Jeanselle Dea

4.4k total citations
7 papers, 451 citations indexed

About

Jeanselle Dea is a scholar working on Molecular Biology, Genetics and Infectious Diseases. According to data from OpenAlex, Jeanselle Dea has authored 7 papers receiving a total of 451 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 5 papers in Genetics and 1 paper in Infectious Diseases. Recurrent topics in Jeanselle Dea's work include Genetics and Neurodevelopmental Disorders (4 papers), Congenital heart defects research (3 papers) and Down syndrome and intellectual disability research (1 paper). Jeanselle Dea is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Congenital heart defects research (3 papers) and Down syndrome and intellectual disability research (1 paper). Jeanselle Dea collaborates with scholars based in United States. Jeanselle Dea's co-authors include Oliver Homann, Alexander D. Johnson, Suzanne M. Noble, A. Jeremy Willsey, Helen Rankin Willsey, Yuxiao Xu, Matthew W. State, Cameron R. T. Exner, Richard M. Harland and Amanda Everitt and has published in prestigious journals such as Nature Communications, Neuron and Development.

In The Last Decade

Jeanselle Dea

7 papers receiving 446 citations

Peers

Jeanselle Dea

ID

MB

EPIDE

GENET

FS

Gwenaëlle André-Leroux France

M. V. Telkov Russia

Valerie Price United States

Chengguo Shen China

Alexander MacKenzie United States

Alena Kozlova United States

Rachel Wright United States

Anna Vanyushkina Russia

Koji Chono Japan

Daniela Albrecht-Eckardt Germany

Gwenaëlle André-Leroux France

Jeanselle Dea

202 ×0.7

ID

355 ×1.5

MB

113 ×0.7

EPIDE

112 ×1.7

GENET

14 ×0.3

FS

Citations per year, relative to Jeanselle Dea Jeanselle Dea (= 1×) peers Gwenaëlle André-Leroux

Countries citing papers authored by Jeanselle Dea

Since Specialization

Citations

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

Fields of papers citing papers by Jeanselle Dea

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jeanselle Dea

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

All Works

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7 of 7 papers shown

1.

Teerikorpi, Nia, Micaela Lasser, Sheng Wang, et al.. (2025). Ciliary biology intersects autism and congenital heart disease. Development. 152(12). 1 indexed citations

2.

Schmidt, James J., Jeanselle Dea, Elise Brimble, et al.. (2025). Autism gene variants disrupt enteric neuron migration and cause gastrointestinal dysmotility. Nature Communications. 16(1). 2238–2238. 4 indexed citations

3.

Lasser, Micaela, Nawei Sun, Yuxiao Xu, et al.. (2023). Pleiotropy of autism-associated chromatin regulators. Development. 150(14). 10 indexed citations

4.

Willsey, Helen Rankin, Cameron R. T. Exner, Yuxiao Xu, et al.. (2021). Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience. Neuron. 109(5). 788–804.e8. 58 indexed citations

5.

Rosenthal, Sara Brin, Helen Rankin Willsey, Yuxiao Xu, et al.. (2021). A convergent molecular network underlying autism and congenital heart disease. Cell Systems. 12(11). 1094–1107.e6. 20 indexed citations

6.

Willsey, Helen Rankin, Yuxiao Xu, Amanda Everitt, et al.. (2020). Neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and brain size in Xenopus embryos. Development. 147(21). 24 indexed citations

7.

Homann, Oliver, Jeanselle Dea, Suzanne M. Noble, & Alexander D. Johnson. (2009). A Phenotypic Profile of the Candida albicans Regulatory Network. PLoS Genetics. 5(12). e1000783–e1000783. 334 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.

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