Erin Conboy

905 citations
28 papers · 481 · h-index 11

Impact in

Papers in

    • Genomics and Rare Diseases 5
    • Genetic Syndromes and Imprinting 4
    • Genomic variations and chromosomal abnormalities 4
    • Genetics and Neurodevelopmental Disorders 3
    • Mitochondrial Function and Pathology 3

Erin Conboy

27 papers receiving 475 citations

Peers

Erin Conboy
Comparison fields: 5 of 78
  • Ophthalmology 118
  • Clinical Biochemistry 58
  • Physiology 164
  • Neurology 31
  • Molecular Biology 241
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Citations per field
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Citations per year

Countries citing papers authored by Erin Conboy

Since Specialization
Citations

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

Fields of papers citing papers by Erin Conboy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 28 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2008148
2 2007133
3 201729
4 201527
5 201717
6 201715
7 201514
8 201713
9 201912
10 201912
11 201910
12 201810
13 200910
14 20087
15 20186
16 20225
17 20173
18 20241
19 20241
20 20241

About Erin Conboy

Erin Conboy is a scholar working on Genetics, Molecular Biology, Epidemiology, Surgery and Clinical Biochemistry, having authored 28 papers that have together received 481 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), Genetic Syndromes and Imprinting (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Metabolism and Genetic Disorders (3 papers), Lysosomal Storage Disorders Research (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Mitochondrial Function and Pathology (3 papers) and Trypanosoma species research and implications (3 papers). The work is most often cited by research in Ophthalmology (118 citations), Clinical Biochemistry (58 citations), Physiology (164 citations), Neurology (31 citations) and Molecular Biology (241 citations). Erin Conboy has collaborated with scholars based in United States, Germany and Brazil. Frequent co-authors include Alistair J. Barber, Sarah K. Bronson, Matthew J. Gastinger, Allen R. Kunselman, David E. Hartigan, Brenda D. Moore, Vijayaraghavan Rangachari, Terrone L. Rosenberry, Dana Kim Reed and Eric W. Klee. Their work appears in journals such as Molecular Case Studies, American Journal of Physiology-Renal Physiology, Ophthalmic Genetics, Clinical Genetics and Molecular Genetics and Metabolism.

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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