M. Kœnig

24.4k total citations · 4 hit papers
301 papers, 12.4k citations indexed

About

M. Kœnig is a scholar working on Nuclear and High Energy Physics, Mechanics of Materials and Geophysics. According to data from OpenAlex, M. Kœnig has authored 301 papers receiving a total of 12.4k indexed citations (citations by other indexed papers that have themselves been cited), including 163 papers in Nuclear and High Energy Physics, 115 papers in Mechanics of Materials and 107 papers in Geophysics. Recurrent topics in M. Kœnig's work include Laser-Plasma Interactions and Diagnostics (159 papers), Laser-induced spectroscopy and plasma (112 papers) and High-pressure geophysics and materials (107 papers). M. Kœnig is often cited by papers focused on Laser-Plasma Interactions and Diagnostics (159 papers), Laser-induced spectroscopy and plasma (112 papers) and High-pressure geophysics and materials (107 papers). M. Kœnig collaborates with scholars based in France, United Kingdom and Italy. M. Kœnig's co-authors include Louis M. Kunkel, Anthony P. Monaco, Corlee J. Bertelson, Eric P. Hoffman, A. Benuzzi‐Mounaix, Alan H. Beggs, Jean‐Louis Mandel, D. Batani, Victoria Campuzano and Chris A. Feener and has published in prestigious journals such as Nature, Cell and Physical Review Letters.

In The Last Decade

M. Kœnig

294 papers receiving 12.1k citations

Hit Papers

align trajectories

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.

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

1987 1.9k citations M. Kœnig, Louis M. Kunkel et al. profile →
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

1988 1.3k citations M. Kœnig, Louis M. Kunkel et al. profile →
Frataxin is Reduced in Friedreich Ataxia Patients and is Associated with Mitochondrial Membranes

1997 602 citations Victoria Campuzano, Laura Montermini et al. Human Molecular Genetics profile →
Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction

1990 577 citations M. Kœnig et al. profile →

Peers

M. Kœnig

NHEP

CMN

GEOPH

R. Mark Henkelman Canada

Takeshi Matsuoka Japan

Ichiro Katayama Japan

Richard D. Leapman United States

Lawrence M. Schwartz United States

W. W. Webb United States

John P. Wikswo United States

Satoshi Ozaki Japan

Naoto Yagi Japan

Simon R. Cherry United States

R. Mark Henkelman Canada

M. Kœnig

7.9k ×1.1

1.8k ×0.6

NHEP

1.6k ×0.7

CMN

254 ×0.1

269 ×0.1

GEOPH

Citations per year, relative to M. Kœnig M. Kœnig (= 1×) peers R. Mark Henkelman

Countries citing papers authored by M. Kœnig

Since Specialization

Citations

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

Fields of papers citing papers by M. Kœnig

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Kœnig

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Marquès, J.-R., A. Ciardi, J. Béard, et al.. (2025). Dynamics and energy dissipation of collisional blast waves in a perpendicular magnetic field. Physics of Plasmas. 32(2). 1 indexed citations

Marquès, J.-R., A. Calisti, A. Ciardi, et al.. (2025). Zeeman splitting observations in laser-produced magnetized blast waves. Matter and Radiation at Extremes. 10(4). 1 indexed citations

Miro, Julie, Charles Van Goethem, Cécile Notarnicola, et al.. (2024). The exon junction complex is required for DMD gene splicing fidelity and myogenic differentiation. Cellular and Molecular Life Sciences. 81(1). 150–150. 2 indexed citations

Harmand, M., B. Albertazzi, A. Benuzzi‐Mounaix, et al.. (2024). Laser-driven shock compression and equation of state of Fe2O3 up to 700 GPa. Physical review. B.. 110(14). 1 indexed citations

Albertazzi, B., M. Kœnig, Pascal Meyer, et al.. (2024). Demonstrating grating-based phase-contrast imaging of laser-driven shock waves. Matter and Radiation at Extremes. 9(4). 2 indexed citations

Vincenti, Maria Aurora, Rosa Maria Montereali, F. Bonfigli, et al.. (2024). Advanced spectroscopic investigation of colour centres in LiF crystals irradiated with monochromatic hard x-rays. Journal of Physics Condensed Matter. 36(20). 205701–205701. 3 indexed citations

