Asma Smahi

8.2k citations

51 papers · 2.5k · h-index 27

Impact in

Dermatology top 1%
- Dermatology and Skin Diseases
Immunology top 2%
- Immunodeficiency and Autoimmune Disorders
- Psoriasis: Treatment and Pathogenesis
- Immune Response and Inflammation

Papers in

Molecular Biology 28
- dental development and anomalies 7
- Hedgehog Signaling Pathway Studies 7
- RNA regulation and disease 5
- Inflammasome and immune disorders 4
Genetics 23
- Genetic and rare skin diseases. 17
- Dermatological and Skeletal Disorders 7

Co-authors: Arnold Münnich (11 shared papers)Gilles Courtois (6 shared papers)S. Hadj‐Rabia (11 shared papers)Christine Bodemer (13 shared papers)Jean‐Laurent Casanova (6 shared papers)Anne Puel (4 shared papers)Alain Israël (6 shared papers)Dominique Hamel‐Teillac (3 shared papers)
Journals: The American Journal of Human Genetics (5 papers)British Journal of Dermatology (3 papers)Human Molecular Genetics (3 papers)Human Mutation (3 papers)Journal of Investigative Dermatology (3 papers)
Partner nations: France United Kingdom Italy

In The Last Decade

Asma Smahi

47 papers receiving 2.4k citations

Peers

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-authors

The 25 scholars most cited alongside Asma Smahi, 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 Asma Smahi Line = papers co-authored together Asma Smahi links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 51 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Claudin-1 gene mutations in neonatal sclerosing cholangitis associated with ichthyosis: A tight junction disease Gastroenterology ·S. Hadj‐Rabia, Lekbir Baala, P. Vabres, Dominique Hamel‐Teillac, Emmanuel Jacquemin, Monique Fabrè, Stanislas Lyonnet, Y. De Prost, Arnold Münnich, Michelle Hadchouel, Asma Smahi	2004	279
2	A hypermorphic IκBα mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency Journal of Clinical Investigation ·Gilles Courtois, Asma Smahi, Janine Reichenbach, Rainer Döffinger, Caterina Cancrini, Marion Bonnet, Anne Puel, Christine Chable-Bessia, Shoji Yamaoka, Jacqueline Feinberg, Sophie Dupuis‐Girod, Christine Bodemer, Susanna Livadiotti, Francesco Novelli, Paolo Rossi, Alain Fischer, Alain Israël, Arnold Munnich, Françoise Le Deist, Jean‐Laurent Casanova	2003	243
3	The NF-kappaB signalling pathway in human diseases: from incontinentia pigmenti to ectodermal dysplasias and immune-deficiency syndromes Human Molecular Genetics ·Asma Smahi	2002	196
4	AP1S3 Mutations Are Associated with Pustular Psoriasis and Impaired Toll-like Receptor 3 Trafficking The American Journal of Human Genetics ·Niovi Setta-Kaffetzi, Michael A. Simpson, Alexander A. Navarini, Varsha Patel, Hui‐Chun Lu, Michael H. Allen, Michael Duckworth, H. Bachelez, A. David Burden, Siew Eng Choon, C.E.M. Griffiths, Brian Kirby, Antonios G.A. Kolios, Marieke M.B. Seyger, Christa Prins, Asma Smahi, Richard C. Trembath, Franca Fraternali, Catherine Smith, (unknown), Francesca Capon	2014	137
5	Inherited disorders of NF-κB-mediated immunity in man Current Opinion in Immunology ·Anne Puel, Capucine Pïcard, Cheng‐Lung Ku, Asma Smahi, Jean‐Laurent Casanova	2003	137
6	Clinical Study of 40 Cases of Incontinentia Pigmenti Archives of Dermatology ·S. Hadj‐Rabia, David Froidevaux, N. Bodak, Dominique Hamel‐Teillac, Asma Smahi, Yasmina Touil, Sylvie Fraïtag, Y. De Prost, Christine Bodemer	2003	122
7	Osteopetrosis, Lymphedema, Anhidrotic Ectodermal Dysplasia, and Immunodeficiency in a Boy and Incontinentia Pigmenti in His Mother PEDIATRICS ·Sophie Dupuis‐Girod, Nadège Corradini, S. Hadj‐Rabia, Jean‐Christophe Fournet, Laurence Faivre, Françoise Le Deist, Philippe Durand, Rainer Döffinger, Asma Smahi, Alain Israël, Gilles Courtois, Nicole Brousse, Stéphane Blanche, Arnold Münnich, Alain Fischer, Jean‐Laurent Casanova, Christine Bodemer	2002	96
8	TAB2, TRAF6 and TAK1 are involved in NF-κB activation induced by the TNF-receptor, Edar and its adaptator Edaradd Human Molecular Genetics ·Aurore Morlon, Arnold Münnich, Asma Smahi	2005	79
9	First Clinical Description of an Infant With Interleukin-36-Receptor Antagonist Deficiency Successfully Treated With Anakinra PEDIATRICS ·Linda Rossi‐Semerano, Maryam Piram, C. Chiavérini, Dominique De Ricaud, Asma Smahi, Isabelle Koné‐Paut	2013	78
10	Alterations of the IKBKG locus and diseases: an update and a report of 13 novel mutations Human Mutation ·Francesca Fusco, Alessandra Pescatore, Élodie Bal, Aïda Ghoul, Mariateresa Paciolla, Maria Brigida Lioi, Michele D’Urso, (unknown), Christine Bodemer, Jean‐Paul Bonnefont, Arnold Münnich, Maria Giuseppina Miano, Asma Smahi, Matilde Valeria Ursini	2008	77
