Marc Trimborn

1.2k total citations
21 papers, 714 citations indexed

About

Marc Trimborn is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Marc Trimborn has authored 21 papers receiving a total of 714 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Genetics and 8 papers in Cell Biology. Recurrent topics in Marc Trimborn's work include Microtubule and mitosis dynamics (8 papers), DNA Repair Mechanisms (7 papers) and Chromosomal and Genetic Variations (7 papers). Marc Trimborn is often cited by papers focused on Microtubule and mitosis dynamics (8 papers), DNA Repair Mechanisms (7 papers) and Chromosomal and Genetic Variations (7 papers). Marc Trimborn collaborates with scholars based in Germany, United States and Japan. Marc Trimborn's co-authors include Heidemarie Neitzel, Detlev Schindler, Karl Sperling, Tatsuya Hirano, Luitgard M. Neumann, Andrew P. Jackson, Ioannis Gavvovidis, Hussain Jafri, Yasmin Abdul Rashid and Sandra Bell and has published in prestigious journals such as The Journal of Cell Biology, PLoS ONE and Scientific Reports.

In The Last Decade

Marc Trimborn

20 papers receiving 654 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marc Trimborn Germany 14 523 305 254 112 76 21 714
Elias O. Silva Brazil 5 494 0.9× 394 1.3× 267 1.1× 56 0.5× 40 0.5× 6 688
Sakura Saburi Japan 9 654 1.3× 216 0.7× 337 1.3× 37 0.3× 44 0.6× 16 815
Eva Pipiras France 15 475 0.9× 424 1.4× 42 0.2× 110 1.0× 79 1.0× 26 744
Takashi Ishiuchi Japan 15 985 1.9× 109 0.4× 326 1.3× 110 1.0× 40 0.5× 21 1.2k
Giovanna Giovinazzo Spain 13 687 1.3× 102 0.3× 184 0.7× 218 1.9× 63 0.8× 18 925
Ninette Cohen United States 15 352 0.7× 229 0.8× 43 0.2× 62 0.6× 55 0.7× 29 691
Natalia Soshnikova Germany 14 900 1.7× 242 0.8× 61 0.2× 150 1.3× 76 1.0× 23 1.0k
Pietro Palumbo Italy 15 314 0.6× 325 1.1× 49 0.2× 40 0.4× 32 0.4× 64 620
Romain Desprat France 11 712 1.4× 179 0.6× 84 0.3× 54 0.5× 29 0.4× 23 801
Divya Jayaraman United States 5 352 0.7× 180 0.6× 217 0.9× 29 0.3× 31 0.4× 7 478

