Pascale Ribaı̈

4.5k total citations
18 papers, 638 citations indexed

About

Pascale Ribaı̈ is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Pascale Ribaı̈ has authored 18 papers receiving a total of 638 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 11 papers in Cellular and Molecular Neuroscience and 7 papers in Neurology. Recurrent topics in Pascale Ribaı̈'s work include Genetic Neurodegenerative Diseases (7 papers), Mitochondrial Function and Pathology (6 papers) and Neurological diseases and metabolism (4 papers). Pascale Ribaı̈ is often cited by papers focused on Genetic Neurodegenerative Diseases (7 papers), Mitochondrial Function and Pathology (6 papers) and Neurological diseases and metabolism (4 papers). Pascale Ribaı̈ collaborates with scholars based in France, Belgium and Italy. Pascale Ribaı̈'s co-authors include Alexandra Dürr, Alexis Brice, Karine Nguyen, Sylvie Forlani, Valérie Hahn‐Barma, Giovanni Stévanin, Christel Depienne, Cyril Goizet, Perrine Charles and Merle Ruberg and has published in prestigious journals such as Brain, Neurology and The American Journal of Human Genetics.

In The Last Decade

Pascale Ribaı̈

18 papers receiving 616 citations

Peers

Pascale Ribaı̈

CMN

NEURO

GENET

Cláudia Melo Portugal

Yaeko Ichikawa Japan

Julia Schicks Germany

Utako Nagaoka Japan

Sandra Martins Portugal

Luigi Di Maio Italy

H. Skre Norway

Corien C. Verschuuren‐Bemelmans Netherlands

Giovanni Airoldi Italy

Carly E. Siskind United States

Cláudia Melo Portugal

Pascale Ribaı̈

386 ×0.8

CMN

221 ×0.6

149 ×0.5

NEURO

130 ×1.0

NEURO

83 ×1.2

GENET

Citations per year, relative to Pascale Ribaı̈ Pascale Ribaı̈ (= 1×) peers Cláudia Melo

Countries citing papers authored by Pascale Ribaı̈

Since Specialization

Citations

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

Fields of papers citing papers by Pascale Ribaı̈

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pascale Ribaı̈

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

All Works

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18 of 18 papers shown

Charles, Perrine, Pascale Ribaı̈, Cyril Goizet, et al.. (2011). Quantitative assessment of the evolution of cerebellar signs in spinocerebellar ataxias. Movement Disorders. 26(3). 534–538. 19 indexed citations

Demonty, J, M Gonce, Pascale Ribaı̈, C. Verellen‐Dumoulin, & R. Hustinx. (2010). CHOREA ASSOCIATED WITH ANTI-PHOSPHOLIPID ANTIBODIES: CASE REPORT. Acta Clinica Belgica. 65(5). 350–353. 6 indexed citations

Cagnoli, Claudia, Giovanni Stévanin, Alessandro Brussino, et al.. (2010). Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias. Human Mutation. 31(10). 1117–1124. 53 indexed citations

Montcel, Sophie Tézenas du, Perrine Charles, Pascale Ribaı̈, et al.. (2008). Composite cerebellar functional severity score: validation of a quantitative score of cerebellar impairment. Brain. 131(5). 1352–1361. 67 indexed citations

Globas, Christoph, Sophie Tézenas du Montcel, Sylvia Boesch, et al.. (2008). Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6. Movement Disorders. 23(15). 2232–2238. 98 indexed citations

Ribaı̈, Pascale, Karine Nguyen, Valérie Hahn‐Barma, et al.. (2007). Psychiatric and Cognitive Difficulties as Indicators of Juvenile Huntington Disease Onset in 29 Patients. Archives of Neurology. 64(6). 813–813. 94 indexed citations

Ribaı̈, Pascale, Françoise Pousset, Marie‐Laure Tanguy, et al.. (2007). Neurological, Cardiological, and Oculomotor Progression in 104 Patients With Friedreich Ataxia During Long-term Follow-up. Archives of Neurology. 64(4). 558–558. 93 indexed citations

Hanein, Sylvain, Alexandra Dürr, Pascale Ribaı̈, et al.. (2007). A novel locus for autosomal dominant “uncomplicated” hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3. Human Genetics. 122(3-4). 261–273. 18 indexed citations

Ribaı̈, Pascale, Christel Depienne, Estelle Fédirko, et al.. (2007). Mental deficiency in three families with SPG4 spastic paraplegia. European Journal of Human Genetics. 16(1). 97–104. 25 indexed citations

10.

Ribaı̈, Pascale, Giovanni Stévanin, Naïma Bouslam, et al.. (2006). A new phenotype linked to SPG27 and refinement of the critical region on chromosome. Journal of Neurology. 253(6). 714–719. 14 indexed citations

11.

Namekawa, Michito, Pascale Ribaı̈, Isabelle Nelson, et al.. (2006). SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years. Neurology. 66(1). 112–114. 80 indexed citations

12.

Ribaı̈, Pascale, et al.. (2005). Usefulness of prolonged video–EEG monitoring and provocative procedure with saline injection for the diagnosis of non epileptic seizures of psychogenic origin. Journal of Neurology. 253(3). 328–332. 22 indexed citations

13.

Abramowicz, Marc, Pascale Ribaı̈, & Monique Cordonnier. (2004). Congenital stationary night blindness: Report of an autosomal recessive family and linkage analysis. American Journal of Medical Genetics Part A. 132A(1). 76–79. 5 indexed citations

14.

Ribaı̈, Pascale, Corinne Liesnard, Georges Rodesch, et al.. (2003). Transient cerebral arteriopathy in infancy associated with enteroviral infection. European Journal of Paediatric Neurology. 7(2). 73–75. 22 indexed citations

15.

Brems, Hilde, et al.. (2003). Second polar body inclusion results in diploid/triploid mixoploidy.. PubMed. 14(4). 425–9. 7 indexed citations

16.

Ribaı̈, Pascale, et al.. (2002). Sensory neuropathy with decreased NCV in Fabry patients with preserved renal function.. The American Journal of Human Genetics. 71(4). 260. 1 indexed citations

17.

Penaloza, Andréa, Christine Decaestecker, Pascale Ribaı̈, et al.. (2000). Sialic acid residues in the labial salivary glands from Sjögren's syndrome patients.. PubMed. 17(6). 713–7. 2 indexed citations

18.

Steinfeld, Serge, Andréa Penaloza, Pascale Ribaı̈, et al.. (1999). D-mannose and N-acetylglucosamine moieties and their respective binding sites in salivary glands of Sjögren's syndrome.. PubMed. 26(4). 833–41. 12 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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