Peter Lichter

98.4k citations
490 papers · 36.6k indexed · 7 hit papers · h-index 100
  • Genetics top 0.01%
    • Chronic Lymphocytic Leukemia Research 100
    • Genomic variations and chromosomal abnormalities 95
    • Glioma Diagnosis and Treatment 59
    • Lymphoma Diagnosis and Treatment 59
    • Cancer Genomics and Diagnostics 42
    • Genomics and Chromatin Dynamics 56
  • Genetics top 0.05%
    • Chronic Lymphocytic Leukemia Research 100
    • Genomic variations and chromosomal abnormalities 95
    • Glioma Diagnosis and Treatment 59
    • Chromosomal and Genetic Variations 47
    • Cancer-related Molecular Pathways 35

Peter Lichter

484 papers receiving 35.9k citations

Hit Papers

Molecular subgroups of medullobla...1.2k198820262000201350010001.5k2.0k

Peers

Peter Lichter
Comparison fields: 5 of 187
  • Genetics 11.9k
  • Pathology and Forensic Medicine 7.5k
  • Cancer Research 6.0k
  • Molecular Biology 19.4k
  • Genetics 7.2k
Replace Louis M. Staudt with:
Louis M. Staudt United States
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Peter Lichter relative to Louis M. Staudt United States Louis M. Staudt's profile →
Citations per field
00.5×3.4×
Louis M. Staudt · 1×
Citations per year

Countries citing papers authored by Peter Lichter

Since Specialization
Citations

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

Fields of papers citing papers by Peter Lichter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Peter Lichter, 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 Lichter Line = papers co-authored together Peter Lichter links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown
#Work
1 20250
2 20231
3 202313
4 202210
5 202130
6 202017
7 20184
8 20171
9 201535
10 2013110
11 2012161
12 2011160
13 2010251
14 201058
15 201055
16 200929
17 2009150
18 2009198
19 200856
20 2005101

About Peter Lichter

Peter Lichter is a scholar working on Genetics, Cancer Research and Genetics, having authored 490 papers that have together received 36.6k indexed citations. Recurring topics across this work include Chronic Lymphocytic Leukemia Research (100 papers), Genomic variations and chromosomal abnormalities (95 papers), Glioma Diagnosis and Treatment (59 papers), Lymphoma Diagnosis and Treatment (59 papers), Genomics and Chromatin Dynamics (56 papers), Chromosomal and Genetic Variations (47 papers), Cancer Genomics and Diagnostics (42 papers) and Cancer-related Molecular Pathways (35 papers). The work is most often cited by research in Genetics (11.9k citations), Pathology and Forensic Medicine (7.5k citations) and Cancer Research (6.0k citations). Peter Lichter has collaborated with scholars based in Germany, United Kingdom and United States. Frequent co-authors include Stephan Stilgenbauer, Hartmut Döhner, Martin Bentz, Axel Benner, David C. Ward, Thomas Cremer, Stefan Joos, Lars Bullinger, Bernhard Radlwimmer and Stefan M. Pfister. Their work appears in journals such as Blood, Genes Chromosomes and Cancer, International Journal of Cancer, Genomics and Cancer 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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