Tommy Gerdes

1.8k total citations
31 papers, 1.4k citations indexed

About

Tommy Gerdes is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Tommy Gerdes has authored 31 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 17 papers in Molecular Biology and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Tommy Gerdes's work include Genomic variations and chromosomal abnormalities (20 papers), Prenatal Screening and Diagnostics (11 papers) and Chromosomal and Genetic Variations (11 papers). Tommy Gerdes is often cited by papers focused on Genomic variations and chromosomal abnormalities (20 papers), Prenatal Screening and Diagnostics (11 papers) and Chromosomal and Genetic Variations (11 papers). Tommy Gerdes collaborates with scholars based in Denmark, United States and Germany. Tommy Gerdes's co-authors include Maria Kirchhoff, Claes Lundsteen, Jan Maahr, Hanne Rose, Thue Bryndorf, Anne Marie Ottesen, Nils Arrigo, Nadir Álvarez, Dorothée Ehrich and Anne‐Marie Lind and has published in prestigious journals such as Experimental Cell Research, BMC Bioinformatics and Pattern Recognition.

In The Last Decade

Tommy Gerdes

31 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tommy Gerdes Denmark 20 859 620 358 283 201 31 1.4k
James T. Mascarello United States 20 866 1.0× 825 1.3× 253 0.7× 217 0.8× 120 0.6× 51 1.6k
Sabina Solinas‐Toldo Germany 12 963 1.1× 786 1.3× 373 1.0× 128 0.5× 369 1.8× 24 1.6k
Gabriele Senger Germany 26 1.1k 1.3× 1.3k 2.0× 596 1.7× 291 1.0× 189 0.9× 56 2.3k
Doris H. Wurster‐Hill United States 27 1.1k 1.3× 1.2k 2.0× 807 2.3× 212 0.7× 162 0.8× 72 2.7k
Nick Sampas United States 7 977 1.1× 856 1.4× 424 1.2× 183 0.6× 170 0.8× 7 1.5k
Felix Kokocinski Germany 16 361 0.4× 1.2k 1.9× 151 0.4× 565 2.0× 384 1.9× 22 2.0k
A. J. Jeffreys United Kingdom 17 470 0.5× 697 1.1× 223 0.6× 95 0.3× 160 0.8× 25 1.2k
W. Krone Germany 24 467 0.5× 856 1.4× 373 1.0× 67 0.2× 77 0.4× 72 1.7k
Brian A. Gray United States 20 567 0.7× 517 0.8× 92 0.3× 164 0.6× 102 0.5× 38 1.1k
Ryuichi Ono Japan 17 1.1k 1.2× 1.6k 2.5× 363 1.0× 625 2.2× 155 0.8× 31 2.0k

Countries citing papers authored by Tommy Gerdes

Since Specialization
Citations

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

Fields of papers citing papers by Tommy Gerdes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tommy Gerdes

