Marisa S. Bartolomei
- Molecular Biology top 0.2%
- Genetics top 0.05%
- Pediatrics, Perinatology and Child Health top 0.05%
- Public Health, Environmental and Occupational Health top 0.5%
- Cancer Research top 1%
- Co-authors
- Shirley M. TilghmanMellissa R.W. MannJoanne L. ThorvaldsenSharon ZemelRichard M. SchultzKimberly D. TremblayJeannie T. LeeDenise P. Barlow
- Topics
- Epigenetics and DNA Methylation (110 papers)Genetic Syndromes and Imprinting (96 papers)Prenatal Screening and Diagnostics (75 papers)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Marisa S. Bartolomei
179 papers receiving 16.2k citations
Hit Papers
Peers
Comparison fields: 5 of 155
- Molecular Biology 12.9k
- Genetics 7.8k
- Pediatrics, Perinatology and Child Health 5.4k
- Public Health, Environmental and Occupational Health 2.0k
- Cancer Research 1.7k
Countries citing papers authored by Marisa S. Bartolomei
This map shows the geographic impact of Marisa S. Bartolomei'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 Marisa S. Bartolomei with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marisa S. Bartolomei more than expected).
Fields of papers citing papers by Marisa S. Bartolomei
This network shows the impact of papers produced by Marisa S. Bartolomei. 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 Marisa S. Bartolomei. The network helps show where Marisa S. Bartolomei may publish in the future.
Co-authorship network of co-authors of Marisa S. Bartolomei
This figure shows the co-authorship network connecting the top 25 collaborators of Marisa S. Bartolomei. A scholar is included among the top collaborators of Marisa S. Bartolomei based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Marisa S. Bartolomei. Marisa S. Bartolomei is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 1 | |
| 3 | 1 | |
| 4 | 8 | |
| 5 | 22 | |
| 6 | 29 | |
| 7 | 23 | |
| 8 | 26 | |
| 9 | 156 | |
| 10 | 5 | |
| 11 | 49 | |
| 12 | Is ART changing the epigenetic landscape of imprinting | 7 |
| 13 | 58 | |
| 14 | 167 | |
| 15 | 35 | |
| 16 | 52 | |
| 17 | 23 | |
| 18 | 52 | |
| 19 | Insulin Resistance and a Diabetes Mellitus-Like Syndrome in Mice Lacking the Protein Kinase Akt2 (PKBβ)breakdown → | 1512 |
| 20 | 70 |
About Marisa S. Bartolomei
Marisa S. Bartolomei is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology, having authored 185 papers that have together received 16.5k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (110 papers), Genetic Syndromes and Imprinting (96 papers) and Prenatal Screening and Diagnostics (75 papers). The work is most often cited by research in Genetics (7.8k citations), Pediatrics, Perinatology and Child Health (5.4k citations) and Molecular Biology (12.9k citations). Marisa S. Bartolomei has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Shirley M. Tilghman, Mellissa R.W. Mann, Joanne L. Thorvaldsen, Sharon Zemel, Richard M. Schultz, Kimberly D. Tremblay, Jeannie T. Lee, Denise P. Barlow, Anne C. Ferguson‐Smith and Raluca Verona. Their work appears in journals such as Nature, Science and Cell.
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.