Heike Fiegler

19.6k citations
53 papers · 7.0k indexed · 2 hit papers · h-index 33
Topics
Genomic variations and chromosomal abnormalities (32 papers)Chromosomal and Genetic Variations (16 papers)Prenatal Screening and Diagnostics (10 papers)

In The Last Decade

Heike Fiegler

53 papers receiving 6.9k citations

Hit Papers

A DNA damage checkpoint response in telomere-initiated se...20032026201020182003200750010001.5k2.0k

Peers

Heike Fiegler
Comparison fields: 5 of 158
  • Molecular Biology 4.3k
  • Genetics 2.2k
  • Physiology 1.8k
  • Plant Science 1.0k
  • Cancer Research 945
Replace Harry Scherthan with:
Harry Scherthan Germany
David I. K. Martin United States
Diego H. Castrillón United States
Yoichi Shinkai Japan
Antoine H.F.M. Peters Switzerland
Victor Guryev Netherlands
Nigel P. Carter United Kingdom
John C. Schimenti United States
Simon Andrews United Kingdom
Toru Nakano Japan
Heike Fiegler relative to Harry Scherthan Germany Harry Scherthan's profile →
Citations per field
00.5×1.6×
Harry Scherthan · 1×
Citations per year

Countries citing papers authored by Heike Fiegler

Since Specialization
Citations

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

Fields of papers citing papers by Heike Fiegler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Heike Fiegler

This figure shows the co-authorship network connecting the top 25 collaborators of Heike Fiegler. A scholar is included among the top collaborators of Heike Fiegler 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 Fiegler. Heike Fiegler 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
#WorkIndexed citations
1 7
2 9
3 17
4 91
5 81
6 30
7 225
8 101
9 13
10 17
11 112
12 59
13 43
14 54
15 157
16 88
17 121
18 7
19
DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones. (vol 36, pg 361, 2003)
14
20 41

About Heike Fiegler

Heike Fiegler is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Plant Science, having authored 53 papers that have together received 7.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (32 papers), Chromosomal and Genetic Variations (16 papers) and Prenatal Screening and Diagnostics (10 papers). The work is most often cited by research in Aging (320 citations), Genetics (2.2k citations) and Physiology (1.8k citations). Heike Fiegler has collaborated with scholars based in United Kingdom, Germany and United States. Frequent co-authors include Nigel P. Carter, Philippa Carr, Stephen P. Jackson, Fabrizio d’Adda di Fagagna, Gabriele Saretzki, Thomas von Zglinicki, Philip M. Reaper, Ian Tomlinson, Richard Redon and Charles Lee. Their work appears in journals such as Nature, Cell and Nucleic Acids Research.

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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