Kim Maincent

821 total citations
9 papers, 297 citations indexed

About

Kim Maincent is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Kim Maincent has authored 9 papers receiving a total of 297 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Neurology. Recurrent topics in Kim Maincent's work include Genomics and Rare Diseases (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Muscle Physiology and Disorders (2 papers). Kim Maincent is often cited by papers focused on Genomics and Rare Diseases (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Muscle Physiology and Disorders (2 papers). Kim Maincent collaborates with scholars based in France, United States and Belgium. Kim Maincent's co-authors include M. Mayer, Adriana Ramirez, Jean Bénard, Sonia Khirani, Brigitte Fauroux, Eric Angevin, Michèle Boulé, C Boccaccio, Olivier Hartmann and Frédéric Lofaso and has published in prestigious journals such as Blood, European Respiratory Journal and Orphanet Journal of Rare Diseases.

In The Last Decade

Kim Maincent

9 papers receiving 292 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kim Maincent France	7	152	104	41	39	35	9	297
Alice Abdel Aleem Egypt	13	216 1.4×	119 1.1×	52 1.3×	28 0.7×	20 0.6×	24	376
Sımona Baldassari Italy	10	247 1.6×	91 0.9×	18 0.4×	30 0.8×	24 0.7×	22	399
M. R. Balestrini Italy	12	196 1.3×	79 0.8×	54 1.3×	40 1.0×	16 0.5×	17	429
Goekhan Uyanik Germany	7	171 1.1×	53 0.5×	75 1.8×	35 0.9×	14 0.4×	7	352
Nam Suk Sim South Korea	13	211 1.4×	175 1.7×	55 1.3×	29 0.7×	21 0.6×	31	531
Roberto Micheli Italy	9	217 1.4×	69 0.7×	13 0.3×	18 0.5×	32 0.9×	16	387
Tomoko Chiyo Japan	10	263 1.7×	72 0.7×	47 1.1×	11 0.3×	15 0.4×	15	347
Zhiyan Shan China	14	253 1.7×	63 0.6×	29 0.7×	36 0.9×	30 0.9×	33	377
Marina Cardano Italy	9	183 1.2×	28 0.3×	50 1.2×	18 0.5×	46 1.3×	14	341
Annabella Salerni Italy	12	76 0.5×	87 0.8×	21 0.5×	13 0.3×	16 0.5×	23	403

Countries citing papers authored by Kim Maincent

Since Specialization

Citations

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

Fields of papers citing papers by Kim Maincent

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kim Maincent

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

All Works

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9 of 9 papers shown

Doummar, Diane, Sandra Whalen, Boris Keren, et al.. (2020). Congenital immobility and stiffness related to biallelic ATAD1 variants. Neurology Genetics. 6(6). e520–e520. 4 indexed citations

Maincent, Kim, Bénédicte Héron, Thierry Billette de Villemeur, & M. Mayer. (2018). Early detection of median nerve compression by Electroneurography can improve outcome in children with Mucopolysaccharidoses. Orphanet Journal of Rare Diseases. 13(1). 209–209. 3 indexed citations

Dimassi, S., Dorothée Ville, Alain Calender, et al.. (2015). Whole‐exome sequencing improves the diagnosis yield in sporadic infantile spasm syndrome. Clinical Genetics. 89(2). 198–204. 58 indexed citations

Servais, Laurent, Nicolas Deconinck, A. Moraux, et al.. (2012). Innovative methods to assess upper limb strength and function in non-ambulant Duchenne patients. Neuromuscular Disorders. 23(2). 139–148. 62 indexed citations

Vuillaumier‐Barrot, Sandrine, C. Bouchet-Séraphin, Caroline Besson, et al.. (2011). Intragenic rearrangements in LARGE and POMGNT1 genes in severe dystroglycanopathies. Neuromuscular Disorders. 21(11). 782–790. 12 indexed citations

Khirani, Sonia, Adriana Ramirez, Frédéric Lofaso, et al.. (2011). Nocturnal hypoxaemia and hypercapnia in children with neuromuscular disorders. European Respiratory Journal. 39(5). 1206–1212. 51 indexed citations

Maincent, Kim, Françoise Baverel, Dominique Le Tessier, et al.. (2009). Molecular cytogenetic characterization of the first reported case of inv dup del 20p compatible with a U‐type exchange model. American Journal of Medical Genetics Part A. 149A(3). 437–445. 16 indexed citations

Portes, Vincent des, Nathalie Boddaert, Silvia Sacco, et al.. (2003). Specific clinical and brain MRI features in mentally retarded patients with mutations in the Oligophrenin‐1 gene. American Journal of Medical Genetics Part A. 124A(4). 364–371. 45 indexed citations

Valteau‐Couanet, Dominique, Kim Maincent, Olivier Hartmann, et al.. (2002). Dendritic cells for NK/LAK activation: rationale for multicellular immunotherapy in neuroblastoma patients. Blood. 100(7). 2554–2561. 46 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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