Peter O'Connell

2.4k citations
18 papers · 2.1k · 1 hit paper · h-index 15

Impact in

Papers in

    • Neurofibromatosis and Schwannoma Cases 5
    • Neurogenetic and Muscular Disorders Research 3
    • Genomic variations and chromosomal abnormalities 2

Peter O'Connell

18 papers receiving 1.9k citations

Peter O'Connell's Hit Papers

Localization of an ataxia-telangiectasia gene to chromosome 11q22–23 1988 · 579 citations
5790+12+25Years since publication100200300400500

Peers

Peter O'Connell
Comparison fields: 5 of 101
  • Cellular and Molecular Neuroscience 434
  • Neurology 301
  • Cancer Research 260
  • Molecular Biology 1.2k
  • Genetics 397
Replace Martine Jaegle with:
Martine Jaegle Netherlands
Satomi Mitsuhashi Japan
Nobutada Tachi Japan
Linda C. Yang United States
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John R. Bermingham United States
Ender Karaca United States
Sachiko Kamakura Japan
Brian J. Krueger United States
Lohith Madireddy United States
Peter O'Connell relative to Martine Jaegle Netherlands Martine Jaegle's profile →
Citations per field
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Citations per year

Countries citing papers authored by Peter O'Connell

Since Specialization
Citations

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

Fields of papers citing papers by Peter O'Connell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter O'Connell. 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 Peter O'Connell. The network helps show where Peter O'Connell may publish in the future.

Co-authors

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

All Works

18 of 18 papers shown
#Work
1
Localization of an ataxia-telangiectasia gene to chromosome 11q22–23
Hit paper breakdown →
1988579
2 1984490
3 1989305
4 1995197
5 198098
6 198890
7
Etiological heterogeneity in X-linked spastic paraplegia.
198765
8 198439
9 199939
10
Diagnosis of neurofibromatosis I by using tightly linked, flanking DNA markers.
199036
11 199233
12 198932
13 198128
14 199021
15
Assaults against general practitioners in Ireland.
199717
16 19886
17 19883
18 19882

About Peter O'Connell

Peter O'Connell is a scholar working on Neurology, Genetics, Molecular Biology, Genetics and Hematology, having authored 18 papers that have together received 2.1k indexed citations. Recurring topics across this work include RNA and protein synthesis mechanisms (5 papers), Neurofibromatosis and Schwannoma Cases (5 papers), Genomics and Chromatin Dynamics (3 papers), Neurogenetic and Muscular Disorders Research (3 papers), Chromatin Remodeling and Cancer (3 papers), Sarcoma Diagnosis and Treatment (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Cancer-related gene regulation (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (434 citations), Neurology (301 citations), Cancer Research (260 citations), Molecular Biology (1.2k citations) and Genetics (397 citations). Peter O'Connell has collaborated with scholars based in United States, Poland and Belgium. Frequent co-authors include Michael Rosbash, Mark Leppert, Yusuke Nakamura, Dora Stauffer, Ray L. White, Jean‐Marc Lalouel, Vernon E. Anderson, Marta Izquierdo, Charles A. Vaslet and Gregory Mark Lathrop. Their work appears in journals such as Nucleic Acids Research, Nature, Genomics, Human Genetics and Trends in 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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