Mitchell R. Vollger

14.0k total citations · 4 hit papers
19 papers, 1.6k citations indexed

About

Mitchell R. Vollger is a scholar working on Molecular Biology, Plant Science and Genetics. According to data from OpenAlex, Mitchell R. Vollger has authored 19 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 12 papers in Plant Science and 10 papers in Genetics. Recurrent topics in Mitchell R. Vollger's work include Chromosomal and Genetic Variations (12 papers), Genomics and Phylogenetic Studies (10 papers) and Genomic variations and chromosomal abnormalities (9 papers). Mitchell R. Vollger is often cited by papers focused on Chromosomal and Genetic Variations (12 papers), Genomics and Phylogenetic Studies (10 papers) and Genomic variations and chromosomal abnormalities (9 papers). Mitchell R. Vollger collaborates with scholars based in United States, Italy and Germany. Mitchell R. Vollger's co-authors include Evan E. Eichler, Glennis A. Logsdon, Adam M. Phillippy, Sergey Koren, Arang Rhie, Sergey Nurk, Karen H. Miga, Brian P. Walenz, Philip C. Dishuck and David Porubský and has published in prestigious journals such as Science, Nature Communications and Nature Biotechnology.

In The Last Decade

Mitchell R. Vollger

17 papers receiving 1.6k citations

Hit Papers

Long-read human genome sequencing and its applications 2020 2026 2022 2024 2020 2020 2022 2022 100 200 300 400 500
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Long-read human genome sequencing and its applications
    2020 589 citations Glennis A. Logsdon, Mitchell R. Vollger et al. Nature Reviews Genetics profile →
  2. HiCanu: accurate assembly of segmental duplications, satellites, and allelic variants from high-fidelity long reads
    2020 384 citations Sergey Nurk, Brian P. Walenz et al. Genome Research profile →
  3. Segmental duplications and their variation in a complete human genome
    2022 152 citations Mitchell R. Vollger, Xavi Guitart et al. Science profile →
  4. Epigenetic patterns in a complete human genome
    2022 146 citations Ariel Gershman, Michael E.G. Sauria et al. Science profile →

Peers

Mitchell R. Vollger
Karen H. Miga United States
Andrew Wu United Kingdom
Marco Mangone United States
Rupali P Patwardhan United States
Glennis A. Logsdon United States
Stuart Stephen Australia
Chun Liang United States
Tatiana V. Tatarinova United States
Sam Kovaka United States
Glenn Proctor United Kingdom
Karen H. Miga United States
Mitchell R. Vollger
Citations per year, relative to Mitchell R. Vollger Mitchell R. Vollger (= 1×) peers Karen H. Miga

Countries citing papers authored by Mitchell R. Vollger

Since Specialization
Citations

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

Fields of papers citing papers by Mitchell R. Vollger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mitchell R. Vollger. 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 Mitchell R. Vollger. The network helps show where Mitchell R. Vollger may publish in the future.

