Ryan E. Mills

40.7k citations

52 papers · 5.3k indexed · 2 hit papers · h-index 30

Impact in

Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
Molecular Biology top 2%
- Genomics and Phylogenetic Studies
- RNA and protein synthesis mechanisms
- RNA Research and Splicing
- RNA modifications and cancer
- CRISPR and Genetic Engineering
- Nuclear Structure and Function

Papers in

Genetics 21
- Genomic variations and chromosomal abnormalities 11
- Genomics and Rare Diseases 4
Molecular Biology 43
- Genomics and Phylogenetic Studies 18
- RNA and protein synthesis mechanisms 14
- CRISPR and Genetic Engineering 5
- Gene expression and cancer classification 4
- Genomics and Chromatin Dynamics 4

Co-authors: Scott E. Devine W. Stephen Pittard Anita H. Corbett Allison Lange Rebecca C. Iskow Murray Stewart E. Andrew Bennett Steve S. Ho
Journals: Genome biology (4 papers)Proceedings of the National Academy of Sciences (4 papers)Genome Research (4 papers)Nucleic Acids Research (3 papers)Current Protocols in Bioinformatics (2 papers)
Partner nations: United States United Kingdom South Korea

In The Last Decade

Ryan E. Mills

51 papers receiving 5.2k citations

Hit Papers

align trajectories log scale

Structural variation in the sequencing era 2019 · 335 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2019 Nature Reviews Genetics
2006 Journal of Biological Chemistry

