Safa Saker

597 total citations
8 papers, 357 citations indexed

About

Safa Saker is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Safa Saker has authored 8 papers receiving a total of 357 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Cell Biology and 3 papers in Genetics. Recurrent topics in Safa Saker's work include Skin and Cellular Biology Research (3 papers), Connective tissue disorders research (3 papers) and Protein Kinase Regulation and GTPase Signaling (2 papers). Safa Saker is often cited by papers focused on Skin and Cellular Biology Research (3 papers), Connective tissue disorders research (3 papers) and Protein Kinase Regulation and GTPase Signaling (2 papers). Safa Saker collaborates with scholars based in France, Lebanon and Syria. Safa Saker's co-authors include Judith Fischer, Florence Jobard, Mark Lathrop, B. Bouadjar, Ayşen Karaduman, Caroline Lefèvre, Meral Özgüç, Jean-François Prud’homme, Juan‐Manuel Anaya and J Sany and has published in prestigious journals such as Human Molecular Genetics, Journal of Investigative Dermatology and Human Genetics.

In The Last Decade

Safa Saker

7 papers receiving 345 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Safa Saker France 7 170 130 113 78 37 8 357
Daniel J. Horan United States 13 410 2.4× 146 1.1× 83 0.7× 48 0.6× 31 0.8× 27 617
Michiko Tojo Japan 14 236 1.4× 65 0.5× 70 0.6× 50 0.6× 26 0.7× 20 480
Päivi M. Hägg Finland 10 120 0.7× 56 0.4× 67 0.6× 30 0.4× 12 0.3× 13 274
Hajimu Oura Japan 12 284 1.7× 117 0.9× 42 0.4× 18 0.2× 31 0.8× 18 585
Maritta Hellström Pigg Sweden 11 204 1.2× 210 1.6× 175 1.5× 19 0.2× 29 0.8× 19 369
Ana V. Perez-Castro United States 9 363 2.1× 79 0.6× 152 1.3× 21 0.3× 43 1.2× 9 448
Castor Cw 12 101 0.6× 145 1.1× 56 0.5× 72 0.9× 57 1.5× 21 401
Melanie K. Marshall United States 8 194 1.1× 29 0.2× 88 0.8× 87 1.1× 34 0.9× 11 357
Jeffrey R. LaDuca United States 11 241 1.4× 85 0.7× 178 1.6× 25 0.3× 21 0.6× 18 607
Yutaka Momota Japan 11 104 0.6× 87 0.7× 29 0.3× 16 0.2× 20 0.5× 31 352

Countries citing papers authored by Safa Saker

Since Specialization
Citations

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

Fields of papers citing papers by Safa Saker

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Safa Saker

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

All Works

8 of 8 papers shown
1.
Clermont, Dominique, et al.. (2014). Assessment of DNA Encapsulation, a New Room-Temperature DNA Storage Method. Biopreservation and Biobanking. 12(3). 176–183. 37 indexed citations
2.
Mégarbané, Hala, Jörn Oliver Sass, Mario Foglio, et al.. (2009). An Autosomal-Recessive Form of Cutis Laxa Is Due to Homozygous Elastin Mutations, and the Phenotype May Be Modified by a Heterozygous Fibulin 5 Polymorphism. Journal of Investigative Dermatology. 129(7). 1650–1655. 20 indexed citations
3.
Fischer, Judith, Hala Mégarbané, André Mégarbané, et al.. (2008). A p.C217R Mutation in Fibulin-5 from Cutis Laxa Patients Is Associated with Incomplete Extracellular Matrix Formation in a Skin Equivalent Model. Journal of Investigative Dermatology. 128(6). 1442–1450. 39 indexed citations
4.
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
5.
Costa, Lydie Da, et al.. (2004). Postmortem diagnosis of Diamond-Blackfan anemia.. PubMed. 26(12). 847–8.
6.
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
7.
Fischer, Judith, Jon Andoni Urtizberea, Sylvana Pavek, et al.. (1998). Genetic linkage of progressive pseudorheumatoid dysplasia to a 3-cM interval of chromosome 6q22. Human Genetics. 103(1). 60–64. 15 indexed citations
8.
Sany, J, Juan‐Manuel Anaya, F. Canovas, et al.. (1993). Influence of methotrexate on the frequency of postoperative infectious complications in patients with rheumatoid arthritis.. PubMed. 20(7). 1129–32. 87 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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