Alain Carrié

6.3k total citations · 1 hit paper
69 papers, 2.8k citations indexed

About

Alain Carrié is a scholar working on Surgery, Molecular Biology and Genetics. According to data from OpenAlex, Alain Carrié has authored 69 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Surgery, 21 papers in Molecular Biology and 16 papers in Genetics. Recurrent topics in Alain Carrié's work include Lipoproteins and Cardiovascular Health (25 papers), Diabetes, Cardiovascular Risks, and Lipoproteins (10 papers) and Cholesterol and Lipid Metabolism (9 papers). Alain Carrié is often cited by papers focused on Lipoproteins and Cardiovascular Health (25 papers), Diabetes, Cardiovascular Risks, and Lipoproteins (10 papers) and Cholesterol and Lipid Metabolism (9 papers). Alain Carrié collaborates with scholars based in France, Lebanon and Italy. Alain Carrié's co-authors include Chérif Beldjord, Marie Claude Vinet, Pierre Billuart, Axel Kahn, Vincent des Portes, Philippe Couvert, Éric Bruckert, Jamel Chelly, Philippe Giral and Jacques Motté and has published in prestigious journals such as Nature, Cell and The Journal of Immunology.

In The Last Decade

Alain Carrié

64 papers receiving 2.7k citations

Hit Papers

A Novel CNS Gene Required for Neuronal Migration and Invo... 1998 2026 2007 2016 1998 100 200 300 400 500
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome
    1998 589 citations Vincent des Portes, Pierre Billuart et al. Cell profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alain Carrié France 26 1.2k 841 653 433 363 69 2.8k
Christopher R. Pierson United States 31 1.1k 0.9× 415 0.5× 440 0.7× 273 0.6× 328 0.9× 103 2.9k
Hiroshi Inoué Japan 29 1.0k 0.8× 652 0.8× 259 0.4× 419 1.0× 178 0.5× 188 3.2k
Ikuko Kondo Japan 33 1.7k 1.4× 561 0.7× 1.2k 1.8× 499 1.2× 119 0.3× 128 3.8k
Qing Lu United States 24 712 0.6× 259 0.3× 426 0.7× 117 0.3× 274 0.8× 47 1.9k
Jeffrey T. Wigle Canada 26 2.2k 1.8× 858 1.0× 218 0.3× 350 0.8× 385 1.1× 55 3.9k
Russell H. Knutsen United States 28 679 0.6× 266 0.3× 834 1.3× 117 0.3× 160 0.4× 49 2.2k
Donal MacGrogan United States 30 2.1k 1.7× 312 0.4× 417 0.6× 321 0.7× 206 0.6× 45 3.9k
Toyoshi Endo Japan 35 1.6k 1.3× 517 0.6× 612 0.9× 307 0.7× 201 0.6× 94 3.4k
Mads Kjølby Denmark 21 660 0.5× 354 0.4× 187 0.3× 236 0.5× 276 0.8× 46 1.8k
Xiaobing Yu United States 23 2.2k 1.8× 356 0.4× 402 0.6× 242 0.6× 124 0.3× 43 3.7k

