Nick Sampas
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Molecular Biology top 10%
- Genomics and Phylogenetic Studies
- Genomics and Chromatin Dynamics
- Gene expression and cancer classification
- Congenital heart defects research
Papers in
- Genetics 6
- Genomic variations and chromosomal abnormalities 6
- Genomics and Rare Diseases 4
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- Genomics and Phylogenetic Studies 2
- Gene expression and cancer classification 2
- Angiogenesis and VEGF in Cancer 1
- Co-authors
- Laurakay Bruhn (7 shared papers)Anya Tsalenko (6 shared papers)Peter Tsang (5 shared papers)Amir Ben‐Dor (4 shared papers)Zohar Yakhini (4 shared papers)Maika Malig (3 shared papers)Stephen Laderman (3 shared papers)Francesca Antonacci (2 shared papers)
- Journals
- The American Journal of Human Genetics (2 papers)Nature Methods (1 paper)Proceedings of the National Academy of Sciences (1 paper)Physiological Genomics (1 paper)Science (1 paper)
- Partner nations
- United StatesItalySouth Korea
In The Last Decade
Nick Sampas
8 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 94
- Genetics 910
- Molecular Biology 742
- Plant Science 355
- Cancer Research 121
- Pediatrics, Perinatology and Child Health 145
Countries citing papers authored by Nick Sampas
This map shows the geographic impact of Nick Sampas'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 Nick Sampas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nick Sampas more than expected).
Fields of papers citing papers by Nick Sampas
This network shows the impact of papers produced by Nick Sampas. 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 Nick Sampas. The network helps show where Nick Sampas may publish in the future.
Co-authors
The 25 scholars most cited alongside Nick Sampas, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 489 | |
| 2 | 2004 | 276 | |
| 3 | 2008 | 266 | |
| 4 | 2007 | 176 | |
| 5 | 2003 | 99 | |
| 6 | 2010 | 97 | |
| 7 | 2011 | 64 | |
| 8 | 2007 | 40 |
About Nick Sampas
Nick Sampas is a scholar working on Genetics, Molecular Biology, Plant Science, Pediatrics, Perinatology and Child Health and Immunology and Allergy, having authored 8 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (4 papers), Chromosomal and Genetic Variations (4 papers), Genomics and Phylogenetic Studies (2 papers), Gene expression and cancer classification (2 papers), Cell Adhesion Molecules Research (1 paper), Angiogenesis and VEGF in Cancer (1 paper) and Prenatal Screening and Diagnostics (1 paper). The work is most often cited by research in Genetics (910 citations), Molecular Biology (742 citations), Plant Science (355 citations), Cancer Research (121 citations) and Pediatrics, Perinatology and Child Health (145 citations). Nick Sampas has collaborated with scholars based in United States, Italy and South Korea. Frequent co-authors include Laurakay Bruhn, Anya Tsalenko, Peter Tsang, Amir Ben‐Dor, Zohar Yakhini, Maika Malig, Stephen Laderman, Francesca Antonacci, Can Alkan and Peter H. Sudmant. Their work appears in journals such as The American Journal of Human Genetics, Nature Methods, Proceedings of the National Academy of Sciences, Physiological Genomics and Science.
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.