Ines Hellmann
Impact in
- Genetics top 0.5%
- Genetic diversity and population structure
- Molecular Biology top 2%
- Epigenetics and DNA Methylation
- Genomics and Phylogenetic Studies
- Genomics and Chromatin Dynamics
- RNA modifications and cancer
- Single-cell and spatial transcriptomics
Papers in
- Genetics 15
- Evolution and Genetic Dynamics 6
- Genetic diversity and population structure 4
- Genetics and Neurodevelopmental Disorders 3
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- Single-cell and spatial transcriptomics 10
- Genomics and Phylogenetic Studies 7
- Genomics and Chromatin Dynamics 4
- CRISPR and Genetic Engineering 3
- Co-authors
- Svante Pääbo (7 shared papers)Wolfgang Enard (17 shared papers)Michael Rebhan (1 shared paper)Dirk Schübeler (1 shared paper)Michael Beda Stadler (1 shared paper)Michael H. Weber (1 shared paper)Liliana Ramos (1 shared paper)Beate Vieth (10 shared papers)
- Journals
- Nature (4 papers)Bioinformatics (3 papers)Nature Genetics (2 papers)PLoS Genetics (2 papers)Genome biology (2 papers)
- Partner nations
- GermanyUnited StatesDenmark
In The Last Decade
Ines Hellmann
37 papers receiving 8.0k citations
Ines Hellmann's Hit Papers
Peers
Comparison fields: 5 of 171
- Genetics 3.1k
- Molecular Biology 4.5k
- Paleontology 438
- Anthropology 546
- Archeology 506
Countries citing papers authored by Ines Hellmann
This map shows the geographic impact of Ines Hellmann'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 Ines Hellmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ines Hellmann more than expected).
Fields of papers citing papers by Ines Hellmann
This network shows the impact of papers produced by Ines Hellmann. 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 Ines Hellmann. The network helps show where Ines Hellmann may publish in the future.
Co-authors
The 25 scholars most cited alongside Ines Hellmann, 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 38 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome Hit paper breakdown → | 2007 | 1731 |
| 2 | The complete genome sequence of a Neanderthal from the Altai Mountains Hit paper breakdown → | 2013 | 1499 |
| 3 | The diploid genome sequence of an Asian individual Hit paper breakdown → | 2008 | 698 |
| 4 | 2005 | 468 | |
| 5 | 2012 | 381 | |
| 6 | 2007 | 377 | |
| 7 | 2009 | 318 | |
| 8 | 2013 | 288 | |
| 9 | 2004 | 271 | |
| 10 | 2018 | 240 | |
| 11 | 2003 | 216 | |
| 12 | 2016 | 216 | |
| 13 | 2016 | 184 | |
| 14 | 2019 | 171 | |
| 15 | 2018 | 171 | |
| 16 | 2004 | 158 | |
| 17 | 2011 | 111 | |
| 18 | 2017 | 101 | |
| 19 | 2015 | 93 | |
| 20 | 2018 | 70 |
About Ines Hellmann
Ines Hellmann is a scholar working on Genetics, Molecular Biology, Cancer Research, Plant Science and Cultural Studies, having authored 38 papers that have together received 8.2k indexed citations. Recurring topics across this work include Single-cell and spatial transcriptomics (10 papers), Chromosomal and Genetic Variations (8 papers), Genomics and Phylogenetic Studies (7 papers), Evolution and Genetic Dynamics (6 papers), Genomics and Chromatin Dynamics (4 papers), Genetic diversity and population structure (4 papers), CRISPR and Genetic Engineering (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). The work is most often cited by research in Genetics (3.1k citations), Molecular Biology (4.5k citations), Paleontology (438 citations), Anthropology (546 citations) and Archeology (506 citations). Ines Hellmann has collaborated with scholars based in Germany, United States and Denmark. Frequent co-authors include Svante Pääbo, Wolfgang Enard, Michael Rebhan, Dirk Schübeler, Michael Beda Stadler, Michael H. Weber, Liliana Ramos, Beate Vieth, Christoph Ziegenhain and Swati Parekh. Their work appears in journals such as Nature, Bioinformatics, Nature Genetics, PLoS Genetics and Genome biology.
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.