Stephanie Dallaire
- Genetics top 5%
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 1
- Genetic Associations and Epidemiology 1
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- Prenatal Screening and Diagnostics 2
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- Chromosomal and Genetic Variations 2
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- Single-cell and spatial transcriptomics 1
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- Viral Infections and Immunology Research 1
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- Acute Myeloid Leukemia Research 1
- Co-authors
- Charles LeeDavid AltshulerSteven A. McCarrollTracy N. HadnottMark J. DalyMichael C. ZodyStacey B. GabrielGeorge H. Perry
- Partner nations
- United StatesMexicoDenmark
In The Last Decade
Stephanie Dallaire
7 papers receiving 616 citations
Hit Papers
Peers
Comparison fields: 5 of 64
- Genetics 476
- Pediatrics, Perinatology and Child Health 96
- Cancer Research 69
- Plant Science 157
- Molecular Biology 274
Countries citing papers authored by Stephanie Dallaire
This map shows the geographic impact of Stephanie Dallaire'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 Stephanie Dallaire with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephanie Dallaire more than expected).
Fields of papers citing papers by Stephanie Dallaire
This network shows the impact of papers produced by Stephanie Dallaire. 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 Stephanie Dallaire. The network helps show where Stephanie Dallaire may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Stephanie Dallaire, 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 | 2019 | 4 | |
| 2 | 2019 | 23 | |
| 3 | 2011 | 33 | |
| 4 | 2009 | 3 | |
| 5 | 2008 | 2 | |
| 6 | 2007 | 38 | |
| 7 | Common deletion polymorphisms in the human genomebreakdown → | 2005 | 527 |
About Stephanie Dallaire
Stephanie Dallaire is a scholar working on Genetics, Genetics and Pediatrics, Perinatology and Child Health, having authored 7 papers that have together received 630 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Chromosomal and Genetic Variations (2 papers), Prenatal Screening and Diagnostics (2 papers), Genomics and Rare Diseases (1 paper), Viral Infections and Immunology Research (1 paper), Genetic Associations and Epidemiology (1 paper), Single-cell and spatial transcriptomics (1 paper) and Acute Myeloid Leukemia Research (1 paper). The work is most often cited by research in Genetics (476 citations), Pediatrics, Perinatology and Child Health (96 citations) and Cancer Research (69 citations). Stephanie Dallaire has collaborated with scholars based in United States, Mexico and Denmark. Frequent co-authors include Charles Lee, David Altshuler, Steven A. McCarroll, Tracy N. Hadnott, Mark J. Daly, Michael C. Zody, Stacey B. Gabriel, George H. Perry, Jeffrey C. Barrett and Pardis C. Sabeti. Their work appears in journals such as Nature Genetics, Blood and BMC Genomics.
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.