M Hartung

798 total citations
36 papers, 640 citations indexed

About

M Hartung is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, M Hartung has authored 36 papers receiving a total of 640 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 14 papers in Genetics and 9 papers in Plant Science. Recurrent topics in M Hartung's work include Genomics and Chromatin Dynamics (10 papers), Chromosomal and Genetic Variations (9 papers) and Animal Genetics and Reproduction (6 papers). M Hartung is often cited by papers focused on Genomics and Chromatin Dynamics (10 papers), Chromosomal and Genetic Variations (9 papers) and Animal Genetics and Reproduction (6 papers). M Hartung collaborates with scholars based in France, Austria and United States. M Hartung's co-authors include A Stahl, M. Devictor, C. Mirre, H. G. Schwarzacher, F. Wachtler, Caroline Fouet, Marie-Roberte Guichaoua, J. M. Luciani, A. M. Vagner‐Capodano and J.-L. Bergé-Lefranc and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Cellular and Molecular Life Sciences and Experimental Cell Research.

In The Last Decade

M Hartung

34 papers receiving 592 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M Hartung France 16 465 260 245 70 68 36 640
J. M. J. C. Scheres Netherlands 14 215 0.5× 305 1.2× 147 0.6× 27 0.4× 122 1.8× 28 457
O. Gabriel-Robez France 16 252 0.5× 466 1.8× 332 1.4× 52 0.7× 133 2.0× 29 610
A.C. Chandley United Kingdom 8 217 0.5× 324 1.2× 199 0.8× 19 0.3× 43 0.6× 8 435
U. Tettenborn Germany 13 215 0.5× 354 1.4× 172 0.7× 16 0.2× 53 0.8× 20 520
A. P. Dyban Russia 11 245 0.5× 173 0.7× 80 0.3× 153 2.2× 104 1.5× 42 417
Áine Rattigan United Kingdom 10 274 0.6× 394 1.5× 91 0.4× 65 0.9× 30 0.4× 10 483
Walter Mills United Kingdom 12 418 0.9× 261 1.0× 180 0.7× 43 0.6× 87 1.3× 21 563
M. Codina‐Pascual Spain 11 175 0.4× 256 1.0× 178 0.7× 70 1.0× 164 2.4× 15 411
Kun Ma United Kingdom 8 543 1.2× 671 2.6× 176 0.7× 67 1.0× 54 0.8× 9 798
C. Ratomponirina France 9 133 0.3× 240 0.9× 200 0.8× 18 0.3× 53 0.8× 12 329

Countries citing papers authored by M Hartung

Since Specialization
Citations

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

Fields of papers citing papers by M Hartung

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M Hartung

This figure shows the co-authorship network connecting the top 25 collaborators of M Hartung. A scholar is included among the top collaborators of M Hartung 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 Hartung. M Hartung 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.
Wachtler, F., Christian Schöfer, W. Mosgöller, et al.. (1992). Human ribosomal RNA gene repeats are localized in the dense fibrillar component of nucleoli: Light and electron microscopic in situ hybridization in human Sertoli cells. Experimental Cell Research. 198(1). 135–143. 52 indexed citations
2.
Stahl, A, F. Wachtler, M Hartung, et al.. (1991). Nucleoli, nucleolar chromosomes and ribosomal genes in the human spermatocyte. Chromosoma. 101(4). 231–244. 46 indexed citations
3.
Wachtler, F., Christian Schöfer, Andreas Schedle, et al.. (1991). Transcribed and nontranscribed parts of the human ribosomal gene repeat show a similar pattern of distribution in nucleoli. Cytogenetic and Genome Research. 57(4). 175–178. 17 indexed citations
4.
Hartung, M, et al.. (1990). Sequential changes in the nucleoli of human spermatogonia with special reference to rDNA location and transcription. Tissue and Cell. 22(1). 25–37. 15 indexed citations
5.
Wachtler, F., M Hartung, M. Devictor, et al.. (1989). Ribosomal DNA is located and transcribed in the dense fibrillar component of human Sertoli cell nucleoli. Experimental Cell Research. 184(1). 61–71. 60 indexed citations
6.
Vagner‐Capodano, A. M., M Hartung, & A Stahl. (1987). Nucleolus, nucleolar chromosomes, and nucleolus-associated chromatin from early diplotene to dictyotene in the human oocyte. Human Genetics. 75(2). 140–146. 13 indexed citations
7.
Guichaoua, Marie-Roberte, M. Devictor, M Hartung, J. M. Luciani, & A Stahl. (1986). Random acrocentric bivalent associations in human pachytene spermatocytes. Cytogenetic and Genome Research. 42(4). 191–197. 27 indexed citations
8.
9.
Hartung, M, et al.. (1983). Nucleoli, micronucleoli, and nucleolus-like structures in human oocytes at meiotic prophase I studied by the silver-NOR technique. Cytogenetic and Genome Research. 35(1). 2–8. 20 indexed citations
10.
Mirre, C., M Hartung, & A Stahl. (1980). Association of ribosomal genes in the fibrillar center of the nucleolus: a factor influencing translocation and nondisjunction in the human meiotic oocyte.. Proceedings of the National Academy of Sciences. 77(10). 6017–6021. 56 indexed citations
11.
Hartung, M & A Stahl. (1978). Autoradiographic study of RNA synthesis during meiotic prophase in the human oocyte. Cytogenetic and Genome Research. 20(1-6). 51–58. 15 indexed citations
12.
Hartung, M, Caroline Fouet, & A Stahl. (1975). [Association of the juxtracentromeric heterochromatin of human chromosome 1 with the nucleolus].. PubMed. 18(4). 247–9. 2 indexed citations
13.
Stahl, A, et al.. (1975). Heterochromatin and nucleolar organizers during first meiotic prophase in quail oocytes. Experimental Cell Research. 91(2). 365–371. 8 indexed citations
14.
Giraud, F, et al.. (1975). [Partial deletion of the short arm of an X chromosome].. PubMed. 31(7). 717–24. 9 indexed citations
15.
Hartung, M, et al.. (1974). [Identification of the W chromosome in Japanese quail, Coturnix coturnix japonica].. PubMed. 278(17). 2157–60. 1 indexed citations
16.
Giraud, F, et al.. (1973). Chromosome Y long (Yq+) et anomalies du phénotype. Etude en fluorescence.. 28(2). 1 indexed citations
17.
Giraud, F, et al.. (1971). [46,XY-45,X mosaicism and 18p- deletion].. PubMed. 14(1). 59–62. 5 indexed citations
18.
Stahl, Andreas, et al.. (1967). [Multiple malformations in a newborn infant presenting a chromosomic triploidy].. PubMed. 22(6). 721–2. 1 indexed citations
19.
Bernard, Rafaëlle, et al.. (1967). [Chromosomal triploidy in a new-born infant with multiple malformations].. PubMed. 10(2). 70–4. 13 indexed citations
20.
Giraud, P, et al.. (1965). [CHROMOSOME MOSAICS. APROPOS OF 4 PERSONAL CASES].. PubMed. 20. 129–38. 1 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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