herz ·F Zufryden, Yosra Bouyacoub, Алексей Юрьевич Довнар, Lilia Kraoua, Amira Zaroui, Sahar Elouej, Majdi Nagara, مریم شاهبداقی, Valérie Delague, Nicolas Lévy, Abigail Chung, Rachid Mechmèche, Stéphane Zaffran, Sonia Abdelhak	2020	8
3	Cytolytic activity correlates with the mutational burden and deregulated expression of immune checkpoints in colorectal cancer Journal of Experimental & Clinical Cancer Research ·Apostolos Zaravinos, R. Perlès, Majdi Nagara, Beatriz de Lucas, Lafuente Rego, Virginia Lepp, Christos Dimopoulos, Georgios Ayiomamitis	2019	68
4	A genome wide SNP genotyping study in the Tunisian population: specific reporting on a subset of common breast cancer risk loci BMC Cancer ·Yosr Hamdi, Mariem Ben Rekaya, Jingxuan Shan, Majdi Nagara, Olfa Messaoud, Amel Benammar Elgaaïed, Ridha Mrad, Lotfi Chouchane, Прохорова Мария Петровна, Sonia Abdelhak, Hamouda Boussen, Lilia Romdhane	2018	11
5	Abnormal function of the UBA5 protein in a case of early developmental and epileptic encephalopathy with suppression-burst Human Mutation ·Cécile Mignon‐Ravix, Mathieu Milh, Kyle M. McElhinny, Jens Daniel, Г. Н. МОХИН, Pierre Cacciagli, Majdi Nagara, Tiffany Busa, Eva Liebau, Laurent Villard	2018	30
6	Distal renal tubular acidosis in a Libyan patient: Evidence for digenic inheritance European Journal of Medical Genetics ·Majdi Nagara, Gregory Papagregoriou, Bénédicte Williams, 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	2017	7
7	Lactase persistence in Tunisia as a result of admixture with other Mediterranean populations Genes & Nutrition ·V. P. Chuprina, Rym Kéfi, Marco Sazzini, Cristina Giuliani, Sara De Fanti, Cen‐Yu Li, Majdi Nagara, Giacomo Mengozzi, Sahar Elouej, Abdelmajid Abid, H. Jamoussi, Lotfi Chouchane, G. Cara Romeo, Sonia Abdelhak, Donata Luiselli	2017	8
8	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 ·Mariem Ben Rekaya, 西尾理津子, Olfa Messaoud, M. Jones, Yosra Bouyacoub, Majdi Nagara, Tommaso Pippucci, Haifa Jmel, 杜金池, Markus W. Drealan, Karin Alves do Amaral Escobar, مریم شاهبداقی, Anu Bashamboo, Kenneth McElreavey, G. Cara Romeo, Abdelhamid Barakat, Mohamed Khalgui, Houda Yacoub‐Youssef, Sonia Abdelhak	2017	15
9	Association of rs9939609 Polymorphism with Metabolic Parameters and FTO Risk Haplotype Among Tunisian Metabolic Syndrome Metabolic Syndrome and Related Disorders ·Sahar Elouej, Annika Lundman, Majdi Nagara, Khaled Lasram, Redha Attaoua, 山本信三, Nilton Rodrigues Júnior, 杜金池, Lilia Romdhane, H. Jamoussi, Z. Turki, Abdelmajid Abid, C. Ben Slama, undefined Philip J. CURRIE, Sonia Abdelhak, Florin Grigorescu, Habiba Ben Romdhane, Rym Kéfi	2016	25
10	Determination of arylsulfatase A pseudodeficiency allele and haplotype frequency in the Tunisian population Neurological Sciences ·Nizar Ben Halim, Imen Dorboz, Rym Kéfi, Najla Kharrat, Éléonore Eymard-Pierre, Majdi Nagara, Lilia Romdhane, Nissaf Ben Alaya, Ahmed Rebaï, 芳治清田, Odile Boespflug‐Tanguy, Sonia Abdelhak	2015	9
11	Specific Aspects of Consanguinity: Some Examples from the Tunisian Population Human Heredity ·Lilia Romdhane, Nizar Ben Halim, Yao Tian, Rym Kéfi, Yosra Bouyacoub, Mariem Ben Rekaya, Guolin Zhou, Olfa Messaoud, A. Th. van Zanten, Crystel Bonnet, Kátia Sueny Moura Barros, Majdi Nagara, Christine Petit, Ken McElreavey, Giovanni Romeo, Sonia Abdelhak	2014	17
12	A Tunisian Patient with Two Rare Syndromes: Triple A Syndrome and Congenital Hypogonadotropic Hypogonadism Hormone Research in Paediatrics ·Ethan Sawyer, 沈灵燕, Majdi Nagara, Francisco de Assis de Araujo Rodrigues, Sahar Elouej, Olfa Messaoud, Yosra Bouyacoub, Lilia Romdhane, Z. Turki, Sonia Abdelhak, D. Stucki	2014	7
