Nabiha Salem

2.7k citations

36 papers · 1.6k indexed · h-index 19

Co-authors: Christine Petit Jacques Loiselet André Mégarbané Elie El‐Zir Mirna Mustapha Shin’ichiro Yasunaga Martine Cohen‐Salmon M’hamed Grati
Topics: Inflammasome and immune disorders (8 papers)Hearing, Cochlea, Tinnitus, Genetics (6 papers)RNA regulation and disease (4 papers)
Cited by: Sensory Systems Neurology Otorhinolaryngology
Journals: Nature Genetics Annals of Neurology Human Molecular Genetics
Partner nations: Lebanon France Jordan

In The Last Decade

Nabiha Salem

35 papers receiving 1.6k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Updates on the molecular spectrum of MEFV variants in lebanese patients with Familial Mediterranean Fever 2025 ·Frontiers in Genetics ·R Feghali,José-Noël Ibrahim,Nabiha Salem,(unknown),(unknown),(unknown),Tony Yammine,(unknown)	2
2	Analysis of ASS1 gene in ten unrelated middle eastern families with citrullinemia type 1 identifies rare and novel variants 2023 ·Molecular Genetics & Genomic Medicine ·(unknown),(unknown),Tony Yammine,Issam Khneisser,Hicham Mansour,Nabiha Salem,(unknown),Johnny Awwad,Adib Moukarzel,Chantal Farra	0
3	Novel SCN9A variant associated with congenital insensitivity to pain 2023 ·Molecular Biology Reports ·Tony Yammine,(unknown),(unknown),Nabiha Salem,Johnny Awwad,Chantal Farra	1
4	FokI vitamin D receptor gene polymorphism and serum 25-hydroxyvitamin D in patients with cardiovascular risk 2019 ·Archives of Medical Science - Atherosclerotic Diseases ·(unknown),Ghassan Sleilaty,Éliane Chouery,Nabiha Salem,Ramez Chahine,Nassim Farès	12
5	Contribution of copy number variants (CNVs) to congenital, unexplained intellectual and developmental disabilities in Lebanese patients 2015 ·Molecular Cytogenetics ·(unknown),Joelle Abou Ghoch,Sandra Corbani,Pierre Cacciagli,Cécile Mignon‐Ravix,Nabiha Salem,Nadine Jalkh,Sandra Sabbagh,Ali Fawaz,Tony Ibrahim,Laurent Villard,André Mégarbané,Éliane Chouery	6
6	Prevalance of BRCA1 and BRCA2 mutations in familial breast cancer patients in Lebanon 2012 ·Hereditary Cancer in Clinical Practice ·Nadine Jalkh,(unknown),Éliane Chouery,Nabiha Salem,(unknown),Lisa Golmard,(unknown),Yves‐Jean Bignon,André Mégarbané	40
7	A whole-genome scan in a large family with leukodystrophy and oligodontia reveals linkage to 10q22 2010 ·Neurogenetics ·Éliane Chouery,Valérie Delague,Nadine Jalkh,Nabiha Salem,(unknown),Diana Rodriguez,B. Chabrol,Odile Boespflug‐Tanguy,Nicolas Lévy,(unknown),André Mégarbané	11
8	Familial Mediterranean fever in a large Lebanese family: Multiple MEFV mutations and evidence for a Founder effect of the p.[M694I] mutation 2010 ·European Journal of Medical Genetics ·Myrna Medlej‐Hashim,Éliane Chouery,Nabiha Salem,Valérie Delague,Marie‐Paule Lefranc,Jacques Loiselet,André Mégarbané	4
9	The molecular basis of familial hypercholesterolemia in Lebanon: Spectrum ofLDLRmutations and role ofPCSK9as a modifier gene 2009 ·Human Mutation ·Marianne Abifadel,(unknown),(unknown),Georges Halaby,(unknown),Antoine Sarkis,(unknown),Mathilde Varret,Nabiha Salem,Sandra Corbani,(unknown),Claudine Junien,Arnold Münnich,Cathérine Boileau	77
10	Pitfalls of homozygosity mapping: an extended consanguineous Bardet–Biedl syndrome family with two mutant genes (BBS2, BBS10), three mutations, but no triallelism 2006 ·European Journal of Human Genetics ·Virginie Laurier,Corinne Stoetzel,Jean Muller,Christelle Thibault-Carpentier,Sandra Corbani,Nadine Jalkh,Nabiha Salem,Éliane Chouery,Olivier Poch,(unknown),Jean-Marc Danse,(unknown),Dominique Bonneau,André Mégarbané,Jean‐Louis Mandel,Hélène Dollfus	43
