Peter Lichter
Impact in
- Genetics top 0.01%
- Glioma Diagnosis and Treatment
- Chronic Lymphocytic Leukemia Research
- Genomic variations and chromosomal abnormalities
- Cancer Research top 0.02%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 210
- Chronic Lymphocytic Leukemia Research 114
- Glioma Diagnosis and Treatment 95
- Genomic variations and chromosomal abnormalities 93
- Cancer Research 112
- Cancer Genomics and Diagnostics 60
- Co-authors
- Stephan Stilgenbauer (93 shared papers)Hartmut Doehner (86 shared papers)Martin Bentz (63 shared papers)Axel Benner (49 shared papers)David C. Ward (13 shared papers)Stefan Joos (59 shared papers)Thomas John Cremer (16 shared papers)Lars Bullinger (15 shared papers)
- Journals
- Blood (58 papers)Genes Chromosomes and Cancer (35 papers)International Journal of Cancer (34 papers)Acta Neuropathologica (25 papers)Nature Communications (22 papers)
- Partner nations
- GermanyUnited KingdomUnited States
In The Last Decade
Peter Lichter
599 papers receiving 73.1k citations
Peter Lichter's Hit Papers
Peers
Comparison fields: 5 of 204
- Genetics 27.0k
- Cancer Research 14.8k
- Pathology and Forensic Medicine 11.4k
- Molecular Biology 36.8k
- Oncology 11.4k
Countries citing papers authored by Peter Lichter
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
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-authors
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.
All Works
Showing the 20 most-cited of 606 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genomic Aberrations and Survival in Chronic Lymphocytic Leukemia Hit paper breakdown → | 2000 | 2710 |
| 2 | The repertoire of mutational signatures in human cancer Hit paper breakdown → | 2020 | 2339 |
| 3 | DNA methylation-based classification of central nervous system tumours Hit paper breakdown → | 2018 | 2183 |
| 4 | Pan-cancer analysis of whole genomes Hit paper breakdown → | 2020 | 2109 |
| 5 | Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma Hit paper breakdown → | 2012 | 2075 |
| 6 | Hotspot Mutations in H3F3A and IDH1 Define Distinct Epigenetic and Biological Subgroups of Glioblastoma Hit paper breakdown → | 2012 | 1513 |
| 7 | Molecular subgroups of medulloblastoma: the current consensus Hit paper breakdown → | 2011 | 1484 |
| 8 | High-Resolution Mapping of Human Chromosome 11 by in Situ Hybridization with Cosmid Clones Hit paper breakdown → | 1990 | 1191 |
| 9 | The landscape of genomic alterations across childhood cancers Hit paper breakdown → | 2018 | 1154 |
| 10 | Resistance Mechanisms for the Bruton's Tyrosine Kinase Inhibitor Ibrutinib Hit paper breakdown → | 2014 | 1064 |
| 11 | Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries Hit paper breakdown → | 1988 | 1009 |
| 12 | Molecular Classification of Ependymal Tumors across All CNS Compartments, Histopathological Grades, and Age Groups Hit paper breakdown → | 2015 | 899 |
| 13 | The whole-genome landscape of medulloblastoma subtypes Hit paper breakdown → | 2017 | 840 |
| 14 | K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas Hit paper breakdown → | 2012 | 810 |
| 15 | Molecular subgroups of medulloblastoma: an international meta-analysis of transcriptome, genetic aberrations, and clinical data of WNT, SHH, Group 3, and Group 4 medulloblastomas Hit paper breakdown → | 2012 | 808 |
| 16 | A Biologic Definition of Burkitt's Lymphoma from Transcriptional and Genomic Profiling Hit paper breakdown → | 2006 | 791 |
| 17 | Matrix-based comparative genomic hybridization: Biochips to screen for genomic imbalances Hit paper breakdown → | 1997 | 750 |
| 18 | New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs Hit paper breakdown → | 2016 | 716 |
| 19 | Dissecting the genomic complexity underlying medulloblastoma Hit paper breakdown → | 2012 | 702 |
| 20 | Genome Sequencing of Pediatric Medulloblastoma Links Catastrophic DNA Rearrangements with TP53 Mutations Hit paper breakdown → | 2012 | 688 |
About Peter Lichter
Peter Lichter is a scholar working on Genetics, Cancer Research, Molecular Biology, Genetics and Pathology and Forensic Medicine, having authored 606 papers that have together received 74.9k indexed citations. Recurring topics across this work include Chronic Lymphocytic Leukemia Research (114 papers), Glioma Diagnosis and Treatment (95 papers), Genomic variations and chromosomal abnormalities (93 papers), Lymphoma Diagnosis and Treatment (67 papers), Genomics and Chromatin Dynamics (65 papers), Cancer Genomics and Diagnostics (60 papers), Chromosomal and Genetic Variations (44 papers) and Epigenetics and DNA Methylation (41 papers). The work is most often cited by research in Genetics (27.0k citations), Cancer Research (14.8k citations), Pathology and Forensic Medicine (11.4k citations), Molecular Biology (36.8k citations) and Oncology (11.4k citations). Peter Lichter has collaborated with scholars based in Germany, United Kingdom and United States. Frequent co-authors include Stephan Stilgenbauer, Hartmut Doehner, Martin Bentz, Axel Benner, David C. Ward, Stefan Joos, Thomas John Cremer, Lars Bullinger, Stefan M. Pfister and Alexander Kröber. Their work appears in journals such as Blood, Genes Chromosomes and Cancer, International Journal of Cancer, Acta Neuropathologica and Nature Communications.
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.