Thomas Liehr
Impact in
- Genetics top 0.05%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 429
- Genomic variations and chromosomal abnormalities 316
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 67
- Genetics and Neurodevelopmental Disorders 33
- Plant Science 275
- Chromosomal and Genetic Variations 270
- Co-authors
- Anja Weise (129 shared papers)Heike Starke (65 shared papers)Kristin Mrasek (79 shared papers)Nadezda Kosyakova (88 shared papers)Uwe Claussen (48 shared papers)U. Claussen (27 shared papers)Ivan Y. Iourov (20 shared papers)Marcelo de Bello Cioffi (81 shared papers)
In The Last Decade
Thomas Liehr
700 papers receiving 11.3k citations
Peers
Comparison fields: 5 of 161
- Genetics 6.3k
- Pediatrics, Perinatology and Child Health 1.8k
- Plant Science 3.7k
- Genetics 652
- Molecular Biology 4.4k
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-authors
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
Showing the 20 most-cited of 742 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 285 | |
| 2 | 2004 | 235 | |
| 3 | 2002 | 184 | |
| 4 | 2007 | 168 | |
| 5 | 2007 | 160 | |
| 6 | 2009 | 157 | |
| 7 | 2001 | 148 | |
| 8 | 2005 | 132 | |
| 9 | 2011 | 130 | |
| 10 | 2001 | 116 | |
| 11 | 2004 | 108 | |
| 12 | 2008 | 104 | |
| 13 | 2010 | 103 | |
| 14 | 2012 | 103 | |
| 15 | 2010 | 103 | |
| 16 | 1994 | 99 | |
| 17 | 2014 | 93 | |
| 18 | 2002 | 91 | |
| 19 | 2020 | 87 | |
| 20 | 2009 | 85 |
About Thomas Liehr
Thomas Liehr is a scholar working on Genetics, Plant Science, Molecular Biology, Pediatrics, Perinatology and Child Health and Hematology, having authored 742 papers that have together received 11.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (316 papers), Chromosomal and Genetic Variations (270 papers), Prenatal Screening and Diagnostics (96 papers), Genomics and Chromatin Dynamics (77 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (67 papers), Acute Myeloid Leukemia Research (38 papers), Genetics and Neurodevelopmental Disorders (33 papers) and Acute Lymphoblastic Leukemia research (32 papers). The work is most often cited by research in Genetics (6.3k citations), Pediatrics, Perinatology and Child Health (1.8k citations), Plant Science (3.7k citations), Genetics (652 citations) and Molecular Biology (4.4k 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, Marcelo de Bello Cioffi, Yuri B. Yurov and Svetlana G. Vorsanova. 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.