Joseph Glessner

30.3k citations
138 papers · 5.5k indexed · 1 hit paper · h-index 39
  • Genetics top 0.2%
    • Genomic variations and chromosomal abnormalities 37
    • Genetic Associations and Epidemiology 27
    • Genetics and Neurodevelopmental Disorders 27
    • Genomics and Rare Diseases 15
    • Congenital heart defects research 15
    • RNA modifications and cancer 13
  • Genetics top 5%
    • Genomic variations and chromosomal abnormalities 37
    • Genetic Associations and Epidemiology 27
    • Genetics and Neurodevelopmental Disorders 27
    • Genomics and Rare Diseases 15
  • Immunology top 5%
    • Autism Spectrum Disorder Research 13
    • Attention Deficit Hyperactivity Disorder 10

Joseph Glessner

129 papers receiving 5.4k citations

Hit Papers

PennCNV: An integrated hidden Markov model designed for h...1.2k20072026201320192505007501000

Peers

Joseph Glessner
Comparison fields: 5 of 139
  • Genetics 3.4k
  • Cancer Research 623
  • Molecular Biology 2.2k
  • Genetics 243
  • Immunology 478
Replace Erik G. Puffenberger with:
Erik G. Puffenberger United States
Bryan Howie United States
Yin Yao Shugart United States
Brendan Blumenstiel United States
Mark Lathrop France
Hans Eiberg Denmark
Lars Feuk Sweden
Yann Hérault France
Brian J. O’Roak United States
Arif B. Ekici Germany
Joseph Glessner relative to Erik G. Puffenberger United States Erik G. Puffenberger's profile →
Citations per field
00.5×
Erik G. Puffenberger · 1×
Citations per year

Countries citing papers authored by Joseph Glessner

Since Specialization
Citations

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

Fields of papers citing papers by Joseph Glessner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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About Joseph Glessner

Joseph Glessner is a scholar working on Genetics, Cancer Research and Molecular Biology, having authored 138 papers that have together received 5.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (37 papers), Genetic Associations and Epidemiology (27 papers), Genetics and Neurodevelopmental Disorders (27 papers), Genomics and Rare Diseases (15 papers), Congenital heart defects research (15 papers), RNA modifications and cancer (13 papers), Autism Spectrum Disorder Research (13 papers) and Attention Deficit Hyperactivity Disorder (10 papers). The work is most often cited by research in Genetics (3.4k citations), Cancer Research (623 citations) and Molecular Biology (2.2k citations). Joseph Glessner has collaborated with scholars based in United States, China and Iceland. Frequent co-authors include Håkon Håkonarson, Kai Wang, Struan F.A. Grant, Mingyao Li, Maja Bućan, Dexter Hadley, Rui Liu, Rosetta Chiavacci, Jonathan P. Bradfield and Edward C. Frackelton. Their work appears in journals such as PLoS ONE, Scientific Reports, Obesity, Journal of Allergy and Clinical Immunology and Nucleic Acids Research.

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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2026