Jochen Hecht
Impact in
- Developmental Biology top 1%
- Genetics top 1%
- Genomics and Rare Diseases
- Connective tissue disorders research
Papers in
- Genetics 29
- Genomics and Rare Diseases 14
- Connective tissue disorders research 6
- Genetics and Neurodevelopmental Disorders 4
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- Congenital limb and hand anomalies 10
- Co-authors
- Stefan Mundlos (30 shared papers)Peter Michael Krawitz (19 shared papers)Peter N. Robinson (26 shared papers)Verena Heinrich (6 shared papers)Christian Haass (1 shared paper)Alexander Hruscha (1 shared paper)Bettina Schmid (1 shared paper)Sigmar Stricker (9 shared papers)
- Journals
- The American Journal of Human Genetics (8 papers)Blood (5 papers)BMC Genomics (5 papers)Nature Communications (3 papers)Journal of Clinical Investigation (3 papers)
- Partner nations
- GermanySpainUnited States
In The Last Decade
Jochen Hecht
93 papers receiving 7.6k citations
Jochen Hecht's Hit Papers
Peers
Comparison fields: 5 of 151
- Developmental Biology 209
- Genetics 1.7k
- Molecular Biology 3.2k
- Clinical Biochemistry 146
- Infectious Diseases 481
Countries citing papers authored by Jochen Hecht
This map shows the geographic impact of Jochen Hecht'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 Jochen Hecht with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jochen Hecht more than expected).
Fields of papers citing papers by Jochen Hecht
This network shows the impact of papers produced by Jochen Hecht. 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 Jochen Hecht. The network helps show where Jochen Hecht may publish in the future.
Co-authors
The 25 scholars most cited alongside Jochen Hecht, 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 95 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 | 1501 |
| 2 | 2013 | 420 | |
| 3 | 2014 | 348 | |
| 4 | 2020 | 290 | |
| 5 | A global metagenomic map of urban microbiomes and antimicrobial resistance Hit paper breakdown → | 2021 | 268 |
| 6 | 2018 | 259 | |
| 7 | 2010 | 254 | |
| 8 | 2013 | 243 | |
| 9 | 2014 | 199 | |
| 10 | 2020 | 192 | |
| 11 | 2013 | 181 | |
| 12 | 2013 | 171 | |
| 13 | 2015 | 134 | |
| 14 | 2012 | 126 | |
| 15 | 2018 | 123 | |
| 16 | 2013 | 119 | |
| 17 | 2012 | 114 | |
| 18 | 2014 | 101 | |
| 19 | 2013 | 96 | |
| 20 | 2014 | 94 |
About Jochen Hecht
Jochen Hecht is a scholar working on Genetics, Developmental Biology, Molecular Biology, Immunology and Periodontics, having authored 95 papers that have together received 7.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (14 papers), Genomics and Phylogenetic Studies (11 papers), Congenital limb and hand anomalies (10 papers), Genomics and Chromatin Dynamics (10 papers), Developmental Biology and Gene Regulation (8 papers), Connective tissue disorders research (6 papers), Acute Lymphoblastic Leukemia research (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). The work is most often cited by research in Developmental Biology (209 citations), Genetics (1.7k citations), Molecular Biology (3.2k citations), Clinical Biochemistry (146 citations) and Infectious Diseases (481 citations). Jochen Hecht has collaborated with scholars based in Germany, Spain and United States. Frequent co-authors include Stefan Mundlos, Peter Michael Krawitz, Peter N. Robinson, Verena Heinrich, Christian Haass, Alexander Hruscha, Bettina Schmid, Sigmar Stricker, Ulrike Krüger and Richard Reinhardt. Their work appears in journals such as The American Journal of Human Genetics, Blood, BMC Genomics, Nature Communications and Journal of Clinical Investigation.
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.