Martine Devillers

4.5k total citations
11 papers, 926 citations indexed

About

Martine Devillers is a scholar working on Surgery, Molecular Biology and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Martine Devillers has authored 11 papers receiving a total of 926 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Surgery, 3 papers in Molecular Biology and 3 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Martine Devillers's work include Lipoproteins and Cardiovascular Health (7 papers), Cholesterol and Lipid Metabolism (3 papers) and Cancer, Lipids, and Metabolism (3 papers). Martine Devillers is often cited by papers focused on Lipoproteins and Cardiovascular Health (7 papers), Cholesterol and Lipid Metabolism (3 papers) and Cancer, Lipids, and Metabolism (3 papers). Martine Devillers collaborates with scholars based in France, Lebanon and United States. Martine Devillers's co-authors include Claudine Junien, Cathérine Boileau, Jean‐Pierre Rabès, Mathilde Varret, Marianne Abifadel, Arnold Münnich, D. Erlich, Françis Brunelle, Claire Nihoul‐Feketé and Jean‐Marie Saudubray and has published in prestigious journals such as Journal of Clinical Investigation, Arteriosclerosis Thrombosis and Vascular Biology and American Journal Of Pathology.

In The Last Decade

Martine Devillers

11 papers receiving 904 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Martine Devillers France	11	649	369	214	169	100	11	926
Suguru Shirotake Japan	20	479 0.7×	81 0.2×	209 1.0×	146 0.9×	17 0.2×	89	1.1k
Tsukasa Teramoto Japan	14	436 0.7×	117 0.3×	150 0.7×	88 0.5×	47 0.5×	70	757
Rossitza P. Naoumova United Kingdom	15	503 0.8×	249 0.7×	197 0.9×	199 1.2×	56 0.6×	19	734
Attila Pethö‐Schramm Switzerland	12	249 0.4×	72 0.2×	192 0.9×	115 0.7×	53 0.5×	34	658
Jorge Peter Netherlands	13	344 0.5×	255 0.7×	157 0.7×	135 0.8×	97 1.0×	25	726
S Bertolini Italy	18	549 0.8×	340 0.9×	252 1.2×	160 0.9×	100 1.0×	53	988
Irmgard Andresen Germany	15	189 0.3×	161 0.4×	169 0.8×	60 0.4×	42 0.4×	41	852
Magdalena Chmara Poland	12	179 0.3×	43 0.1×	294 1.4×	73 0.4×	73 0.7×	32	679
Francesca Schiavi Italy	18	1.1k 1.8×	1.0k 2.7×	415 1.9×	882 5.2×	69 0.7×	63	1.8k
Karoliina Tuppurainen Finland	10	372 0.6×	563 1.5×	285 1.3×	229 1.4×	64 0.6×	10	1.3k

Countries citing papers authored by Martine Devillers

Since Specialization

Citations

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

Fields of papers citing papers by Martine Devillers

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martine Devillers

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

All Works

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11 of 11 papers shown

Carrié, Alain, Agnès Sassolas, Martine Devillers, et al.. (2010). Molecular Spectrum of Autosomal Dominant Hypercholesterolemia in France. Human Mutation. 31(11). E1811–E1824. 84 indexed citations

Rabès, Jean‐Pierre, Martine Devillers, Delphine Allard, et al.. (2010). A fourth locus for autosomal dominant hypercholesterolemia maps at 16q22.1. European Journal of Human Genetics. 18(11). 1236–1242. 30 indexed citations

Debret, Romain, Valérie Cenizo, Valérie André, et al.. (2010). Epigenetic Silencing of Lysyl Oxidase-Like-1 through DNA Hypermethylation in an Autosomal Recessive Cutis Laxa Case. Journal of Investigative Dermatology. 130(11). 2594–2601. 17 indexed citations

Abifadel, Marianne, Jean‐Pierre Rabès, Martine Devillers, et al.. (2009). Mutations and polymorphisms in the proprotein convertase subtilisin kexin 9 (PCSK9) gene in cholesterol metabolism and disease. Human Mutation. 30(4). 520–529. 198 indexed citations

Abifadel, Marianne, L. Bernier, Geneviève Dubuc, et al.. (2008). A PCSK9 variant and familial combined hyperlipidaemia. Journal of Medical Genetics. 45(12). 780–786. 38 indexed citations

Fischer, Judith, Hala Mégarbané, André Mégarbané, et al.. (2008). A p.C217R Mutation in Fibulin-5 from Cutis Laxa Patients Is Associated with Incomplete Extracellular Matrix Formation in a Skin Equivalent Model. Journal of Investigative Dermatology. 128(6). 1442–1450. 39 indexed citations

Allard, Delphine, Sabine Amsellem, Marianne Abifadel, et al.. (2005). Novel mutations of thePCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia. Human Mutation. 26(5). 497–497. 164 indexed citations

Fournet, Jean‐Christophe, Pascale de Lonlay, Virginie Verkarre, et al.. (2001). Unbalanced Expression of 11p15 Imprinted Genes in Focal Forms of Congenital Hyperinsulinism. American Journal Of Pathology. 158(6). 2177–2184. 91 indexed citations

Saint-Jore, Bruno, Mathilde Varret, Christiane Dachet, et al.. (2000). Autosomal dominant type IIa hypercholesterolemia: evaluation of the respective contributions of LDLR and APOB gene defects as well as a third major group of defects. European Journal of Human Genetics. 8(8). 621–630. 10 indexed citations

10.

Rabès, Jean‐Pierre, Mathilde Varret, Martine Devillers, et al.. (2000). R3531C Mutation in the Apolipoprotein B Gene Is Not Sufficient to Cause Hypercholesterolemia. Arteriosclerosis Thrombosis and Vascular Biology. 20(10). E76–82. 25 indexed citations

11.

Verkarre, Virginie, Jean‐Christophe Fournet, Pascale de Lonlay, et al.. (1998). Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia.. Journal of Clinical Investigation. 102(7). 1286–1291. 230 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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