Vincenti, Maria Aurora, Rosa Maria Montereali, E. Nichelatti, et al.. (2023). Optical characterization of lithium fluoride thin-film imaging detectors for monochromatic hard X-rays. Journal of Instrumentation. 18(4). C04012–C04012. 2 indexed citations

Albertazzi, B., P. Mabey, Th. Michel, et al.. (2021). Exploring the Atwood-number dependence of the highly nonlinear Rayleigh-Taylor instability regime in high-energy-density conditions. Physical review. E. 104(4). 45213–45213. 9 indexed citations

Perrin, Aurélien, Corinne Métay, Marcello Villanova, et al.. (2020). A new congenital multicore titinopathy associated with fast myosin heavy chain deficiency. Annals of Clinical and Translational Neurology. 7(5). 846–854. 9 indexed citations

10.

Bergougnoux, Anne, et al.. (2020). miRNA repertoires of cystic fibrosis ex vivo models highlight miR‐181a and miR‐101 that regulate WISP1 expression. The Journal of Pathology. 253(2). 186–197. 8 indexed citations

11.

Perrin, Aurélien, Raúl Juntas‐Morales, François Rivier, et al.. (2020). The importance of an integrated genotype-phenotype strategy to unravel the molecular bases of titinopathies. Neuromuscular Disorders. 30(11). 877–887. 14 indexed citations

12.

Ramaekers, V., Karin Segers, J.M. Sequeira, et al.. (2018). Genetic assessment and folate receptor autoantibodies in infantile-onset cerebral folate deficiency (CFD) syndrome. Molecular Genetics and Metabolism. 124(1). 87–93. 18 indexed citations

13.

Guissart, Claire, Caroline Raynal, Anne Girardet, et al.. (2016). Non-invasive prenatal diagnosis (NIPD) of cystic fibrosis: an optimized protocol using MEMO fluorescent PCR to detect the p.Phe508del mutation. Journal of Cystic Fibrosis. 16(2). 198–206. 12 indexed citations

14.

Alame, Mélissa, et al.. (2016). Implementation of a Reliable Next-Generation Sequencing Strategy for Molecular Diagnosis of Dystrophinopathies. Journal of Molecular Diagnostics. 18(5). 731–740. 15 indexed citations

15.

Guissart, Claire, Bruno Leheup, Nathalie Drouot, et al.. (2014). Mutation of SLC9A1, encoding the major Na+/H+ exchanger, causes ataxia-deafness Lichtenstein-Knorr syndrome. Human Molecular Genetics. 24(2). 463–470. 37 indexed citations

16.

Salih, Mustafa A., Emeline Mundwiller, Arif O. Khan, et al.. (2013). New Findings in a Global Approach to Dissect the Whole Phenotype of PLA2G6 Gene Mutations. PLoS ONE. 8(10). e76831–e76831. 38 indexed citations

17.

Drake, R. P., K. Killebrew, Daniel Kremer, et al.. (2005). Collapsing Radiative Shocks in Xenon Gas on the Omega Laser. Bulletin of the American Physical Society. 45. 2 indexed citations

18.

Batani, D., Andrea Morelli, M Tomasini, et al.. (2002). Equation of State Data for Iron at Pressures beyond 10 Mbar. Physical Review Letters. 88(23). 235502–235502. 57 indexed citations

19.

Campuzano, Victoria, Laura Montermini, Yves Lutz, et al.. (1997). Frataxin is Reduced in Friedreich Ataxia Patients and is Associated with Mitochondrial Membranes. Human Molecular Genetics. 6(11). 1771–1780. 602 indexed citations breakdown →

20.

McCabe, Edward R.B., Jeffrey A. Towbin, Jeffrey S. Chamberlain, et al.. (1989). Complementary DNA probes for the Duchenne muscular dystrophy locus demonstrate a previously undetectable deletion in a patient with dystrophic myopathy, glycerol kinase deficiency, and congenital adrenal hypoplasia.. Journal of Clinical Investigation. 83(1). 95–99. 48 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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