Asma Smahi

8.3k total citations
50 papers, 2.4k citations indexed

About

Asma Smahi is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Asma Smahi has authored 50 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 23 papers in Genetics and 12 papers in Immunology. Recurrent topics in Asma Smahi's work include Genetic and rare skin diseases. (17 papers), NF-κB Signaling Pathways (11 papers) and Dermatological and Skeletal Disorders (9 papers). Asma Smahi is often cited by papers focused on Genetic and rare skin diseases. (17 papers), NF-κB Signaling Pathways (11 papers) and Dermatological and Skeletal Disorders (9 papers). Asma Smahi collaborates with scholars based in France, Italy and United Kingdom. Asma Smahi's co-authors include Arnold Münnich, Gilles Courtois, S. Hadj‐Rabia, Christine Bodemer, Jean‐Laurent Casanova, Anne Puel, Alain Israël, Dominique Hamel‐Teillac, Y. De Prost and Cheng‐Lung Ku and has published in prestigious journals such as Journal of Clinical Investigation, Nature Communications and Gastroenterology.

In The Last Decade

Asma Smahi

48 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Asma Smahi France 26 1.1k 804 671 467 456 50 2.4k
Elisha Roberson United States 17 1.4k 1.3× 838 1.0× 289 0.4× 282 0.6× 258 0.6× 29 2.8k
Jill F. Wright United States 16 946 0.9× 1.0k 1.3× 226 0.3× 83 0.2× 188 0.4× 20 2.2k
Françoise Meylan United States 23 566 0.5× 2.1k 2.7× 333 0.5× 172 0.4× 120 0.3× 39 3.1k
Caren Furlonger Canada 21 1.1k 1.0× 2.2k 2.7× 219 0.3× 201 0.4× 116 0.3× 29 3.5k
Shingo Ichimiya Japan 29 857 0.8× 797 1.0× 90 0.1× 197 0.4× 139 0.3× 100 2.3k
Kotaro Suzuki Japan 30 638 0.6× 1.7k 2.1× 100 0.1× 249 0.5× 246 0.5× 77 2.9k
Christoph Schwärzler Austria 17 767 0.7× 639 0.8× 105 0.2× 140 0.3× 154 0.3× 29 1.6k
Blair R. Renshaw United States 15 829 0.8× 1.9k 2.4× 136 0.2× 182 0.4× 423 0.9× 20 2.6k
Martin Hafner Germany 13 643 0.6× 786 1.0× 111 0.2× 250 0.5× 100 0.2× 17 1.8k
Lee Ann Garrett‐Sinha United States 29 1.1k 1.1× 926 1.2× 334 0.5× 319 0.7× 52 0.1× 49 2.5k

Countries citing papers authored by Asma Smahi

Since Specialization
Citations

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

Fields of papers citing papers by Asma Smahi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Asma Smahi

