Wolfram Hoeps
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetic Mapping and Diversity in Plants and Animals
-
- Genomics and Phylogenetic Studies
- Genomics and Chromatin Dynamics
- RNA and protein synthesis mechanisms
- CRISPR and Genetic Engineering
Papers in
- Genetics 10
- Genomic variations and chromosomal abnormalities 7
- Genomics and Rare Diseases 5
-
- Genomics and Phylogenetic Studies 4
- RNA and protein synthesis mechanisms 3
- CRISPR and Genetic Engineering 2
- RNA modifications and cancer 1
- Co-authors
- David Porubskỳ (2 shared papers)Evan E. Eichler (2 shared papers)Tobias Marschall (2 shared papers)Ashley D. Sanders (2 shared papers)Jan O. Korbel (2 shared papers)Ludovica Mercuri (1 shared paper)Mario Ventura (1 shared paper)Stuart Cantsilieris (1 shared paper)
- Journals
- F1000Research (3 papers)Nature (2 papers)Science (1 paper)Nature Genetics (1 paper)Cell Genomics (1 paper)
- Partner nations
- United StatesGermanyUnited Kingdom
In The Last Decade
Wolfram Hoeps
14 papers receiving 713 citations
Wolfram Hoeps's Hit Papers
Peers
Comparison fields: 5 of 65
- Genetics 386
- Molecular Biology 410
- Plant Science 201
- Cancer Research 55
- Developmental Biology 3
Countries citing papers authored by Wolfram Hoeps
This map shows the geographic impact of Wolfram Hoeps'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 Wolfram Hoeps with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Wolfram Hoeps more than expected).
Fields of papers citing papers by Wolfram Hoeps
This network shows the impact of papers produced by Wolfram Hoeps. 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 Wolfram Hoeps. The network helps show where Wolfram Hoeps may publish in the future.
Co-authors
The 25 scholars most cited alongside Wolfram Hoeps, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Haplotype-resolved diverse human genomes and integrated analysis of structural variation Hit paper breakdown → | 2021 | 429 |
| 2 | 2022 | 90 | |
| 3 | 2023 | 61 | |
| 4 | 2020 | 43 | |
| 5 | 2025 | 27 | |
| 6 | 2023 | 21 | |
| 7 | 2025 | 16 | |
| 8 | 2024 | 12 | |
| 9 | 2018 | 9 | |
| 10 | 2024 | 6 | |
| 11 | 2022 | 3 | |
| 12 | 2024 | 2 | |
| 13 | 2025 | 1 | |
| 14 | 2026 | 1 |
About Wolfram Hoeps
Wolfram Hoeps is a scholar working on Genetics, Molecular Biology, Plant Science, Pathology and Forensic Medicine and Pediatrics, Perinatology and Child Health, having authored 14 papers that have together received 721 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (5 papers), Genomics and Rare Diseases (5 papers), Genomics and Phylogenetic Studies (4 papers), RNA and protein synthesis mechanisms (3 papers), CRISPR and Genetic Engineering (2 papers), Biomedical and Engineering Education (2 papers) and RNA modifications and cancer (1 paper). The work is most often cited by research in Genetics (386 citations), Molecular Biology (410 citations), Plant Science (201 citations), Cancer Research (55 citations) and Developmental Biology (3 citations). Wolfram Hoeps has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include David Porubskỳ, Evan E. Eichler, Tobias Marschall, Ashley D. Sanders, Jan O. Korbel, Ludovica Mercuri, Mario Ventura, Stuart Cantsilieris, Arvis Sulovari and Shwetha Canchi Murali. Their work appears in journals such as F1000Research, Nature, Science, Nature Genetics and Cell Genomics.
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.