Bernhard Horsthemke

21.2k citations
222 papers · 12.9k indexed · 3 hit papers · h-index 57
Topics
Genetic Syndromes and Imprinting (105 papers)Epigenetics and DNA Methylation (96 papers)Prenatal Screening and Diagnostics (56 papers)

In The Last Decade

Bernhard Horsthemke

220 papers receiving 12.5k citations

Hit Papers

Association of a human G-protein β3 subunit variant with ...1998202620072016199820022013200400600

Peers

Bernhard Horsthemke
Comparison fields: 5 of 151
  • Molecular Biology 8.2k
  • Genetics 6.7k
  • Pediatrics, Perinatology and Child Health 3.3k
  • Oncology 1.1k
  • Ophthalmology 1.1k
Replace Han G. Brunner with:
Han G. Brunner Netherlands
Cynthia C. Morton United States
Niels Tommerup Denmark
Andrew O.M. Wilkie United Kingdom
Ethylin Wang Jabs United States
Paul A. Overbeek United States
David Fitzpatrick United Kingdom
Fowzan S. Alkuraya Saudi Arabia
Philippe Soriano United States
Robert S. Sparkes United States
Bernhard Horsthemke relative to Han G. Brunner Netherlands Han G. Brunner's profile →
Citations per field
00.5×2.6×
Han G. Brunner · 1×
Citations per year

Countries citing papers authored by Bernhard Horsthemke

Since Specialization
Citations

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

Fields of papers citing papers by Bernhard Horsthemke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bernhard Horsthemke

This figure shows the co-authorship network connecting the top 25 collaborators of Bernhard Horsthemke. A scholar is included among the top collaborators of Bernhard Horsthemke 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 Bernhard Horsthemke. Bernhard Horsthemke 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 1
2 38
3 4
4 2
5 242
6 22
7 54
8 15
9 49
10 78
11 208
12 66
13
Intracytoplasmic Sperm Injection May Increase the Risk of Imprinting Defectsbreakdown →
519
14 23
15
Molekulare Genetik und Diagnostik des Retinoblastoms : Bedeutung für die Ophthalmologische Praxis
1
16 3
17 50
18 6
19
Somatic mosaicism in a patient with bilateral retinoblastoma.
29
20 387

About Bernhard Horsthemke

Bernhard Horsthemke is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Ophthalmology, having authored 222 papers that have together received 12.9k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (105 papers), Epigenetics and DNA Methylation (96 papers) and Prenatal Screening and Diagnostics (56 papers). The work is most often cited by research in Genetics (6.7k citations), Pediatrics, Perinatology and Child Health (3.3k citations) and Ophthalmology (1.1k citations). Bernhard Horsthemke has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Karin Buiting, Robert D. Nicholls, Shinji Saitoh, Eberhard Passarge, Dietmar Lohmann, Hermann‐Josef Lüdecke, Valerie Greger, Gabriele Gillessen‐Kaesbach, Bärbel Dittrich and Stephanie Groß. Their work appears in journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026