Peter Krusche

4.1k citations
15 papers · 1.6k · 1 hit paper · h-index 9

Impact in

Papers in

    • Genomics and Phylogenetic Studies 5
    • Epigenetics and DNA Methylation 2
    • Genomics and Rare Diseases 3
    • Genetic Associations and Epidemiology 3

Peter Krusche

14 papers receiving 1.6k citations

Peter Krusche's Hit Papers

Strelka2: fast and accurate calling of germline and somatic variants 2018 · 715 citations
7150+2+5Years since publication200400600

Peers

Peter Krusche
Comparison fields: 5 of 109
  • Cancer Research 385
  • Aging 48
  • Endocrine and Autonomic Systems 143
  • Genetics 417
  • Molecular Biology 794
Replace Andrew M. Gross with:
Andrew M. Gross United States
Daniel E. Newburger United States
Giovanna Ambrosini Switzerland
Volker Matys Germany
Wouter Meuleman Netherlands
Robin Andersson Denmark
Patrick Kemmeren Netherlands
Eric Batchelor United States
Timothy Durham United States
A. Kasprzyk United Kingdom
Peter Krusche relative to Andrew M. Gross United States Andrew M. Gross's profile →
Citations per field
00.5×2.6×
Andrew M. Gross · 1×
Citations per year

Countries citing papers authored by Peter Krusche

Since Specialization
Citations

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

Fields of papers citing papers by Peter Krusche

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Peter Krusche, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Peter Krusche Line = papers co-authored together Peter Krusche links everyone, so they are left out of the graph.

All Works

15 of 15 papers shown
#Work
1
Strelka2: fast and accurate calling of germline and somatic variants
Hit paper breakdown →
2018715
2 2016221
3 2019189
4 2014161
5 2019104
6 201253
7 201346
8 201730
9 201027
10 20108
11 20157
12 20243
13
Efficient parallel string comparison
20073
14 20082
15
Zur Theorie und Praxis der Predigtarbeit : Bericht von einer homiletischen Arbeitstagung September 1967 - Esslingen
19680

About Peter Krusche

Peter Krusche is a scholar working on Molecular Biology, Genetics, Plant Science, Hardware and Architecture and Artificial Intelligence, having authored 15 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genomics and Phylogenetic Studies (5 papers), Genomics and Rare Diseases (3 papers), Genetic Associations and Epidemiology (3 papers), Plant Molecular Biology Research (3 papers), Circadian rhythm and melatonin (2 papers), Epigenetics and DNA Methylation (2 papers), Network Packet Processing and Optimization (2 papers) and Algorithms and Data Compression (2 papers). The work is most often cited by research in Cancer Research (385 citations), Aging (48 citations), Endocrine and Autonomic Systems (143 citations), Genetics (417 citations) and Molecular Biology (794 citations). Peter Krusche has collaborated with scholars based in United Kingdom, United States and Switzerland. Frequent co-authors include Morten Källberg, Aaron L. Halpern, Mitchell A. Bekritsky, Eunho Noh, Christopher T. Saunders, Doruk Beyter, Sangtae Kim, Konrad Scheffler, Michael A. Eberle and Benjamin L. Moore. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Methods, Genome Research, Scientific Reports and BMC Evolutionary Biology.

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