J. Beckmann

78.9k total citations · 7 hit papers
289 papers, 21.3k citations indexed

About

J. Beckmann is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, J. Beckmann has authored 289 papers receiving a total of 21.3k indexed citations (citations by other indexed papers that have themselves been cited), including 203 papers in Molecular Biology, 88 papers in Genetics and 55 papers in Cell Biology. Recurrent topics in J. Beckmann's work include Muscle Physiology and Disorders (62 papers), Calpain Protease Function and Regulation (35 papers) and Genetic Mapping and Diversity in Plants and Animals (23 papers). J. Beckmann is often cited by papers focused on Muscle Physiology and Disorders (62 papers), Calpain Protease Function and Regulation (35 papers) and Genetic Mapping and Diversity in Plants and Animals (23 papers). J. Beckmann collaborates with scholars based in France, Switzerland and United States. J. Beckmann's co-authors include M. Soller, Françoise Fougerousse, J. L. Weber, Stylianos E. Antonarakis, Isabelle Richard, Matthias Soller, Michel Fardeau, Margaret M. Tarpey, Peter G. Anderson and Jianjun Chen and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

J. Beckmann

282 papers receiving 20.5k citations

Hit Papers

Targeted Disruption of the Mouse Caspase 8 Gene Ablates C... 1993 2026 2004 2015 1998 1994 1995 2005 1998 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J. Beckmann France 74 13.8k 5.3k 3.4k 2.7k 2.4k 289 21.3k
Anthony R. Means United States 96 23.7k 1.7× 3.8k 0.7× 4.7k 1.4× 3.6k 1.3× 2.1k 0.9× 379 33.9k
William B. Guggino United States 75 13.5k 1.0× 4.7k 0.9× 1.5k 0.4× 2.3k 0.9× 912 0.4× 248 22.4k
Shigeo Ohno Japan 100 22.3k 1.6× 4.0k 0.8× 8.0k 2.3× 2.6k 1.0× 910 0.4× 598 34.3k
Paul A. Krieg United States 46 12.3k 0.9× 2.9k 0.6× 1.7k 0.5× 2.2k 0.8× 1.1k 0.5× 115 16.9k
Frank Grosveld Netherlands 105 27.5k 2.0× 7.1k 1.3× 5.2k 1.5× 1.9k 0.7× 815 0.3× 391 38.5k
Anthony Wynshaw‐Boris United States 85 18.8k 1.4× 5.9k 1.1× 4.6k 1.3× 3.3k 1.2× 580 0.2× 204 27.9k
Eisuke Nishida Japan 104 26.9k 1.9× 2.9k 0.6× 9.9k 2.9× 2.7k 1.0× 1.2k 0.5× 332 37.5k
Uta Francke United States 99 24.1k 1.7× 14.5k 2.7× 4.0k 1.2× 3.8k 1.4× 1.5k 0.6× 503 41.9k
Stylianos E. Antonarakis Switzerland 102 21.9k 1.6× 13.3k 2.5× 1.9k 0.6× 1.8k 0.7× 951 0.4× 602 40.8k
Nobuyoshi Shimizu Japan 70 12.5k 0.9× 5.2k 1.0× 2.2k 0.6× 3.5k 1.3× 422 0.2× 541 27.6k

Countries citing papers authored by J. Beckmann

Since Specialization
Citations

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

Fields of papers citing papers by J. Beckmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. Beckmann