11	Familial Mediterranean fever (FMF) in Lebanon and Jordan: a population genetics study and report of three novel mutations 2005 ·European Journal of Medical Genetics ·Myrna Medlej‐Hashim,Jean‐Louis Serre,Sandra Corbani,(unknown),Nadine Jalkh,Valérie Delague,Éliane Chouery,Nabiha Salem,Jacques Loiselet,Marie‐Paule Lefranc,André Mégarbané	46
12	Amyloidosis in familial Mediterranean fever patients: correlation with MEFV genotype and SAA1 and MICA polymorphisms effects 2004 ·BMC Medical Genetics ·Myrna Medlej‐Hashim,Valérie Delague,Éliane Chouery,Nabiha Salem,M. O. Rawashdeh,Marie‐Paule Lefranc,Jacques Loiselet,André Mégarbané	51
13	Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutations 2002 ·European Journal of Human Genetics ·Myrna Medlej‐Hashim,Mirna Mustapha,Éliane Chouery,Dominique Weil,(unknown),Nabiha Salem,Valérie Delague,Jacques Loiselet,Mark Lathrop,Christine Petit,André Mégarbané	25
14	A new autosomal recessive non-progressive congenital cerebellar ataxia associated with mental retardation, optic atrophy, and skin abnormalities (CAMOS) maps to chromosome 15q24-q26 in a large consanguineous Lebanese Druze family 2002 ·Neurogenetics ·Valérie Delague,Corinne Bareil,Patrice Bouvagnet,Nabiha Salem,Éliane Chouery,Jacques Loiselet,André Mégarbané,Mireille Claustres	17
15	Familial Mediterranean Fever: association of elevated IgD plasma levels with specific MEFV mutations 2001 ·European Journal of Human Genetics ·Myrna Medlej‐Hashim,Isabelle Petit,(unknown),Éliane Chouery,Nabiha Salem,Valérie Delague,M. O. Rawashdeh,Issam Mansour,Marie‐Paule Lefranc,Roger Naman,Jacques Loiselet,Jean‐Claude Lecron,Jean‐Louis Serre,André Mégarbané	18
16	A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C 2000 ·Nature Genetics ·Elisabeth Verpy,Michel Leibovici,Ingrid Zwaenepoel,Xue-Zhong Liu,Andreas Gal,Nabiha Salem,Ahmad M. Mansour,Stéphane Blanchard,Ichiro Kobayashi,Bronya J.B. Keats,Rima Slim,Christine Petit	357
17	X-linked transposition of the great arteries and incomplete penetrance among males with a nonsense mutation in ZIC3 2000 ·European Journal of Human Genetics ·André Mégarbané,Nabiha Salem,(unknown),(unknown),(unknown),Valérie Delague,Roland Kassab,Jacques Loiselet,Patrice Bouvagnet	88
18	A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness 1999 ·Nature Genetics ·Shin’ichiro Yasunaga,M’hamed Grati,Martine Cohen‐Salmon,A. Amraoui,Mirna Mustapha,Nabiha Salem,Elie El‐Zir,Jacques Loiselet,Christine Petit	429
19	Identification of a locus on chromosome 7q31, DFNB14, responsible for prelingual sensorineural non-syndromic deafness 1998 ·European Journal of Human Genetics ·Mirna Mustapha,Nabiha Salem,Dominique Weil,Elie El‐Zir,Jacques Loiselet,Christine Petit	16
20	A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36 1998 ·European Journal of Human Genetics ·Mirna Mustapha,Sébastien Chardenoux,(unknown),Nabiha Salem,Jean Weissenbach,Elie El‐Zir,Jacques Loiselet,Christine Petit	29

About Nabiha Salem

Nabiha Salem is a scholar working on Sensory Systems, Neurology and Otorhinolaryngology, having authored 36 papers that have together received 1.6k indexed citations. Recurring topics across this work include Inflammasome and immune disorders (8 papers), Hearing, Cochlea, Tinnitus, Genetics (6 papers) and RNA regulation and disease (4 papers). The work is most often cited by research in Sensory Systems (664 citations), Neurology (208 citations) and Otorhinolaryngology (72 citations). Nabiha Salem has collaborated with scholars based in Lebanon, France and Jordan. Frequent co-authors include Christine Petit, Jacques Loiselet, André Mégarbané, Elie El‐Zir, Mirna Mustapha, Shin’ichiro Yasunaga, Martine Cohen‐Salmon, M’hamed Grati, A. Amraoui and Valérie Delague. Their work appears in journals such as Nature Genetics, Annals of Neurology and Human Molecular Genetics.

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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