Co-authorship network of co-authors of Mitchell R. Vollger

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

All Works

19 of 19 papers shown
1.
Bubb, Kerry L., Joseph Min, Erik J. Bergstrom, et al.. (2025). The regulatory potential of transposable elements in maize. Nature Plants. 11(6). 1181–1192. 2 indexed citations
2.
Swanson, Elliott, Benjamin J. Mallory, Mitchell R. Vollger, et al.. (2025). Mapping single-cell diploid chromatin fiber architectures using DAF-seq. Nature Biotechnology.
3.
Li, Chang, Benjamin J. Mallory, Elliott Swanson, et al.. (2024). Resolving the chromatin impact of mosaic variants with targeted Fiber-seq. Genome Research. 34(12). 2269–2278. 4 indexed citations
4.
Peter, Cyril, Risa Watanabe, Bibi Kassim, et al.. (2024). Single chromatin fiber profiling and nucleosome position mapping in the human brain. Cell Reports Methods. 4(12). 100911–100911.
5.
Jha, Anupama, Jane Ranchalis, Benjamin J. Mallory, et al.. (2024). DNA-m6A calling and integrated long-read epigenetic and genetic analysis with fibertools. Genome Research. 34(11). 1976–1986. 15 indexed citations
6.
Yang, Xiangyu, Yawen Zou, Shilong Zhang, et al.. (2023). Characterization of large-scale genomic differences in the first complete human genome. Genome biology. 24(1). 157–157. 10 indexed citations
7.
Porubský, David, Mitchell R. Vollger, William T. Harvey, et al.. (2023). Gaps and complex structurally variant loci in phased genome assemblies. Genome Research. 33(4). 496–510. 23 indexed citations
8.
DeWitt, William S., Luke Zhu, Mitchell R. Vollger, et al.. (2023). mutyper: assigning and summarizing mutation types foranalyzing germline mutation spectra. The Journal of Open Source Software. 8(85). 5227–5227. 2 indexed citations
9.
Vollger, Mitchell R., Xavi Guitart, Philip C. Dishuck, et al.. (2022). Segmental duplications and their variation in a complete human genome. Science. 376(6588). eabj6965–eabj6965. 152 indexed citations breakdown →
10.
Vollger, Mitchell R., Peter Kerpedjiev, Adam M. Phillippy, & Evan E. Eichler. (2022). StainedGlass: interactive visualization of massive tandem repeat structures with identity heatmaps. Bioinformatics. 38(7). 2049–2051. 67 indexed citations
11.
Gershman, Ariel, Michael E.G. Sauria, Xavi Guitart, et al.. (2022). Epigenetic patterns in a complete human genome. Science. 376(6588). eabj5089–eabj5089. 146 indexed citations breakdown →
12.
Hsieh, PingHsun, Vy Dang, Mitchell R. Vollger, et al.. (2021). Evidence for opposing selective forces operating on human-specific duplicated TCAF genes in Neanderthals and humans. Nature Communications. 12(1). 5118–5118. 9 indexed citations
13.
Vollger, Mitchell R.. (2021). Data files for: Segmental duplications and their variation in a complete human genome.. Zenodo (CERN European Organization for Nuclear Research). 1 indexed citations
14.
Logsdon, Glennis A., Mitchell R. Vollger, & Evan E. Eichler. (2020). Long-read human genome sequencing and its applications. Nature Reviews Genetics. 21(10). 597–614. 589 indexed citations breakdown →
15.
Nurk, Sergey, Brian P. Walenz, Arang Rhie, et al.. (2020). HiCanu: accurate assembly of segmental duplications, satellites, and allelic variants from high-fidelity long reads. Genome Research. 30(9). 1291–1305. 384 indexed citations breakdown →
16.
Vollger, Mitchell R., Glennis A. Logsdon, Peter A. Audano, et al.. (2019). Improved assembly and variant detection of a haploid human genome using single‐molecule, high‐fidelity long reads. Annals of Human Genetics. 84(2). 125–140. 81 indexed citations
17.
Hsieh, PingHsun, Mitchell R. Vollger, Vy Dang, et al.. (2019). Adaptive archaic introgression of copy number variants and the discovery of previously unknown human genes. Science. 366(6463). 51 indexed citations
18.
Maggiolini, Flavia Angela Maria, Stuart Cantsilieris, Pietro D’Addabbo, et al.. (2019). Genomic inversions and GOLGA core duplicons underlie disease instability at the 15q25 locus. PLoS Genetics. 15(3). e1008075–e1008075. 16 indexed citations
19.
Vollger, Mitchell R., Philip C. Dishuck, Melanie Sorensen, et al.. (2018). Long-read sequence and assembly of segmental duplications. Nature Methods. 16(1). 88–94. 95 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 Karen H. Miga Breakdown of academic impact, for papers by Andrew Wu Breakdown of academic impact, for papers by Marco Mangone Breakdown of academic impact, for papers by Rupali P Patwardhan Breakdown of academic impact, for papers by Glennis A. Logsdon Breakdown of academic impact, for papers by Stuart Stephen Breakdown of academic impact, for papers by Chun Liang Breakdown of academic impact, for papers by Tatiana V. Tatarinova Breakdown of academic impact, for papers by Sam Kovaka Breakdown of academic impact, for papers by Glenn Proctor
Rankless by CCL
2026