Peyton Greenside

13.7k citations
13 papers · 1.6k indexed · 1 hit paper · h-index 11

Impact in

    • Cancer Genomics and Diagnostics
    • Genomics and Chromatin Dynamics
    • Single-cell and spatial transcriptomics
    • Epigenetics and DNA Methylation
    • RNA Research and Splicing
    • RNA modifications and cancer
    • CRISPR and Genetic Engineering
    • RNA and protein synthesis mechanisms

Papers in

    • Cancer Genomics and Diagnostics 2
    • Genomics and Chromatin Dynamics 5
    • RNA Research and Splicing 3
    • CRISPR and Genetic Engineering 2

Peyton Greenside

13 papers receiving 1.6k citations

Hit Papers

Lineage-specific and single-cell chromatin accessibility charts human hematopoiesis and leukemia evolution 2016 · 656 citations
6562016202620192022200400600

Peers

Peyton Greenside
Comparison fields: 5 of 97
  • Cancer Research 312
  • Molecular Biology 1.3k
  • Hematology 148
  • Immunology 204
  • Oncology 238
Replace Matthias Muhar with:
Matthias Muhar Austria
Hauke Cornils Switzerland
Abraham S. Weintraub United States
Ivo J. Huijbers Netherlands
Olga Anczuków United States
Grzegorz Nalepa United States
Joanne Kamens United States
Heather A. Hoke United States
Ramya Raviram United States
Warren A. Whyte United States
Peyton Greenside relative to Matthias Muhar Austria Matthias Muhar's profile →
Citations per field
00.5×1.5×1.9×
Matthias Muhar · 1×
Citations per year

Countries citing papers authored by Peyton Greenside

Since Specialization
Citations

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

Fields of papers citing papers by Peyton Greenside

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peyton Greenside. 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 Peyton Greenside. The network helps show where Peyton Greenside may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Peyton Greenside, 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 Peyton Greenside Line = papers co-authored together Peyton Greenside links everyone, so they are left out of the graph.

All Works

13 of 13 papers shown
#Work
1 2020113
2 201959
3 201851
4 2018104
5 20182
6 2017128
7 20177
8 2017111
9 201778
10
Lineage-specific and single-cell chromatin accessibility charts human hematopoiesis and leukemia evolution
Hit paper breakdown →
2016656
11 201685
12 2015212
13 201544

About Peyton Greenside

Peyton Greenside is a scholar working on Cancer Research, Molecular Biology, Computational Theory and Mathematics, Pathology and Forensic Medicine and Oncology, having authored 13 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (5 papers), RNA Research and Splicing (3 papers), Cancer Mechanisms and Therapy (2 papers), Computational Drug Discovery Methods (2 papers), CRISPR and Genetic Engineering (2 papers), Cancer Genomics and Diagnostics (2 papers), Acute Myeloid Leukemia Research (1 paper) and Genomics and Rare Diseases (1 paper). The work is most often cited by research in Cancer Research (312 citations), Molecular Biology (1.3k citations), Hematology (148 citations), Immunology (204 citations) and Oncology (238 citations). Peyton Greenside has collaborated with scholars based in United States, Germany and Austria. Frequent co-authors include Anshul Kundaje, M Snyder, Jonathan K. Pritchard, William J. Greenleaf, M. Ryan Corces, Ravindra Majeti, Jason D. Buenrostro, Julie L. Koenig, Steven M. Chan and Howard Y. Chang. Their work appears in journals such as Cancer Discovery, Nature Genetics, PLoS Biology, Nature Medicine and CPT Pharmacometrics & Systems Pharmacology.

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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