N. Abbas
Impact in
- Reproductive Medicine top 2%
- Sperm and Testicular Function
- Genetics top 2%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Animal Genetics and Reproduction
Papers in
-
- Sexual Differentiation and Disorders 7
- Mitochondrial Function and Pathology 3
- Ubiquitin and proteasome pathways 2
- Genetics 11
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
- Co-authors
- Éric Vilain (5 shared papers)Ken McElreavey (4 shared papers)M Fellous (2 shared papers)Marc Fellous (6 shared papers)Ira Herskowitz (1 shared paper)C. Boucekkine (5 shared papers)Andrew Sinclair (1 shared paper)Peter N. Goodfellow (1 shared paper)
- Journals
- Proceedings of the National Academy of Sciences (2 papers)Human Molecular Genetics (2 papers)European Journal of Pediatrics (1 paper)Human Genetics (1 paper)Nature (1 paper)
- Partner nations
- FranceAlgeriaUnited Kingdom
In The Last Decade
N. Abbas
18 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 58
- Reproductive Medicine 343
- Genetics 852
- Cellular and Molecular Neuroscience 252
- Urology 72
- Molecular Biology 829
Countries citing papers authored by N. Abbas
This map shows the geographic impact of N. Abbas'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 N. Abbas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites N. Abbas more than expected).
Fields of papers citing papers by N. Abbas
This network shows the impact of papers produced by N. Abbas. 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 N. Abbas. The network helps show where N. Abbas may publish in the future.
Co-authors
The 25 scholars most cited alongside N. Abbas, 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 | 1993 | 280 | |
| 2 | 1989 | 222 | |
| 3 | 1992 | 132 | |
| 4 | 1994 | 92 | |
| 5 | Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado-Joseph disease locus. | 1995 | 87 |
| 6 | 1990 | 67 | |
| 7 | 1990 | 54 | |
| 8 | The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locus. | 1996 | 53 |
| 9 | Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group. | 1996 | 44 |
| 10 | A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies. | 1995 | 39 |
| 11 | Familial case of 46,XX male and 46,XX true hermaphrodite associated with a paternal-derived SRY-bearing X chromosome. | 1993 | 33 |
| 12 | 1996 | 27 | |
| 13 | 1995 | 16 | |
| 14 | 1995 | 15 | |
| 15 | 1993 | 12 | |
| 16 | 1992 | 11 | |
| 17 | 1990 | 2 | |
| 18 | 1988 | 2 |
About N. Abbas
N. Abbas is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Reproductive Medicine and Neurology, having authored 18 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Sexual Differentiation and Disorders (7 papers), Sperm and Testicular Function (6 papers), Genetic Neurodegenerative Diseases (5 papers), Hereditary Neurological Disorders (4 papers), Mitochondrial Function and Pathology (3 papers), Ubiquitin and proteasome pathways (2 papers) and Chromosomal and Genetic Variations (2 papers). The work is most often cited by research in Reproductive Medicine (343 citations), Genetics (852 citations), Cellular and Molecular Neuroscience (252 citations), Urology (72 citations) and Molecular Biology (829 citations). N. Abbas has collaborated with scholars based in France, Algeria and United Kingdom. Frequent co-authors include Éric Vilain, Ken McElreavey, M Fellous, Marc Fellous, Ira Herskowitz, C. Boucekkine, Andrew Sinclair, Peter N. Goodfellow, Mark S. Palmer and Philippe Berta. Their work appears in journals such as Proceedings of the National Academy of Sciences, Human Molecular Genetics, European Journal of Pediatrics, Human Genetics and Nature.
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.