Dan Röhme

732 total citations
26 papers, 546 citations indexed

About

Dan Röhme is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Dan Röhme has authored 26 papers receiving a total of 546 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 10 papers in Genetics and 9 papers in Plant Science. Recurrent topics in Dan Röhme's work include Chromosomal and Genetic Variations (8 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genomics and Chromatin Dynamics (6 papers). Dan Röhme is often cited by papers focused on Chromosomal and Genetic Variations (8 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genomics and Chromatin Dynamics (6 papers). Dan Röhme collaborates with scholars based in Sweden, United States and United Kingdom. Dan Röhme's co-authors include Jan‐Erik Edström, Anna‐Maria Frischauf, Howard S. Fox, Bernhard G. Herrmann, Paul E. Mains, Lee M. Silver, Hans Lehrach, Mattias Höglund, Rolf Kaiser and Göran Levan and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Cell Science.

In The Last Decade

Dan Röhme

26 papers receiving 509 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dan Röhme Sweden 7 356 198 163 118 71 26 546
Héra Der‐Sarkissian France 11 400 1.1× 416 2.1× 120 0.7× 67 0.6× 126 1.8× 13 628
Andrew P. Salinger United States 8 512 1.4× 196 1.0× 100 0.6× 58 0.5× 67 0.9× 11 591
Mintie Pu United States 7 659 1.9× 51 0.3× 129 0.8× 61 0.5× 27 0.4× 10 750
M Härle Germany 6 333 0.9× 55 0.3× 83 0.5× 19 0.2× 166 2.3× 7 461
Nobuko Katoku-Kikyo United States 12 529 1.5× 73 0.4× 60 0.4× 29 0.2× 25 0.4× 14 621
Jan Fröhlich Czechia 13 196 0.6× 74 0.4× 116 0.7× 23 0.2× 104 1.5× 31 377
Abbhirami Rajagopal United States 8 217 0.6× 45 0.2× 74 0.5× 30 0.3× 25 0.4× 9 467
Robert N. Plasschaert United States 6 343 1.0× 91 0.5× 163 1.0× 14 0.1× 29 0.4× 7 449
Zhaohui Kou China 18 1.4k 4.1× 108 0.5× 249 1.5× 29 0.2× 41 0.6× 32 1.6k
Shruti Bhide United States 9 306 0.9× 77 0.4× 169 1.0× 13 0.1× 18 0.3× 14 498

Countries citing papers authored by Dan Röhme

Since Specialization
Citations

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

Fields of papers citing papers by Dan Röhme

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dan Röhme

This figure shows the co-authorship network connecting the top 25 collaborators of Dan Röhme. A scholar is included among the top collaborators of Dan Röhme 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 Dan Röhme. Dan Röhme 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.
Heneen, W. K., et al.. (2009). Studies on certified and suspected HeLa cells. Preliminary report. Hereditas. 81(1). 119–124. 3 indexed citations
2.
Röhme, Dan. (2009). Evidence suggesting chromosome continuity during the S phase of Indian muntjac cells. Hereditas. 80(1). 145–149. 1 indexed citations
3.
4.
Adamović, Tatjana, et al.. (2008). Rearrangement and allelic imbalance on chromosome 5 leads to homozygous deletions in the CDKN2A/2B tumor suppressor gene region in rat endometrial cancer. Cancer Genetics and Cytogenetics. 184(1). 9–21. 6 indexed citations
5.
Sjöling, Åsa, Anna Walentinsson, Åsa Karlsson, et al.. (2005). Assessment of allele dosage at polymorphic microsatellite loci displaying allelic imbalance in tumors by means of quantitative competitive-polymerase chain reaction. Cancer Genetics and Cytogenetics. 157(2). 97–103. 5 indexed citations
6.
Sjöling, Åsa, Emma Samuelson, Tatjana Adamović, et al.. (2002). Recurrent allelic imbalance at the rat Pten locus in DMBA‐induced fibrosarcomas. Genes Chromosomes and Cancer. 36(1). 70–79. 6 indexed citations
7.
Behboudi, Afrouz, et al.. (2002). Detailed chromosomal and radiation hybrid mapping in the proximal part of rat Chromosome 10 and gene order comparison with mouse and human. Mammalian Genome. 13(6). 302–309. 7 indexed citations
8.
Larsson, Maria E. H., et al.. (1998). Sublocalizing the centromeric region in linkage groups from three metacentric rat chromosomes by FISH. Mammalian Genome. 9(6). 479–481. 3 indexed citations
9.
Zhou, Jian‐Nian, Jamileh Hashemi, Khalil Helou, et al.. (1998). Analysis of mechanisms and frequency of CDKN2A/B gene loss during progression of RAS-transformed rat embryo fibroblast clones.. Somatic Cell and Molecular Genetics. 24(6). 327–339. 2 indexed citations
10.
Helou, Khalil, et al.. (1997). Isolation of DNA markers for the ratSai 1 gene for suppression of anchorage independence by using representational difference analysis. Somatic Cell and Molecular Genetics. 23(1). 63–74. 2 indexed citations
11.
Zhou, Jian‐Nian, et al.. (1997). Codeletion of theJUN proto-oncogene and theCDKN2A tumor-suppressor gene inHRAS-transformed rat embryo fibroblast cell lines. Genes Chromosomes and Cancer. 20(1). 82–89. 5 indexed citations
12.
Maarel, Silvère M. van der, D. Olde Weghuis, I Huber, et al.. (1995). Cloning of candidate genes for X-linked mental retardation by use of chromosome aberrations. American Journal of Medical Genetics Part A. 64(1). 19. 1 indexed citations
13.
Golembieski, William, et al.. (1994). Physical map of small cell lung cancer deletion region on short arm of human chromosome 3 (3p13–22) based on radiation fusion hybrid analysis. Somatic Cell and Molecular Genetics. 20(2). 121–132. 3 indexed citations
14.
Kumlien, Johan, et al.. (1994). Identification of human chromosome region 3p14.2–21.3-specific YAC clones using Alu-PCR products from a radiation hybrid. Somatic Cell and Molecular Genetics. 20(2). 137–142. 1 indexed citations
15.
16.
Höglund, Mattias, et al.. (1992). The Isolation of Evolutionarily Conserved Eag I End-Clones from Mouse Chromosome 17 Using Cloned DNA. DNA and Cell Biology. 11(8). 613–619. 1 indexed citations
17.
Höglund, Mattias, Torbjörn Säll, & Dan Röhme. (1990). On the origin of coding sequences from random open reading frames. Journal of Molecular Evolution. 30(2). 104–108. 11 indexed citations
18.
Stubbs, Lisa, Annemarie Poustka, Dan Röhme, Liane B. Russell, & Hans Lehrach. (1988). Approaching the Mouse Steel Locus from Closely Linked Molecular Markers. Current topics in microbiology and immunology. 137. 47–52. 3 indexed citations
19.
Edström, Jan‐Erik, Rolf Kaiser, & Dan Röhme. (1987). [37] Microcloning of mammalian metaphase chromosomes. Methods in enzymology on CD-ROM/Methods in enzymology. 151. 503–516. 18 indexed citations
20.
Heneen, W. K., et al.. (1980). Heteromorphism of constitutive heterochromatin in carcinoma and dysplasia of the uterine cervix. European Journal of Obstetrics & Gynecology and Reproductive Biology. 10(3). 173–182. 7 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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