Ryan Poplin
Impact in
- Genetics top 0.1%
- Genomics and Rare Diseases
- Genetic diversity and population structure
- Genetic Mapping and Diversity in Plants and Animals
- Genetic and phenotypic traits in livestock
- Genomic variations and chromosomal abnormalities
- Health Informatics top 0.5%
Papers in ⓘ
- Genetics 6
- Genomics and Rare Diseases 5
- Genomic variations and chromosomal abnormalities 4
- Genetic Associations and Epidemiology 1
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- Cell Image Analysis Techniques 1
- Co-authors
- Mark A. DePristo (6 shared papers)Eric Banks (3 shared papers)Stacey Gabriel (2 shared papers)David Altshuler (2 shared papers)Guillermo del Angel (2 shared papers)Christopher Hartl (2 shared papers)Kiran Garimella (2 shared papers)Manuel A. Rivas (1 shared paper)
- Journals
- Nature Biomedical Engineering (1 paper)Nature Genetics (1 paper)BMC Genomics (1 paper)JAMA (1 paper)Quantitative Biology (1 paper)
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
Ryan Poplin
12 papers receiving 14.0k citations
Hit Papers
Peers
Comparison fields: 5 of 187
- Genetics 5.3k
- Health Informatics 196
- Cancer Research 2.0k
- Molecular Biology 6.7k
- Biophysics 317
Countries citing papers authored by Ryan Poplin
This map shows the geographic impact of Ryan Poplin'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 Poplin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ryan Poplin more than expected).
Fields of papers citing papers by Ryan Poplin
This network shows the impact of papers produced by Ryan Poplin. 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 Poplin. The network helps show where Ryan Poplin may publish in the future.
Co-authors
The 25 scholars most cited alongside Ryan Poplin, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | A framework for variation discovery and genotyping using next-generation DNA sequencing data Hit paper breakdown → | 2011 | 7268 |
| 2 | From FastQ Data to High‐Confidence Variant Calls: The Genome Analysis Toolkit Best Practices Pipeline Hit paper breakdown → | 2013 | 4252 |
| 3 | Prediction of cardiovascular risk factors from retinal fundus photographs via deep learning Hit paper breakdown → | 2018 | 1029 |
| 4 | A universal SNP and small-indel variant caller using deep neural networks Hit paper breakdown → | 2018 | 757 |
| 5 | In Silico Labeling: Predicting Fluorescent Labels in Unlabeled Images Hit paper breakdown → | 2018 | 394 |
| 6 | Identifying viruses from metagenomic data using deep learning Hit paper breakdown → | 2020 | 361 |
| 7 | 2021 | 27 | |
| 8 | 2015 | 9 | |
| 9 | 2021 | 5 | |
| 10 | 2017 | 3 | |
| 11 | 2019 | 3 | |
| 12 | 2018 | 2 |
About Ryan Poplin
Ryan Poplin is a scholar working on Genetics, Biophysics, Cancer Research, Ophthalmology and Molecular Biology, having authored 12 papers that have together received 14.1k indexed citations. Recurring topics across this work include Genomics and Phylogenetic Studies (6 papers), Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Cancer Genomics and Diagnostics (2 papers), Advanced biosensing and bioanalysis techniques (1 paper), Genetic Associations and Epidemiology (1 paper), Cell Image Analysis Techniques (1 paper) and Digital Imaging for Blood Diseases (1 paper). The work is most often cited by research in Genetics (5.3k citations), Health Informatics (196 citations), Cancer Research (2.0k citations), Molecular Biology (6.7k citations) and Biophysics (317 citations). Ryan Poplin has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Mark A. DePristo, Eric Banks, Stacey Gabriel, David Altshuler, Guillermo del Angel, Christopher Hartl, Kiran Garimella, Manuel A. Rivas, Aaron McKenna and Jared Maguire. Their work appears in journals such as Nature Biomedical Engineering, Nature Genetics, BMC Genomics, JAMA and Quantitative Biology.
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.