Erin Conboy

945 citations
28 papers · 490 · h-index 12

Impact in

Papers in

    • Genomics and Rare Diseases 6
    • Genetics and Neurodevelopmental Disorders 3
    • Genetic Syndromes and Imprinting 3
    • Mitochondrial Function and Pathology 3
    • Congenital heart defects research 2

Erin Conboy

27 papers receiving 484 citations

Peers

Erin Conboy
Comparison fields: 5 of 75
  • Ophthalmology 106
  • Clinical Biochemistry 54
  • Physiology 164
  • Neurology 28
  • Molecular Biology 216
Replace Anandalakshmi Venkatraman with:
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Citations per field
00.5×3.5×
Anandalakshmi Venkatraman · 1×
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 201528
5 201717
6 201715
7 201514
8 201713
9 201912
10 201812
11 201912
12 201911
13 200910
14 20088
15 20186
16 20225
17 20173
18 20223
19 20242
20 20232

About Erin Conboy

Erin Conboy is a scholar working on Genetics, Molecular Biology, Surgery, Epidemiology and Clinical Biochemistry, having authored 28 papers that have together received 490 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (3 papers), Metabolism and Genetic Disorders (3 papers), Genetic Syndromes and Imprinting (3 papers), Mitochondrial Function and Pathology (3 papers), Lysosomal Storage Disorders Research (3 papers), Trypanosoma species research and implications (2 papers) and Congenital heart defects research (2 papers). The work is most often cited by research in Ophthalmology (106 citations), Clinical Biochemistry (54 citations), Physiology (164 citations), Neurology (28 citations) and Molecular Biology (216 citations). Erin Conboy has collaborated with scholars based in United States, Brazil and Germany. Frequent co-authors include Alistair J. Barber, Sarah K. Bronson, Allen R. Kunselman, Matthew J. Gastinger, David E. Hartigan, Brenda D. Moore, Terrone L. Rosenberry, Dana Kim Reed, Vijayaraghavan Rangachari and Filippo Pinto e Vairo. Their work appears in journals such as Molecular Case Studies, Clinical Genetics, Ophthalmic Genetics, American Journal of Physiology-Renal Physiology and Journal of Medical Genetics.

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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