Heike Starke

3.5k total citations
70 papers, 2.2k citations indexed

About

Heike Starke is a scholar working on Genetics, Plant Science and Molecular Biology. According to data from OpenAlex, Heike Starke has authored 70 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Genetics, 48 papers in Plant Science and 37 papers in Molecular Biology. Recurrent topics in Heike Starke's work include Genomic variations and chromosomal abnormalities (58 papers), Chromosomal and Genetic Variations (48 papers) and Genomics and Chromatin Dynamics (21 papers). Heike Starke is often cited by papers focused on Genomic variations and chromosomal abnormalities (58 papers), Chromosomal and Genetic Variations (48 papers) and Genomics and Chromatin Dynamics (21 papers). Heike Starke collaborates with scholars based in Germany, Poland and Russia. Heike Starke's co-authors include Thomas Liehr, U. Claussen, Anita Heller, Anja Weise, Uwe Claussen, Kristin Mrasek, Vladimir A. Trifonov, Н. Б. Рубцов, M. Oliver‐Bonet and J. Navarro and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and The Journal of Urology.

In The Last Decade

Heike Starke

70 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Heike Starke Germany 25 1.7k 1.2k 967 686 150 70 2.2k
Sharon W. Horsley United Kingdom 19 1.3k 0.8× 436 0.4× 882 0.9× 367 0.5× 23 0.2× 30 1.8k
L. Tiepolo Italy 24 1.8k 1.1× 677 0.6× 1.6k 1.7× 277 0.4× 26 0.2× 73 2.6k
Philippos C. Patsalis Cyprus 27 1.2k 0.7× 266 0.2× 1.0k 1.1× 705 1.0× 21 0.1× 100 2.0k
Helena Ayyub United Kingdom 27 1.0k 0.6× 329 0.3× 2.7k 2.8× 270 0.4× 52 0.3× 43 3.5k
R. Sid Wilroy United States 21 778 0.5× 167 0.1× 635 0.7× 275 0.4× 77 0.5× 53 1.3k
Nick Sampas United States 7 977 0.6× 424 0.4× 856 0.9× 183 0.3× 15 0.1× 7 1.5k
P Maraschio Italy 25 1.1k 0.7× 480 0.4× 1.0k 1.1× 263 0.4× 10 0.1× 73 1.7k
James Tepperberg United States 15 532 0.3× 149 0.1× 362 0.4× 284 0.4× 37 0.2× 28 889
Susan Pfeifer‐Ohlsson Sweden 16 519 0.3× 94 0.1× 1.1k 1.1× 287 0.4× 35 0.2× 23 1.6k
Heinz‐Ulrich G. Weier United States 17 507 0.3× 174 0.1× 712 0.7× 153 0.2× 27 0.2× 47 1.3k

Countries citing papers authored by Heike Starke

Since Specialization
Citations

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

Fields of papers citing papers by Heike Starke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Heike Starke