Countries citing papers authored by Marc Trimborn

Since Specialization
Citations

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

Fields of papers citing papers by Marc Trimborn

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marc Trimborn

This figure shows the co-authorship network connecting the top 25 collaborators of Marc Trimborn. A scholar is included among the top collaborators of Marc Trimborn 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 Marc Trimborn. Marc Trimborn 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.
Müller, Petra, Christian Sell, Thorsten Hadrys, et al.. (2019). Inter-laboratory study on standardized MPS libraries: evaluation of performance, concordance, and sensitivity using mixtures and degraded DNA. International Journal of Legal Medicine. 134(1). 185–198. 20 indexed citations
2.
Kuriyama, Ryoko, Marc Trimborn, Daniel Keifenheim, et al.. (2017). MCPH1, mutated in primary microcephaly, is required for efficient chromosome alignment during mitosis. Scientific Reports. 7(1). 13019–13019. 17 indexed citations
3.
Wegner, Rolf‐Dieter, Marc Trimborn, Markus Stümm, & Peter Wieacker. (2016). Humangenetische Grundlagen für Gynäkologen. 1 indexed citations
4.
Trimborn, Marc, et al.. (2015). Chromosome structure deficiencies in MCPH1 syndrome. Chromosoma. 124(4). 491–501. 9 indexed citations
5.
Villavicencio‐Lorini, Pablo, Eva Klopocki, Marc Trimborn, et al.. (2012). Phenotypic variant of Brachydactyly-mental retardation syndrome in a family with an inherited interstitial 2q37.3 microdeletion including HDAC4. European Journal of Human Genetics. 21(7). 743–748. 52 indexed citations
6.
Ghani, Mahdi, Peter N. Robinson, Susanne Morlot, et al.. (2012). Two Missense Mutations in the Primary Autosomal Recessive Microcephaly Gene MCPH1 Disrupt the Function of the Highly Conserved N-Terminal BRCT Domain of Microcephalin. Molecular Syndromology. 3(1). 6–13. 15 indexed citations
7.
Gavvovidis, Ioannis, Marc Trimborn, Frank J. Kaiser, et al.. (2012). A Novel MCPH1 Isoform Complements the Defective Chromosome Condensation of Human MCPH1-Deficient Cells. PLoS ONE. 7(8). e40387–e40387. 24 indexed citations
8.
9.
Marchal, Juan Alberto, Mahdi Ghani, Detlev Schindler, et al.. (2011). Misregulation of mitotic chromosome segregation in a new type of autosomal recessive primary microcephaly. Cell Cycle. 10(17). 2967–2977. 7 indexed citations
10.
Trimborn, Marc, Michaela Endres, Christiane Bommer, et al.. (2011). Karyotyping of human chondrocytes in scaffold-assisted cartilage tissue engineering. Acta Biomaterialia. 8(4). 1519–1529. 12 indexed citations
11.
Yamashita, Daisuke, Keishi Shintomi, Takao Ono, et al.. (2011). MCPH1 regulates chromosome condensation and shaping as a composite modulator of condensin II. The Journal of Cell Biology. 194(6). 841–854. 66 indexed citations
12.
Gavvovidis, Ioannis, Juan Alberto Marchal, Markus Stümm, et al.. (2010). MCPH1 patient cells exhibit delayed release from DNA damage-induced G2/M checkpoint arrest . Cell Cycle. 9(24). 4893–4899. 19 indexed citations
13.
Klopocki, Eva, Ran Wei, Christiane Bommer, et al.. (2009). De novo 9 Mb deletion of 6q23.2q24.1 disrupting the gene EYA4 in a patient with sensorineural hearing loss, cardiac malformation, and mental retardation. European Journal of Medical Genetics. 52(6). 450–453. 9 indexed citations
14.
Trimborn, Marc, et al.. (2006). Prenatal diagnosis and molecular cytogenetic characterisation of a small de novo interstitial duplication 16q11.2‐q13. Prenatal Diagnosis. 26(3). 273–276. 9 indexed citations
15.
Trimborn, Marc, Nadine Sternberg, Ioannis Gavvovidis, et al.. (2005). The first missense alteration in the MCPH1 gene causes autosomal recessive microcephaly with an extremely mild cellular and clinical phenotype. Human Mutation. 26(5). 496–496. 44 indexed citations
16.
Trimborn, Marc, Detlev Schindler, Heidemarie Neitzel, & Tatsuya Hirano. (2005). Misregulated Chromosome Condensation in MCPH1 Primary Microcephaly is Mediated by Condensin II. Cell Cycle. 5(3). 322–326. 60 indexed citations
17.
Trimborn, Marc, Thomas Liehr, Britta Belitz, et al.. (2005). Prenatal Diagnosis and Molecular Cytogenetic Characterization of an Unusual Complex Structural Rearrangement in a Pregnancy Following Intracytoplasmic Sperm Injection (ICSI). Journal of Histochemistry & Cytochemistry. 53(3). 351–354. 5 indexed citations
18.
Trimborn, Marc, Sandra Bell, Yasmin Abdul Rashid, et al.. (2004). Mutations in Microcephalin Cause Aberrant Regulation of Chromosome Condensation. The American Journal of Human Genetics. 75(2). 261–266. 190 indexed citations
19.
20.
Neitzel, Heidemarie, Luitgard M. Neumann, Detlev Schindler, et al.. (2002). Premature Chromosome Condensation in Humans Associated with Microcephaly and Mental Retardation: A Novel Autosomal Recessive Condition. The American Journal of Human Genetics. 70(4). 1015–1022. 82 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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