Devin McQuaid
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Glioma Diagnosis and Treatment
- Cognitive Neuroscience top 10%
- Autism Spectrum Disorder Research
Papers in
- Genetics 8
- Genomic variations and chromosomal abnormalities 7
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- Gene expression and cancer classification 2
- Chromatin Remodeling and Cancer 2
- Genomics and Chromatin Dynamics 2
- DNA Repair Mechanisms 1
- Co-authors
- Norma J. Nowak (12 shared papers)Jeffrey M. Conroy (10 shared papers)John K. Cowell (5 shared papers)Samer Karamohamed (1 shared paper)Edwin H. Cook (1 shared paper)T. Conrad Gilliam (1 shared paper)Jyotsna Sudi (1 shared paper)Ravinesh A. Kumar (1 shared paper)
- Journals
- Genes Chromosomes and Cancer (2 papers)British Journal of Cancer (2 papers)Biological Psychiatry (1 paper)Molecular Cancer Therapeutics (1 paper)Birth Defects Research Part A Clinical and Molecular Teratology (1 paper)
- Partner nations
- United StatesCanadaGreece
In The Last Decade
Devin McQuaid
12 papers receiving 577 citations
Peers
Comparison fields: 5 of 62
- Genetics 321
- Cognitive Neuroscience 139
- Cancer Research 94
- Genetics 52
- Molecular Biology 289
Countries citing papers authored by Devin McQuaid
This map shows the geographic impact of Devin McQuaid'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 Devin McQuaid with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Devin McQuaid more than expected).
Fields of papers citing papers by Devin McQuaid
This network shows the impact of papers produced by Devin McQuaid. 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 Devin McQuaid. The network helps show where Devin McQuaid may publish in the future.
Co-authors
The 25 scholars most cited alongside Devin McQuaid, 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 | 2008 | 241 | |
| 2 | 2005 | 97 | |
| 3 | 2004 | 55 | |
| 4 | 2005 | 51 | |
| 5 | 2005 | 34 | |
| 6 | 2005 | 32 | |
| 7 | 2004 | 31 | |
| 8 | 2005 | 23 | |
| 9 | 2004 | 17 | |
| 10 | 2007 | 11 | |
| 11 | 2006 | 7 | |
| 12 | 2007 | 2 |
About Devin McQuaid
Devin McQuaid is a scholar working on Genetics, Molecular Biology, Cancer Research, Pediatrics, Perinatology and Child Health and Plant Science, having authored 12 papers that have together received 601 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Cancer Genomics and Diagnostics (3 papers), Gene expression and cancer classification (2 papers), Chromosomal and Genetic Variations (2 papers), Chromatin Remodeling and Cancer (2 papers), Genomics and Chromatin Dynamics (2 papers), Prenatal Screening and Diagnostics (2 papers) and DNA Repair Mechanisms (1 paper). The work is most often cited by research in Genetics (321 citations), Cognitive Neuroscience (139 citations), Cancer Research (94 citations), Genetics (52 citations) and Molecular Biology (289 citations). Devin McQuaid has collaborated with scholars based in United States, Canada and Greece. Frequent co-authors include Norma J. Nowak, Jeffrey M. Conroy, John K. Cowell, Samer Karamohamed, Edwin H. Cook, T. Conrad Gilliam, Jyotsna Sudi, Ravinesh A. Kumar, Susan L. Christian and Elliot S. Gershon. Their work appears in journals such as Genes Chromosomes and Cancer, British Journal of Cancer, Biological Psychiatry, Molecular Cancer Therapeutics and Birth Defects Research Part A Clinical and Molecular Teratology.
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.