Amandine Boyer

1.1k total citations
15 papers, 797 citations indexed

About

Amandine Boyer is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, Amandine Boyer has authored 15 papers receiving a total of 797 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 6 papers in Cell Biology. Recurrent topics in Amandine Boyer's work include Hereditary Neurological Disorders (6 papers), Nuclear Structure and Function (5 papers) and RNA Research and Splicing (4 papers). Amandine Boyer is often cited by papers focused on Hereditary Neurological Disorders (6 papers), Nuclear Structure and Function (5 papers) and RNA Research and Splicing (4 papers). Amandine Boyer collaborates with scholars based in France, Germany and Netherlands. Amandine Boyer's co-authors include Nicolas Lévy, Rafaëlle Bernard, Annachiara De Sandre‐Giovannoli, Pierre Cau, Claire Navarro, Raoul C. M. Hennekam, Irène Boccaccio, Frits A. Beemer, Catherine Badens and Sébastien Courrier and has published in prestigious journals such as Stroke, Human Molecular Genetics and Clinical Chemistry.

In The Last Decade

Amandine Boyer

14 papers receiving 782 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Amandine Boyer France	11	587	143	136	57	52	15	797
Judit Symmank Germany	12	170 0.3×	55 0.4×	88 0.6×	71 1.2×	25 0.5×	27	367
Kriti Mohan United States	11	132 0.2×	69 0.5×	55 0.4×	72 1.3×	14 0.3×	32	498
Juliette Bitard France	10	227 0.4×	100 0.7×	52 0.4×	11 0.2×	10 0.2×	15	346
Koichiro Higashi Japan	12	347 0.6×	50 0.3×	13 0.1×	141 2.5×	78 1.5×	29	596
Jinu Han South Korea	15	226 0.4×	53 0.4×	32 0.2×	73 1.3×	42 0.8×	81	672
Jing-Qi Zhang Japan	11	155 0.3×	20 0.1×	56 0.4×	13 0.2×	14 0.3×	20	332
Enrique Garcia-Valenzuela United States	13	349 0.6×	30 0.2×	89 0.7×	26 0.5×	129 2.5×	20	942
Karsten Hufendiek Germany	11	184 0.3×	28 0.2×	20 0.1×	32 0.6×	17 0.3×	38	448
Lekbir Baala France	7	289 0.5×	69 0.5×	28 0.2×	101 1.8×	157 3.0×	9	602
Henk Veldman Netherlands	16	182 0.3×	64 0.4×	163 1.2×	21 0.4×	18 0.3×	20	484

Countries citing papers authored by Amandine Boyer

Since Specialization

Citations

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

Fields of papers citing papers by Amandine Boyer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amandine Boyer

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

All Works

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15 of 15 papers shown

Salort‐Campana, Emmanuelle, Amandine Boyer, Florence Esselin, et al.. (2022). HINT1 neuropathy: Expanding the genotype and phenotype spectrum. Clinical Genetics. 102(5). 379–390. 3 indexed citations

Stojkovic, Tanya, Amandine Boyer, Nathalie Martini, et al.. (2018). Molecular diagnosis of inherited peripheral neuropathies by targeted next-generation sequencing: molecular spectrum delineation. BMJ Open. 8(10). e021632–e021632. 40 indexed citations

Boyer, Amandine. (2015). La diarrhée aiguë du nourrisson et du jeune enfant : évaluation de la prise en charge ambulatoire dans le département de l'Isère. HAL (Le Centre pour la Communication Scientifique Directe).

Chen, Jian‐Min, Rafaëlle Bernard, Bernard de Massy, et al.. (2013). Dissecting the Structure and Mechanism of a Complex Duplication-Triplication Rearrangement in theDMDGene. Human Mutation. 34(8). 1080–1084. 23 indexed citations

Navarro, Claire, Sébastien Courrier, Amandine Boyer, et al.. (2013). New ZMPSTE24 (FACE1) mutations in patients affected with restrictive dermopathy or related progeroid syndromes and mutation update. European Journal of Human Genetics. 22(8). 1002–1011. 40 indexed citations

Boyer, Amandine, Emna Kerkeni, Joël Courageot, et al.. (2013). A Novel Mutation in FGD4/FRABIN Causes Charcot Marie Tooth Disease Type 4H in Patients from a Consanguineous Tunisian Family. Annals of Human Genetics. 77(4). 336–343. 15 indexed citations

Gaudy‐Marqueste, Caroline, Amandine Boyer, Claire Navarro, et al.. (2009). LMNA , ZMPSTE24 , and LBR Are Not Mutated in Scleroderma. Genetic Testing and Molecular Biomarkers. 13(5). 635–639. 2 indexed citations

Renard, Dimitri, Didier Milhaud, D. Bessis, et al.. (2008). Novel LMNA Mutation in Atypical Werner Syndrome Presenting With Ischemic Disease. Stroke. 40(2). e11–4. 25 indexed citations

Navarro, Claire, Juan Cadiñanos, Annachiara De Sandre‐Giovannoli, et al.. (2005). Loss of ZMPSTE24 (FACE-1) causes autosomal recessive restrictive dermopathy and accumulation of Lamin A precursors. Human Molecular Genetics. 14(11). 1503–1513. 217 indexed citations

10.

Navarro, Claire, Annachiara De Sandre‐Giovannoli, Rafaëlle Bernard, et al.. (2004). Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy. Human Molecular Genetics. 13(20). 2493–2503. 266 indexed citations

11.

Hunter, Michael, Rafaëlle Bernard, Elizabeth Freitas, et al.. (2003). Mutation screening of the N-myc downstream-regulated gene 1 (NDRG1) in patients with Charcot-Marie-Tooth Disease. Human Mutation. 22(2). 129–135. 41 indexed citations

12.

Bernard, Rafaëlle, Amandine Boyer, Perrine Malzac, et al.. (2002). Prenatal detection of the 17p11.2 duplication in Charcot-Marie-Tooth disease type 1A: necessity of a multidisciplinary approach for heterogeneous disorders. European Journal of Human Genetics. 10(5). 297–302. 7 indexed citations

13.

Latour, Philippe, Laetitia Boutrand, Nicolas Lévy, et al.. (2001). Polymorphic Short Tandem Repeats for Diagnosis of the Charcot-Marie-Tooth 1A Duplication. Clinical Chemistry. 47(5). 829–837. 55 indexed citations

14.

Bettega, G., et al.. (2000). A simulator for maxillofacial surgery integrating 3D cephalometry and orthodontia. Computer Aided Surgery. 5(3). 156–165. 36 indexed citations

15.

Bettega, G., et al.. (2000). A Simulator for Maxillofacial Surgery Integrating 3D Cephalometry and Orthodontia. Computer Aided Surgery. 5(3). 156–165. 27 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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