Denise E. Mauldin
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
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- Cancer Genomics and Diagnostics
Papers in
- Genetics 7
- Genomics and Rare Diseases 4
- Genetic Associations and Epidemiology 3
- Genetic Mapping and Diversity in Plants and Animals 2
- Genomic variations and chromosomal abnormalities 2
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- Genomics and Phylogenetic Studies 3
- Co-authors
- Leroy Hood (6 shared papers)Gustavo Glusman (6 shared papers)Jared C. Roach (5 shared papers)Robert M. Hubley (2 shared papers)David J. Galas (2 shared papers)Stephen L. Guthery (1 shared paper)Katherine S. Pollard (1 shared paper)Hong Li (1 shared paper)
- Journals
- Frontiers in Genetics (2 papers)Proceedings of the National Academy of Sciences (2 papers)Bioinformatics (1 paper)The Prostate (1 paper)The American Journal of Human Genetics (1 paper)
- Partner nations
- United StatesLuxembourgCanada
In The Last Decade
Denise E. Mauldin
10 papers receiving 923 citations
Denise E. Mauldin's Hit Papers
Peers
Comparison fields: 5 of 114
- Genetics 337
- Cancer Research 108
- Biological Psychiatry 15
- Molecular Biology 415
- Psychiatry and Mental health 52
Countries citing papers authored by Denise E. Mauldin
This map shows the geographic impact of Denise E. Mauldin'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 Denise E. Mauldin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Denise E. Mauldin more than expected).
Fields of papers citing papers by Denise E. Mauldin
This network shows the impact of papers produced by Denise E. Mauldin. 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 Denise E. Mauldin. The network helps show where Denise E. Mauldin may publish in the future.
Co-authors
The 25 scholars most cited alongside Denise E. Mauldin, 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 | An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge Hit paper breakdown → | 2014 | 406 |
| 2 | 2011 | 180 | |
| 3 | 2015 | 139 | |
| 4 | 2014 | 58 | |
| 5 | 2019 | 56 | |
| 6 | 2011 | 49 | |
| 7 | 2015 | 16 | |
| 8 | 2007 | 16 | |
| 9 | 2016 | 14 | |
| 10 | 2017 | 9 |
About Denise E. Mauldin
Denise E. Mauldin is a scholar working on Genetics, Molecular Biology, Cancer Research, Nutrition and Dietetics and Endocrinology, Diabetes and Metabolism, having authored 10 papers that have together received 943 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (4 papers), Genomics and Phylogenetic Studies (3 papers), Genetic Associations and Epidemiology (3 papers), Genetic Mapping and Diversity in Plants and Animals (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Cancer Genomics and Diagnostics (1 paper), interferon and immune responses (1 paper) and Preterm Birth and Chorioamnionitis (1 paper). The work is most often cited by research in Genetics (337 citations), Cancer Research (108 citations), Biological Psychiatry (15 citations), Molecular Biology (415 citations) and Psychiatry and Mental health (52 citations). Denise E. Mauldin has collaborated with scholars based in United States, Luxembourg and Canada. Frequent co-authors include Leroy Hood, Gustavo Glusman, Jared C. Roach, Robert M. Hubley, David J. Galas, Stephen L. Guthery, Katherine S. Pollard, Hong Li, N.A. Shankaracharya and Max Robinson. Their work appears in journals such as Frontiers in Genetics, Proceedings of the National Academy of Sciences, Bioinformatics, The Prostate and The American Journal of Human 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.