Cécile Laroche

574 total citations
3 papers, 126 citations indexed

About

Cécile Laroche is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Cécile Laroche has authored 3 papers receiving a total of 126 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Genetics, 1 paper in Surgery and 1 paper in Molecular Biology. Recurrent topics in Cécile Laroche's work include Muscle and Compartmental Disorders (1 paper), Genetic Syndromes and Imprinting (1 paper) and Muscle metabolism and nutrition (1 paper). Cécile Laroche is often cited by papers focused on Muscle and Compartmental Disorders (1 paper), Genetic Syndromes and Imprinting (1 paper) and Muscle metabolism and nutrition (1 paper). Cécile Laroche collaborates with scholars based in France and Denmark. Cécile Laroche's co-authors include Catherine Yardin, Sylvie Bourthoumieu, Odile Rigal, Cécile Acquaviva, Anne‐Laure Bédat‐Millet, B. Chabrol, Odile Boespflug‐Tanguy, Christine Vianey‐Saban, I. Pénisson-Besnier and I. Delèvaux and has published in prestigious journals such as Archives of Disease in Childhood, Neuromuscular Disorders and American Journal of Medical Genetics Part A.

In The Last Decade

Cécile Laroche

3 papers receiving 124 citations

Peers

Countries citing papers authored by Cécile Laroche

Since Specialization

Citations

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

Fields of papers citing papers by Cécile Laroche

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cécile Laroche

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

All Works

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3 of 3 papers shown

#	Work	Indexed citations
1	Towards a new point of view on the phenotype of patients with a 17q12 microdeletion syndrome 2014 ·Archives of Disease in Childhood ·Fanny Laffargue, Sylvie Bourthoumieu, Brigitte Llanas, Véronique Baudouin, Annie Lahoche, Denis Morin, Lucie Bessenay, L de Parscau, Sylvie Cloarec, Marie‐Ange Delrue, (unknown), (unknown), Cécile Laroche, Claire Bahans, Catherine Yardin, Didier Lacombe, Vincent Guigonis	39
2	Diagnostic assessment and long-term follow-up of 13 patients with Very Long-Chain Acyl-Coenzyme A dehydrogenase (VLCAD) deficiency 2009 ·Neuromuscular Disorders ·Pascal Laforêt, Cécile Acquaviva, Odile Rigal, M. Brivet, I. Pénisson-Besnier, B. Chabrol, Denys Chaigne, Odile Boespflug‐Tanguy, Cécile Laroche, Anne‐Laure Bédat‐Millet, Anthony Béhin, I. Delèvaux, Anne Lombès, Brage Storstein Andresen, B. Eymard, Christine Vianey‐Saban	66
3	Monozygotic twins concordant for blood karyotype, but phenotypically discordant: A case of “mosaic chimerism” 2005 ·American Journal of Medical Genetics Part A ·Sylvie Bourthoumieu, Catherine Yardin, Faraj Terro, Brigitte Gilbert, Cécile Laroche, Robert Saura, Marie‐Claire Vincent, Françoise Esclaire	21

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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