Solenn Legallic

2.2k total citations
6 papers, 382 citations indexed

About

Solenn Legallic is a scholar working on Genetics, Molecular Biology and Neurology. According to data from OpenAlex, Solenn Legallic has authored 6 papers receiving a total of 382 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Neurology. Recurrent topics in Solenn Legallic's work include Parkinson's Disease Mechanisms and Treatments (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Solenn Legallic is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Solenn Legallic collaborates with scholars based in France, Italy and Ireland. Solenn Legallic's co-authors include Dominique Campion, Didier Hannequin, Alexis Brice, Catherine Thomas-Antérion, M. Décousus, Vincent Meininger, Eric Guedj, William Camu, Bruno Dubois and Lina Benajiba and has published in prestigious journals such as Annals of Neurology, Neurobiology of Disease and Journal of Alzheimer s Disease.

In The Last Decade

Solenn Legallic

6 papers receiving 380 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Solenn Legallic France	5	286	130	109	103	101	6	382
Kevin McAvoy United States	9	229 0.8×	77 0.6×	190 1.7×	118 1.1×	90 0.9×	11	400
Tomoyo Hashimoto Japan	9	291 1.0×	105 0.8×	139 1.3×	101 1.0×	77 0.8×	24	448
Olubunmi Abel United Kingdom	5	312 1.1×	52 0.4×	133 1.2×	172 1.7×	101 1.0×	6	379
Tsz Hang Wong Netherlands	10	127 0.4×	145 1.1×	146 1.3×	39 0.4×	70 0.7×	13	308
Rachel A.K. Atkinson Australia	10	408 1.4×	166 1.3×	236 2.2×	198 1.9×	83 0.8×	16	638
Isabella Fogh Italy	12	157 0.5×	60 0.5×	152 1.4×	100 1.0×	39 0.4×	17	345
N. Siddique United States	6	326 1.1×	53 0.4×	143 1.3×	197 1.9×	108 1.1×	8	399
Younghwi Kwon South Korea	9	214 0.7×	117 0.9×	207 1.9×	61 0.6×	67 0.7×	13	432
Rohini Raman United Kingdom	5	146 0.5×	109 0.8×	150 1.4×	100 1.0×	96 1.0×	6	330
Janis Bennion Callister United Kingdom	8	309 1.1×	92 0.7×	135 1.2×	142 1.4×	60 0.6×	8	368

Countries citing papers authored by Solenn Legallic

Since Specialization

Citations

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

Fields of papers citing papers by Solenn Legallic

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Solenn Legallic

This figure shows the co-authorship network connecting the top 25 collaborators of Solenn Legallic. A scholar is included among the top collaborators of Solenn Legallic 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 Solenn Legallic. Solenn Legallic 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:

6 of 6 papers shown

1.

Rovelet‐Lecrux, Anne, Solenn Legallic, David Wallon, et al.. (2011). A genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer disease. European Journal of Human Genetics. 20(6). 613–617. 44 indexed citations

2.

Rovelet‐Lecrux, Anne, Didier Hannequin, Olivier Guillin, et al.. (2010). Frontotemporal Dementia Phenotype Associated with MAPT Gene Duplication. Journal of Alzheimer s Disease. 21(3). 897–902. 33 indexed citations

3.

Benajiba, Lina, Isabelle Le Ber, Agnès Camuzat, et al.. (2009). TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration. Annals of Neurology. 65(4). 470–473. 239 indexed citations

4.

Rosa, Gabriella Di, Giuseppina Pustorino, Maria Spanò, et al.. (2008). Type I hyperprolinemia and proline dehydrogenase (PRODH) mutations in four Italian children with epilepsy and mental retardation. Psychiatric Genetics. 18(1). 40–42. 20 indexed citations

5.

Legallic, Solenn, Jacqueline Bou, Sadeq Haouzir, et al.. (2008). No pathogenic rearrangement within the DISC 1 gene in psychosis. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(1). 148–150. 1 indexed citations

6.

Rovelet‐Lecrux, Anne, Vincent Deramecourt, Solenn Legallic, et al.. (2008). Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease. Neurobiology of Disease. 31(1). 41–45. 45 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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