Joseph Glessner

30.4k citations
137 papers · 5.4k · 1 hit paper · h-index 39

Impact in

  • Genetics top 0.2%
    • Genomic variations and chromosomal abnormalities
    • Genetic Associations and Epidemiology
    • Genomics and Rare Diseases
    • Genetics and Neurodevelopmental Disorders
    • Cancer Genomics and Diagnostics

Papers in

    • Genomic variations and chromosomal abnormalities 31
    • Genetic Associations and Epidemiology 23
    • Genetics and Neurodevelopmental Disorders 18
    • Genomics and Rare Diseases 12
    • Congenital heart defects research 11
    • RNA modifications and cancer 10

Joseph Glessner

129 papers receiving 5.3k citations

Joseph Glessner's Hit Papers

PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data 2007 · 1.2k citations
1.2k0+6+12Years since publication2505007501000

Peers

Joseph Glessner
Comparison fields: 5 of 134
  • Genetics 2.9k
  • Cancer Research 453
  • Molecular Biology 1.7k
  • Immunology 405
  • Endocrine and Autonomic Systems 113
Replace Erik G. Puffenberger with:
Erik G. Puffenberger United States
Harald H.H. Göring United States
Arif B. Ekici Germany
Joseph E. Powell Australia
Brendan Blumenstiel United States
Hossein Najmabadi Iran
Alexander Gusev United States
Marwan Shinawi United States
Thierry Bienvenu France
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Joseph Glessner relative to Erik G. Puffenberger United States Erik G. Puffenberger's profile →
Citations per field
00.5×1.7×
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-authors

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

20 of 20 papers shown

Showing the 20 most-cited of 137 papers — load more, or switch the sort, to bring in the rest.

#Work
1
PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
Hit paper breakdown →
20071177
2 2008234
3 2011231
4 2009207
5 2009155
6 2008153
7 2009150
8 2011138
9 2011135
10 2011128
11 2009109
12 201396
13 201395
14 201085
15 201178
16 201174
17 201269
18 200968
19 200967
20 201063

About Joseph Glessner

Joseph Glessner is a scholar working on Genetics, Molecular Biology, Surgery, Cognitive Neuroscience and Epidemiology, having authored 137 papers that have together received 5.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (31 papers), Genetic Associations and Epidemiology (23 papers), Genetics and Neurodevelopmental Disorders (18 papers), Genomics and Rare Diseases (12 papers), Congenital heart defects research (11 papers), RNA modifications and cancer (10 papers), Autism Spectrum Disorder Research (9 papers) and Attention Deficit Hyperactivity Disorder (9 papers). The work is most often cited by research in Genetics (2.9k citations), Cancer Research (453 citations), Molecular Biology (1.7k citations), Immunology (405 citations) and Endocrine and Autonomic Systems (113 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, Journal of Allergy and Clinical Immunology, Obesity and Molecular Psychiatry.

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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