Gabriele Senger

3.0k total citations
56 papers, 2.3k citations indexed

About

Gabriele Senger is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Gabriele Senger has authored 56 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Genetics, 29 papers in Molecular Biology and 17 papers in Plant Science. Recurrent topics in Gabriele Senger's work include Genomic variations and chromosomal abnormalities (26 papers), Chromosomal and Genetic Variations (17 papers) and Prenatal Screening and Diagnostics (8 papers). Gabriele Senger is often cited by papers focused on Genomic variations and chromosomal abnormalities (26 papers), Chromosomal and Genetic Variations (17 papers) and Prenatal Screening and Diagnostics (8 papers). Gabriele Senger collaborates with scholars based in Germany, United Kingdom and France. Gabriele Senger's co-authors include Uwe Claussen, Bernhard Horsthemke, Denise Sheer, Richard A. Kroczek, Hans Werner Mages, John Trowsdale, Hermann‐Josef Lüdecke, Ulf Korthäuer, U. Claussen and Daniel Graf and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Current Biology.

In The Last Decade

Gabriele Senger

54 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gabriele Senger Germany 26 1.3k 1.1k 596 526 291 56 2.3k
J. E. Landegent Netherlands 16 1.4k 1.1× 1.0k 0.9× 793 1.3× 200 0.4× 276 0.9× 22 2.4k
Niall Dillon United Kingdom 34 4.4k 3.5× 996 0.9× 706 1.2× 523 1.0× 180 0.6× 64 5.1k
J Couturier France 29 1.6k 1.2× 1.1k 1.0× 645 1.1× 313 0.6× 235 0.8× 110 3.3k
Cameron S. Osborne United Kingdom 23 3.1k 2.4× 625 0.6× 593 1.0× 338 0.6× 95 0.3× 40 3.6k
Cordelia Langford United Kingdom 20 1.7k 1.3× 591 0.5× 196 0.3× 372 0.7× 88 0.3× 26 2.5k
Pino J. Poddighe Netherlands 25 1.0k 0.8× 623 0.6× 184 0.3× 185 0.4× 176 0.6× 58 2.1k
Anne Gégonne United States 26 2.3k 1.8× 604 0.5× 183 0.3× 714 1.4× 82 0.3× 44 3.2k
Robert‐Jan Palstra Netherlands 24 3.4k 2.7× 630 0.6× 645 1.1× 340 0.6× 129 0.4× 33 4.0k
Ian R. Adams United Kingdom 29 3.2k 2.5× 809 0.7× 517 0.9× 279 0.5× 151 0.5× 55 3.7k
Shelagh Boyle United Kingdom 30 5.1k 4.0× 933 0.8× 1.2k 1.9× 269 0.5× 97 0.3× 53 5.7k

Countries citing papers authored by Gabriele Senger

Since Specialization
Citations

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

Fields of papers citing papers by Gabriele Senger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gabriele Senger

This figure shows the co-authorship network connecting the top 25 collaborators of Gabriele Senger. A scholar is included among the top collaborators of Gabriele Senger 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 Gabriele Senger. Gabriele Senger 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.
Liehr, Thomas, Heike Starke, Gabriele Senger, et al.. (2005). Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC. American Journal of Medical Genetics Part A. 140A(1). 46–51. 23 indexed citations
2.
Chudoba, Ilse, et al.. (2004). mBAND: a high resolution multicolor banding technique for the detection of complex intrachromosomal aberrations. Cytogenetic and Genome Research. 104(1-4). 390–393. 35 indexed citations
3.
4.
Lemke, Johannes R., Ilse Chudoba, Gabriele Senger, et al.. (2001). Improved definition of chromosomal breakpoints using high-resolution multicolour banding. Human Genetics. 108(6). 478–483. 17 indexed citations
5.
Starke, Heike, Gabriele Senger, Н. Б. Рубцов, et al.. (2001). Maternal insertion of 18q11.2–q12.2 in 18p11.3 of the same chromosome analysed by microdissection and multicolour banding (MCB). Prenatal Diagnosis. 21(12). 1049–1052. 16 indexed citations
6.
Chudoba, Ilse, Andreas Plesch, T. Lörch, et al.. (1999). High resolution multicolor-banding: a new technique for refined FISH analysis of human chromosomes. Cytogenetic and Genome Research. 84(3-4). 156–160. 169 indexed citations
7.
Humphray, Sean, Angela Davies, Jethro Herberg, et al.. (1998). Physical Map of Human 6p21.2–6p21.3: Region Flanking the Centromeric End of the Major Histocompatibility Complex. Genome Research. 8(6). 631–643. 30 indexed citations
8.
Buiting, Karin, Stefan Größ, Y. Ji, et al.. (1998). Expressed copies of the MN7 (D15F37) gene family map close to the common deletion breakpoints in the Prader-Willi/Angelman syndromes. Cytogenetic and Genome Research. 81(3-4). 247–253. 21 indexed citations
9.
Рубцов, Н. Б., et al.. (1996). Interstitial deletion of chromosome 6q: Precise definition of the breakpoints by microdissection, DNA amplification, and reverse painting. Human Genetics. 97(6). 705–709. 48 indexed citations
10.
Olavesen, Mark G., Angela Davies, Jo Wixon, et al.. (1995). An integrated map of human chromosome 6p23.. Genome Research. 5(4). 342–358. 14 indexed citations
11.
Senger, Gabriele, et al.. (1994). Released chromatin: linearized DNA for high resolution fluorescence in situ hybridization. Human Molecular Genetics. 3(8). 1275–1280. 41 indexed citations
12.
Sanséau, Philippe, Amanda Jackson, Gabriele Senger, et al.. (1994). Cloning of the region between HLA-DMB and LMP2 in the human major histocompatibility complex. Human Immunology. 40(1). 1–7. 6 indexed citations
13.
Bardenheuer, Walter, Andreas Lux, H.-J. Lüdecke, et al.. (1994). Characterization of a Microdissection Library from Human Chromosome Region 3p14. Genomics. 19(2). 291–297. 13 indexed citations
14.
Ragoussis, Jiannis, Gabriele Senger, Ian Mockridge, et al.. (1992). A testis-expressed Zn finger gene (ZNF76) in human 6p21.3 centromeric to the MHC is closely linked to the human homolog of the t-complex gene tcp-11. Genomics. 14(3). 673–679. 43 indexed citations
15.
Graf, Daniel, Ulf Korthäuer, Hans Werner Mages, Gabriele Senger, & Richard A. Kroczek. (1992). Cloning of TRAP, a ligand for CD40 on human T cells. European Journal of Immunology. 22(12). 3191–3194. 232 indexed citations
16.
Puech, Anne, H.‐J. Lüdecke, Gabriele Senger, et al.. (1992). 11p15.5-Specific libraries for identification of potential gene sequences involved in Beckwith-Wiedemann syndrome and tumorigenesis. Genomics. 13(4). 1274–1280. 7 indexed citations
17.
Davis, Lisa M., Bernhard Zabel, Gabriele Senger, et al.. (1991). A tumor chromosome rearrangement further defines the 11p13 Wilms tumor locus. Genomics. 10(3). 588–592. 17 indexed citations
18.
19.
Senger, Gabriele, et al.. (1990). Microdissection of banded human chromosomes. Human Genetics. 84(6). 507–11. 81 indexed citations
20.
Lüdecke, Hermann‐Josef, Gabriele Senger, Uwe Claussen, & Bernhard Horsthemke. (1989). Cloning defined regions of the human genome by microdissection of banded chromosomes and enzymatic amplification. Nature. 338(6213). 348–350. 261 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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