Robert Carlier

947 total citations
28 papers, 464 citations indexed

About

Robert Carlier is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Surgery. According to data from OpenAlex, Robert Carlier has authored 28 papers receiving a total of 464 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 8 papers in Cardiology and Cardiovascular Medicine and 6 papers in Surgery. Recurrent topics in Robert Carlier's work include Muscle Physiology and Disorders (9 papers), Cardiomyopathy and Myosin Studies (7 papers) and Nuclear Structure and Function (5 papers). Robert Carlier is often cited by papers focused on Muscle Physiology and Disorders (9 papers), Cardiomyopathy and Myosin Studies (7 papers) and Nuclear Structure and Function (5 papers). Robert Carlier collaborates with scholars based in France, Italy and Spain. Robert Carlier's co-authors include Susana Quijano-Roy, Dirk Fischer, B. Estournet, D. Mompoint, David Orlikowski, Susana Quijano‐Roy, Pascale Richard, Abdallah Fayssoil, Djillali Annane and Hélène Prigent and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Radiology.

In The Last Decade

Robert Carlier

25 papers receiving 449 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert Carlier France 11 232 145 99 92 83 28 464
Macarena Cabrera‐Serrano Spain 11 207 0.9× 54 0.4× 58 0.6× 38 0.4× 21 0.3× 31 360
Volker Schick Germany 12 140 0.6× 34 0.2× 29 0.3× 115 1.3× 133 1.6× 44 580
Shay Ben‐Shachar Israel 12 148 0.6× 47 0.3× 108 1.1× 59 0.6× 58 0.7× 26 394
Joaquin Camara‐Quintana United States 12 64 0.3× 75 0.5× 22 0.2× 52 0.6× 200 2.4× 39 473
Jin Nishimiya Japan 6 204 0.9× 97 0.7× 110 1.1× 32 0.3× 25 0.3× 10 369
James Miller United Kingdom 13 239 1.0× 106 0.7× 74 0.7× 20 0.2× 42 0.5× 28 573
Franco Salerno Italy 14 123 0.5× 21 0.1× 73 0.7× 110 1.2× 114 1.4× 29 646
I Krivosic France 12 175 0.8× 36 0.2× 145 1.5× 48 0.5× 113 1.4× 43 407
George Kleinman United States 14 64 0.3× 61 0.4× 136 1.4× 294 3.2× 194 2.3× 35 608
Nahide Gökçora Türkiye 13 35 0.2× 59 0.4× 81 0.8× 83 0.9× 83 1.0× 41 467

Countries citing papers authored by Robert Carlier

Since Specialization
Citations

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

Fields of papers citing papers by Robert Carlier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Robert Carlier

