Mads Bak
Impact in
- Spectroscopy top 0.2%
- Advanced NMR Techniques and Applications
- Cancer Research top 0.5%
- MicroRNA in disease regulation
- Cancer-related molecular mechanisms research
Papers in
-
- Epigenetics and DNA Methylation 11
- Circular RNAs in diseases 7
- RNA regulation and disease 7
- Genetics 33
- Genomic variations and chromosomal abnormalities 20
- Genetics and Neurodevelopmental Disorders 13
- Co-authors
- Niels Chr. Nielsen (12 shared papers)Jan T. Rasmussen (1 shared paper)Niels Tommerup (47 shared papers)Sakari Kauppinen (9 shared papers)Asli Silahtaroglu (7 shared papers)Mette Christensen (3 shared papers)Lorenzo F. Sempere (4 shared papers)Kristian Helin (3 shared papers)
- Journals
- European Journal of Human Genetics (6 papers)Journal of Magnetic Resonance (5 papers)Molecular Cytogenetics (3 papers)Human Mutation (3 papers)Scientific Reports (2 papers)
- Partner nations
- DenmarkUnited StatesGermany
In The Last Decade
Mads Bak
83 papers receiving 7.3k citations
Mads Bak's Hit Papers
Peers
Comparison fields: 5 of 150
- Spectroscopy 2.4k
- Cancer Research 2.2k
- Nuclear and High Energy Physics 957
- Molecular Biology 3.8k
- Biophysics 280
Countries citing papers authored by Mads Bak
This map shows the geographic impact of Mads Bak'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 Mads Bak with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mads Bak more than expected).
Fields of papers citing papers by Mads Bak
This network shows the impact of papers produced by Mads Bak. 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 Mads Bak. The network helps show where Mads Bak may publish in the future.
Co-authors
The 25 scholars most cited alongside Mads Bak, 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 84 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | SIMPSON: A General Simulation Program for Solid-State NMR Spectroscopy Hit paper breakdown → | 2000 | 1475 |
| 2 | SIMPSON: A general simulation program for solid-state NMR spectroscopy Hit paper breakdown → | 2011 | 770 |
| 3 | Antagonism of microRNA-122 in mice by systemically administered LNA-antimiR leads to up-regulation of a large set of predicted target mRNAs in the liver Hit paper breakdown → | 2007 | 543 |
| 4 | 2007 | 473 | |
| 5 | 2010 | 443 | |
| 6 | 2011 | 411 | |
| 7 | 2008 | 396 | |
| 8 | 2010 | 328 | |
| 9 | 1997 | 321 | |
| 10 | Genetic analysis of human esophageal tumors from two high incidence geographic areas: frequent p53 base substitutions and absence of ras mutations. | 1991 | 173 |
| 11 | 2010 | 172 | |
| 12 | 2011 | 156 | |
| 13 | 2009 | 151 | |
| 14 | 2012 | 126 | |
| 15 | 2001 | 104 | |
| 16 | 2002 | 91 | |
| 17 | 2013 | 73 | |
| 18 | 2015 | 72 | |
| 19 | 2011 | 68 | |
| 20 | 2017 | 68 |
About Mads Bak
Mads Bak is a scholar working on Molecular Biology, Genetics, Cancer Research, Plant Science and Spectroscopy, having authored 84 papers that have together received 7.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (20 papers), Chromosomal and Genetic Variations (14 papers), Genetics and Neurodevelopmental Disorders (13 papers), Advanced NMR Techniques and Applications (12 papers), MicroRNA in disease regulation (11 papers), Epigenetics and DNA Methylation (11 papers), Circular RNAs in diseases (7 papers) and RNA regulation and disease (7 papers). The work is most often cited by research in Spectroscopy (2.4k citations), Cancer Research (2.2k citations), Nuclear and High Energy Physics (957 citations), Molecular Biology (3.8k citations) and Biophysics (280 citations). Mads Bak has collaborated with scholars based in Denmark, United States and Germany. Frequent co-authors include Niels Chr. Nielsen, Jan T. Rasmussen, Niels Tommerup, Sakari Kauppinen, Asli Silahtaroglu, Mette Christensen, Lorenzo F. Sempere, Kristian Helin, Juri Rappsilber and Jens Vilstrup Johansen. Their work appears in journals such as European Journal of Human Genetics, Journal of Magnetic Resonance, Molecular Cytogenetics, Human Mutation and Scientific Reports.
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.