Countries citing papers authored by Alain Carrié

Since Specialization
Citations

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

Fields of papers citing papers by Alain Carrié

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alain Carrié

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

All Works

20 of 20 papers shown
1.
Carrié, Alain, et al.. (2025). Millimeter-wave high frequency 5G (26 GHz) electromagnetic fields do not modulate human brain electrical activity. Environmental Research. 289. 123349–123349.
2.
3.
Carreau, Valérie, Maryse Guérin, Éric Frisdal, et al.. (2023). Transcriptomic profile helps to identify high-risk heterozygous familial hypercholesterolemia patients. Archives of cardiovascular diseases. 117(1). S107–S108. 1 indexed citations
4.
Bluteau, Olivier, Bertrand Cariou, Valérie Carreau, et al.. (2023). Additive Effect of APOE Rare Variants on the Phenotype of Familial Hypercholesterolemia. Arteriosclerosis Thrombosis and Vascular Biology. 43(7). e270–e278. 3 indexed citations
5.
Gallo, Antonio, Philippe Giral, David Rosenbaum, et al.. (2021). Myocardial fibrosis assessed by magnetic resonance imaging in asymptomatic heterozygous familial hypercholesterolemia: the cholcoeur study. EBioMedicine. 74. 103735–103735. 6 indexed citations
6.
Small, Lewin, Lars R. Ingerslev, Rhianna C. Laker, et al.. (2021). Ablation of DNA-methyltransferase 3A in skeletal muscle does not affect energy metabolism or exercise capacity. PLoS Genetics. 17(1). e1009325–e1009325. 11 indexed citations
7.
Dargent, Auguste, Jean-Paul Paı̈s de Barros, Samir Saheb, et al.. (2020). LDL apheresis as an alternate method for plasma LPS purification in healthy volunteers and dyslipidemic and septic patients. Journal of Lipid Research. 61(12). 1776–1783. 4 indexed citations
8.
Mattina, Alessandro, Antonina Giammanco, Philippe Giral, et al.. (2019). Polyvascular subclinical atherosclerosis in familial hypercholesterolemia: The role of cholesterol burden and gender. Nutrition Metabolism and Cardiovascular Diseases. 29(10). 1068–1076. 12 indexed citations
9.
Béliard, Sophie, Antonio Gallo, Emilie Duchêne, et al.. (2018). Lipoprotein-apheresis in familial hypercholesterolemia: Long-term patient compliance in a French cohort. Atherosclerosis. 277. 66–71. 9 indexed citations
10.
Gallo, Antonio, Philippe Giral, Alain Carrié, et al.. (2017). Early coronary calcifications are related to cholesterol burden in heterozygous familial hypercholesterolemia. Journal of clinical lipidology. 11(3). 704–711.e2. 30 indexed citations
11.
Melenotte, Cléa, Alain Carrié, Jacques Serratrice, & Pierre‐Jean Weiller. (2014). Sitosterolemia: A new mutation in a Mediterranean patient. Journal of clinical lipidology. 8(4). 451–454. 4 indexed citations
12.
Szalat, Raphaël, John Pirault, Jean‐Paul Fermand, et al.. (2014). Physiopathology of necrobiotic xanthogranuloma with monoclonal gammopathy. Journal of Internal Medicine. 276(3). 269–284. 25 indexed citations
13.
Duong, T.A., S. Oro, Nicolas de Prost, et al.. (2011). Syndrome de Stevens-Johnson/nécrolyse épidermique toxique : évaluation de la fonction respiratoire à distance. Annales de Dermatologie et de Vénéréologie. 138(12). A89–A90. 1 indexed citations
14.
Carrié, Alain, et al.. (2010). Protutor : a pronunciation tutor that uses historic open learner models. 30(4). 86–90. 1 indexed citations
15.
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
16.
Poirier, Karine, Céline Chalas, Frédérique Tissier, et al.. (2003). Loss of parental‐specific methylation at the IGF2 locus in human hepatocellular carcinoma. The Journal of Pathology. 201(3). 473–479. 27 indexed citations
17.
Girard, M, Philippe Couvert, Alain Carrié, et al.. (2001). Parental origin of de novo MECP2 mutations in Rett syndrome. European Journal of Human Genetics. 9(3). 231–236. 92 indexed citations
18.
19.
Portes, Vincent des, Pierre Billuart, Marie Claude Vinet, et al.. (1998). A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome. Cell. 92(1). 51–61. 589 indexed citations breakdown →
20.
Billuart, Pierre, T. Bienvenu, Nathalie Ronce, et al.. (1998). Oligophrenin 1 encodes a rho-GAP protein involved in X-linked mental retardation.. PubMed. 46(9). 678–678. 33 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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