Pascale Hince

1.3k total citations
14 papers, 630 citations indexed

About

Pascale Hince is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Pascale Hince has authored 14 papers receiving a total of 630 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Neurology and 5 papers in Genetics. Recurrent topics in Pascale Hince's work include Neurogenetic and Muscular Disorders Research (5 papers), Amyotrophic Lateral Sclerosis Research (4 papers) and Mitochondrial Function and Pathology (2 papers). Pascale Hince is often cited by papers focused on Neurogenetic and Muscular Disorders Research (5 papers), Amyotrophic Lateral Sclerosis Research (4 papers) and Mitochondrial Function and Pathology (2 papers). Pascale Hince collaborates with scholars based in Canada, France and United States. Pascale Hince's co-authors include Guy A. Rouleau, Patrick A. Dion, Daniel Rochefort, Nicolas Dupré, Véronique Belzil, Hussein Daoud, Simon Girard, Anne Noreau, Paul N. Valdmanis and William Camu and has published in prestigious journals such as Science, Journal of Clinical Investigation and Journal of Neuroscience.

In The Last Decade

Pascale Hince

14 papers receiving 624 citations

Peers

Pascale Hince

NEURO

CMN

GENET

NEURO

So Yoen Choi South Korea

Mito Shiote Japan

Olga Tarabal Spain

Benjamin Dombert Germany

Georgia Karadima Greece

Haviryaji S. G. Kalluri United States

Μάριος Πάνας Greece

O. Garofalo United Kingdom

Toshiya Shiojima Japan

Catherine Gelsthorpe United Kingdom

So Yoen Choi South Korea

Pascale Hince

510 ×1.8

244 ×0.9

NEURO

158 ×0.9

CMN

96 ×0.6

GENET

64 ×0.8

NEURO

Citations per year, relative to Pascale Hince Pascale Hince (= 1×) peers So Yoen Choi

Countries citing papers authored by Pascale Hince

Since Specialization

Citations

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

Fields of papers citing papers by Pascale Hince

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pascale Hince

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

All Works

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14 of 14 papers shown

Cruceanu, Cristiana, Susana G. Torres‐Platas, Juan Pablo López, et al.. (2017). Rare susceptibility variants for bipolar disorder suggest a role for G protein-coupled receptors. Molecular Psychiatry. 23(10). 2050–2056. 15 indexed citations

Bowerman, Mélissa, Véronique Bernard, Annie Dionne, et al.. (2017). KCC3 loss-of-function contributes to Andermann syndrome by inducing activity-dependent neuromuscular junction defects. Neurobiology of Disease. 106. 35–48. 6 indexed citations

Blondeau, F, Martine Girard, Pascale Hince, et al.. (2017). A polyalanine antibody for the diagnosis of oculopharyngeal muscular dystrophy and polyalanine-related diseases. 1. 1–1. 1 indexed citations

Blondeau, F, Martine Girard, Pascale Hince, et al.. (2017). A Polyalanine Antibody For The Diagnosis Of Oculopharyngeal Muscular Dystrophy And Polyalanine-Related Diseases. Zenodo (CERN European Organization for Nuclear Research). 1 indexed citations

Zhou, Sirui, Amirthagowri Ambalavanan, Daniel Rochefort, et al.. (2016). RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population. The American Journal of Human Genetics. 99(5). 1072–1085. 41 indexed citations

Jouan, Loubna, Bouchra Ouled Amar Bencheikh, Hussein Daoud, et al.. (2015). Exome sequencing identifies recessive CDK5RAP2 variants in patients with isolated agenesis of corpus callosum. European Journal of Human Genetics. 24(4). 607–610. 17 indexed citations

Kaneb, Hannah, Andrew W. Folkmann, Véronique Belzil, et al.. (2014). Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis. Human Molecular Genetics. 24(5). 1363–1373. 101 indexed citations

Shekarabi, Masoud, Randal X. Moldrich, Janet Laganière, et al.. (2012). Loss of Neuronal Potassium/Chloride Cotransporter 3 (KCC3) Is Responsible for the Degenerative Phenotype in a Conditional Mouse Model of Hereditary Motor and Sensory Neuropathy Associated with Agenesis of the Corpus Callosum. Journal of Neuroscience. 32(11). 3865–3876. 27 indexed citations

Srour, Myriam, Jean‐Baptiste Rivière, Marie‐Pierre Dubé, et al.. (2010). Mutations in DCC Cause Congenital Mirror Movements. Science. 328(5978). 592–592. 128 indexed citations

10.

Valdmanis, Paul N., Véronique Belzil, Patrick A. Dion, et al.. (2009). A Mutation that Creates a Pseudoexon in SOD1 Causes Familial ALS. Annals of Human Genetics. 73(6). 652–657. 31 indexed citations

11.

Belzil, Véronique, Paul N. Valdmanis, Patrick A. Dion, et al.. (2009). Mutations in FUS cause FALS and SALS in French and French Canadian populations. Neurology. 73(15). 1176–1179. 114 indexed citations

12.

Shekarabi, Masoud, Sébastien Holbert, Patrick A. Dion, et al.. (2008). HMSN/ACC truncation mutations disrupt brain-type creatine kinase-dependant activation of K+/Cl− co-transporter 3. Human Molecular Genetics. 17(17). 2703–2711. 23 indexed citations

13.

Shekarabi, Masoud, Jean‐Baptiste Rivière, Patrick A. Dion, et al.. (2008). Mutations in the nervous system–specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II. Journal of Clinical Investigation. 118(7). 2496–505. 81 indexed citations

14.

Valdmanis, Paul N., Edor Kabashi, Pascale Hince, et al.. (2008). Association of paraoxonase gene cluster polymorphisms with ALS in France, Quebec, and Sweden. Neurology. 71(7). 514–520. 44 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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