N. Abbas

2.6k total citations
18 papers, 1.2k citations indexed

About

N. Abbas is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, N. Abbas has authored 18 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 11 papers in Genetics and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in N. Abbas's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Sexual Differentiation and Disorders (8 papers) and Sperm and Testicular Function (7 papers). N. Abbas is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Sexual Differentiation and Disorders (8 papers) and Sperm and Testicular Function (7 papers). N. Abbas collaborates with scholars based in France, Algeria and United Kingdom. N. Abbas's co-authors include Éric Vilain, Ken McElreavey, M Fellous, Marc Fellous, Ira Herskowitz, C. Boucekkine, Andrew Sinclair, Peter N. Goodfellow, Nathanael A. Ellis and Philippe Berta and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Human Molecular Genetics.

In The Last Decade

N. Abbas

18 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
N. Abbas France 14 905 881 393 251 105 18 1.2k
Antonella Pragliola Italy 9 484 0.5× 486 0.6× 526 1.3× 109 0.4× 11 0.1× 10 958
Isabelle Stévant Switzerland 16 985 1.1× 489 0.6× 251 0.6× 58 0.2× 11 0.1× 26 1.3k
Catherine Boucher United Kingdom 12 530 0.6× 336 0.4× 58 0.1× 191 0.8× 45 0.4× 15 681
Bryan P. Haines Australia 15 430 0.5× 164 0.2× 41 0.1× 117 0.5× 24 0.2× 16 662
Marjorie Withers United States 17 925 1.0× 1.1k 1.3× 13 0.0× 56 0.2× 26 0.2× 23 1.6k
Caitlin Collin Australia 16 554 0.6× 240 0.3× 32 0.1× 136 0.5× 6 0.1× 20 847
Stan R. Blecher Canada 15 418 0.5× 323 0.4× 160 0.4× 13 0.1× 4 0.0× 43 632
Natalia Tulina United States 9 572 0.6× 192 0.2× 72 0.2× 205 0.8× 3 0.0× 11 880
Karolina Piotrowska-Nitsche United States 9 682 0.8× 186 0.2× 39 0.1× 159 0.6× 67 0.6× 13 849
Miranda Gomperts United Kingdom 8 946 1.0× 251 0.3× 72 0.2× 63 0.3× 2 0.0× 9 1.1k

Countries citing papers authored by N. Abbas

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 of co-authors of N. Abbas

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

All Works

18 of 18 papers shown
1.
David, Gilles, Paola Giunti, N. Abbas, et al.. (1996). 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.. PubMed. 59(6). 1328–36. 52 indexed citations
2.
Ravisé, N., Judith Lopes, N. Abbas, et al.. (1996). A de Novo Case of Hereditary Neuropathy with Liability to Pressure Palsies (HNPP) of Maternal Origin: A New Mechanism for Deletion in 17p11.2?. Human Molecular Genetics. 5(1). 103–106. 27 indexed citations
3.
Lopes, Judith, Éric Leguern, Riadh Gouider, et al.. (1996). 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.. PubMed. 58(6). 1223–30. 44 indexed citations
4.
Cancel‐Tassin, Géraldine, N. Abbas, Giovanni Stévanin, et al.. (1995). Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado-Joseph disease locus.. PubMed. 57(4). 809–16. 87 indexed citations
5.
Stévanin, Giovanni, Géraldine Cancel‐Tassin, N. Abbas, et al.. (1995). Characterisation of the unstable expanded CAG repeat in the MJD1 gene in four Brazilian families of Portuguese descent with Machado-Joseph disease. Journal of Medical Genetics. 32(10). 827–830. 16 indexed citations
6.
Lorenzetti, Diego, Davide Pareyson, Angelo Sghirlanzoni, et al.. (1995). A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies.. PubMed. 56(1). 91–8. 39 indexed citations
7.
Leguern, Éric, Riadh Gouider, Judith Lopes, et al.. (1995). Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: a study of 30 unrelated cases. Human Molecular Genetics. 4(9). 1673–1674. 15 indexed citations
8.
Boucekkine, C., Jean‐Edmond Toublanc, N. Abbas, et al.. (1994). Clinical and anatomical spectrum in XX sex reversed patients. Relationship to the presence of Y specific DNA‐sequences. Clinical Endocrinology. 40(6). 733–742. 92 indexed citations
9.
Abbas, N., Éric Vilain, Francis Jaubert, et al.. (1993). Familial case of 46,XX male and 46,XX true hermaphrodite associated with a paternal-derived SRY-bearing X chromosome.. PubMed. 316(4). 375–83. 33 indexed citations
10.
Toublanc, J E, C. Boucekkine, N. Abbas, et al.. (1993). Hormonal and molecular genetic findings in 46,XX subjects with sexual ambiguity and testicular differentiation. European Journal of Pediatrics. 152(S2). S70–S75. 12 indexed citations
11.
McElreavey, Ken, Éric Vilain, N. Abbas, Ira Herskowitz, & M Fellous. (1993). A regulatory cascade hypothesis for mammalian sex determination: SRY represses a negative regulator of male development.. Proceedings of the National Academy of Sciences. 90(8). 3368–3372. 280 indexed citations
12.
Vilain, Éric, N. Abbas, J.‐M. Costa, et al.. (1992). XY sex reversal associated with a deletion 5' to the SRY "HMG box" in the testis-determining region.. Proceedings of the National Academy of Sciences. 89(22). 11016–11020. 132 indexed citations
13.
Boucekkine, C., J E Toublanc, N. Abbas, et al.. (1992). The Sole Presence of the Testis-Determining Region of the Y Chromosome <i>(SRY)</i> in 46, XX Patients Is Associated with Phenot&gamma;pic Variability. Hormone Research. 37(6). 236–240. 11 indexed citations
14.
Lucotte, G, et al.. (1990). Rétro-transposition de la séquence humaine homologue á la p49f sur le chromosome y au cours de l'evolution des singes anthropoïdes. Biochemical Systematics and Ecology. 18(2-3). 199–204. 2 indexed citations
15.
Abbas, N., Jean‐Edmond Toublanc, C. Boucekkine, et al.. (1990). A possible common origin of ?Y-negative? human XX males and XX true hermaphrodites. Human Genetics. 84(4). 356–60. 67 indexed citations
16.
Semino, Ornella, Rosaria Scozzari, Giorgio Sirugo, et al.. (1990). Y chromosome DNA polymorphisms in human populations: differences between Caucasoids and Africans detected by 49a and 49f probes. Annals of Human Genetics. 54(4). 287–296. 54 indexed citations
17.
Palmer, Mark S., Andrew Sinclair, Philippe Berta, et al.. (1989). Genetic evidence that ZFY is not the testis-determining factor. Nature. 342(6252). 937–939. 222 indexed citations
18.
Abbas, N., et al.. (1988). Séquences Y-chromosome humain spécifiques présentes chez les singes anthropoïdes. Biochemical Systematics and Ecology. 16(1). 105–109. 2 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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