This figure shows the co-authorship network connecting the top 25 collaborators of Tommy Gerdes. A scholar is included among the top collaborators of Tommy Gerdes 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 Tommy Gerdes. Tommy Gerdes 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.
Stockhausen, Marie‐Thérése, Helle Broholm, Mette Villingshøj, et al.. (2011). Maintenance of EGFR and EGFRvIII expressions in an in vivo and in vitro model of human glioblastoma multiforme. Experimental Cell Research. 317(11). 1513–1526. 43 indexed citations
2.
Kjærgaard, Søren K., Karin Sundberg, Finn Stener Jørgensen, et al.. (2010). Diagnostic yield by supplementing prenatal metaphase karyotyping with MLPA for microdeletion syndromes and subtelomere imbalances. Prenatal Diagnosis. 30(10). 995–999. 20 indexed citations
3.
Ottesen, Anne Marie, Lise Aksglæde, Nicole Tartaglia, et al.. (2010). Increased number of sex chromosomes affects height in a nonlinear fashion: A study of 305 patients with sex chromosome aneuploidy. American Journal of Medical Genetics Part A. 152A(5). 1206–1212. 141 indexed citations
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Huang, Chien‐Hao, et al.. (2007). Copy number analysis of survival motor neuron genes by multiplex ligation-dependent probe amplification. Genetics in Medicine. 9(4). 241–248. 51 indexed citations
7.
Kirchhoff, Maria, Anne‐Marie Bisgaard, Thue Bryndorf, & Tommy Gerdes. (2006). MLPA analysis for a panel of syndromes with mental retardation reveals imbalances in 5.8% of patients with mental retardation and dysmorphic features, including duplications of the Sotos syndrome and Williams–Beuren syndrome regions. European Journal of Medical Genetics. 50(1). 33–42. 79 indexed citations
8.
Gerdes, Tommy, Maria Kirchhoff, & Thue Bryndorf. (2005). Automatic analysis of multiplex ligation‐dependent probe amplification products (exemplified by a commercial kit for prenatal aneuploidy detection). Electrophoresis. 26(22). 4327–4332. 19 indexed citations
9.
Ottesen, Anne Marie, Jacob Larsen, Tommy Gerdes, et al.. (2004). Cytogenetic investigation of testicular carcinoma in situ and early seminoma by high-resolution comparative genomic hybridization analysis of subpopulations flow sorted according to DNA content. Cancer Genetics and Cytogenetics. 149(2). 89–97. 10 indexed citations
10.
Gerdes, Tommy, et al.. (2004). Computer-assisted prenatal aneuploidy screening for chromosome 13, 18, 21, X and Y based on multiplex ligation-dependent probe amplification (MLPA). European Journal of Human Genetics. 13(2). 171–175. 44 indexed citations
11.
Kirchhoff, Maria, Hanne Rose, Bodil Laub Petersen, et al.. (2001). Comparative genomic hybridization reveals non-random chromosomal aberrations in early preinvasive cervical lesions. Cancer Genetics and Cytogenetics. 129(1). 47–51. 37 indexed citations
12.
Kirchhoff, Maria, Hanne Rose, Jan Maahr, et al.. (2000). High resolution comparative genomic hybridisation analysis reveals imbalances in dyschromosomal patients with normal or apparently balanced conventional karyotypes. European Journal of Human Genetics. 8(9). 661–668. 38 indexed citations
13.
Larsen, Jacob, Maria Kirchhoff, Hanne Rose, et al.. (1999). Improved Sensitivity in Comparative Genomic Hybridization Analysis of DNA Heteroploid Cell Mixtures after Pre‐Enrichment of Subpopulations by Fluorescence Activated Cell Sorting. Analytical Cellular Pathology. 19(3-4). 119–124. 5 indexed citations
14.
Kirchhoff, Maria, Tommy Gerdes, Jan Maahr, et al.. (1999). Deletions below 10 megabasepairs are detected in comparative genomic hybridization by standard reference intervals. Genes Chromosomes and Cancer. 25(4). 410–413. 107 indexed citations
15.
Lundsteen, Claes, Jan Maahr, Britta Christensen, et al.. (1995). Image analysis in comparative genomic hybridization. Cytometry. 19(1). 42–50. 49 indexed citations
16.
Manoir, Stanislas du, Olli Kallioniemi, Jim Piper, et al.. (1995). Hardware and software requirements for quantitative analysis of comparative genomic hybridization. Cytometry. 19(1). 4–9. 62 indexed citations
17.
Lundsteen, Claes, Jan Maahr, & Tommy Gerdes. (1994). Metaphase quality can be monitored by automatic counting of bands. Clinical Genetics. 45(2). 62–66. 1 indexed citations
18.
Lundsteen, Claes, Tommy Gerdes, Jan Maahr, & J. Philip. (1987). Clinical performance of a system for semiautomated chromosome analysis.. Europe PMC (PubMed Central). 41(3). 493–502. 16 indexed citations
19.
Lundsteen, Claes, et al.. (1982). A model for selection of attributes for automatic pattern recognition. Stepwise data compression monitored by visual classification. Pattern Recognition. 15(3). 243–251. 1 indexed citations
20.
Lundsteen, Claes, et al.. (1981). Automatic chromosome analysis. Clinical Genetics. 19(1). 26–36. 17 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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