Nabiha Salem

2.7k total citations
36 papers, 1.6k citations indexed

About

Nabiha Salem is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Nabiha Salem has authored 36 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 10 papers in Genetics and 8 papers in Immunology. Recurrent topics in Nabiha Salem's work include Inflammasome and immune disorders (8 papers), Hearing, Cochlea, Tinnitus, Genetics (6 papers) and RNA regulation and disease (4 papers). Nabiha Salem is often cited by papers focused on Inflammasome and immune disorders (8 papers), Hearing, Cochlea, Tinnitus, Genetics (6 papers) and RNA regulation and disease (4 papers). Nabiha Salem collaborates with scholars based in Lebanon, France and United States. Nabiha Salem's co-authors include Christine Petit, Jacques Loiselet, André Mégarbané, Elie El‐Zir, Mirna Mustapha, M’hamed Grati, A. Amraoui, Shin’ichiro Yasunaga, Martine Cohen‐Salmon and Valérie Delague and has published in prestigious journals such as Nature Genetics, Annals of Neurology and Human Molecular Genetics.

In The Last Decade

Nabiha Salem

35 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nabiha Salem Lebanon 19 1.1k 664 252 208 203 36 1.6k
Shin’ichiro Yasunaga Japan 21 741 0.7× 430 0.6× 237 0.9× 162 0.8× 325 1.6× 60 1.7k
Jianyong Shou United States 24 1.2k 1.1× 862 1.3× 188 0.7× 85 0.4× 137 0.7× 41 2.2k
Isabelle Schrauwen United States 25 690 0.6× 525 0.8× 336 1.3× 323 1.6× 136 0.7× 105 1.8k
Miguel A. Moreno‐Pelayo Spain 19 1.4k 1.3× 1.2k 1.8× 162 0.6× 384 1.8× 151 0.7× 59 2.3k
Jinwoong Bok South Korea 26 1.1k 1.0× 951 1.4× 281 1.1× 226 1.1× 62 0.3× 82 2.0k
Jun Shen United States 20 807 0.8× 555 0.8× 307 1.2× 116 0.6× 71 0.3× 44 1.6k
Anand N. Mhatre United States 24 866 0.8× 916 1.4× 189 0.8× 327 1.6× 38 0.2× 46 1.8k
Duygu Duman Türkiye 19 697 0.6× 601 0.9× 303 1.2× 268 1.3× 205 1.0× 42 1.4k
J. Hikke van Doorninck Netherlands 15 971 0.9× 328 0.5× 249 1.0× 72 0.3× 56 0.3× 17 1.8k
Héla Azaiez United States 20 860 0.8× 1.2k 1.7× 260 1.0× 393 1.9× 113 0.6× 45 1.7k

