Lukas Soellner
Impact in
- Genetics top 5%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 20
- Genetic Syndromes and Imprinting 19
- Genomic variations and chromosomal abnormalities 2
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- Epigenetics and DNA Methylation 8
- Renal and related cancers 2
- Co-authors
- Thomas Eggermann (22 shared papers)Matthias Begemann (18 shared papers)Karin Buiting (3 shared papers)Dieter Kotzot (1 shared paper)Gerhard Binder (3 shared papers)Elisa Wirthgen (1 shared paper)Birgit Zirn (1 shared paper)Wilbert van Workum (1 shared paper)
In The Last Decade
Lukas Soellner
22 papers receiving 589 citations
Peers
Comparison fields: 5 of 46
- Genetics 434
- Pediatrics, Perinatology and Child Health 263
- Endocrinology, Diabetes and Metabolism 65
- Molecular Biology 273
- Obstetrics and Gynecology 22
Countries citing papers authored by Lukas Soellner
This map shows the geographic impact of Lukas Soellner'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 Lukas Soellner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lukas Soellner more than expected).
Fields of papers citing papers by Lukas Soellner
This network shows the impact of papers produced by Lukas Soellner. 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 Lukas Soellner. The network helps show where Lukas Soellner may publish in the future.
Co-authors
The 25 scholars most cited alongside Lukas Soellner, 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 22 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 148 | |
| 2 | 2016 | 85 | |
| 3 | 2014 | 80 | |
| 4 | 2016 | 44 | |
| 5 | 2014 | 36 | |
| 6 | 2017 | 35 | |
| 7 | 2012 | 33 | |
| 8 | 2015 | 27 | |
| 9 | 2012 | 23 | |
| 10 | 2017 | 21 | |
| 11 | 2016 | 17 | |
| 12 | 2015 | 11 | |
| 13 | 2018 | 10 | |
| 14 | 2015 | 10 | |
| 15 | 2017 | 9 | |
| 16 | 2015 | 7 | |
| 17 | 2015 | 7 | |
| 18 | 2013 | 5 | |
| 19 | 2013 | 4 | |
| 20 | 2018 | 2 |
About Lukas Soellner
Lukas Soellner is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Pathology and Forensic Medicine and Public Health, Environmental and Occupational Health, having authored 22 papers that have together received 616 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (19 papers), Prenatal Screening and Diagnostics (11 papers), Epigenetics and DNA Methylation (8 papers), Tumors and Oncological Cases (4 papers), Gestational Trophoblastic Disease Studies (3 papers), Renal and related cancers (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Gastrointestinal disorders and treatments (1 paper). The work is most often cited by research in Genetics (434 citations), Pediatrics, Perinatology and Child Health (263 citations), Endocrinology, Diabetes and Metabolism (65 citations), Molecular Biology (273 citations) and Obstetrics and Gynecology (22 citations). Lukas Soellner has collaborated with scholars based in Germany, Poland and Hungary. Frequent co-authors include Thomas Eggermann, Matthias Begemann, Karin Buiting, Dieter Kotzot, Gerhard Binder, Elisa Wirthgen, Birgit Zirn, Wilbert van Workum, Roland Schweizer and Gijs W.E. Santen. Their work appears in journals such as European Journal of Human Genetics, The Journal of Pediatrics, Clinical Genetics, European Journal of Medical Genetics and Journal of Perinatal Medicine.
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.