Denise E. Mauldin

1.1k total citations
7 papers, 302 citations indexed

About

Denise E. Mauldin is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Denise E. Mauldin has authored 7 papers receiving a total of 302 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 1 paper in Pulmonary and Respiratory Medicine. Recurrent topics in Denise E. Mauldin's work include Genomics and Phylogenetic Studies (3 papers), Genomics and Rare Diseases (2 papers) and Genetic Associations and Epidemiology (2 papers). Denise E. Mauldin is often cited by papers focused on Genomics and Phylogenetic Studies (3 papers), Genomics and Rare Diseases (2 papers) and Genetic Associations and Epidemiology (2 papers). Denise E. Mauldin collaborates with scholars based in United States, Luxembourg and Canada. Denise E. Mauldin's co-authors include Leroy Hood, Gustavo Glusman, Jared C. Roach, Juan Caballero-Pérez, Robert Hubley, Hao Hu, Lynn B. Jorde, Stephen L. Guthery, Max Robinson and Hong Li and has published in prestigious journals such as Bioinformatics, The American Journal of Human Genetics and PLoS Genetics.

In The Last Decade

Denise E. Mauldin

7 papers receiving 297 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Denise E. Mauldin United States 7 178 177 39 18 17 7 302
Efren Sandoval United States 4 183 1.0× 258 1.5× 47 1.2× 15 0.8× 13 0.8× 4 393
Ligia Mateiu Belgium 12 157 0.9× 285 1.6× 46 1.2× 19 1.1× 18 1.1× 29 480
Gundula Povysil United States 9 141 0.8× 131 0.7× 37 0.9× 8 0.4× 17 1.0× 18 314
Shruti Marwaha United States 6 123 0.7× 131 0.7× 29 0.7× 6 0.3× 15 0.9× 19 283
Harry Clifford United Kingdom 8 98 0.6× 86 0.5× 69 1.8× 12 0.7× 9 0.5× 12 247
Zachary Zappala United States 6 244 1.4× 266 1.5× 73 1.9× 28 1.6× 14 0.8× 6 420
Sandra C. Doelken Germany 14 251 1.4× 294 1.7× 30 0.8× 17 0.9× 6 0.4× 16 425
Thomas Juettemann United Kingdom 3 106 0.6× 285 1.6× 43 1.1× 24 1.3× 40 2.4× 3 360
Jennifer L. Asimit United Kingdom 11 397 2.2× 206 1.2× 54 1.4× 24 1.3× 17 1.0× 22 501
Robin Steinhaus Germany 7 97 0.5× 142 0.8× 33 0.8× 9 0.5× 20 1.2× 11 249

Countries citing papers authored by Denise E. Mauldin

Since Specialization
Citations

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

Fields of papers citing papers by Denise E. Mauldin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Denise E. Mauldin. 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 Denise E. Mauldin. The network helps show where Denise E. Mauldin may publish in the future.

Co-authorship network of co-authors of Denise E. Mauldin

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

All Works

7 of 7 papers shown
1.
Glusman, Gustavo, Denise E. Mauldin, Leroy Hood, & Max Robinson. (2017). Ultrafast Comparison of Personal Genomes via Precomputed Genome Fingerprints. Frontiers in Genetics. 8. 136–136. 11 indexed citations
2.
Stittrich, Anna, J. R. Ashworth, Mude Shi, et al.. (2016). Genomic architecture of inflammatory bowel disease in five families with multiple affected individuals. Human Genome Variation. 3(1). 15060–15060. 11 indexed citations
3.
Glusman, Gustavo, Varsha Dhankani, Max Robinson, et al.. (2015). Identification of copy number variants in whole-genome data using Reference Coverage Profiles. Frontiers in Genetics. 6. 45–45. 15 indexed citations
4.
Li, Hong, Gustavo Glusman, Hao Hu, et al.. (2014). Relationship Estimation from Whole-Genome Sequence Data. PLoS Genetics. 10(1). e1004144–e1004144. 54 indexed citations
5.
Roach, Jared C., Gustavo Glusman, Robert Hubley, et al.. (2011). Chromosomal Haplotypes by Genetic Phasing of Human Families. The American Journal of Human Genetics. 89(3). 382–397. 45 indexed citations
6.
Glusman, Gustavo, Juan Caballero-Pérez, Denise E. Mauldin, Leroy Hood, & Jared C. Roach. (2011). Kaviar: an accessible system for testing SNV novelty. Bioinformatics. 27(22). 3216–3217. 151 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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