Christiane Penet

4.6k total citations · 2 hit papers
27 papers, 2.9k citations indexed

About

Christiane Penet is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Physiology. According to data from OpenAlex, Christiane Penet has authored 27 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Cellular and Molecular Neuroscience and 9 papers in Physiology. Recurrent topics in Christiane Penet's work include Alzheimer's disease research and treatments (9 papers), Genetic Neurodegenerative Diseases (7 papers) and Mitochondrial Function and Pathology (6 papers). Christiane Penet is often cited by papers focused on Alzheimer's disease research and treatments (9 papers), Genetic Neurodegenerative Diseases (7 papers) and Mitochondrial Function and Pathology (6 papers). Christiane Penet collaborates with scholars based in France, Sweden and Norway. Christiane Penet's co-authors include Alexis Brice, Yves Agid, Alexandra Dürr, Mireille Cossée, Claude Mignard, Victoria Campuzano, Jean‐Louis Mandel, Michel Kœnig, María Martínez and Giovanni Stévanin and has published in prestigious journals such as New England Journal of Medicine, Nature Genetics and Neurology.

In The Last Decade

Christiane Penet

27 papers receiving 2.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia

1996 769 citations Alexandra Dürr, Mireille Cossée et al. New England Journal of Medicine profile →
Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum

1999 544 citations Dominique Campion, Cécile Dumanchin et al. The American Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Christiane Penet France	17	1.7k	1.5k	769	763	566	27	2.9k
Ornit Chiba‐Falek United States	29	1.1k 0.6×	673 0.5×	934 1.2×	532 0.7×	400 0.7×	82	2.5k
Grazia Annesi Italy	27	1.1k 0.6×	1.2k 0.8×	1.2k 1.5×	263 0.3×	462 0.8×	94	2.7k
Mario Ezquerra Spain	28	1.3k 0.8×	782 0.5×	1.7k 2.2×	1.1k 1.4×	177 0.3×	85	3.0k
Janet Alder United States	26	1.2k 0.7×	1.1k 0.8×	258 0.3×	317 0.4×	183 0.3×	46	2.4k
Gloria J. Klapstein United States	15	1.3k 0.8×	1.9k 1.3×	960 1.2×	259 0.3×	110 0.2×	18	2.5k
Albert Giralt Spain	31	1.7k 1.0×	1.6k 1.1×	672 0.9×	447 0.6×	151 0.3×	73	2.8k
Kay Seidel Germany	30	1.5k 0.9×	1.7k 1.2×	1.1k 1.4×	392 0.5×	83 0.1×	50	2.7k
Paul Mohapel Sweden	26	632 0.4×	1.5k 1.0×	346 0.4×	299 0.4×	117 0.2×	37	2.5k
Ebba Lohmann Türkiye	26	826 0.5×	1.2k 0.8×	2.1k 2.7×	801 1.0×	218 0.4×	73	3.3k
Richard Grondin United States	35	908 0.5×	2.2k 1.5×	1.6k 2.1×	361 0.5×	141 0.2×	69	3.5k

Countries citing papers authored by Christiane Penet

Since Specialization

Citations

This map shows the geographic impact of Christiane Penet'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 Christiane Penet with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christiane Penet more than expected).

Fields of papers citing papers by Christiane Penet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christiane Penet. 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 Christiane Penet. The network helps show where Christiane Penet may publish in the future.

Co-authorship network of co-authors of Christiane Penet

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

All Works

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20 of 20 papers shown

Philippe, Anne, María Martínez, Christopher Gillberg, et al.. (2002). Analysis of ten candidate genes in autism by association and linkage. American Journal of Medical Genetics. 114(2). 125–128. 19 indexed citations

Penet, Christiane, et al.. (2001). Walnut blight - new knowledge for an old disease. Summary of research (1995-2000). 171. 27–30. 4 indexed citations

Campion, Dominique, Cécile Dumanchin, Didier Hannequin, et al.. (1999). Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum. The American Journal of Human Genetics. 65(3). 664–670. 544 indexed citations breakdown →

