Thomas Liehr
- Genetics top 0.05%
- Genomic variations and chromosomal abnormalities 339
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 71
- Genetics and Neurodevelopmental Disorders 41
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- Prenatal Screening and Diagnostics 120
- Plant Science top 0.2%
- Chromosomal and Genetic Variations 308
- Genetics top 1%
- Genomic variations and chromosomal abnormalities 339
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 71
- Genetics and Neurodevelopmental Disorders 41
- Molecular Biology top 1%
- Genomics and Chromatin Dynamics 88
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- Acute Myeloid Leukemia Research 45
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- Acute Lymphoblastic Leukemia research 39
Thomas Liehr
692 papers receiving 11.2k citations
Peers
Comparison fields: 5 of 163
- Genetics 6.8k
- Pediatrics, Perinatology and Child Health 2.4k
- Plant Science 4.4k
- Genetics 796
- Molecular Biology 5.1k
Countries citing papers authored by Thomas Liehr
This map shows the geographic impact of Thomas Liehr'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 Thomas Liehr with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thomas Liehr more than expected).
Fields of papers citing papers by Thomas Liehr
This network shows the impact of papers produced by Thomas Liehr. 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 Thomas Liehr. The network helps show where Thomas Liehr may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Thomas Liehr, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2024 | 6 | |
| 2 | 2024 | 0 | |
| 3 | 2024 | 4 | |
| 4 | 2024 | 2 | |
| 5 | 2024 | 1 | |
| 6 | 2024 | 3 | |
| 7 | 2024 | 4 | |
| 8 | 2023 | 5 | |
| 9 | 2022 | 4 | |
| 10 | 2021 | 2 | |
| 11 | 2020 | 9 | |
| 12 | 2019 | 1 | |
| 13 | 2019 | 2 | |
| 14 | 2019 | 8 | |
| 15 | 2017 | 32 | |
| 16 | 2015 | 28 | |
| 17 | 2014 | 2 | |
| 18 | 2010 | 30 | |
| 19 | 2008 | 9 | |
| 20 | The use of pyrosequencing to identify copy number variation of 16p11.2 in euchromatic variant carriers and the normal population | 2006 | 1 |
About Thomas Liehr
Thomas Liehr is a scholar working on Genetics, Plant Science, Pediatrics, Perinatology and Child Health, Hematology and Genetics, having authored 735 papers that have together received 11.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (339 papers), Chromosomal and Genetic Variations (308 papers), Prenatal Screening and Diagnostics (120 papers), Genomics and Chromatin Dynamics (88 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (71 papers), Acute Myeloid Leukemia Research (45 papers), Genetics and Neurodevelopmental Disorders (41 papers) and Acute Lymphoblastic Leukemia research (39 papers). The work is most often cited by research in Genetics (6.8k citations), Pediatrics, Perinatology and Child Health (2.4k citations), Plant Science (4.4k citations), Genetics (796 citations) and Molecular Biology (5.1k citations). Thomas Liehr has collaborated with scholars based in Germany, Brazil and Russia. Frequent co-authors include Anja Weise, Heike Starke, Kristin Mrasek, Nadezda Kosyakova, Uwe Claussen, U. Claussen, Ivan Y. Iourov, Yuri B. Yurov, Svetlana G. Vorsanova and Marcelo de Bello Cioffi. Their work appears in journals such as Molecular Cytogenetics, Cytogenetic and Genome Research, International Journal of Molecular Sciences, Journal of Histochemistry & Cytochemistry and International Journal of Oncology.
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.