Peter O'Connell

2.4k citations

17 papers · 1.4k indexed · 1 hit paper · h-index 14

Impact in

Cellular and Molecular Neuroscience top 5%
- Neurobiology and Insect Physiology Research
Neurology top 5%
- Neurofibromatosis and Schwannoma Cases

Papers in

Neurology 5
- Neurofibromatosis and Schwannoma Cases 5
Genetics 3
- Neurogenetic and Muscular Disorders Research 3
- Genomic variations and chromosomal abnormalities 2

Co-authors: Michael Rosbash Yusuke Nakamura Mark Leppert Dora Stauffer R. White Vernon Anderson Jean‐Marc Lalouel Marta Izquierdo
Journals: Nucleic Acids Research (6 papers)Nature (2 papers)Genomics (2 papers)The EMBO Journal (1 paper)Human Genetics (1 paper)
Partner nations: United States Belgium Ireland

In The Last Decade

Peter O'Connell

17 papers receiving 1.4k citations

Hit Papers

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Sequence, structure, and codon preference of theDrosophilaribosomal protein 49 gene 1984 · 502 citations

Peers

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-authorship network

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

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17 of 17 papers shown

#	Work
1	Gene expression patterns in cell lines from patients with 18q- syndrome Human Genetics ·Keely J. Higbie, Jannine D. Cody, Robin J. Leach, Peter O'Connell	1999	24
2	Assaults against general practitioners in Ireland. PubMed ·Peter O'Connell, Gerard Bury	1997	16
3	Genomic organization of the neurofibromatosis 1 gene (NF1) Genomics ·Y Li, Peter O'Connell, Riley Ck, Richard Cawthon, J. Castañer, Lester B. Ball, Susie O’Brien, Margaret Robertson, Bernd Jäger, David Viskochil	1995	179
4	Characterization of human adenylate kinase 3 (AK3) cDNA and mapping of the AK3 pseudogene to an intron of the NF1 gene Genomics ·Gangfeng Xu, Peter O'Connell, Jeff Stevens, Ray White	1992	31
5	A chromosome jump crosses a translocation breakpoint in the von recklinghausen neurofibromatosis region Genes Chromosomes and Cancer ·Margaret R. Wallace, Lone B. Andersen, Jane W. Fountain, Hana M. Odeh, David Viskochil, Douglas A. Marchuk, Peter O'Connell, R. White, Francis S. Collins	1990	19
6	Diagnosis of neurofibromatosis I by using tightly linked, flanking DNA markers. PubMed ·Niesler Tr, Peter O'Connell, John C. Carey, Mark Leppert, Justas Bajarskas, Rosemarie Plaetke, Barbara Ogden, R. White	1990	32
7	Benign familial neonatal convulsions linked to genetic markers on chromosome 20 Nature ·Mark Leppert, Vernon Anderson, Jernstrom Eeva, Dora Stauffer, Peter O'Connell, Yusuke Nakamura, Jean‐Marc Lalouel, R. White	1989	266
8	Progress towards identifying the neurofibromatosis (NF1) gene Trends in Genetics ·Francis S. Collins, Peter O'Connell, Bruce A.J. Ponder, Bernd R. Seizinger	1989	30
9	Isotation and mapping of a polymorphic DNA sequence (pEFD134.7) on chromosome 3 [D3S45] Nucleic Acids Research ·Yusuke Nakamura, E. Fujimoto, Peter O'Connell, M. Leppert, G.M. Lathrop, Jean-Marc Lalouel, R. White	1988	2
10	Isolation and mapping of a polymorphic DNA sequence (pYNZ22) on chromosome 17p [D17S30] Nucleic Acids Research ·Yusuke Nakamura, L. Ballard, M. Leppert, Peter O'Connell, G.M. Lathrop, J.-M. Lalouel, R. White	1988	90
11	Isolation and mapping of a polymorphic DNA sequence (pYNZ132) on chromosome 6 [D6S40] Nucleic Acids Research ·В В Янко, Melanie Culver, Mark Leppert, Brian V. Jensen, Peter O'Connell, G.M. Lathrop, J.-M. Lalouel, R. White	1988	3
12	Isolation and mapping of a polymorphic DNA sequence (pEFD64.1) on chromosome 3 [D3S42] Nucleic Acids Research ·Yusuke Nakamura, E. Fujimoto, Peter O'Connell, M. Leppert, G.M. Lathrop, Jean-Marc Lalouel, R. White	1988	6
13	Etiological heterogeneity in X-linked spastic paraplegia. PubMed ·Laura Davis Keppen, Mark Leppert, Peter O'Connell, Yusuke Nakamura, Dora Stauffer, Mark Lathrop, J.-M. Lalouel, R. White	1987	62
14	Drosophila maternal and embryo mRNAs transcribed from a single transcription unit use alternate combinations of exons. The EMBO Journal ·Alain Vincent, Peter O'Connell, M GRAY, Michael Rosbash	1984	38
15	Sequence, structure, and codon preference of theDrosophilaribosomal protein 49 gene Nucleic Acids Research ·Peter O'Connell, Michael Rosbash Hit paper breakdown →	1984	502
16	DNase I hypersensitive sites of the chromatin for Drosophila melanogaster ribosomal protein 49 gene Nucleic Acids Research ·Yuk‐Chor Wong, Peter O'Connell, Michael Rosbash, Sarah C. R. Elgin	1981	27
17	Isolation and mapping of a cloned ribosomal protein gene of Drosophila melanogaster Nature ·Charles A. Vaslet, Peter O'Connell, Marta Izquierdo, Michael Rosbash	1980	95

About Peter O'Connell

Peter O'Connell is a scholar working on Neurology, Genetics, Genetics, Pharmacy and Gastroenterology, having authored 17 papers that have together received 1.4k indexed citations. Recurring topics across this work include RNA and protein synthesis mechanisms (5 papers), Neurofibromatosis and Schwannoma Cases (5 papers), Neurogenetic and Muscular Disorders Research (3 papers), Chromatin Remodeling and Cancer (3 papers), Genomics and Chromatin Dynamics (3 papers), Genomic variations and chromosomal abnormalities (2 papers), Sarcoma Diagnosis and Treatment (2 papers) and DNA and Nucleic Acid Chemistry (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (356 citations), Neurology (265 citations), Molecular Biology (808 citations), Aging (19 citations) and Genetics (295 citations). Peter O'Connell has collaborated with scholars based in United States, Belgium and Ireland. Frequent co-authors include Michael Rosbash, Yusuke Nakamura, Mark Leppert, Dora Stauffer, R. White, Vernon Anderson, Jean‐Marc Lalouel, Marta Izquierdo, Charles A. Vaslet and R. White. Their work appears in journals such as Nucleic Acids Research, Nature, Genomics, The EMBO Journal and Human 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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