Matthew Flickinger

16.8k citations
6 papers · 449 · 1 hit paper · h-index 5

Impact in

  • Genetics top 10%
    • Genetic Associations and Epidemiology
    • Genomics and Rare Diseases
    • Forensic and Genetic Research
    • Genomic variations and chromosomal abnormalities
    • Genetic Mapping and Diversity in Plants and Animals
    • Cancer Genomics and Diagnostics

Papers in

    • Genetic Associations and Epidemiology 3
    • Genomics and Rare Diseases 1
    • Forensic and Genetic Research 1
    • Molecular Biology Techniques and Applications 3
    • Genomics and Phylogenetic Studies 2
    • Gene expression and cancer classification 2

Matthew Flickinger

6 papers receiving 446 citations

Matthew Flickinger's Hit Papers

LocusZoom.js: interactive and embeddable visualization of genetic association study results 2021 · 145 citations
1450+1+3Years since publication4080120

Peers

Matthew Flickinger
Comparison fields: 5 of 84
  • Genetics 220
  • Cancer Research 56
  • Molecular Biology 189
  • Clinical Biochemistry 7
  • Nephrology 6
Replace Chaowei Tian with:
Chaowei Tian China
Emmanuelle Souzeau Australia
Kerith‐Rae Dias Australia
Ninon Mounier Switzerland
Kurt N. Hetrick United States
Ivone Leong United States
Natalia T. Leach United States
Lori Iwasaki United States
Angli Xue Australia
Vlad Makarov United States
Matthew Flickinger relative to Chaowei Tian China Chaowei Tian's profile →
Citations per field
00.5×1.5×2.2×
Chaowei Tian · 1×
Citations per year

Countries citing papers authored by Matthew Flickinger

Since Specialization
Citations

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

Fields of papers citing papers by Matthew Flickinger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

6 of 6 papers shown
#Work
1 2012215
2
LocusZoom.js: interactive and embeddable visualization of genetic association study results
Hit paper breakdown →
2021145
3 202036
4 201530
5 201422
6 20221

About Matthew Flickinger

Matthew Flickinger is a scholar working on Genetics, Molecular Biology, Information Systems, Information Systems and Management and Artificial Intelligence, having authored 6 papers that have together received 449 indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (3 papers), Molecular Biology Techniques and Applications (3 papers), Genomics and Phylogenetic Studies (2 papers), Gene expression and cancer classification (2 papers), Research Data Management Practices (1 paper), Scientific Computing and Data Management (1 paper), Genomics and Rare Diseases (1 paper) and Forensic and Genetic Research (1 paper). The work is most often cited by research in Genetics (220 citations), Cancer Research (56 citations), Molecular Biology (189 citations), Clinical Biochemistry (7 citations) and Nephrology (6 citations). Matthew Flickinger has collaborated with scholars based in United States and Poland. Frequent co-authors include Gonçalo R. Abecasis, Michael Boehnke, Hyun Min Kang, Goo Jun, Kimberly F. Doheny, Kurt N. Hetrick, Jane Romm, Andrew P. Boughton, Ryan Welch and Peter VandeHaar. Their work appears in journals such as The American Journal of Human Genetics, Bioinformatics, Psychophysiology, Genome Research and PubMed.

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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