Peter Lichter
Impact in
- Genetics top 0.01%
- Chronic Lymphocytic Leukemia Research
- Genomic variations and chromosomal abnormalities
- Glioma Diagnosis and Treatment
- Pathology and Forensic Medicine top 0.05%
- Lymphoma Diagnosis and Treatment
Papers in
-
- Genomics and Chromatin Dynamics 56
- Genetics 159
- Chronic Lymphocytic Leukemia Research 100
- Genomic variations and chromosomal abnormalities 95
- Glioma Diagnosis and Treatment 59
- Co-authors
- Stephan Stilgenbauer (94 shared papers)Hartmut Döhner (85 shared papers)Martin Bentz (60 shared papers)Axel Benner (52 shared papers)David C. Ward (13 shared papers)Thomas Cremer (17 shared papers)Stefan Joos (57 shared papers)Lars Bullinger (15 shared papers)
- Journals
- Blood (52 papers)Genes Chromosomes and Cancer (32 papers)International Journal of Cancer (26 papers)Genomics (21 papers)Cancer Research (16 papers)
- Partner nations
- GermanyUnited KingdomUnited States
In The Last Decade
Peter Lichter
484 papers receiving 35.9k citations
Peter Lichter's Hit Papers
Peers
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
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 490 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 | 2266 |
| 2 | Molecular subgroups of medulloblastoma: the current consensus Hit paper breakdown → | 2011 | 1241 |
| 3 | High-Resolution Mapping of Human Chromosome 11 by in Situ Hybridization with Cosmid Clones Hit paper breakdown → | 1990 | 1149 |
| 4 | Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries Hit paper breakdown → | 1988 | 962 |
| 5 | Matrix-based comparative genomic hybridization: Biochips to screen for genomic imbalances Hit paper breakdown → | 1997 | 699 |
| 6 | V H mutation status, CD38 expression level, genomic aberrations, and survival in chronic lymphocytic leukemia Hit paper breakdown → | 2002 | 597 |
| 7 | p53 gene deletion predicts for poor survival and non-response to therapy with purine analogs in chronic B-cell leukemias Hit paper breakdown → | 1995 | 576 |
| 8 | 2008 | 470 | |
| 9 | 2012 | 449 | |
| 10 | 1993 | 448 | |
| 11 | 1988 | 435 | |
| 12 | 2014 | 402 | |
| 13 | 1993 | 394 | |
| 14 | 2006 | 389 | |
| 15 | 2015 | 377 | |
| 16 | Missense mutations in SMOH in sporadic basal cell carcinomas of the skin and primitive neuroectodermal tumors of the central nervous system. | 1998 | 336 |
| 17 | 2013 | 323 | |
| 18 | 1997 | 322 | |
| 19 | 1997 | 309 | |
| 20 | 1995 | 266 |
About Peter Lichter
Peter Lichter is a scholar working on Molecular Biology, Genetics, Genetics, Oncology and Pathology and Forensic Medicine, 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), Cancer Research (6.0k citations), Molecular Biology (19.4k citations) and Genetics (7.2k 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.