B. Bouadjar

2.6k total citations
27 papers, 1.8k citations indexed

About

B. Bouadjar is a scholar working on Molecular Biology, Cell Biology and Dermatology. According to data from OpenAlex, B. Bouadjar has authored 27 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 10 papers in Cell Biology and 8 papers in Dermatology. Recurrent topics in B. Bouadjar's work include Skin and Cellular Biology Research (9 papers), Hedgehog Signaling Pathway Studies (5 papers) and Genetic and rare skin diseases. (5 papers). B. Bouadjar is often cited by papers focused on Skin and Cellular Biology Research (9 papers), Hedgehog Signaling Pathway Studies (5 papers) and Genetic and rare skin diseases. (5 papers). B. Bouadjar collaborates with scholars based in Algeria, France and Morocco. B. Bouadjar's co-authors include Judith Fischer, Nicolás Ramoz, Michel Fãvre, Gérard Orth, Caroline Lefèvre, Mark Lathrop, Jean-François Prud’homme, Florence Jobard, Ayşen Karaduman and Meral Özgüç and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Cancer Research.

In The Last Decade

B. Bouadjar

26 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
B. Bouadjar Algeria 21 943 608 359 354 306 27 1.8k
Nathalie Jonca France 17 438 0.5× 574 0.9× 64 0.2× 121 0.3× 488 1.6× 36 1.3k
Mikyoung Chang United States 21 1.2k 1.3× 74 0.1× 198 0.6× 129 0.4× 102 0.3× 24 2.6k
Cory L. Simpson United States 15 965 1.0× 562 0.9× 124 0.3× 130 0.4× 236 0.8× 32 1.8k
F C Ramaekers Netherlands 21 840 0.9× 398 0.7× 99 0.3× 273 0.8× 133 0.4× 27 1.5k
Heidemarie Rossiter Austria 20 470 0.5× 310 0.5× 368 1.0× 58 0.2× 323 1.1× 32 1.4k
Weihong Xu United States 20 1.6k 1.7× 628 1.0× 378 1.1× 356 1.0× 24 0.1× 39 2.6k
Annika Sääf Sweden 16 1.0k 1.1× 120 0.2× 59 0.2× 388 1.1× 148 0.5× 25 1.6k
Show‐Li Chen Taiwan 26 799 0.8× 98 0.2× 282 0.8× 224 0.6× 29 0.1× 66 1.5k
Joshua N. Finger United States 15 1.4k 1.5× 164 0.3× 204 0.6× 189 0.5× 35 0.1× 18 2.1k
Stephanie Rieder United States 10 810 0.9× 900 1.5× 272 0.8× 54 0.2× 45 0.1× 16 1.5k

Countries citing papers authored by B. Bouadjar

Since Specialization
Citations

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

Fields of papers citing papers by B. Bouadjar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of B. Bouadjar