This figure shows the co-authorship network connecting the top 25 collaborators of Robert Carlier. A scholar is included among the top collaborators of Robert Carlier 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 Robert Carlier. Robert Carlier 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.
Perrin, Aurélien, Tanya Stojkovic, Céline Tard, et al.. (2024). Congenital Titinopathies Linked to Mutations in TTN Metatranscript-Only Exons. International Journal of Molecular Sciences. 25(23). 12994–12994. 1 indexed citations
2.
Métay, Corinne, Michael Frank, Nicolas Denarié, et al.. (2023). A severe case of PLOD1‐related kyphoscoliotic Ehlers–Danlos syndrome associated with several arterial and venous complications: A case report. SHILAP Revista de lepidopterología. 11(2). e6760–e6760. 2 indexed citations
3.
Gouze, Hélène, et al.. (2023). Clinical image: atypical calcification of dorsal spine. Annals of the Rheumatic Diseases. 82(11). 1495–1495.
4.
Mazancourt, Philippe de, et al.. (2022). Classical Ehlers–Danlos syndrome with severe kyphoscoliosis due to a novel pathogenic variant of COL5A2. SHILAP Revista de lepidopterología. 10(11). e06338–e06338. 2 indexed citations
5.
Malfatti, Edoardo, Sonia Nouioua, Emmanuel Fournier, et al.. (2021). A TOR1AIP1 variant segregating with an early onset limb girdle myasthenia—Support for the role of LAP1 in NMJ function and disease. Neuropathology and Applied Neurobiology. 48(1). e12743–e12743. 6 indexed citations
6.
Mazancourt, Philippe de, Corinne Métay, Robert Carlier, et al.. (2021). A novel COL1A1 variant in a family with clinical features of hypermobile Ehlers‐Danlos syndrome that proved to be a COL1‐related overlap disorder. SHILAP Revista de lepidopterología. 9(9). e04128–e04128. 6 indexed citations
7.
Hauguel‐Moreau, Marie, et al.. (2021). Spontaneous Coronary Artery Rupture in Patients With Ehlers-Danlos Syndrome: Mini Review. Cardiovascular revascularization medicine. 40. 231–234. 1 indexed citations
8.
Fayssoil, Abdallah, Lee S. Nguyen, Tanya Stojkovic, et al.. (2021). Determinants of diaphragm inspiratory motion, diaphragm thickening, and its performance for predicting respiratory restrictive pattern in Duchenne muscular dystrophy. Muscle & Nerve. 65(1). 89–95. 6 indexed citations
9.
Hauguel‐Moreau, Marie, Mostafa El Hajjam, Antoine Vieillard‐Baron, et al.. (2020). Occurrence of pulmonary embolism related to COVID-19. Journal of Thrombosis and Thrombolysis. 52(1). 69–75. 10 indexed citations
10.
Hajjam, Mostafa El, Ahmed Mekki, Mélanie Eyries, et al.. (2020). RASA1 phenotype overlaps with hereditary haemorrhagic telangiectasia: two case reports. Journal of Medical Genetics. 58(9). 645–647. 7 indexed citations
11.
Lornage, Xavière, Norma B. Romero, Sandra Donkervoort, et al.. (2019). ACTN2 mutations cause “Multiple structured Core Disease” (MsCD). Acta Neuropathologica. 137(3). 501–519. 35 indexed citations
12.
Fayssoil, Abdallah, Lee S. Nguyen, Adam Ogna, et al.. (2019). Diaphragm sniff ultrasound: Normal values, relationship with sniff nasal pressure and accuracy for predicting respiratory involvement in patients with neuromuscular disorders. PLoS ONE. 14(4). e0214288–e0214288. 31 indexed citations
13.
Fayssoil, Abdallah, Anthony Béhin, Adam Ogna, et al.. (2017). Diaphragm: Pathophysiology and Ultrasound Imaging in Neuromuscular Disorders. Journal of Neuromuscular Diseases. 5(1). 1–10. 76 indexed citations
14.
Quijano‐Roy, Susana, Sonia Khirani, Marina Colella, et al.. (2013). Diaphragmatic dysfunction in Collagen VI myopathies. Neuromuscular Disorders. 24(2). 125–133. 29 indexed citations
15.
Béhin, Anthony, Pascal Laforêt, N. Pellegrini, et al.. (2013). P.15.10 Megaconial myopathy presenting as a progressive limb-girdle myopathy. Neuromuscular Disorders. 23(9-10). 821–821. 1 indexed citations
16.
Dieterich, Klaus, Susana Quijano-Roy, Nicole Monnier, et al.. (2012). The neuronal endopeptidase ECEL1 is associated with a distinct form of recessive distal arthrogryposis. Human Molecular Genetics. 22(8). 1483–1492. 51 indexed citations
17.
Quijano-Roy, Susana, Robert Carlier, & Dirk Fischer. (2011). Muscle Imaging in Congenital Myopathies. Seminars in Pediatric Neurology. 18(4). 221–229. 50 indexed citations
18.
Quijano‐Roy, Susana, Itxaso Martì, S. Makri, et al.. (2005). Brain MRI abnormalities in muscular dystrophy due to FKRP mutations. Brain and Development. 28(4). 232–242. 26 indexed citations
19.
Vallat‐Decouvelaere, Anne‐Valérie, Fabrice Chrétien, Geoffroy Lorin de la Grandmaison, et al.. (2003). [The neuropathology of HIV infection in the era of highly active antiretroviral therapy].. PubMed. 23(5). 408–23. 13 indexed citations
20.
Carlier, Robert, Jean-Marc Pinard, D. Mompoint, et al.. (1998). Congenital muscular dystrophy: use of brain MR imaging findings to predict merosin deficiency.. Radiology. 206(3). 811–816. 28 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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