Amelie Pandraud

1.0k total citations
7 papers, 523 citations indexed

About

Amelie Pandraud is a scholar working on Neurology, Molecular Biology and Genetics. According to data from OpenAlex, Amelie Pandraud has authored 7 papers receiving a total of 523 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Neurology, 3 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in Amelie Pandraud's work include Neurogenetic and Muscular Disorders Research (3 papers), Genetic Neurodegenerative Diseases (3 papers) and Hereditary Neurological Disorders (2 papers). Amelie Pandraud is often cited by papers focused on Neurogenetic and Muscular Disorders Research (3 papers), Genetic Neurodegenerative Diseases (3 papers) and Hereditary Neurological Disorders (2 papers). Amelie Pandraud collaborates with scholars based in United Kingdom, India and United States. Amelie Pandraud's co-authors include Henry Houlden, Mary M. Reilly, Sinéad M. Murphy, James M. Polke, Yo‐Tsen Liu, Hadi Manji, Matilde Laurá, Gita Ramdharry, Mary B. Davis and Alexander M. Rossor and has published in prestigious journals such as Brain, Human Molecular Genetics and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Amelie Pandraud

7 papers receiving 498 citations

Peers

Amelie Pandraud

CMN

NEURO

MB

NEURO

CB

Stefania Magri Italy

Anna Sailer United Kingdom

Dolores Martínez‐Rubio Spain

Janel O. Johnson United States

Naïma Bouslam Morocco

Laurie Robak United States

S. A. Klyushnikov Russia

Elena Sánchez-Ferrero Spain

Claudia Stendel Germany

Paola Saveri Italy

Stefania Magri Italy

Amelie Pandraud

271 ×0.8

CMN

115 ×0.6

NEURO

296 ×1.8

MB

66 ×0.5

NEURO

32 ×0.5

CB

Citations per year, relative to Amelie Pandraud Amelie Pandraud (= 1×) peers Stefania Magri

Countries citing papers authored by Amelie Pandraud

Since Specialization

Citations

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

Fields of papers citing papers by Amelie Pandraud

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amelie Pandraud

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

All Works

Sort: Min cites: Since: Top N: Style:

7 of 7 papers shown

1.

Kalmár, Bernadett, Amy Innes, Klaus Wanisch, et al.. (2017). Mitochondrial deficits and abnormal mitochondrial retrograde axonal transport play a role in the pathogenesis of mutant Hsp27-induced Charcot Marie Tooth Disease. Human Molecular Genetics. 26(17). 3313–3326. 44 indexed citations

2.

Kara, Eleanna, Aoife P. Kiely, Christos Proukakis, et al.. (2014). A 6.4 Mb Duplication of the α-Synuclein Locus Causing Frontotemporal Dementia and Parkinsonism. JAMA Neurology. 71(9). 1162–1162. 54 indexed citations

3.

Nalini, Atchayaram, Amelie Pandraud, Kin Y. Mok, & Henry Houlden. (2013). Madras motor neuron disease (MMND) is distinct from the riboflavin transporter genetic defects that cause Brown–Vialetto–Van Laere syndrome. Journal of the Neurological Sciences. 334(1-2). 119–122. 6 indexed citations

4.

Murphy, Sinéad M., Matilde Laurá, Katherine A. Fawcett, et al.. (2012). Charcot–Marie–Tooth disease: frequency of genetic subtypes and guidelines for genetic testing. Journal of Neurology Neurosurgery & Psychiatry. 83(7). 706–710. 257 indexed citations

5.

Koutsis, Georgios, Georgia Karadima, Amelie Pandraud, et al.. (2012). Genetic screening of Greek patients with Huntington's disease phenocopies identifies an SCA8 expansion. Journal of Neurology. 259(9). 1874–1878. 13 indexed citations

6.

Johnson, Janel O., J. Raphael Gibbs, André Mégarbané, et al.. (2012). Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease. Brain. 135(9). 2875–2882. 99 indexed citations

7.

Bryson, J. Barney, Carl Hobbs, Michael Parsons, et al.. (2012). Amyloid precursor protein (APP) contributes to pathology in the SOD1G93A mouse model of amyotrophic lateral sclerosis. Human Molecular Genetics. 21(17). 3871–3882. 50 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.

Explore authors with similar magnitude of impact