Mads Bak
Impact in
- Cancer Research top 1%
- MicroRNA in disease regulation
- Cancer-related molecular mechanisms research
- Spectroscopy top 0.2%
- Advanced NMR Techniques and Applications
Papers in
- Genetics 36
- Genomic variations and chromosomal abnormalities 24
- Genetics and Neurodevelopmental Disorders 10
- Genomics and Rare Diseases 8
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- MicroRNA in disease regulation 10
- Co-authors
- Niels Chr. Nielsen (14 shared papers)Niels Tommerup (45 shared papers)Sakari Kauppinen (8 shared papers)Asli Silahtaroglu (7 shared papers)Mette Christensen (3 shared papers)Lorenzo F. Sempere (3 shared papers)Kristian Helin (4 shared papers)Juri Rappsilber (3 shared papers)
- Journals
- European Journal of Human Genetics (7 papers)Journal of Magnetic Resonance (6 papers)Clinical Genetics (5 papers)PLoS Genetics (3 papers)Human Mutation (3 papers)
- Partner nations
- DenmarkUnited StatesGermany
In The Last Decade
Mads Bak
92 papers receiving 8.8k citations
Mads Bak's Hit Papers
Peers
Comparison fields: 5 of 175
- Cancer Research 2.1k
- Spectroscopy 2.5k
- Nuclear and High Energy Physics 1.0k
- Molecular Biology 4.1k
- Biophysics 289
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 98 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 | 1554 |
| 2 | SIMPSON: A general simulation program for solid-state NMR spectroscopy Hit paper breakdown → | 2011 | 811 |
| 3 | Ancient human genome sequence of an extinct Palaeo-Eskimo Hit paper breakdown → | 2010 | 607 |
| 4 | 2007 | 583 | |
| 5 | 2007 | 503 | |
| 6 | 2010 | 463 | |
| 7 | 2011 | 429 | |
| 8 | 2008 | 411 | |
| 9 | 2010 | 345 | |
| 10 | 1997 | 338 | |
| 11 | 2014 | 282 | |
| 12 | 2010 | 184 | |
| 13 | Genetic analysis of human esophageal tumors from two high incidence geographic areas: frequent p53 base substitutions and absence of ras mutations. | 1991 | 177 |
| 14 | 2011 | 164 | |
| 15 | 2009 | 155 | |
| 16 | 2012 | 133 | |
| 17 | 2011 | 120 | |
| 18 | 2001 | 106 | |
| 19 | 2002 | 100 | |
| 20 | 2013 | 84 |
About Mads Bak
Mads Bak is a scholar working on Genetics, Cancer Research, Molecular Biology, Spectroscopy and Pediatrics, Perinatology and Child Health, having authored 98 papers that have together received 9.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (24 papers), Chromosomal and Genetic Variations (15 papers), Advanced NMR Techniques and Applications (13 papers), Genetics and Neurodevelopmental Disorders (10 papers), MicroRNA in disease regulation (10 papers), Prenatal Screening and Diagnostics (9 papers), Genomics and Rare Diseases (8 papers) and Solid-state spectroscopy and crystallography (8 papers). The work is most often cited by research in Cancer Research (2.1k citations), Spectroscopy (2.5k citations), Nuclear and High Energy Physics (1.0k citations), Molecular Biology (4.1k citations) and Biophysics (289 citations). Mads Bak has collaborated with scholars based in Denmark, United States and Germany. Frequent co-authors include Niels Chr. Nielsen, Niels Tommerup, Sakari Kauppinen, Asli Silahtaroglu, Mette Christensen, Lorenzo F. Sempere, Kristian Helin, Juri Rappsilber, Charles N. Cole and Jens Vilstrup Johansen. Their work appears in journals such as European Journal of Human Genetics, Journal of Magnetic Resonance, Clinical Genetics, PLoS Genetics and Human Mutation.
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.