N. Abbas
- Reproductive Medicine top 2%
- Sperm and Testicular Function 7
- Genetics top 2%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
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- Genetic Neurodegenerative Diseases 5
- Hereditary Neurological Disorders 4
- Molecular Biology top 10%
- Sexual Differentiation and Disorders 8
- Mitochondrial Function and Pathology 3
- Ubiquitin and proteasome pathways 2
- Urology top 5%
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- Neurological diseases and metabolism 2
- Co-authors
- Éric VilainKen McElreaveyM FellousMarc FellousIra HerskowitzC. BoucekkineAndrew SinclairPhilippe Berta
- Journals
- Human Molecular Genetics (2 papers)Proceedings of the National Academy of Sciences (2 papers)Annals of Human Genetics (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 393
- Genetics 881
- Cellular and Molecular Neuroscience 251
- Molecular Biology 905
- Urology 79
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-authorship network
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 | 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 | 52 |
| 2 | 1996 | 27 | |
| 3 | 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 |
| 4 | 1995 | 16 | |
| 5 | 1995 | 15 | |
| 6 | Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado-Joseph disease locus. | 1995 | 87 |
| 7 | 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 |
| 8 | 1994 | 92 | |
| 9 | 1993 | 12 | |
| 10 | Familial case of 46,XX male and 46,XX true hermaphrodite associated with a paternal-derived SRY-bearing X chromosome. | 1993 | 33 |
| 11 | 1993 | 280 | |
| 12 | 1992 | 11 | |
| 13 | 1992 | 132 | |
| 14 | 1990 | 67 | |
| 15 | 1990 | 2 | |
| 16 | 1990 | 54 | |
| 17 | 1989 | 222 | |
| 18 | 1988 | 2 |
About N. Abbas
N. Abbas is a scholar working on Reproductive Medicine, Genetics and Cellular and Molecular Neuroscience, 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 (8 papers), Sperm and Testicular Function (7 papers), Genetic Neurodegenerative Diseases (5 papers), Hereditary Neurological Disorders (4 papers), Mitochondrial Function and Pathology (3 papers), Neurological diseases and metabolism (2 papers) and Ubiquitin and proteasome pathways (2 papers). The work is most often cited by research in Reproductive Medicine (393 citations), Genetics (881 citations) and Cellular and Molecular Neuroscience (251 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, Philippe Berta, Peter N. Goodfellow and Nathanael A. Ellis. Their work appears in journals such as Human Molecular Genetics, Proceedings of the National Academy of Sciences, Annals of Human Genetics, European Journal of Pediatrics 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.