Justin E. Paschall
Impact in
- Genetics top 0.2%
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetic Mapping and Diversity in Plants and Animals
- Cancer Research top 2%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 23
- Genomics and Rare Diseases 12
- Genetic Associations and Epidemiology 12
- Genomic variations and chromosomal abnormalities 9
- Genetic Syndromes and Imprinting 3
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- Genomics and Phylogenetic Studies 7
- Gene expression and cancer classification 6
- Bioinformatics and Genomic Networks 3
- Co-authors
- Elizabeth Wyn Pugh (2 shared papers)Kimberly Floy Doheny (3 shared papers)William K. Scott (1 shared paper)Albert Tenesa (1 shared paper)Cyrus P. Zabetian (1 shared paper)Haydeh Payami (1 shared paper)Denise M. Kay (1 shared paper)Jennifer S. Montimurro (1 shared paper)
- Journals
- Nature Genetics (5 papers)The American Journal of Human Genetics (3 papers)Genetic Epidemiology (3 papers)Proceedings of the National Academy of Sciences (2 papers)Genetics in Medicine (2 papers)
- Partner nations
- United StatesUnited KingdomChina
In The Last Decade
Justin E. Paschall
37 papers receiving 12.4k citations
Justin E. Paschall's Hit Papers
Peers
Comparison fields: 5 of 188
- Genetics 6.0k
- Cancer Research 1.2k
- Molecular Biology 5.4k
- Neurology 359
- Neurology 583
Countries citing papers authored by Justin E. Paschall
This map shows the geographic impact of Justin E. Paschall'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 Justin E. Paschall with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Justin E. Paschall more than expected).
Fields of papers citing papers by Justin E. Paschall
This network shows the impact of papers produced by Justin E. Paschall. 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 Justin E. Paschall. The network helps show where Justin E. Paschall may publish in the future.
Co-authors
The 25 scholars most cited alongside Justin E. Paschall, 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 38 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A map of human genome variation from population-scale sequencing Hit paper breakdown → | 2010 | 6317 |
| 2 | The NCBI dbGaP database of genotypes and phenotypes Hit paper breakdown → | 2007 | 896 |
| 3 | Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease Hit paper breakdown → | 2010 | 663 |
| 4 | Demographic history and rare allele sharing among human populations Hit paper breakdown → | 2011 | 475 |
| 5 | 2010 | 416 | |
| 6 | 2015 | 378 | |
| 7 | 2010 | 375 | |
| 8 | Open Targets: a platform for therapeutic target identification and validation Hit paper breakdown → | 2016 | 362 |
| 9 | 2011 | 352 | |
| 10 | International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases Hit paper breakdown → | 2017 | 314 |
| 11 | 2009 | 303 | |
| 12 | 2015 | 276 | |
| 13 | 2011 | 275 | |
| 14 | 2012 | 213 | |
| 15 | 2017 | 168 | |
| 16 | 2014 | 151 | |
| 17 | 2010 | 133 | |
| 18 | 2010 | 78 | |
| 19 | 2020 | 76 | |
| 20 | 2011 | 67 |
About Justin E. Paschall
Justin E. Paschall is a scholar working on Genetics, Molecular Biology, Cancer Research, Rheumatology and Immunology and Allergy, having authored 38 papers that have together received 12.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (12 papers), Genetic Associations and Epidemiology (12 papers), Genomic variations and chromosomal abnormalities (9 papers), Genomics and Phylogenetic Studies (7 papers), Gene expression and cancer classification (6 papers), Cancer Genomics and Diagnostics (3 papers), Genetic Syndromes and Imprinting (3 papers) and Bioinformatics and Genomic Networks (3 papers). The work is most often cited by research in Genetics (6.0k citations), Cancer Research (1.2k citations), Molecular Biology (5.4k citations), Neurology (359 citations) and Neurology (583 citations). Justin E. Paschall has collaborated with scholars based in United States, United Kingdom and China. Frequent co-authors include Elizabeth Wyn Pugh, Kimberly Floy Doheny, William K. Scott, Albert Tenesa, Cyrus P. Zabetian, Haydeh Payami, Denise M. Kay, Jennifer S. Montimurro, Alida Griffith and John W. Roberts. Their work appears in journals such as Nature Genetics, The American Journal of Human Genetics, Genetic Epidemiology, Proceedings of the National Academy of Sciences and Genetics in Medicine.
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.