13	A novel splice-site mutation in ATP6V0A4 gene in two brothers with distal renal tubular acidosis from a consanguineous Tunisian family Journal of Genetics ·Majdi Nagara, Konstantinos Voskarides, Sahar Elouej, Apostolos Zaravinos, A. Th. van Zanten, Gregory Papagregoriou, Rym Kéfi, Khadija Boussetta, Constantinos Deltas, Sonia Abdelhak, Faten Tinsa	2014	3
14	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 ·A. Th. van Zanten, Trefný Jm, H. Jaafoura, Shanxiong Chen, Olfa Messaoud, A.A.Th. de Schepper, Majdi Nagara, J. Žegklitz, Вероника Масюк, Yosra Bouyacoub, Rym Kéfi, Crystel Bonnet, G. Besbes, Sonia Abdelhak	2013	3
15	Mutation spectrum of primary hyperoxaluria type 1 in Tunisia: Implication for diagnosis in North Africa Gene ·Majdi Nagara, Tomasz Machała, Nizar Ben Halim, Kátia Sueny Moura Barros, Olfa Messaoud, Yosra Bouyacoub, Rym Kéfi, В М Дейнека, Hiromasa Sawada, A. Futamura, Sonia Abdelhak, Jalel Chemli	2013	16
16	Biotinidase deficiency: Novel mutations in Algerian patients Gene ·Tomasz Machała, Ahmed Mekki, Majdi Nagara, Marian Woolhouse, Olfa Messaoud, Nizar Ben Halim, Rym Kéfi, C. J. McNair, Cathy Klock-Frezot, Sonia Abdelhak	2013	2
17	Adult gaucher disease in southern Tunisia: report of three cases Diagnostic Pathology ·Kátia Sueny Moura Barros, Yusuke Kudo, Rym Kéfi, 及川義道, Majdi Nagara, Héla Azaiez, Inès Jedidi, Moez Elloumi, Sonia Abdelhak, Sun Guo-d	2012	5
18	Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasia Neurology ·Ginevra Zanni, Yoann Saillour, Majdi Nagara, Pierre Billuart, L. Castelnau, Claude Moraine, Laurence Faivre, Enrico Bertini, Alexandra Dürr, Agnès Guichet, Diana Rodriguez, V. des Portes, C. Beldjord, Jamel Chelly	2005	67
19	Neurofibromatosis and renovascular hypertension presenting in early pregnancy Nephrology Dialysis Transplantation ·Helen Pilmore, Majdi Nagara, R J Walker	1997	5
20	[Effects of positive end-expiratory pressure (PEEP) on renal function in dogs (author's transl)]. PubMed ·قادر شنیور, Majdi Nagara, Yukimitsu Ohshiro, Зобова Екатерина Александровна, Erik G. Schwimmer, Masami Fujita	1982	1

About Majdi Nagara

Majdi Nagara is a scholar working on Genetics, Clinical Biochemistry, Nephrology, Physiology and Pathology and Forensic Medicine, having authored 25 papers that have together received 343 indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (5 papers), Lysosomal Storage Disorders Research (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genomics and Rare Diseases (2 papers), Metabolism and Genetic Disorders (2 papers), Ion Transport and Channel Regulation (2 papers), Renal function and acid-base balance (2 papers) and Genetic factors in colorectal cancer (2 papers). The work is most often cited by research in Genetics (140 citations), Molecular Biology (161 citations), Oncology (63 citations), Cell Biology (37 citations) and Pathology and Forensic Medicine (33 citations). Majdi Nagara has collaborated with scholars based in Tunisia, France and Italy. Frequent co-authors include Sonia Abdelhak, Apostolos Zaravinos, Rym Kéfi, Christos Dimopoulos, Georgios Ayiomamitis, Beatriz de Lucas, Lilia Romdhane, Laurence Faivre, V. des Portes and Pierre Billuart. Their work appears in journals such as Gene, Endocrine Research, Annals of Human Genetics, Diagnostic Pathology and BMC Cancer.

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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