Peers

Countries citing papers authored by Ryan E. Mills

Since Specialization

Citations

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

Fields of papers citing papers by Ryan E. Mills

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Ryan E. Mills, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Ryan E. Mills Line = papers co-authored together Ryan E. Mills links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Somatic nuclear mitochondrial DNA insertions are prevalent in the human brain and accumulate over time in fibroblasts PLoS Biology ·Weichen Zhou, Kalpita R. Karan, Asad Alhroob, Hans‐Ulrich Klein, Gabriel Sturm, Philip L. De Jager, David A. Bennett, Michio Hirano, Martin Picard, Ryan E. Mills	2024	10
2	Candida albicans selection for human commensalism results in substantial within-host diversity without decreasing fitness for invasive disease PLoS Biology ·Márcio Ferro, Noelle D. Visser, Kevin R. Amses, Andrea Hodgins-Davis, Ricardo Nieto González, 中田亨, Michael J. McFadden, Ryan E. Mills, Matthew J. O’Meara, Timothy Y. James, Teresa R. O’Meara	2023	30
3	Cas9 targeted enrichment of mobile elements using nanopore sequencing Nature Communications ·T. L. McDonald, Weichen Zhou, Pirniyazova Gulzira Jamalovna, Gao Zhi, Mohammed S. Abu Ajrah, Ryan E. Mills, Alan P. Boyle	2021	39
4	Characterization of nuclear mitochondrial insertions in the whole genomes of primates NAR Genomics and Bioinformatics ·Gargi Dayama, Weichen Zhou, Javier Prado-Martinez, Tomàs Marquès‐Bonet, Ryan E. Mills	2020	16
5	Structural variation in the sequencing era Nature Reviews Genetics ·Steve S. Ho, Alexander E. Urban, Ryan E. Mills Hit paper breakdown →	2019	335
6	Translation of upstream open reading frames in a model of neuronal differentiation BMC Genomics ·Caitlin M. Rodriguez, Sang Y. Chun, Ryan E. Mills, Peter K. Todd	2019	28
7	FusorSV: an algorithm for optimally combining data from multiple structural variation detection methods Genome biology ·戴道扬, Wan‐Ping Lee, Joseph F. Leone, Qihui Zhu, Chengsheng Zhang, Silvia Liu, Masaki Ban, WANG Xin'gang, Adam Mil-Homens, Eliza Cerveira, Paul Veravanich, Elizabeth Christman, Fábio C. P. Navarro, Timur R. Galeev, Mark Gerstein, Ryan E. Mills, Dong‐Guk Shin, Charles Lee, Ankit Malhotra	2018	38
8	A recurrence-based approach for validating structural variation using long-read sequencing technology GigaScience ·Xuefang Zhao, Ricardo Nieto González, Ryan E. Mills	2017	14
9	The Mobile Element Locator Tool (MELT): population-scale mobile element discovery and biology Genome Research ·Eugene J. Gardner, Vincent Kwok Lim Lam, Daniel Harris, Nelson T. Chuang, Emma Scott, W. Stephen Pittard, Ryan E. Mills, Scott E. Devine	2017	205
10	Resolving complex structural genomic rearrangements using a randomized approach Genome biology ·Xuefang Zhao, Sarah B. Emery, Bridget Myers, Jeffrey M. Kidd, Ryan E. Mills	2016	25
11	SPECtre: a spectral coherence-based classifier of actively translated transcripts from ribosome profiling sequence data BMC Bioinformatics ·Sang Y. Chun, Caitlin M. Rodriguez, Peter K. Todd, Ryan E. Mills	2016	35
12	CodonShuffle: a tool for generating and analyzing synonymously mutated sequences Virus Evolution ·Lidia Henrieke van der Helm, Ryan E. Mills, Adam S. Lauring	2015	17
13	The genomic landscape of polymorphic human nuclear mitochondrial insertions Nucleic Acids Research ·Gargi Dayama, Sarah B. Emery, Jeffrey M. Kidd, Ryan E. Mills	2014	127
14	CGG Repeat-Associated Translation Mediates Neurodegeneration in Fragile X Tremor Ataxia Syndrome Neuron ·Peter K. Todd, Seok Yoon Oh, Amy Krans, Fang He, Chantal Sellier, 信之山内, Abigail J. Renoux, А. А. Малахова, K. Matthew Scaglione, Venkatesha Basrur, Kojo S.J. Elenitoba‐Johnson, Jean Paul Vonsattel, Elan D. Louis, Michael A. Sutton, Masanobu Kodama, Ryan E. Mills, Nicolas Charlet‐Berguerand, Henry L. Paulson	2013	1
15	Small insertions and deletions (INDELs) in human genomes Human Molecular Genetics ·Julienne M. Mullaney, Ryan E. Mills, W. Stephen Pittard, Scott E. Devine	2010	225
16	Natural Mutagenesis of Human Genomes by Endogenous Retrotransposons Cell ·Rebecca C. Iskow, Michael T. McCabe, Ryan E. Mills, Aqsa Wadood, W. Stephen Pittard, Andrew F. Neuwald, Erwin G. Van Meir, Paula M. Vertino, Scott E. Devine	2010	418
17	Active Alu retrotransposons in the human genome Genome Research ·E. Andrew Bennett, Heiko Keller, Ryan E. Mills, Steffen Schmidt, John V. Moran, Oliver Weichenrieder, Scott E. Devine	2008	198
18	Which transposable elements are active in the human genome? Trends in Genetics ·Ryan E. Mills, E. Andrew Bennett, Rebecca C. Iskow, Scott E. Devine	2007	343
19	Recently Mobilized Transposons in the Human and Chimpanzee Genomes The American Journal of Human Genetics ·Ryan E. Mills, E. Andrew Bennett, Rebecca C. Iskow, Hanis Wan Husin, Circe Tsui, W. Stephen Pittard, Scott E. Devine	2006	115
20	Improving gene annotation of complete viral genomes Nucleic Acids Research ·Ryan E. Mills	2003	41

About Ryan E. Mills

Ryan E. Mills is a scholar working on Genetics, Molecular Biology, Aging, Plant Science and Cancer Research, having authored 52 papers that have together received 5.3k indexed citations. Recurring topics across this work include Genomics and Phylogenetic Studies (18 papers), Chromosomal and Genetic Variations (15 papers), RNA and protein synthesis mechanisms (14 papers), Genomic variations and chromosomal abnormalities (11 papers), CRISPR and Genetic Engineering (5 papers), Genomics and Rare Diseases (4 papers), Gene expression and cancer classification (4 papers) and Genomics and Chromatin Dynamics (4 papers). The work is most often cited by research in Genetics (1.9k citations), Molecular Biology (3.9k citations), Plant Science (1.5k citations), Cancer Research (390 citations) and Aging (31 citations). Ryan E. Mills has collaborated with scholars based in United States, United Kingdom and South Korea. Frequent co-authors include Scott E. Devine, W. Stephen Pittard, Anita H. Corbett, Allison Lange, Rebecca C. Iskow, Murray Stewart, E. Andrew Bennett, Steve S. Ho, Alexander E. Urban and Circe Tsui. Their work appears in journals such as Genome biology, Proceedings of the National Academy of Sciences, Genome Research, Nucleic Acids Research and Current Protocols in Bioinformatics.

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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