Mark Seielstad
Impact in
- Genetics top 0.5%
- Forensic and Genetic Research
- Genetic diversity and population structure
- Genetic Associations and Epidemiology
- Genetic and phenotypic traits in livestock
- Genetic Mapping and Diversity in Plants and Animals
- Race, Genetics, and Society
- Statistics and Probability top 2%
- Markov Chains and Monte Carlo Methods
Papers in
- Genetics 36
- Genetic Associations and Epidemiology 15
- Forensic and Genetic Research 14
- Genetic diversity and population structure 11
- Genomic variations and chromosomal abnormalities 6
- Genomics and Rare Diseases 5
- Race, Genetics, and Society 5
- Co-authors
- Kristin Ardlie (2 shared papers)Leonid Kruglyak (1 shared paper)Anna Pérez-Lezaun (2 shared papers)M.W. Feldman (1 shared paper)Jonathan K. Pritchard (1 shared paper)Eric Minch (1 shared paper)L. Luca Cavalli-Sforza (1 shared paper)Xueling Sim (10 shared papers)
- Journals
- The American Journal of Human Genetics (6 papers)PLoS ONE (4 papers)Genes and Immunity (4 papers)Human Molecular Genetics (3 papers)Ophthalmology (2 papers)
- Partner nations
- United StatesSingaporeUnited Kingdom
In The Last Decade
Mark Seielstad
69 papers receiving 5.8k citations
Mark Seielstad's Hit Papers
Peers
Comparison fields: 5 of 170
- Genetics 2.8k
- Statistics and Probability 257
- Infectious Diseases 499
- Immunology 521
- Rheumatology 296
Countries citing papers authored by Mark Seielstad
This map shows the geographic impact of Mark Seielstad'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 Mark Seielstad with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark Seielstad more than expected).
Fields of papers citing papers by Mark Seielstad
This network shows the impact of papers produced by Mark Seielstad. 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 Mark Seielstad. The network helps show where Mark Seielstad may publish in the future.
Co-authors
The 25 scholars most cited alongside Mark Seielstad, 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 69 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Patterns of linkage disequilibrium in the human genome Hit paper breakdown → | 2002 | 859 |
| 2 | Population growth of human Y chromosomes: a study of Y chromosome microsatellites Hit paper breakdown → | 1999 | 695 |
| 3 | 1998 | 453 | |
| 4 | 2000 | 363 | |
| 5 | 2009 | 218 | |
| 6 | 2008 | 206 | |
| 7 | 2000 | 204 | |
| 8 | 2010 | 199 | |
| 9 | 2007 | 187 | |
| 10 | 2012 | 177 | |
| 11 | 2002 | 175 | |
| 12 | 2008 | 132 | |
| 13 | 2009 | 122 | |
| 14 | 2010 | 112 | |
| 15 | 2008 | 108 | |
| 16 | 2011 | 107 | |
| 17 | 2008 | 100 | |
| 18 | 2011 | 96 | |
| 19 | 2010 | 93 | |
| 20 | 2012 | 80 |
About Mark Seielstad
Mark Seielstad is a scholar working on Genetics, Molecular Biology, Epidemiology, Infectious Diseases and Immunology, having authored 69 papers that have together received 5.9k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (15 papers), Forensic and Genetic Research (14 papers), Genetic diversity and population structure (11 papers), Tuberculosis Research and Epidemiology (7 papers), Genomic variations and chromosomal abnormalities (6 papers), Mycobacterium research and diagnosis (5 papers), Genomics and Rare Diseases (5 papers) and Race, Genetics, and Society (5 papers). The work is most often cited by research in Genetics (2.8k citations), Statistics and Probability (257 citations), Infectious Diseases (499 citations), Immunology (521 citations) and Rheumatology (296 citations). Mark Seielstad has collaborated with scholars based in United States, Singapore and United Kingdom. Frequent co-authors include Kristin Ardlie, Leonid Kruglyak, Anna Pérez-Lezaun, M.W. Feldman, Jonathan K. Pritchard, Eric Minch, L. Luca Cavalli-Sforza, Xueling Sim, Kathryn L. Lunetta and Martin L. Hibberd. Their work appears in journals such as The American Journal of Human Genetics, PLoS ONE, Genes and Immunity, Human Molecular Genetics and Ophthalmology.
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.