This figure shows the co-authorship network connecting the top 25 collaborators of J. Beckmann. A scholar is included among the top collaborators of J. Beckmann 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 J. Beckmann. J. Beckmann 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.
Beckmann, J.. (2017). From evidence-based to precision medicine: Challenges and opportunities. 1 indexed citations
2.
Bonafé, Luisa, Jinlong Liang, Maria W. Górna, et al.. (2014). MMP13 mutations are the cause of recessive metaphyseal dysplasia, Spahr type. American Journal of Medical Genetics Part A. 164(5). 1175–1179. 12 indexed citations
3.
Lupo, Vincenzo, Eduardo Calpena, Luca Bartesaghi, et al.. (2013). Sh3tc2 deficiency affects neuregulin‐1/ErbB signaling. Glia. 61(7). 1041–1051. 36 indexed citations
4.
Marek, Diana, Stéphanie Papin, Kim Ellefsen, et al.. (2012). Carriers of the fragile X mental retardation 1 (FMR1) premutation allele present with increased levels of cytokine IL-10. Journal of Neuroinflammation. 9(1). 238–238. 17 indexed citations
5.
Beckmann, J., et al.. (2010). [R74W;R1070W;D1270N]: A new complex allele responsible for cystic fibrosis. Journal of Cystic Fibrosis. 9(6). 447–449. 6 indexed citations
6.
Michaud, Katarzyna, Florence Fellmann, Hugues Abriel, et al.. (2009). Molecular autopsy in sudden cardiac death and its implication for families: discussion of the practical, legal and ethical aspects of the multidisciplinary collaboration. SERVAL (Université de Lausanne). 8 indexed citations
7.
Rivolta, Carlo, Terri L. McGee, Nicholas M. Wade, et al.. (2009). A Single-Base Substitution Within an Intronic Repetitive Element in PRPF31 Causes Dominant Retinitis Pigmentosa With Reduced Penetrance. Investigative Ophthalmology & Visual Science. 50(13). 2318–2318. 6 indexed citations
8.
Argov, Zohar, Dov Soffer, Esther Kahana, et al.. (2000). Muscular dystrophy due to dysferlin deficiency in Libyan Jews. Brain. 123(6). 1229–1237. 77 indexed citations
9.
Chami, Mounia, Devrim Gözüaçık, Kenichi Saigo, et al.. (2000). Hepatitis B virus-related insertional mutagenesis implicates SERCA1 gene in the control of apoptosis. Oncogene. 19(25). 2877–2886. 55 indexed citations
10.
Varfolomeev, Eugene, Marcus Schuchmann, Victor Luria, et al.. (1998). Targeted Disruption of the Mouse Caspase 8 Gene Ablates Cell Death Induction by the TNF Receptors, Fas/Apo1, and DR3 and Is Lethal Prenatally. Immunity. 9(2). 267–276. 999 indexed citations breakdown →
11.
Henskens, Yvonne, Wim van’t Hof, Enno C.I. Veerman, et al.. (1996). Short Communication. Biological Chemistry Hoppe-Seyler. 377(12). 847–864. 3 indexed citations
13.
Fougerousse, Françoise, Odile Broux, Isabelle Richard, et al.. (1994). Mapping of a chromosome 15 region involved in limb girdle muscular dystrophy. Human Molecular Genetics. 3(2). 285–293. 44 indexed citations
14.
Belal, Samir, Giorgio Sirugo, P.A. Ioannou, et al.. (1992). Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locus.. PubMed. 51(6). 1372–6. 11 indexed citations
15.
Gafni, Yedidya, et al.. (1990). RFLP analysis of a hybrid cultivar of pepper (Capsicum annuum) and its use in distinguishing between parental lines and in hybrid identification.. Seed Science and Technology. 18(2). 209–214. 11 indexed citations
16.
Hallerman, Eric M., et al.. (1988). Screening of Israeli Holstein-Friesian Cattle for Restriction Fragment Length Polymorphisms Using Homologous and Heterologous Deoxyribonucleic Acid Probes. Journal of Dairy Science. 71(12). 3378–3389. 10 indexed citations
17.
Soller, Matthias, et al.. (1987). Trait-based analyses for the detection of linkage between marker loci and quantitative trait loci in crosses between inbred lines. Theoretical and Applied Genetics. 73(4). 556–562. 157 indexed citations
18.
Kashi, Yechezkel, et al.. (1986). Restriction fragment length polymorphisms in dairy cattle genetic improvement.. Proceedings of the World Congress on Genetics applied to Livestock Production. 57–63. 8 indexed citations
19.
Beckmann, J. & Matthias Soller. (1983). Restriction fragment length polymorphisms in genetic improvement: methodologies, mapping and costs. Theoretical and Applied Genetics. 67(1). 35–43. 257 indexed citations
20.
Ogden, Richard C., Gayle Knapp, Craig L. Peebles, et al.. (1980). Enzymatic Removal of Intervening Sequences in the Synthesis of Yeast tRNAs. Cold Spring Harbor Monograph Archive. 173–190. 3 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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