This figure shows the co-authorship network connecting the top 25 collaborators of B. Bouadjar. A scholar is included among the top collaborators of B. Bouadjar 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 B. Bouadjar. B. Bouadjar 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.
Zimmer, Andreas, et al.. (2016). Whole-Exome-Sequencing Reveals Small Deletions in CASP14 in Patients with Autosomal Recessive Inherited Ichthyosis. Acta Dermato Venereologica. 97(1). 102–104. 27 indexed citations
2.
Ammar-Khodja, A, B. Bouadjar, H. Benchikhi, et al.. (2015). EPIMAG: International Cross-Sectional Epidemiological Psoriasis Study in the Maghreb. Dermatology. 231(2). 134–144. 21 indexed citations
3.
Soufir, Nadem, Cécile Ged, Agnès Bourillon, et al.. (2010). A Prevalent Mutation with Founder Effect in Xeroderma Pigmentosum Group C from North Africa. Journal of Investigative Dermatology. 130(6). 1537–1542. 69 indexed citations
4.
Klar, Joakim, Martina Schweiger, Robert J. Zimmerman, et al.. (2009). Mutations in the Fatty Acid Transport Protein 4 Gene Cause the Ichthyosis Prematurity Syndrome. The American Journal of Human Genetics. 85(2). 248–253. 120 indexed citations
5.
Rezvani, Hamid, Cécile Ged, B. Bouadjar, Hubert de Verneuil, & Alain Taı̈eb. (2008). Catalase overexpression reduces UVB-induced apoptosis in a human xeroderma pigmentosum reconstructed epidermis. Cancer Gene Therapy. 15(4). 241–251. 28 indexed citations
6.
Lefèvre, Caroline, B. Bouadjar, Gianluca Tadini, et al.. (2006). Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3. Human Molecular Genetics. 15(5). 767–776. 148 indexed citations
7.
Lesueur, Fabienne, B. Bouadjar, Caroline Lefèvre, et al.. (2006). Novel Mutations in ALOX12B in Patients with Autosomal Recessive Congenital Ichthyosis and Evidence for Genetic Heterogeneity on Chromosome 17p13. Journal of Investigative Dermatology. 127(4). 829–834. 33 indexed citations
8.
Lefèvre, Caroline, B. Bouadjar, Ayşen Karaduman, et al.. (2004). Mutations in ichthyin a new gene on chromosome 5q33 in a new form of autosomal recessive congenital ichthyosis. Human Molecular Genetics. 13(20). 2473–2482. 126 indexed citations
9.
10.
Couvé-Privat, Sophie, B. Bouadjar, M.-F. Avril, Alain Sarasin, & Leela Daya–Grosjean. (2002). Significantly high levels of ultraviolet-specific mutations in the smoothened gene in basal cell carcinomas from DNA repair-deficient xeroderma pigmentosum patients.. PubMed. 62(24). 7186–9. 44 indexed citations
11.
Ramoz, Nicolás, et al.. (2002). Mutations in two adjacent novel genes are associated with epidermodysplasia verruciformis. Nature Genetics. 32(4). 579–581. 276 indexed citations
12.
Lefèvre, Caroline, Florence Jobard, F. Caux, et al.. (2001). Mutations in CGI-58, the Gene Encoding a New Protein of the Esterase/Lipase/Thioesterase Subfamily, in Chanarin-Dorfman Syndrome. The American Journal of Human Genetics. 69(5). 1002–1012. 346 indexed citations
13.
Blanchet‐Bardon, C, B. Bouadjar, J.‐F. Stalder, et al.. (2001). Novel Point Mutations, Deletions, and Polymorphisms in the Cathepsin C Gene in Nine Families from Europe and North Africa with Papillon–Lefèvre Syndrome. Journal of Investigative Dermatology. 117(6). 1657–1661. 30 indexed citations
14.
Bouadjar, B., et al.. (2000). Clinical and Genetic Studies of 3 Large, Consanguineous, Algerian Families With Mal de Meleda. Archives of Dermatology. 136(10). 1247–52. 26 indexed citations
15.
Ramoz, Nicolás, et al.. (2000). Evidence for a Nonallelic Heterogeneity of Epidermodysplasia Verruciformis with Two Susceptibility Loci Mapped to Chromosome Regions 2p21–p24 and 17q25. Journal of Investigative Dermatology. 114(6). 1148–1153. 89 indexed citations
16.
Fischer, Judith, B. Bouadjar, C Blanchet‐Bardon, et al.. (2000). Two New Loci for Autosomal Recessive Ichthyosis on Chromosomes 3p21 and 19p12-q12 and Evidence for Further Genetic Heterogeneity. The American Journal of Human Genetics. 66(3). 904–913. 59 indexed citations
17.
Bodak, N., Sophie Queillé, M.-F. Avril, et al.. (1999). High levels of patched gene mutations in basal-cell carcinomas from patients with xeroderma pigmentosum. Proceedings of the National Academy of Sciences. 96(9). 5117–5122. 94 indexed citations
18.
19.
Fischer, Judith, B. Bouadjar, Roland Heilig, et al.. (1998). Genetic linkage of Meleda disease to chromosome 8qter. European Journal of Human Genetics. 6(6). 542–547. 34 indexed citations
20.
Bouadjar, B., et al.. (1992). [Multiple pilomatrixoma and myotonic dystrophy].. PubMed. 119(11). 899–900. 5 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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