This figure shows the co-authorship network connecting the top 25 collaborators of Heike Starke. A scholar is included among the top collaborators of Heike Starke 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 Heike Starke. Heike Starke 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.
Starke, Heike, Günther Ernst, Nadezda Kosyakova, et al.. (2007). A further case with a small supernumerary marker chromosome (sSMC) derived from chromosome 1—evidence for high variability in mosaicism in different tissues of sSMC carriers. Prenatal Diagnosis. 27(8). 783–785. 29 indexed citations
2.
Brečević, Lukrecija, S. Michel, Heike Starke, et al.. (2006). Multicolor FISH used for the characterization of small supernumerary marker chromosomes (sSMC) in commercially available immortalized cell lines. Cytogenetic and Genome Research. 114(3-4). 319–324. 11 indexed citations
3.
Dufke, Andreas, Sylke Singer, Ulrike A. Mau‐Holzmann, et al.. (2006). De novostructural chromosomal imbalances: molecular cytogenetic characterization of partial trisomies. Cytogenetic and Genome Research. 114(3-4). 342–350. 11 indexed citations
4.
Bartels, Iris, et al.. (2006). An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype. European Journal of Medical Genetics. 50(2). 133–138. 42 indexed citations
5.
Tönnies, H., et al.. (2006). Molecular cytogenetic identification and characterization of a de novo supernumerary neocentromeric derivative chromosome 13. Cytogenetic and Genome Research. 114(3-4). 325–329. 6 indexed citations
6.
Barber, John, Shuai Zhang, Amanda Collins, et al.. (2006). Duplications of proximal 16q flanked by heterochromatin are not euchromatic variants and show no evidence of heterochromatic position effect. Cytogenetic and Genome Research. 114(3-4). 351–358. 18 indexed citations
7.
Polityko, A., et al.. (2005). Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding. Cytogenetic and Genome Research. 111(2). 171–174. 13 indexed citations
8.
Liehr, Thomas, Gabriele Gillessen‐Kaesbach, Rainer König, et al.. (2005). Prader–Willi syndrome with a karyotype 47,XY,+min(15)(pter->q11.1:) and maternal UPD 15—case report plus review of similar cases. European Journal of Medical Genetics. 48(2). 175–181. 21 indexed citations
9.
Vermeesch, Joris, Cindy Melotte, Mariluce Riegel, et al.. (2005). Tetrasomy 12pter-12p13.31 in a girl with partial Pallister–Killian syndrome phenotype. European Journal of Medical Genetics. 48(3). 319–327. 19 indexed citations
10.
Codina‐Pascual, M., M. Oliver‐Bonet, J. Navarro, et al.. (2004). FISH characterization of a dicentric Yq (p11.32) isochromosome in an azoospermic male. American Journal of Medical Genetics Part A. 127A(3). 302–306. 34 indexed citations
11.
12.
Weise, Anja, Heike Starke, Kristin Mrasek, U. Claussen, & Thomas Liehr. (2004). New insights into the evolution of chromosome 1. Cytogenetic and Genome Research. 108(1-3). 217–222. 17 indexed citations
13.
Sun, Fei, M. Oliver‐Bonet, Thomas Liehr, et al.. (2004). Human Male Recombination Maps for Individual Chromosomes. The American Journal of Human Genetics. 74(3). 521–531. 108 indexed citations
14.
Weise, Anja, Anita Heller, Heike Starke, et al.. (2003). Multitude multicolor chromosome banding (mMCB) – a comprehensive one-step multicolor FISH banding method. Cytogenetic and Genome Research. 103(1-2). 34–39. 32 indexed citations
15.
Grasshoff, Ute, Sylke Singer, Thomas Liehr, et al.. (2003). A complex chromosomal rearrangement with a translocation 4;10;14 in a fertile male carrier: ascertainment through an offspring with partial trisomy 14q24→1q22 and partial monosomy 4q27→q28. Cytogenetic and Genome Research. 103(1-2). 17–23. 26 indexed citations
16.
Liehr, Thomas, Matthias Schmidt, Heike Starke, et al.. (2002). First Case of Trisomy 13 plus Mosaic Trisomy 1q. Fetal Diagnosis and Therapy. 17(3). 133–136. 5 indexed citations
17.
Liehr, Thomas, Anita Heller, Heike Starke, & Uwe Claussen. (2002). FISH banding methods: applications in research and diagnostics. Expert Review of Molecular Diagnostics. 2(3). 217–225. 29 indexed citations
18.
Starke, Heike, Martin Kristian Raida, Vladimir A. Trifonov, et al.. (2001). Molecular cytogenetic characterization of an acquired minute supernumerary marker chromosome as the sole abnormality in a case clinically diagnosed as atypical Philadelphia‐negative chronic myelogenous leukaemia. British Journal of Haematology. 113(2). 435–438. 18 indexed citations
19.
Mrasek, Kristin, Anita Heller, Н. Б. Рубцов, et al.. (2001). Reconstruction of the female <i>Gorilla gorilla</i> karyotype using 25-color FISH and multicolor banding (MCB). Cytogenetic and Genome Research. 93(3-4). 242–248. 41 indexed citations
20.
Thiele, Hannelore, et al.. (2001). Kabuki syndrome-like features associated with a small ring chromosome X andXIST gene expression. American Journal of Medical Genetics. 102(3). 286–292. 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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