Volkmar Beensen

692 total citations
17 papers, 430 citations indexed

About

Volkmar Beensen is a scholar working on Genetics, Plant Science and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Volkmar Beensen has authored 17 papers receiving a total of 430 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 7 papers in Plant Science and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Volkmar Beensen's work include Genomic variations and chromosomal abnormalities (12 papers), Chromosomal and Genetic Variations (7 papers) and Prenatal Screening and Diagnostics (5 papers). Volkmar Beensen is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Chromosomal and Genetic Variations (7 papers) and Prenatal Screening and Diagnostics (5 papers). Volkmar Beensen collaborates with scholars based in Germany, Poland and United States. Volkmar Beensen's co-authors include Thomas Liehr, Uwe Claussen, U. Claussen, Heike Starke, Angela Nietzel, Anita Heller, Gabriele Senger, Wolfgang Fiedler, Ivan Lončarević and Mariano Rocchi and has published in prestigious journals such as Journal of Histochemistry & Cytochemistry, Arthritis Research & Therapy and Human Genetics.

In The Last Decade

Volkmar Beensen

17 papers receiving 409 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Volkmar Beensen Germany 10 275 165 159 135 93 17 430
H.‐J. Lüdecke Germany 8 166 0.6× 29 0.2× 180 1.1× 26 0.2× 42 0.5× 12 279
Anna Sowińska‐Seidler Poland 13 237 0.9× 23 0.1× 254 1.6× 74 0.5× 34 0.4× 38 409
Vida Petrovic Australia 10 301 1.1× 256 1.6× 390 2.5× 64 0.5× 22 0.2× 19 600
Joyce Andrade Brazil 7 126 0.5× 53 0.3× 195 1.2× 32 0.2× 36 0.4× 14 331
Renqian Du China 11 167 0.6× 42 0.3× 209 1.3× 19 0.1× 23 0.2× 13 304
Raymond Lewandowski United States 14 272 1.0× 88 0.5× 140 0.9× 119 0.9× 13 0.1× 16 380
Koh‐ichiro Yoshiura Japan 14 170 0.6× 32 0.2× 181 1.1× 185 1.4× 37 0.4× 35 549
Grange S. Coffin United States 8 294 1.1× 66 0.4× 274 1.7× 82 0.6× 19 0.2× 12 467
Marina Manvelyan Germany 13 228 0.8× 131 0.8× 190 1.2× 93 0.7× 23 0.2× 22 402
G Venti Italy 11 118 0.4× 23 0.1× 131 0.8× 35 0.3× 19 0.2× 25 253

Countries citing papers authored by Volkmar Beensen

Since Specialization
Citations

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

Fields of papers citing papers by Volkmar Beensen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Volkmar Beensen

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

All Works

17 of 17 papers shown
1.
Hyckel, Peter, Alexander Berndt, Peter Schleier, et al.. (2005). Cherubism – new hypotheses on pathogenesis and therapeutic consequences. Journal of Cranio-Maxillofacial Surgery. 33(1). 61–68. 70 indexed citations
2.
Schreyer, Isolde, Volkmar Beensen, Karl‐Heinz Eichhorn, et al.. (2005). Dup(13)(q14.2-q14.3): Yet Another New Differential Diagnostic Aspect for Short Stature–like Phenotype. Journal of Histochemistry & Cytochemistry. 53(3). 365–366. 1 indexed citations
3.
Kinne, Raimund W., Elke Kunisch, Volkmar Beensen, et al.. (2003). Synovial fibroblasts and synovial macrophages from patients with rheumatoid arthritis and other inflammatory joint diseases show chromosomal aberrations. Genes Chromosomes and Cancer. 38(1). 53–67. 17 indexed citations
4.
5.
Liehr, Thomas, Heike Starke, Anja Weise, et al.. (2003). Evidence for a new microdeletion syndrome in 15q21. International Journal of Molecular Medicine. 11(5). 575–7. 15 indexed citations
6.
Starke, Heike, Beate Mitulla, Angela Nietzel, et al.. (2002). First patient with trisomy 21 accompanied by an additional der(4)(:p11 → q11:) plus partial uniparental disomy 4p15‐16. American Journal of Medical Genetics Part A. 116A(1). 26–30. 12 indexed citations
7.
Kinne, Raimund W., Thomas Liehr, Volkmar Beensen, et al.. (2001). Mosaic chromosomal aberrations in synovial fibroblasts of patients with rheumatoid arthritis, osteoarthritis, and other inflammatory joint diseases. Arthritis Research & Therapy. 3(5). 319–30. 37 indexed citations
8.
Nietzel, Angela, Mariano Rocchi, Heike Starke, et al.. (2001). A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH). Human Genetics. 108(3). 199–204. 115 indexed citations
9.
Seidel, J., Simone Schiller, Christina Kelbova, et al.. (2001). Brachytelephalangic dwarfism due to the loss of ARSE and SHOX genes resulting from an X;Y translocation. Clinical Genetics. 59(2). 115–121. 23 indexed citations
10.
Seidel, James S., E Kauf, Dirk Schramm, et al.. (2000). Insulin-like Growth Factor Serum Concentrations Reflect Insufficient Growth in a Hypoplastic Infant with Partial Trisomy 9q in the 12th Week of Life. Journal of Pediatric Endocrinology and Metabolism. 13(4). 445–50. 1 indexed citations
11.
Dufke, Andreas, M. Schöning, Christina Kelbova, et al.. (2000). Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn syndrome. Cytogenetic and Genome Research. 91(1-4). 81–84. 7 indexed citations
12.
Starke, Heike, Isolde Schreyer, Wolfgang Fiedler, et al.. (1999). Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8. Prenatal Diagnosis. 19(12). 1169–1174. 2 indexed citations
13.
Chudoba, Ilse, Gabriele Senger, Stanislas Demuth, et al.. (1999). Maternal UPD 20 in a hyperactive child with severe growth retardation. European Journal of Human Genetics. 7(5). 533–540. 54 indexed citations
14.
Starke, Heike, Isolde Schreyer, Wolfgang Fiedler, et al.. (1999). Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8. Prenatal Diagnosis. 19(12). 1169–1174. 17 indexed citations
15.
Liehr, Thomas, et al.. (1999). Translocation trisomy dup(21q) and free trisomy 21 can be distinguished by interphase-FISH.. International Journal of Molecular Medicine. 3(1). 11–4. 4 indexed citations
16.
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
17.
Рубцов, Н. Б., Gabriele Senger, Christina Kelbova, 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. 4 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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