A. Sefiani
Impact in
- Genetics top 10%
- Genetic and rare skin diseases.
- Dermatological and Skeletal Disorders
- Genetics and Neurodevelopmental Disorders
- Connective tissue disorders research
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- Cancer and Skin Lesions
Papers in
- Genetics 8
- Genetic and rare skin diseases. 5
- Genetics and Neurodevelopmental Disorders 1
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- Hedgehog Signaling Pathway Studies 3
- Ubiquitin and proteasome pathways 1
- Glycosylation and Glycoproteins Research 1
- Co-authors
- S. Heuertz (5 shared papers)M. C. Hors‐Cayla (5 shared papers)Damian Labuda (3 shared papers)Daniel Sinnett (2 shared papers)Laurent Abel (2 shared papers)J Frézal (2 shared papers)P Maroteaux (1 shared paper)M Guilloud-Bataille (1 shared paper)
In The Last Decade
A. Sefiani
15 papers receiving 233 citations
Peers
Comparison fields: 5 of 39
- Genetics 189
- Dermatology 28
- Cell Biology 39
- Reproductive Medicine 17
- Molecular Biology 125
Countries citing papers authored by A. Sefiani
This map shows the geographic impact of A. Sefiani'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 A. Sefiani with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A. Sefiani more than expected).
Fields of papers citing papers by A. Sefiani
This network shows the impact of papers produced by A. Sefiani. 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 A. Sefiani. The network helps show where A. Sefiani may publish in the future.
Co-authors
The 25 scholars most cited alongside A. Sefiani, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1989 | 95 | |
| 2 | 1991 | 33 | |
| 3 | 1988 | 29 | |
| 4 | 1988 | 28 | |
| 5 | 2011 | 20 | |
| 6 | 2016 | 9 | |
| 7 | A gene for non-specific X-linked mental retardation (MRX55) is located in Xp11. | 1998 | 9 |
| 8 | Incontinentia pigmenti: Xp breakpoint is not the same in a case of r(X) and in X/autosome translocations. | 1989 | 9 |
| 9 | 2012 | 5 | |
| 10 | 2008 | 4 | |
| 11 | 2011 | 3 | |
| 12 | 1996 | 2 | |
| 13 | 2007 | 2 | |
| 14 | 1996 | 1 | |
| 15 | 1997 | 1 |
About A. Sefiani
A. Sefiani is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Cell Biology and Infectious Diseases, having authored 15 papers that have together received 250 indexed citations. Recurring topics across this work include Genetic and rare skin diseases. (5 papers), Hedgehog Signaling Pathway Studies (3 papers), Genetics and Neurodevelopmental Disorders (1 paper), Ubiquitin and proteasome pathways (1 paper), Hemophilia Treatment and Research (1 paper), Glycosylation and Glycoproteins Research (1 paper), Global Health and Surgery (1 paper) and Sperm and Testicular Function (1 paper). The work is most often cited by research in Genetics (189 citations), Dermatology (28 citations), Cell Biology (39 citations), Reproductive Medicine (17 citations) and Molecular Biology (125 citations). A. Sefiani has collaborated with scholars based in France, Morocco and Canada. Frequent co-authors include S. Heuertz, M. C. Hors‐Cayla, Damian Labuda, Daniel Sinnett, Laurent Abel, J Frézal, P Maroteaux, M Guilloud-Bataille, B. Le Marec and Karim Ouldim. Their work appears in journals such as Human Genetics, Neuromuscular Disorders, Gene, European Journal of Neurology and Genomics.
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.