N. Abbas
Impact in
- Cellular and Molecular Neuroscience top 0.5%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
- Neurology top 1%
- Parkinson's Disease Mechanisms and Treatments
- Amyotrophic Lateral Sclerosis Research
Papers in
-
- Genetic Neurodegenerative Diseases 11
- Hereditary Neurological Disorders 5
- Genetics 12
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 11
- Forensic and Genetic Research 1
- Co-authors
- Yves Agid (15 shared papers)Alexis Brice (16 shared papers)Alexandra Dürr (10 shared papers)Marc Fellous (10 shared papers)Giovanni Stévanin (10 shared papers)Géraldine Cancel‐Tassin (9 shared papers)Eric J. N. Vilain (7 shared papers)Ken McElreavey (6 shared papers)
- Journals
- Human Molecular Genetics (5 papers)Nature Genetics (3 papers)Human Genetics (3 papers)The American Journal of Human Genetics (2 papers)Proceedings of the National Academy of Sciences (2 papers)
- Partner nations
- FranceItalyUnited Kingdom
In The Last Decade
N. Abbas
34 papers receiving 4.4k citations
N. Abbas's Hit Papers
Peers
Comparison fields: 5 of 53
- Cellular and Molecular Neuroscience 2.0k
- Neurology 755
- Genetics 942
- Molecular Biology 298
- Reproductive Medicine 43
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
Showing the 20 most-cited of 35 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats Hit paper breakdown → | 1996 | 753 |
| 2 | 1997 | 661 | |
| 3 | 1999 | 474 | |
| 4 | 1996 | 381 | |
| 5 | 1993 | 308 | |
| 6 | 1994 | 271 | |
| 7 | 1989 | 260 | |
| 8 | 1997 | 223 | |
| 9 | 1998 | 160 | |
| 10 | 1992 | 152 | |
| 11 | 1994 | 107 | |
| 12 | 1992 | 96 | |
| 13 | Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado-Joseph disease locus. | 1995 | 93 |
| 14 | 1990 | 80 | |
| 15 | 2003 | 69 | |
| 16 | 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 | 58 |
| 17 | 1998 | 58 | |
| 18 | 1990 | 55 | |
| 19 | 1998 | 54 | |
| 20 | 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 | 47 |
About N. Abbas
N. Abbas is a scholar working on Cellular and Molecular Neuroscience, Genetics, Neurology, Plant Science and Nuclear Energy and Engineering, having authored 35 papers that have together received 4.7k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers), Genetic Neurodegenerative Diseases (11 papers), Parkinson's Disease Mechanisms and Treatments (6 papers), Hereditary Neurological Disorders (5 papers), Forensic and Genetic Research (1 paper) and Chromosomal and Genetic Variations (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (2.0k citations), Neurology (755 citations), Genetics (942 citations), Molecular Biology (298 citations) and Reproductive Medicine (43 citations). N. Abbas has collaborated with scholars based in France, Italy and United Kingdom. Frequent co-authors include Yves Agid, Alexis Brice, Alexandra Dürr, Marc Fellous, Giovanni Stévanin, Géraldine Cancel‐Tassin, Eric J. N. Vilain, Ken McElreavey, Olivier Didierjean and Frédéric Saudou. Their work appears in journals such as Human Molecular Genetics, Nature Genetics, Human Genetics, The American Journal of Human Genetics and Proceedings of the National Academy of Sciences.
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.