Emily Bonkowski

1.1k total citations
11 papers, 277 citations indexed

About

Emily Bonkowski is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Emily Bonkowski has authored 11 papers receiving a total of 277 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Emily Bonkowski's work include Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and BRCA gene mutations in cancer (3 papers). Emily Bonkowski is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and BRCA gene mutations in cancer (3 papers). Emily Bonkowski collaborates with scholars based in United States, Czechia and Israel. Emily Bonkowski's co-authors include Wendy H. Raskind, Thomas D. Bird, Deborah A. Nickerson, Youngmee Sul, Mark Matsushita, Dong-Hui Chen, John Wolff, Thalia Papayannopoulou, Sioḃán Keel and Toshiyasu Taniguchi and has published in prestigious journals such as Neurology, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Emily Bonkowski

8 papers receiving 277 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Emily Bonkowski United States 4 118 72 68 51 37 11 277
Francesca Bertola Italy 10 66 0.6× 43 0.6× 76 1.1× 11 0.2× 35 0.9× 20 291
Fong Ct United States 6 141 1.2× 74 1.0× 15 0.2× 19 0.4× 23 0.6× 186 296
Leïla Lazaro France 8 254 2.2× 103 1.4× 21 0.3× 30 0.6× 96 2.6× 9 411
Sara Lewis United States 7 79 0.7× 37 0.5× 33 0.5× 34 0.7× 61 1.6× 13 227
Daniel Nachun United States 11 193 1.6× 64 0.9× 18 0.3× 11 0.2× 58 1.6× 16 300
Frédérique Sloan‐Béna Switzerland 9 123 1.0× 87 1.2× 26 0.4× 40 0.8× 16 0.4× 23 263
Sharan Goobie Canada 15 162 1.4× 281 3.9× 41 0.6× 150 2.9× 55 1.5× 29 504
Marije Meuwissen Belgium 11 153 1.3× 186 2.6× 28 0.4× 9 0.2× 23 0.6× 23 368
Xiaodan Ding China 9 199 1.7× 30 0.4× 41 0.6× 103 2.0× 10 0.3× 10 339
Emmanuelle Ranza Switzerland 12 137 1.2× 103 1.4× 8 0.1× 56 1.1× 36 1.0× 22 295

Countries citing papers authored by Emily Bonkowski

Since Specialization
Citations

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

Fields of papers citing papers by Emily Bonkowski

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emily Bonkowski

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

All Works

11 of 11 papers shown
1.
Wang, Yong‐Dong, Nicolas Koehler, Renata Mendonça Moraes, et al.. (2025). Patient-derived models of UBA5- associated encephalopathy identify defects in neurodevelopment and highlight potential therapeutic avenues. Science Translational Medicine. 17(797). eadn8417–eadn8417.
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Bonkowski, Emily, et al.. (2024). A roadmap to cure CHD2-related disorders. PubMed. 5. 931193509–931193509. 2 indexed citations
5.
Smith, Hadley Stevens, et al.. (2023). Clinically Indicated Genomic Sequencing of Children in Foster Care: Legal and Ethical Issues. The Journal of Pediatrics. 262. 113612–113612. 1 indexed citations
6.
Smith, Hadley Stevens, et al.. (2023). Framing the Family: A Qualitative Exploration of Factors That Shape Family-Level Experience of Pediatric Genomic Sequencing. Children. 10(5). 774–774. 3 indexed citations
7.
Smith, Hadley Stevens, Emily Bonkowski, Amanda M. Gutierrez, et al.. (2022). Key drivers of family-level utility of pediatric genomic sequencing: a qualitative analysis to support preference research. European Journal of Human Genetics. 31(4). 445–452. 8 indexed citations
8.
Chen, Dong-Hui, Jennifer E. Below, Akiko Shimamura, et al.. (2016). Ataxia-Pancytopenia Syndrome Is Caused by Missense Mutations in SAMD9L. The American Journal of Human Genetics. 98(6). 1146–1158. 119 indexed citations
9.
Chen, Donghui, Emily Bonkowski, Olena Korvatska, et al.. (2015). ADCY5-related movement disorder: broader spectrum and genotype/phenotype correlations including new cases (P2.140). Neurology. 84(14_supplement). 2 indexed citations
10.
Korvatska, Olena, Nicholas S. Strand, Jason D. Berndt, et al.. (2013). Altered splicing of ATP6AP2 causes X-linked parkinsonism with spasticity (XPDS). Human Molecular Genetics. 22(16). 3259–3268. 101 indexed citations
11.
Chen, Dong-Hui, Alipi V. Naydenov, Jacqueline L. Blankman, et al.. (2013). Two Novel Mutations inABHD12: Expansion of the Mutation Spectrum in PHARC and Assessment of Their Functional Effects. Human Mutation. 34(12). 1672–1678. 41 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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2026