E Seemanová
Impact in
- Developmental Biology top 2%
- Cancer Research top 2%
- Carcinogens and Genotoxicity Assessment
Papers in
-
- DNA Repair Mechanisms 21
- Genetics 39
- Genomic variations and chromosomal abnormalities 12
- Genetics and Neurodevelopmental Disorders 11
- Genetic Syndromes and Imprinting 7
- Co-authors
- Karl Sperling (13 shared papers)Raymonda Varon (9 shared papers)Krystyńa Chrzańowska (8 shared papers)Martin Digweed (8 shared papers)André Reis (6 shared papers)Corry M.R. Weemaes (2 shared papers)Markus Stümm (2 shared papers)Kathrin Saar (2 shared papers)
- Journals
- Human Genetics (7 papers)European Journal of Human Genetics (5 papers)Journal of Inherited Metabolic Disease (2 papers)Cytogenetic and Genome Research (2 papers)Scientific Reports (1 paper)
- Partner nations
- CzechiaGermanyUnited States
In The Last Decade
E Seemanová
88 papers receiving 3.3k citations
E Seemanová's Hit Papers
Peers
Comparison fields: 5 of 111
- Developmental Biology 120
- Cancer Research 677
- Genetics 1.1k
- Molecular Biology 2.4k
- Oncology 575
Countries citing papers authored by E Seemanová
This map shows the geographic impact of E Seemanová'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 E Seemanová with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites E Seemanová more than expected).
Fields of papers citing papers by E Seemanová
This network shows the impact of papers produced by E Seemanová. 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 E Seemanová. The network helps show where E Seemanová may publish in the future.
Co-authors
The 25 scholars most cited alongside E Seemanová, 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 92 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome Hit paper breakdown → | 1998 | 811 |
| 2 | 2007 | 201 | |
| 3 | 1998 | 140 | |
| 4 | 1992 | 133 | |
| 5 | 2000 | 129 | |
| 6 | 2000 | 101 | |
| 7 | 2001 | 94 | |
| 8 | Nonsyndromic cleft lip with or without cleft palate: evidence of linkage to BCL3 in 17 multigenerational families. | 1995 | 87 |
| 9 | 1994 | 86 | |
| 10 | The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21. | 1997 | 85 |
| 11 | 2005 | 83 | |
| 12 | 1985 | 81 | |
| 13 | 1971 | 79 | |
| 14 | 2003 | 68 | |
| 15 | 1989 | 67 | |
| 16 | 2007 | 66 | |
| 17 | 1990 | 63 | |
| 18 | 2004 | 61 | |
| 19 | 2006 | 51 | |
| 20 | 2004 | 48 |
About E Seemanová
E Seemanová is a scholar working on Molecular Biology, Genetics, Cancer Research, Oncology and Plant Science, having authored 92 papers that have together received 3.4k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (21 papers), Carcinogens and Genotoxicity Assessment (18 papers), Genomic variations and chromosomal abnormalities (12 papers), Genetics and Neurodevelopmental Disorders (11 papers), Cancer-related Molecular Pathways (8 papers), Genetic Syndromes and Imprinting (7 papers), Metabolism and Genetic Disorders (7 papers) and Plant Genetic and Mutation Studies (6 papers). The work is most often cited by research in Developmental Biology (120 citations), Cancer Research (677 citations), Genetics (1.1k citations), Molecular Biology (2.4k citations) and Oncology (575 citations). E Seemanová has collaborated with scholars based in Czechia, Germany and United States. Frequent co-authors include Karl Sperling, Raymonda Varon, Krystyńa Chrzańowska, Martin Digweed, André Reis, Corry M.R. Weemaes, Markus Stümm, Kathrin Saar, Patrick Concannon and Karen Cerosaletti. Their work appears in journals such as Human Genetics, European Journal of Human Genetics, Journal of Inherited Metabolic Disease, Cytogenetic and Genome Research and Scientific Reports.
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.