11	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 ·Orianne Philippe, Marlène Rio, Astrid Carioux, Jean-Marc Plaza, Philippe Guigue, Florence Molinari, Nathalie Boddaert, Christine Bôle‐Feysot, Patrick Nitschké, Asma Smahi, Arnold Münnich, Laurence Colleaux	2009	74
12	The NEMO Mutation Creating the Most-Upstream Premature Stop Codon Is Hypomorphic Because of a Reinitiation of Translation The American Journal of Human Genetics ·Anne Puel, Janine Reichenbach, Jacinta Bustamante, Cheng‐Lung Ku, Jacqueline Feinberg, Rainer Döffinger, Marion Bonnet, Orchidée Filipe‐Santos, Ludovic de Beaucoudrey, Anne Durandy, Gerd Horneff, Francesco Novelli, V. Wahn, Asma Smahi, Alain Israël, Tim Niehues, Jean‐Laurent Casanova	2006	72
13	IL36RN Mutations Affect Protein Expression and Function: A Basis for Genotype-Phenotype Correlation in Pustular Diseases Journal of Investigative Dermatology ·M. Tauber, Élodie Bal, Xue-Yuan Pei, Marine Madrange, Amel Haj Khelil, H. Sahel, Akila Zenati, Mohamed Makrelouf, Khaled Boubridaa, Amel Chiali, Naima Smahi, F. Otsmane, Bakar Bouajar, Slaheddine Marrakchi, H. Turki, E. Bourrat, M. Viguier, Yamina Hamel, H. Bachelez, Asma Smahi	2016	71
14	A Gene for X-Linked Idiopathic Congenital Nystagmus (NYS1) Maps to Chromosome Xp11.4-p11.3 The American Journal of Human Genetics ·Annick Cabot, Jean‐Michel Rozet, S. Gerber, Isabelle Perrault, Dominique Ducroq, Asma Smahi, Eric H. Souied, Arnold Munnich, Josseline Kaplan	1999	66
15	NF-κB-related genetic diseases Cell Death and Differentiation ·Gilles Courtois, Asma Smahi	2006	61
16	Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus Human Mutation ·Élodie Bal, Lekbir Baala, Céline Cluzeau, F. El Kerch, Karim Ouldim, S. Hadj‐Rabia, Christine Bodemer, Arnold Münnich, Gilles Courtois, Abdelaziz Sefiani, Asma Smahi	2007	61
17	A new mutation in exon 7 of NEMO gene: late skewed X-chromosome inactivation in an incontinentia pigmenti female patient with immunodeficiency Human Genetics ·Natalia Martínez‐Pomar, Iván Muñoz-Saá, Damián Heine‐Suñer, Ana Martín, Asma Smahi, N Matamoros	2005	57
18	NEMO/IKKγ: linking NF-κB to human disease Trends in Molecular Medicine ·Gilles Courtois, Asma Smahi, Alain Israël	2001	57
19	Insight intoIKBKG/NEMOLocus: Report of New Mutations and Complex Genomic Rearrangements Leading to Incontinentia Pigmenti Disease Human Mutation ·Matilde Immacolata Conte, Alessandra Pescatore, Mariateresa Paciolla, Elio Esposito, Maria Giuseppina Miano, Maria Brigida Lioi, Maeve A. McAleer, Giuliana Giardino, Claudio Pignata, Alan D. Irvine, Angela E. Scheuerle, Ghislaine Royer, S. Hadj‐Rabia, Christine Bodemer, Jean‐Paul Bonnefont, Arnold Münnich, Asma Smahi, Julie Steffann, Francesca Fusco, Matilde Valeria Ursini	2013	53
20	Genomic architecture at the Incontinentia Pigmenti locus favours de novo pathological alleles through different mechanisms Human Molecular Genetics ·Francesca Fusco, Mariateresa Paciolla, Federico Napolitano, Alessandra Pescatore, Irene D’Addario, Élodie Bal, Maria Brigida Lioi, Asma Smahi, Maria Giuseppina Miano, Matilde Valeria Ursini	2011	46

About Asma Smahi

Asma Smahi is a scholar working on Molecular Biology, Genetics, Immunology, Cancer Research and Cell Biology, having authored 51 papers that have together received 2.5k indexed citations. Recurring topics across this work include Genetic and rare skin diseases. (17 papers), NF-κB Signaling Pathways (11 papers), Dermatological and Skeletal Disorders (7 papers), dental development and anomalies (7 papers), Hedgehog Signaling Pathway Studies (7 papers), Psoriasis: Treatment and Pathogenesis (5 papers), RNA regulation and disease (5 papers) and Inflammasome and immune disorders (4 papers). The work is most often cited by research in Dermatology (414 citations), Immunology (842 citations), Cancer Research (433 citations), Genetics (639 citations) and Neurology (178 citations). Asma Smahi has collaborated with scholars based in France, United Kingdom and Italy. Frequent 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. Their work appears in journals such as The American Journal of Human Genetics, British Journal of Dermatology, Human Molecular Genetics, Human Mutation and Journal of Investigative Dermatology.

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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Asma Smahi

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