Brieana Fregeau

969 total citations
3 papers, 120 citations indexed

About

Brieana Fregeau is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Brieana Fregeau has authored 3 papers receiving a total of 120 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Molecular Biology, 2 papers in Genetics and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in Brieana Fregeau's work include Genetics and Neurodevelopmental Disorders (2 papers), Congenital heart defects research (1 paper) and Fetal and Pediatric Neurological Disorders (1 paper). Brieana Fregeau is often cited by papers focused on Genetics and Neurodevelopmental Disorders (2 papers), Congenital heart defects research (1 paper) and Fetal and Pediatric Neurological Disorders (1 paper). Brieana Fregeau collaborates with scholars based in United States, Netherlands and India. Brieana Fregeau's co-authors include Elliott H. Sherr, A. James Barkovich, Danielle Mizuiri, Nizar Smaoui, Esther Leshinsky‐Silver, John F. Houde, Katrina W. Lexa, Carly Demopoulos, Ronald D. Vale and Thomas Andrew Burrow and has published in prestigious journals such as Scientific Reports, Journal of Medical Genetics and Annals of Clinical and Translational Neurology.

In The Last Decade

Brieana Fregeau

3 papers receiving 120 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Brieana Fregeau United States 3 48 47 39 33 21 3 120
Elise Ng‐Cordell United Kingdom 8 68 1.4× 28 0.6× 82 2.1× 23 0.7× 66 3.1× 13 196
Laura C. Murphy United Kingdom 8 116 2.4× 36 0.8× 64 1.6× 17 0.5× 44 2.1× 14 197
David V.C. Brito Germany 9 144 3.0× 19 0.4× 81 2.1× 68 2.1× 59 2.8× 15 244
Lia Boyle United States 4 83 1.7× 34 0.7× 135 3.5× 19 0.6× 98 4.7× 4 207
Elisa Cappuyns Belgium 4 78 1.6× 18 0.4× 78 2.0× 47 1.4× 52 2.5× 5 187
Ines Heise United Kingdom 8 120 2.5× 14 0.3× 19 0.5× 36 1.1× 40 1.9× 9 228
Christopher Krasniak United States 4 80 1.7× 81 1.7× 30 0.8× 53 1.6× 10 0.5× 4 155
Junyeop Daniel Roh South Korea 5 86 1.8× 33 0.7× 35 0.9× 70 2.1× 28 1.3× 7 143
Caterina Montani Italy 7 101 2.1× 23 0.5× 41 1.1× 63 1.9× 21 1.0× 10 180
Jessica Root United States 6 63 1.3× 36 0.8× 16 0.4× 18 0.5× 31 1.5× 8 253

Countries citing papers authored by Brieana Fregeau

Since Specialization
Citations

This map shows the geographic impact of Brieana Fregeau'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 Brieana Fregeau with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Brieana Fregeau more than expected).

Fields of papers citing papers by Brieana Fregeau

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Brieana Fregeau. 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 Brieana Fregeau. The network helps show where Brieana Fregeau may publish in the future.

Co-authorship network of co-authors of Brieana Fregeau

This figure shows the co-authorship network connecting the top 25 collaborators of Brieana Fregeau. A scholar is included among the top collaborators of Brieana Fregeau 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 Brieana Fregeau. Brieana Fregeau is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

3 of 3 papers shown
1.
Matalon, Dena R., Brieana Fregeau, Ingvild Aukrust, et al.. (2020). De novo variants in SUPT16H cause neurodevelopmental disorders associated with corpus callosum abnormalities. Journal of Medical Genetics. 57(7). 461–465. 12 indexed citations
2.
Demopoulos, Carly, Hardik Kothare, Danielle Mizuiri, et al.. (2018). Abnormal Speech Motor Control in Individuals with 16p11.2 Deletions. Scientific Reports. 8(1). 1274–1274. 32 indexed citations
3.
Nieh, Sahar Esmaeeli, Minhajuddin Sirajuddin, Brieana Fregeau, et al.. (2015). De novo mutations in KIF1A cause progressive encephalopathy and brain atrophy. Annals of Clinical and Translational Neurology. 2(6). 623–635. 76 indexed citations

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Elise Ng‐Cordell Breakdown of academic impact, for papers by Laura C. Murphy Breakdown of academic impact, for papers by David V.C. Brito Breakdown of academic impact, for papers by Lia Boyle Breakdown of academic impact, for papers by Elisa Cappuyns Breakdown of academic impact, for papers by Ines Heise Breakdown of academic impact, for papers by Christopher Krasniak Breakdown of academic impact, for papers by Junyeop Daniel Roh Breakdown of academic impact, for papers by Caterina Montani Breakdown of academic impact, for papers by Jessica Root
Rankless by CCL
2026