Jacek Majewski
Impact in
- Genetics top 0.5%
- Genomics and Rare Diseases
- Connective tissue disorders research
- Molecular Biology top 1%
- RNA modifications and cancer
- RNA Research and Splicing
- RNA and protein synthesis mechanisms
- Mitochondrial Function and Pathology
- Epigenetics and DNA Methylation
Papers in
-
- RNA modifications and cancer 30
- RNA Research and Splicing 24
- RNA and protein synthesis mechanisms 21
- Mitochondrial Function and Pathology 19
- Epigenetics and DNA Methylation 16
- Genomics and Chromatin Dynamics 12
- Genetics 62
- Genomics and Rare Diseases 21
- Co-authors
- Jürg Ott (14 shared papers)Jeremy Schwartzentruber (51 shared papers)Frederick M. Cohan (4 shared papers)Kym M. Boycott (49 shared papers)Somayyeh Fahiminiya (32 shared papers)Jasmin Coulombe‐Huntington (5 shared papers)Nada Jabado (14 shared papers)Tomi Pastinen (4 shared papers)
- Journals
- The American Journal of Human Genetics (18 papers)Journal of Medical Genetics (15 papers)Clinical Genetics (11 papers)Human Mutation (9 papers)Human Molecular Genetics (7 papers)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Jacek Majewski
214 papers receiving 9.5k citations
Peers
Comparison fields: 5 of 142
- Genetics 2.7k
- Molecular Biology 5.6k
- Clinical Biochemistry 488
- Cancer Research 927
- Genetics 547
Countries citing papers authored by Jacek Majewski
This map shows the geographic impact of Jacek Majewski'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 Jacek Majewski with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jacek Majewski more than expected).
Fields of papers citing papers by Jacek Majewski
This network shows the impact of papers produced by Jacek Majewski. 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 Jacek Majewski. The network helps show where Jacek Majewski may publish in the future.
Co-authors
The 25 scholars most cited alongside Jacek Majewski, 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 217 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 404 | |
| 2 | 2011 | 246 | |
| 3 | 2002 | 246 | |
| 4 | 2008 | 233 | |
| 5 | 2014 | 214 | |
| 6 | 2013 | 164 | |
| 7 | 2010 | 162 | |
| 8 | 2016 | 154 | |
| 9 | 2003 | 153 | |
| 10 | 2015 | 151 | |
| 11 | 2014 | 149 | |
| 12 | 2018 | 146 | |
| 13 | 2000 | 145 | |
| 14 | 2012 | 132 | |
| 15 | 2013 | 132 | |
| 16 | 2005 | 126 | |
| 17 | 2014 | 123 | |
| 18 | 2006 | 120 | |
| 19 | 1999 | 116 | |
| 20 | 2015 | 105 |
About Jacek Majewski
Jacek Majewski is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Genetics and Immunology, having authored 217 papers that have together received 9.7k indexed citations. Recurring topics across this work include RNA modifications and cancer (30 papers), RNA Research and Splicing (24 papers), Genomics and Rare Diseases (21 papers), RNA and protein synthesis mechanisms (21 papers), Mitochondrial Function and Pathology (19 papers), Metabolism and Genetic Disorders (19 papers), Epigenetics and DNA Methylation (16 papers) and Genomics and Chromatin Dynamics (12 papers). The work is most often cited by research in Genetics (2.7k citations), Molecular Biology (5.6k citations), Clinical Biochemistry (488 citations), Cancer Research (927 citations) and Genetics (547 citations). Jacek Majewski has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Jürg Ott, Jeremy Schwartzentruber, Frederick M. Cohan, Kym M. Boycott, Somayyeh Fahiminiya, Jasmin Coulombe‐Huntington, Nada Jabado, Tomi Pastinen, Emilie Lalonde and Dennis E. Bulman. Their work appears in journals such as The American Journal of Human Genetics, Journal of Medical Genetics, Clinical Genetics, Human Mutation and Human Molecular Genetics.
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.