Cassandra Runke

469 total citations
5 papers, 84 citations indexed

About

Cassandra Runke is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Cassandra Runke has authored 5 papers receiving a total of 84 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Molecular Biology, 2 papers in Pediatrics, Perinatology and Child Health and 2 papers in Genetics. Recurrent topics in Cassandra Runke's work include Prenatal Screening and Diagnostics (2 papers), Ethics in Clinical Research (1 paper) and Wnt/β-catenin signaling in development and cancer (1 paper). Cassandra Runke is often cited by papers focused on Prenatal Screening and Diagnostics (2 papers), Ethics in Clinical Research (1 paper) and Wnt/β-catenin signaling in development and cancer (1 paper). Cassandra Runke collaborates with scholars based in United States, Canada and Saudi Arabia. Cassandra Runke's co-authors include Jennifer L. Hand, Jennelle C. Hodge, McKinsey L. Goodenberger, Margaret Lilley, Susan Christian, Umut Aypar, Ruth M. Farrell, Wayne W. Grody, Marsha Michie and Richard R. Sharp and has published in prestigious journals such as Journal of the American Academy of Dermatology, Journal of Speech Language and Hearing Research and Clinical Genetics.

In The Last Decade

Cassandra Runke

5 papers receiving 83 citations

Peers

Cassandra Runke
Liliana Fernández United States
Julie McCarrier United States
Leigh Anne Flore United States
C. Rauscher Austria
Caroline McGowan United States
Stacy Gabriel United States
Liliana Fernández United States
Cassandra Runke
Citations per year, relative to Cassandra Runke Cassandra Runke (= 1×) peers Liliana Fernández

Countries citing papers authored by Cassandra Runke

Since Specialization
Citations

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

Fields of papers citing papers by Cassandra Runke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cassandra Runke

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

All Works

5 of 5 papers shown
1.
Chenausky, Karen, Becky S. Baas, Ruth Stoeckel, et al.. (2023). Comorbidity and Severity in Childhood Apraxia of Speech: A Retrospective Chart Review. Journal of Speech Language and Hearing Research. 66(3). 791–803. 11 indexed citations
2.
Allyse, Megan, Umut Aypar, Natasha Bonhomme, et al.. (2017). Offering Prenatal Screening in the Age of Genomic Medicine: A Practical Guide. Journal of Women s Health. 26(7). 755–761. 9 indexed citations
3.
Runke, Cassandra, et al.. (2016). Further Defining the Role of the Laboratory Genetic Counselor. Journal of Genetic Counseling. 25(4). 786–798. 28 indexed citations
4.
Hand, Jennifer L., Cassandra Runke, & Jennelle C. Hodge. (2015). The phenotype spectrum of X-linked ichthyosis identified by chromosomal microarray. Journal of the American Academy of Dermatology. 72(4). 617–627. 26 indexed citations
5.
Čuturilo, Goran, Cassandra Runke, Erik C. Thorland, et al.. (2015). Phenotype analysis impacts testing strategy in patients with Currarino syndrome. Clinical Genetics. 89(1). 109–114. 10 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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