Julia Kolarova
Impact in
- Genetics top 10%
- Genetic Syndromes and Imprinting
- Chronic Lymphocytic Leukemia Research
- Pathology and Forensic Medicine top 10%
- Lymphoma Diagnosis and Treatment
Papers in
- Genetics 10
- Genetic Syndromes and Imprinting 9
- Chronic Lymphocytic Leukemia Research 3
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- Prenatal Screening and Diagnostics 4
- Co-authors
- Reiner Siebert (14 shared papers)Ole Ammerpohl (11 shared papers)Susanne Bens (8 shared papers)Almuth Caliebe (5 shared papers)Gabriele Gillessen‐Kaesbach (3 shared papers)Karin Buiting (3 shared papers)Jasmin Beygo (2 shared papers)Constantin von Kaisenberg (1 shared paper)
- Journals
- Epigenomics (2 papers)Epigenetics (2 papers)Leukemia (2 papers)PLoS ONE (2 papers)European Journal of Human Genetics (2 papers)
- Partner nations
- GermanySpainNetherlands
In The Last Decade
Julia Kolarova
26 papers receiving 1.1k citations
Julia Kolarova's Hit Papers
Peers
Comparison fields: 5 of 66
- Genetics 160
- Pathology and Forensic Medicine 190
- Epidemiology 274
- Pediatrics, Perinatology and Child Health 148
- Cancer Research 107
Countries citing papers authored by Julia Kolarova
This map shows the geographic impact of Julia Kolarova'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 Julia Kolarova with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Julia Kolarova more than expected).
Fields of papers citing papers by Julia Kolarova
This network shows the impact of papers produced by Julia Kolarova. 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 Julia Kolarova. The network helps show where Julia Kolarova may publish in the future.
Co-authors
The 25 scholars most cited alongside Julia Kolarova, 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 26 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | DNA Methylation Analysis in Nonalcoholic Fatty Liver Disease Suggests Distinct Disease-Specific and Remodeling Signatures after Bariatric Surgery Hit paper breakdown → | 2013 | 456 |
| 2 | 2014 | 123 | |
| 3 | 2018 | 121 | |
| 4 | 2015 | 117 | |
| 5 | 2018 | 53 | |
| 6 | 2012 | 29 | |
| 7 | 2018 | 29 | |
| 8 | 2015 | 26 | |
| 9 | 2016 | 25 | |
| 10 | 2016 | 21 | |
| 11 | 2016 | 20 | |
| 12 | 2012 | 16 | |
| 13 | 2015 | 13 | |
| 14 | 2022 | 11 | |
| 15 | 2014 | 10 | |
| 16 | 2020 | 10 | |
| 17 | 2017 | 9 | |
| 18 | 2015 | 8 | |
| 19 | 2016 | 7 | |
| 20 | 2025 | 4 |
About Julia Kolarova
Julia Kolarova is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Oncology, Molecular Biology and Pathology and Forensic Medicine, having authored 26 papers that have together received 1.1k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (12 papers), Genetic Syndromes and Imprinting (9 papers), RNA modifications and cancer (4 papers), Prenatal Screening and Diagnostics (4 papers), Lymphoma Diagnosis and Treatment (4 papers), Chronic Lymphocytic Leukemia Research (3 papers), Viral-associated cancers and disorders (3 papers) and Acute Myeloid Leukemia Research (2 papers). The work is most often cited by research in Genetics (160 citations), Pathology and Forensic Medicine (190 citations), Epidemiology (274 citations), Pediatrics, Perinatology and Child Health (148 citations) and Cancer Research (107 citations). Julia Kolarova has collaborated with scholars based in Germany, Spain and Netherlands. Frequent co-authors include Reiner Siebert, Ole Ammerpohl, Susanne Bens, Almuth Caliebe, Gabriele Gillessen‐Kaesbach, Karin Buiting, Jasmin Beygo, Constantin von Kaisenberg, Simone Heidemann and Bernhard Horsthemke. Their work appears in journals such as Epigenomics, Epigenetics, Leukemia, PLoS ONE and European Journal of Human Genetics.
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.