James M. Havrilla

649 total citations
15 papers, 277 citations indexed

About

James M. Havrilla is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, James M. Havrilla has authored 15 papers receiving a total of 277 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Genetics and 3 papers in Epidemiology. Recurrent topics in James M. Havrilla's work include Genomics and Rare Diseases (8 papers), Biomedical Text Mining and Ontologies (8 papers) and Urinary Tract Infections Management (3 papers). James M. Havrilla is often cited by papers focused on Genomics and Rare Diseases (8 papers), Biomedical Text Mining and Ontologies (8 papers) and Urinary Tract Infections Management (3 papers). James M. Havrilla collaborates with scholars based in United States, Australia and Iceland. James M. Havrilla's co-authors include Aaron R. Quinlan, Ryan M. Layer, Brent S. Pedersen, Cong Liu, Chunhua Weng, Jacqueline Peng, Leandros Boukas, Kasper D. Hansen, Peter F. Hickey and Hans T. Björnsson and has published in prestigious journals such as Nature Genetics, Genome Research and The American Journal of Human Genetics.

In The Last Decade

James M. Havrilla

13 papers receiving 272 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
James M. Havrilla United States 7 182 174 29 19 13 15 277
John Garner United States 3 142 0.8× 208 1.2× 46 1.6× 8 0.4× 5 0.4× 3 298
Michael Boehnke United States 7 279 1.5× 149 0.9× 15 0.5× 4 0.2× 6 0.5× 10 372
Kyung Dae Ko United States 9 37 0.2× 261 1.5× 28 1.0× 6 0.3× 3 0.2× 18 324
Zhanye Zheng China 6 107 0.6× 159 0.9× 25 0.9× 2 0.1× 8 0.6× 7 255
Diego Garrido-Martín Spain 6 64 0.4× 196 1.1× 42 1.4× 3 0.2× 6 0.5× 10 275
Federico López United Kingdom 4 58 0.3× 121 0.7× 16 0.6× 8 0.4× 3 0.2× 7 195
Tracy Dudding‐Byth Australia 10 146 0.8× 147 0.8× 8 0.3× 4 0.2× 24 1.8× 18 272
Ada J. S. Chan Canada 5 158 0.9× 103 0.6× 38 1.3× 2 0.1× 29 2.2× 7 212
Scott Ronquist United States 8 35 0.2× 148 0.9× 16 0.6× 7 0.4× 7 0.5× 13 232
Muhammed Hasan Çelik Germany 7 99 0.5× 265 1.5× 29 1.0× 5 0.3× 2 0.2× 11 330

Countries citing papers authored by James M. Havrilla

Since Specialization
Citations

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

Fields of papers citing papers by James M. Havrilla

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by James M. Havrilla. 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 James M. Havrilla. The network helps show where James M. Havrilla may publish in the future.

Co-authorship network of co-authors of James M. Havrilla

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

All Works

15 of 15 papers shown
1.
Festa, Richard A., F. R. Cockerill, Mohit Mathur, et al.. (2025). Full Validation of Pooled Antibiotic Susceptibility Testing Using CLSI Methods and Performance Criteria in UTI Pathogens. Antibiotics. 14(11). 1168–1168.
2.
Festa, Richard A., F. R. Cockerill, Mohit Mathur, et al.. (2025). Pooled Antibiotic Susceptibility Testing for Polymicrobial UTI Performs Within CLSI Validation Standards. Antibiotics. 14(2). 143–143. 2 indexed citations
3.
4.
5.
Havrilla, James M., et al.. (2022). PheNominal: an EHR-integrated web application for structured deep phenotyping at the point of care. BMC Medical Informatics and Decision Making. 22(S2). 198–198. 6 indexed citations
6.
Liu, Cong, Casey Ta, James M. Havrilla, et al.. (2022). OARD: Open annotations for rare diseases and their phenotypes based on real-world data. The American Journal of Human Genetics. 109(9). 1591–1604. 4 indexed citations
7.
Havrilla, James M., Jacqueline Peng, W. Spencer Guthrie, et al.. (2022). Development of a phenotype ontology for autism spectrum disorder by natural language processing on electronic health records. Journal of Neurodevelopmental Disorders. 14(1). 32–32. 5 indexed citations
8.
Havrilla, James M., et al.. (2021). PhenCards: a data resource linking human phenotype information to biomedical knowledge. Genome Medicine. 13(1). 91–91. 4 indexed citations
9.
Havrilla, James M., Cong Liu, Chunhua Weng, et al.. (2021). Clinical Phenotypic Spectrum of 4095 Individuals with Down Syndrome from Text Mining of Electronic Health Records. Genes. 12(8). 1159–1159. 6 indexed citations
10.
Havrilla, James M., Fang Li, Ying Chen, et al.. (2020). Phen2Gene: rapid phenotype-driven gene prioritization for rare diseases. NAR Genomics and Bioinformatics. 2(2). lqaa032–lqaa032. 44 indexed citations
11.
Peng, Jacqueline, James M. Havrilla, Cong Liu, et al.. (2020). Natural language processing (NLP) tools in extracting biomedical concepts from research articles: a case study on autism spectrum disorder. BMC Medical Informatics and Decision Making. 20(S11). 322–322. 20 indexed citations
12.
Boukas, Leandros, James M. Havrilla, Peter F. Hickey, et al.. (2019). Coexpression patterns define epigenetic regulators associated with neurological dysfunction. Genome Research. 29(4). 532–542. 30 indexed citations
13.
Belyeu, Jonathan R., T. Nicholas, Brent S. Pedersen, et al.. (2018). SV-plaudit: A cloud-based framework for manually curating thousands of structural variants. GigaScience. 7(7). 25 indexed citations
14.
Havrilla, James M., Brent S. Pedersen, Ryan M. Layer, & Aaron R. Quinlan. (2018). A map of constrained coding regions in the human genome. Nature Genetics. 51(1). 88–95. 122 indexed citations
15.
Havrilla, James M. & Ahmet Saçan. (2012). Meta-analysis of protein structural alignment. 7. 72–76. 1 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 John Garner Breakdown of academic impact, for papers by Michael Boehnke Breakdown of academic impact, for papers by Kyung Dae Ko Breakdown of academic impact, for papers by Zhanye Zheng Breakdown of academic impact, for papers by Diego Garrido-Martín Breakdown of academic impact, for papers by Federico López Breakdown of academic impact, for papers by Tracy Dudding‐Byth Breakdown of academic impact, for papers by Ada J. S. Chan Breakdown of academic impact, for papers by Scott Ronquist Breakdown of academic impact, for papers by Muhammed Hasan Çelik
Rankless by CCL
2026