Peter Michael Krawitz
Impact in
- Genetics top 1%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Health Informatics top 2%
Papers in
- Genetics 76
- Genomics and Rare Diseases 36
- Genomic variations and chromosomal abnormalities 19
- Genetics and Neurodevelopmental Disorders 17
- Genetic Associations and Epidemiology 15
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- RNA regulation and disease 8
- Genomics and Phylogenetic Studies 7
- Co-authors
- Peter N. Robinson (30 shared papers)Stefan Mundlos (25 shared papers)Jochen Hecht (19 shared papers)Denise Horn (10 shared papers)Verena Heinrich (8 shared papers)Bettina Schmid (2 shared papers)Christian Haass (2 shared papers)Sebastian Bauer (6 shared papers)
- Journals
- The American Journal of Human Genetics (16 papers)European Journal of Human Genetics (13 papers)Bioinformatics (7 papers)Human Mutation (6 papers)Genetics in Medicine (6 papers)
- Partner nations
- GermanyUnited StatesUnited Kingdom
In The Last Decade
Peter Michael Krawitz
161 papers receiving 7.8k citations
Peter Michael Krawitz's Hit Papers
Peers
Comparison fields: 5 of 171
- Genetics 2.4k
- Health Informatics 101
- Molecular Biology 4.2k
- Aging 66
- Developmental Biology 81
Countries citing papers authored by Peter Michael Krawitz
This map shows the geographic impact of Peter Michael Krawitz'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 Peter Michael Krawitz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Michael Krawitz more than expected).
Fields of papers citing papers by Peter Michael Krawitz
This network shows the impact of papers produced by Peter Michael Krawitz. 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 Peter Michael Krawitz. The network helps show where Peter Michael Krawitz may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter Michael Krawitz, 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 169 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Disruptions of Topological Chromatin Domains Cause Pathogenic Rewiring of Gene-Enhancer Interactions Hit paper breakdown → | 2015 | 1477 |
| 2 | Identifying facial phenotypes of genetic disorders using deep learning Hit paper breakdown → | 2018 | 526 |
| 3 | 2013 | 412 | |
| 4 | 2009 | 406 | |
| 5 | 2010 | 254 | |
| 6 | 2013 | 242 | |
| 7 | 2014 | 197 | |
| 8 | 2020 | 194 | |
| 9 | 2013 | 181 | |
| 10 | 2015 | 134 | |
| 11 | 2022 | 133 | |
| 12 | 2012 | 126 | |
| 13 | 2013 | 96 | |
| 14 | 2014 | 94 | |
| 15 | 2012 | 93 | |
| 16 | 2017 | 92 | |
| 17 | 2014 | 91 | |
| 18 | 2016 | 86 | |
| 19 | 2013 | 83 | |
| 20 | 2010 | 83 |
About Peter Michael Krawitz
Peter Michael Krawitz is a scholar working on Genetics, Molecular Biology, Physiology, Cell Biology and Immunology, having authored 169 papers that have together received 8.0k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (36 papers), Genomic variations and chromosomal abnormalities (19 papers), Genetics and Neurodevelopmental Disorders (17 papers), Genetic Associations and Epidemiology (15 papers), Cancer Genomics and Diagnostics (8 papers), Lysosomal Storage Disorders Research (8 papers), RNA regulation and disease (8 papers) and Genomics and Phylogenetic Studies (7 papers). The work is most often cited by research in Genetics (2.4k citations), Health Informatics (101 citations), Molecular Biology (4.2k citations), Aging (66 citations) and Developmental Biology (81 citations). Peter Michael Krawitz has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Peter N. Robinson, Stefan Mundlos, Jochen Hecht, Denise Horn, Verena Heinrich, Bettina Schmid, Christian Haass, Sebastian Bauer, Alexander Hruscha and Nicole Fleischer. Their work appears in journals such as The American Journal of Human Genetics, European Journal of Human Genetics, Bioinformatics, Human Mutation and Genetics in 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.