Stephanie Dallaire

5.2k total citations · 1 hit paper
7 papers, 630 citations indexed

About

Stephanie Dallaire is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Stephanie Dallaire has authored 7 papers receiving a total of 630 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Stephanie Dallaire's work include Genomic variations and chromosomal abnormalities (4 papers), Chromosomal and Genetic Variations (2 papers) and Prenatal Screening and Diagnostics (2 papers). Stephanie Dallaire is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Chromosomal and Genetic Variations (2 papers) and Prenatal Screening and Diagnostics (2 papers). Stephanie Dallaire collaborates with scholars based in United States, Mexico and United Kingdom. Stephanie Dallaire's co-authors include Charles Lee, Tracy N. Hadnott, Jeffrey C. Barrett, George H. Perry, Mark J. Daly, Pardis C. Sabeti, Steven A. McCarroll, David Altshuler, Stacey B. Gabriel and Michael C. Zody and has published in prestigious journals such as Nature Genetics, Blood and BMC Genomics.

In The Last Decade

Stephanie Dallaire

7 papers receiving 616 citations

Hit Papers

Common deletion polymorphisms in the human genome 2005 2026 2012 2019 2005 100 200 300 400 500
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Common deletion polymorphisms in the human genome
    2005 527 citations Steven A. McCarroll, Tracy N. Hadnott et al. Nature Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Stephanie Dallaire United States 5 476 274 157 96 69 7 630
Tracy N. Hadnott United States 7 507 1.1× 333 1.2× 140 0.9× 107 1.1× 66 1.0× 11 752
Sara Benito‐Sanz Spain 14 501 1.1× 395 1.4× 41 0.3× 29 0.3× 53 0.8× 22 637
Rajini Haraksingh United States 8 217 0.5× 245 0.9× 59 0.4× 36 0.4× 96 1.4× 12 425
Kênia Balbi El-Jaick Brazil 11 284 0.6× 546 2.0× 40 0.3× 47 0.5× 34 0.5× 20 675
H. Shuen Lo United States 6 191 0.4× 522 1.9× 61 0.4× 21 0.2× 61 0.9× 7 647
Gregor Schlüter Germany 13 186 0.4× 246 0.9× 29 0.2× 37 0.4× 28 0.4× 25 486
Yoichi Sekita Japan 15 325 0.7× 526 1.9× 63 0.4× 310 3.2× 59 0.9× 22 775
Rika Wakao Japan 9 216 0.5× 727 2.7× 74 0.5× 17 0.2× 64 0.9× 18 914
Ko–ichiro Yoshiura Japan 12 251 0.5× 304 1.1× 69 0.4× 107 1.1× 39 0.6× 22 505
Gaetano Verde Italy 14 591 1.2× 934 3.4× 63 0.4× 335 3.5× 86 1.2× 16 1.1k

Countries citing papers authored by Stephanie Dallaire

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 of co-authors of Stephanie Dallaire

This figure shows the co-authorship network connecting the top 25 collaborators of Stephanie Dallaire. A scholar is included among the top collaborators of Stephanie Dallaire based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Stephanie Dallaire. Stephanie Dallaire is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

7 of 7 papers shown
1.
Vimbela, Gina V., et al.. (2019). Rapid electrophoretic recovery of DNA from dried blood spots. Electrophoresis. 40(14). 1812–1819. 4 indexed citations
2.
Gutiérrez-Mateo, Cristina, David M. Hougaard, Jonas Bybjerg‐Grauholm, et al.. (2019). Development of a Multiplex Real-Time PCR Assay for the Newborn Screening of SCID, SMA, and XLA. International Journal of Neonatal Screening. 5(4). 39–39. 23 indexed citations
3.
Shaffer, Lisa G., Justine Coppinger, Sarah Alliman, et al.. (2011). The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes. Prenatal Diagnosis. 31(8). 778–787. 33 indexed citations
4.
Tirado, Carlos A, S Henderson, Erin Matthews, et al.. (2009). Cytogenetic and molecular characterization of a partial trisomy 2p arising from inverted duplication of 2p with terminal deletion of 2pter. American Journal of Medical Genetics Part A. 149A(11). 2507–2512. 3 indexed citations
5.
Andreeff, Michael, Teresa McQueen, Christopher Williams, et al.. (2008). Clonal Abnormalities in MSC Derived from AML Bone Marrows. Blood. 112(11). 2428–2428. 2 indexed citations
6.
Freeman, Jennifer L., Ruby Banerjee, Stephanie Dallaire, et al.. (2007). Definition of the zebrafish genome using flow cytometry and cytogenetic mapping. BMC Genomics. 8(1). 195–195. 38 indexed citations
7.
McCarroll, Steven A., Tracy N. Hadnott, George H. Perry, et al.. (2005). Common deletion polymorphisms in the human genome. Nature Genetics. 38(1). 86–92. 527 indexed citations breakdown →

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.

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