Philippe, Anne, María Martínez, M Guilloud-Bataille, et al.. (1999). Genome-Wide Scan for Autism Susceptibility Genes. Human Molecular Genetics. 8(5). 805–812. 385 indexed citations

Dumanchin, Cécile, A. Camuzat, Dominique Campion, et al.. (1998). Segregation of a Missense Mutation in the Microtubule-Associated Protein Tau Gene with Familial Frontotemporal Dementia and Parkinsonism. Human Molecular Genetics. 7(11). 1825–1829. 184 indexed citations

Didierjean, Olivier, María Martínez, Dominique Campion, et al.. (1997). No effect of the alpha 1-antichymotrypsin A allele in Alzheimer's disease. Journal of Neurology Neurosurgery & Psychiatry. 63(1). 103–105. 14 indexed citations

Dürr, Alexandra, Giovanni Stévanin, Géraldine Cancel‐Tassin, et al.. (1996). Spinocerebellar ataxia 3 and machado‐joseph disease: Clinical, molecular, and neuropathological features. Annals of Neurology. 39(4). 490–499. 350 indexed citations

Dürr, Alexandra, Mireille Cossée, Yves Agid, et al.. (1996). Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia. New England Journal of Medicine. 335(16). 1169–1175. 769 indexed citations breakdown →

Campion, Dominique, Alexis Brice, Cécile Dumanchin, et al.. (1996). A novel presenilin 1 mutation resulting in familial Alzheimerʼs disease with an onset age of 29 years. Neuroreport. 7(10). 1582–1584. 56 indexed citations

10.

Benomar, Ali, Giovanni Stévanin, Géraldine Cancel‐Tassin, et al.. (1995). The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12–p21.1. Nature Genetics. 10(1). 84–88. 126 indexed citations

11.

Fontaine, Bertrand, Jamïlé Hazan, Alexandra Dürr, et al.. (1995). Exclusion of the candidate locus FSP1 in six families with late-onset autosomal dominant spastic paraplegia. Neuromuscular Disorders. 5(1). 11–17. 5 indexed citations

12.

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

13.

Cancel‐Tassin, Géraldine, Giovanni Stévanin, Alexandra Dürr, et al.. (1995). SCA2 is not a major locus for ADCA type I in French families. American Journal of Medical Genetics. 60(5). 382–385. 8 indexed citations

14.

Brice, Alexis, Sandrine Tardieu, Dominique Campion, et al.. (1995). Allelic association at the D14S43 locus in early onset Alzheimer's disease. American Journal of Medical Genetics. 60(2). 91–93. 3 indexed citations

15.

Dubourg, Olivier, Alexandra Dürr, Géraldine Cancel‐Tassin, et al.. (1995). Analysis of the SCAI CAG repeat in a large number of families with dominant ataxia: Clinical and molecular correlations. Annals of Neurology. 37(2). 176–180. 62 indexed citations

16.

Campion, Dominique, Alexis Brice, Didier Hannequin, et al.. (1995). A large pedigree with early-onset Alzheimer's disease. Neurology. 45(1). 80–85. 39 indexed citations

17.

Guern, E. Le, N. Ravisé, Michel Gugenheim, et al.. (1994). Linkage analyses between dominant X-linked Charcot-Marie-Tooth disease, and 15 Xq11–Xq21 microsatellites in a new large family: Three new markers are closely linked to the gene. Neuromuscular Disorders. 4(5-6). 463–469. 8 indexed citations

18.

Dürr, Alexandra, Giovanni Stévanin, C P Jedynak, et al.. (1993). Familial essential tremor and idiopathic torsion dystonia are different genetic entities. Neurology. 43(11). 2212–2212. 33 indexed citations

19.

Brice, Alexis, Giovanni Stévanin, Michel Gugenheim, et al.. (1992). Duplication within chromosome 17p11.2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type 1a. The French CMT Research Group.. Journal of Medical Genetics. 29(11). 807–812. 29 indexed citations

20.

Pierrot‐Deseilligny, C., et al.. (1989). Increased wave P 300 latency in progressive supranuclear palsy.. Journal of Neurology Neurosurgery & Psychiatry. 52(5). 656–658. 15 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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