Mark A. McElwain
Impact in
- Genetics top 10%
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Papers in
-
- Genomics and Phylogenetic Studies 2
- Gene expression and cancer classification 1
- Genetics 3
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 1
- Genomics and Rare Diseases 1
- Genetic Syndromes and Imprinting 1
- Co-authors
- Brock A. Peters (4 shared papers)Radoje Drmanac (3 shared papers)Arthur L. Beaudet (1 shared paper)Yaping Yang (1 shared paper)C. Thomas Caskey (1 shared paper)Christian P. Schaaf (1 shared paper)Lorraine Potocki (1 shared paper)Fan Xia (1 shared paper)
- Journals
- Blood (1 paper)Molecular Biology of the Cell (1 paper)Nature Genetics (1 paper)Genome Research (1 paper)PLoS ONE (1 paper)
- Partner nations
- United StatesChina
In The Last Decade
Mark A. McElwain
7 papers receiving 295 citations
Peers
Comparison fields: 5 of 43
- Genetics 179
- Aging 6
- Structural Biology 4
- Pediatrics, Perinatology and Child Health 44
- Molecular Biology 164
Countries citing papers authored by Mark A. McElwain
This map shows the geographic impact of Mark A. McElwain'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 A. McElwain with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark A. McElwain more than expected).
Fields of papers citing papers by Mark A. McElwain
This network shows the impact of papers produced by Mark A. McElwain. 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 A. McElwain. The network helps show where Mark A. McElwain may publish in the future.
Co-authors
The 25 scholars most cited alongside Mark A. McElwain, 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 | 2013 | 212 | |
| 2 | 2015 | 37 | |
| 3 | 2004 | 23 | |
| 4 | 2011 | 19 | |
| 5 | 2017 | 4 | |
| 6 | A Critical Review of Gene Prediction Software | 2007 | 3 |
| 7 | 2022 | 1 | |
| 8 | 2023 | 0 |
About Mark A. McElwain
Mark A. McElwain is a scholar working on Molecular Biology, Genetics, Cancer Research, Pediatrics, Perinatology and Child Health and Hematology, having authored 8 papers that have together received 299 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Cancer Genomics and Diagnostics (2 papers), Genomics and Phylogenetic Studies (2 papers), Acute Myeloid Leukemia Research (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Genomics and Rare Diseases (1 paper), Gene expression and cancer classification (1 paper) and Genetic Syndromes and Imprinting (1 paper). The work is most often cited by research in Genetics (179 citations), Aging (6 citations), Structural Biology (4 citations), Pediatrics, Perinatology and Child Health (44 citations) and Molecular Biology (164 citations). Mark A. McElwain has collaborated with scholars based in United States and China. Frequent co-authors include Brock A. Peters, Radoje Drmanac, Arthur L. Beaudet, Yaping Yang, C. Thomas Caskey, Christian P. Schaaf, Lorraine Potocki, Fan Xia, Manuel L. Gonzalez‐Garay and Karen W. Gripp. Their work appears in journals such as Blood, Molecular Biology of the Cell, Nature Genetics, Genome Research and PLoS ONE.
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.