Countries citing papers authored by Nabiha Salem

Since Specialization
Citations

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

Fields of papers citing papers by Nabiha Salem

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nabiha Salem

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

All Works

20 of 20 papers shown
1.
Feghali, R, et al.. (2025). Updates on the molecular spectrum of MEFV variants in lebanese patients with Familial Mediterranean Fever. Frontiers in Genetics. 15. 1506656–1506656. 2 indexed citations
2.
Yammine, Tony, Issam Khneisser, Hicham Mansour, et al.. (2023). Analysis of ASS1 gene in ten unrelated middle eastern families with citrullinemia type 1 identifies rare and novel variants. Molecular Genetics & Genomic Medicine. 11(2). e2058–e2058.
3.
Yammine, Tony, et al.. (2023). Novel SCN9A variant associated with congenital insensitivity to pain. Molecular Biology Reports. 50(7). 6293–6298. 1 indexed citations
4.
Sleilaty, Ghassan, et al.. (2019). FokI vitamin D receptor gene polymorphism and serum 25-hydroxyvitamin D in patients with cardiovascular risk. Archives of Medical Science - Atherosclerotic Diseases. 4(1). 298–303. 12 indexed citations
5.
Ghoch, Joelle Abou, Sandra Corbani, Pierre Cacciagli, et al.. (2015). Contribution of copy number variants (CNVs) to congenital, unexplained intellectual and developmental disabilities in Lebanese patients. Molecular Cytogenetics. 8(1). 26–26. 6 indexed citations
6.
Jalkh, Nadine, Éliane Chouery, Nabiha Salem, et al.. (2012). Prevalance of BRCA1 and BRCA2 mutations in familial breast cancer patients in Lebanon. Hereditary Cancer in Clinical Practice. 10(1). 7–7. 40 indexed citations
7.
Chouery, Éliane, Valérie Delague, Nadine Jalkh, et al.. (2010). A whole-genome scan in a large family with leukodystrophy and oligodontia reveals linkage to 10q22. Neurogenetics. 12(1). 73–78. 11 indexed citations
8.
Medlej‐Hashim, Myrna, Éliane Chouery, Nabiha Salem, et al.. (2010). Familial Mediterranean fever in a large Lebanese family: Multiple MEFV mutations and evidence for a Founder effect of the p.[M694I] mutation. European Journal of Medical Genetics. 54(1). 50–54. 4 indexed citations
9.
Abifadel, Marianne, Georges Halaby, Antoine Sarkis, et al.. (2009). The molecular basis of familial hypercholesterolemia in Lebanon: Spectrum ofLDLRmutations and role ofPCSK9as a modifier gene. Human Mutation. 30(7). E682–E691. 77 indexed citations
10.
Laurier, Virginie, Corinne Stoetzel, Jean Muller, et al.. (2006). Pitfalls of homozygosity mapping: an extended consanguineous Bardet–Biedl syndrome family with two mutant genes (BBS2, BBS10), three mutations, but no triallelism. European Journal of Human Genetics. 14(11). 1195–1203. 43 indexed citations
11.
Medlej‐Hashim, Myrna, Jean‐Louis Serre, Sandra Corbani, et al.. (2005). Familial Mediterranean fever (FMF) in Lebanon and Jordan: a population genetics study and report of three novel mutations. European Journal of Medical Genetics. 48(4). 412–420. 46 indexed citations
12.
Medlej‐Hashim, Myrna, Valérie Delague, Éliane Chouery, et al.. (2004). Amyloidosis in familial Mediterranean fever patients: correlation with MEFV genotype and SAA1 and MICA polymorphisms effects. BMC Medical Genetics. 5(1). 4–4. 51 indexed citations
13.
Medlej‐Hashim, Myrna, Mirna Mustapha, Éliane Chouery, et al.. (2002). Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutations. European Journal of Human Genetics. 10(6). 391–394. 25 indexed citations
14.
15.
Stéphan, E., André Mégarbané, Roland Kassab, et al.. (2000). [Autosomal dominant Mendelian midline complex. Secundum atrial septal defect associated with cardiac and facial-thoracic defects. A familial case].. PubMed. 93(5). 641–7. 4 indexed citations
16.
Verpy, Elisabeth, Michel Leibovici, Ingrid Zwaenepoel, et al.. (2000). A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C. Nature Genetics. 26(1). 51–55. 357 indexed citations
17.
Mégarbané, André, Nabiha Salem, Valérie Delague, et al.. (2000). X-linked transposition of the great arteries and incomplete penetrance among males with a nonsense mutation in ZIC3. European Journal of Human Genetics. 8(9). 704–708. 88 indexed citations
18.
Yasunaga, Shin’ichiro, M’hamed Grati, Martine Cohen‐Salmon, et al.. (1999). A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness. Nature Genetics. 21(4). 363–369. 429 indexed citations
19.
Mustapha, Mirna, Sébastien Chardenoux, Nabiha Salem, et al.. (1998). A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36. European Journal of Human Genetics. 6(3). 245–250. 29 indexed citations
20.
Mustapha, Mirna, Nabiha Salem, Dominique Weil, et al.. (1998). Identification of a locus on chromosome 7q31, DFNB14, responsible for prelingual sensorineural non-syndromic deafness. European Journal of Human Genetics. 6(6). 548–551. 16 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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