This figure shows the co-authorship network connecting the top 25 collaborators of Asma Smahi. A scholar is included among the top collaborators of Asma Smahi 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 Asma Smahi. Asma Smahi 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.
Rinaldi, Giulia, Joseph Ng, Asma Smahi, et al.. (2023). In Silico and In Vitro Analysis of IL36RN Alterations Reveals Critical Residues for the Function of the Interleukin-36 Receptor Complex. Journal of Investigative Dermatology. 143(12). 2468–2475.e6. 3 indexed citations
2.
Park, Hyun‐Sook, Daniel Bachmann, Markus Plomann, et al.. (2021). ARP-T1-associated Bazex–Dupré–Christol syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies. Communications Biology. 4(1). 544–544. 6 indexed citations
3.
Assan, Florence, J. Gottlieb, Florence Tubach, et al.. (2020). Anti-Saccharomyces cerevisiae IgG and IgA antibodies are associated with systemic inflammation and advanced disease in hidradenitis suppurativa. Journal of Allergy and Clinical Immunology. 146(2). 452–455.e5. 31 indexed citations
4.
Bal, Élodie, Emmanuel Laplantine, Yamina Hamel, et al.. (2017). Lack of interaction between NEMO and SHARPIN impairs linear ubiquitination and NF-κB activation and leads to incontinentia pigmenti. Journal of Allergy and Clinical Immunology. 140(6). 1671–1682.e2. 13 indexed citations
5.
Tauber, M., Élodie Bal, Xue-Yuan Pei, et al.. (2016). IL36RN Mutations Affect Protein Expression and Function: A Basis for Genotype-Phenotype Correlation in Pustular Diseases. Journal of Investigative Dermatology. 136(9). 1811–1819. 71 indexed citations
6.
Hadj‐Rabia, S., Asma Smahi, Sylvie Fraïtag, et al.. (2011). Clinical and histologic features of incontinentia pigmenti in adults with nuclear factor-κB essential modulator gene mutations. Journal of the American Academy of Dermatology. 64(3). 508–515. 28 indexed citations
7.
Salomon, Julie, Yolanda Espinosa‐Parrilla, Olivier Goulet, et al.. (2011). A founder effect at the EPCAM locus in Congenital Tufting Enteropathy in the Arabic Gulf. European Journal of Medical Genetics. 54(3). 319–322. 27 indexed citations
8.
Clauss, François, Nicolas Chassaing, Asma Smahi, et al.. (2010). X‐linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic‐dental phenotypic findings. Clinical Genetics. 78(3). 257–266. 24 indexed citations
9.
Rio, Marlène, Jean-Marc Plaza, Philippe Guigue, et al.. (2009). Combination of Linkage Mapping and Microarray-Expression Analysis Identifies NF-κB Signaling Defect as a Cause of Autosomal-Recessive Mental Retardation. The American Journal of Human Genetics. 85(6). 903–908. 73 indexed citations
10.
Mégarbané, Hala, Céline Cluzeau, Christine Bodemer, et al.. (2008). Unusual presentation of a severe autosomal recessive anhydrotic ectodermal dysplasia with a novel mutation in the EDAR gene. American Journal of Medical Genetics Part A. 146A(20). 2657–2662. 20 indexed citations
11.
Martínez‐Pomar, Natalia, et al.. (2005). A new mutation in exon 7 of NEMO gene: late skewed X-chromosome inactivation in an incontinentia pigmenti female patient with immunodeficiency. Human Genetics. 118(3-4). 458–465. 56 indexed citations
12.
Morlon, Aurore, Arnold Münnich, & Asma Smahi. (2005). TAB2, TRAF6 and TAK1 are involved in NF-κB activation induced by the TNF-receptor, Edar and its adaptator Edaradd. Human Molecular Genetics. 14(23). 3751–3757. 78 indexed citations
13.
Puel, Anne, Capucine Pïcard, Cheng‐Lung Ku, Asma Smahi, & Jean‐Laurent Casanova. (2003). Inherited disorders of NF-κB-mediated immunity in man. Current Opinion in Immunology. 16(1). 34–41. 138 indexed citations
14.
Hadj‐Rabia, S., N. Bodak, Dominique Hamel‐Teillac, et al.. (2003). Clinical Study of 40 Cases of Incontinentia Pigmenti. Archives of Dermatology. 139(9). 1163–70. 121 indexed citations
15.
Mégarbané, André, et al.. (2002). Linear and whorled nevoid hypermelanosis with bilateral giant cerebral aneurysms. American Journal of Medical Genetics. 112(1). 95–98. 8 indexed citations
16.
Smahi, Asma. (2002). The NF-kappaB signalling pathway in human diseases: from incontinentia pigmenti to ectodermal dysplasias and immune-deficiency syndromes. Human Molecular Genetics. 11(20). 2371–2375. 196 indexed citations
17.
Aradhya, Swaroop, Richard A. Lewis, David L. Nelson, et al.. (2000). Filamin (FLN1),plexin (SEX), major palmitoylated proteinp55 (MPP1), and von-Hippel Lindau binding protein (VBP1) are not involved in incontinentia pigmenti type 2. American Journal of Medical Genetics. 94(1). 79–84. 3 indexed citations
18.
Cabot, Annick, Jean‐Michel Rozet, S. Gerber, et al.. (1999). A Gene for X-Linked Idiopathic Congenital Nystagmus (NYS1) Maps to Chromosome Xp11.4-p11.3. The American Journal of Human Genetics. 64(4). 1141–1146. 66 indexed citations
19.
Smahi, Asma, et al.. (1999). Pseudotumeur inflammatoire du poumon. Étude anatomoclinique d'une observation. Chirurgie. 124(1). 73–76. 3 indexed citations
20.
Hors‐Cayla, M. C., S. Heuertz, & Asma Smahi. (1994). Refinement of the localization of the gene responsible for spondylo epiphyseal dysplasia in Xp22. The American Journal of Human Genetics. 55. 1 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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