Danielle S. Rudd

2.0k total citations
12 papers, 392 citations indexed

About

Danielle S. Rudd is a scholar working on Genetics, Molecular Biology and Ophthalmology. According to data from OpenAlex, Danielle S. Rudd has authored 12 papers receiving a total of 392 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Ophthalmology. Recurrent topics in Danielle S. Rudd's work include Genomic variations and chromosomal abnormalities (7 papers), Congenital heart defects research (3 papers) and Genetic Associations and Epidemiology (2 papers). Danielle S. Rudd is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Congenital heart defects research (3 papers) and Genetic Associations and Epidemiology (2 papers). Danielle S. Rudd collaborates with scholars based in United States and India. Danielle S. Rudd's co-authors include Thomas H. Wassink, Eric A. Epping, Kacie J. Meyer, Val C. Sheffield, Lea K. Davis, Nancy C. Andreasen, Beng‐Choon Ho, Michael G. Anderson, Matthew M. Harper and Laura M. Dutca and has published in prestigious journals such as Scientific Reports, Investigative Ophthalmology & Visual Science and Experimental Eye Research.

In The Last Decade

Danielle S. Rudd

11 papers receiving 388 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Danielle S. Rudd United States 10 212 135 95 74 60 12 392
Defne A. Amado United States 11 270 1.3× 93 0.7× 63 0.7× 169 2.3× 15 0.3× 22 548
Valerio Castoldi Italy 12 332 1.6× 172 1.3× 46 0.5× 58 0.8× 58 1.0× 26 586
Khanh-Nhat Tran-Viet United States 13 186 0.9× 102 0.8× 220 2.3× 72 1.0× 84 1.4× 16 735
Xiaohe Yan China 10 99 0.5× 34 0.3× 102 1.1× 21 0.3× 152 2.5× 31 438
J A Maat-Kievit Netherlands 9 288 1.4× 92 0.7× 27 0.3× 214 2.9× 31 0.5× 10 536
Akiko Takeda Japan 9 192 0.9× 28 0.2× 53 0.6× 21 0.3× 37 0.6× 22 401
Gidon Karmon Israel 9 158 0.7× 94 0.7× 13 0.1× 15 0.2× 57 0.9× 14 322
Margaret A. Cooper United States 12 269 1.3× 65 0.5× 21 0.2× 18 0.2× 26 0.4× 20 564
Elisa Murenu Germany 7 318 1.5× 76 0.6× 39 0.4× 10 0.1× 56 0.9× 8 457
Mihailo Vujic Sweden 11 797 3.8× 466 3.5× 304 3.2× 11 0.1× 76 1.3× 14 1.1k

Countries citing papers authored by Danielle S. Rudd

Since Specialization
Citations

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

Fields of papers citing papers by Danielle S. Rudd

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Danielle S. Rudd. 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 Danielle S. Rudd. The network helps show where Danielle S. Rudd may publish in the future.

Co-authorship network of co-authors of Danielle S. Rudd

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

All Works

12 of 12 papers shown
1.
Harper, Matthew M., Danielle S. Rudd, Kacie J. Meyer, et al.. (2020). Identification of chronic brain protein changes and protein targets of serum auto-antibodies after blast-mediated traumatic brain injury. Heliyon. 6(2). e03374–e03374. 26 indexed citations
2.
Dutca, Laura M., et al.. (2018). Effects of sustained daily latanoprost application on anterior chamber anatomy and physiology in mice. Scientific Reports. 8(1). 13088–13088.
3.
Hedberg‐Buenz, Adam, Mark Christopher, Kacie J. Meyer, et al.. (2015). RetFM-J, an ImageJ-based module for automated counting and quantifying features of nuclei in retinal whole-mounts. Experimental Eye Research. 146. 386–392. 20 indexed citations
4.
5.
Rudd, Danielle S., et al.. (2014). A genome‐wide CNV analysis of schizophrenia reveals a potential role for a multiple‐hit model. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 165(8). 619–626. 21 indexed citations
6.
Dutca, Laura M., Steven F. Stasheff, Adam Hedberg‐Buenz, et al.. (2014). Early Detection of Subclinical Visual Damage After Blast-Mediated TBI Enables Prevention of Chronic Visual Deficit by Treatment With P7C3-S243. Investigative Ophthalmology & Visual Science. 55(12). 8330–8341. 73 indexed citations
7.
Wassink, Thomas H., Eric A. Epping, Danielle S. Rudd, et al.. (2012). Influence of ZNF804a on Brain Structure Volumes and Symptom Severity in Individuals With Schizophrenia. Archives of General Psychiatry. 69(9). 885–885. 42 indexed citations
8.
Davis, Lea K., Kacie J. Meyer, Emily I. Schindler, et al.. (2011). Copy Number Variations and Primary Open-Angle Glaucoma. Investigative Ophthalmology & Visual Science. 52(10). 7122–7122. 29 indexed citations
9.
Meyer, Kacie J., Lea K. Davis, Emily I. Schindler, et al.. (2010). Genome-wide analysis of copy number variants in age-related macular degeneration. Human Genetics. 129(1). 91–100. 32 indexed citations
10.
Davis, Lea K., Kacie J. Meyer, Danielle S. Rudd, et al.. (2009). Novel copy number variants in children with autism and additional developmental anomalies. Journal of Neurodevelopmental Disorders. 1(4). 292–301. 28 indexed citations
11.
Hartz, Sarah M., Beng‐Choon Ho, Nancy C. Andreasen, et al.. (2009). G72 influences longitudinal change in frontal lobe volume in schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(2). 640–647. 20 indexed citations
12.
Davis, Lea K., Kacie J. Meyer, Danielle S. Rudd, et al.. (2008). Pax6 3′ deletion results in aniridia, autism and mental retardation. Human Genetics. 123(4). 371–378. 94 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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