Peter O'Connell
Impact in
- Neurology top 0.2%
- Neurofibromatosis and Schwannoma Cases
- Neuroblastoma Research and Treatments
- Cancer Research top 1%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 70
- Genomic variations and chromosomal abnormalities 37
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- DNA and Nucleic Acid Chemistry 44
- DNA Repair Mechanisms 27
- Genomics and Chromatin Dynamics 18
- CRISPR and Genetic Engineering 11
- Co-authors
- Ray L. White (98 shared papers)Richard Cawthon (13 shared papers)Melanie Culver (19 shared papers)David H. Viskochil (13 shared papers)Mark Leppert (16 shared papers)Yusuke Nakamura (96 shared papers)Donald Craig Allred (14 shared papers)Gregory Mark Lathrop (112 shared papers)
- Journals
- Nucleic Acids Research (101 papers)Genomics (25 papers)Breast Cancer Research and Treatment (5 papers)Cell (4 papers)Science (4 papers)
- Partner nations
- United StatesIrelandUnited Kingdom
In The Last Decade
Peter O'Connell
245 papers receiving 16.1k citations
Peter O'Connell's Hit Papers
Peers
Comparison fields: 5 of 172
- Neurology 4.0k
- Cancer Research 2.0k
- Genetics 3.8k
- Pathology and Forensic Medicine 1.7k
- Molecular Biology 6.7k
Countries citing papers authored by Peter O'Connell
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
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.
All Works
Showing the 20 most-cited of 248 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Variable Number of Tandem Repeat (VNTR) Markers for Human Gene Mapping Hit paper breakdown → | 1987 | 1426 |
| 2 | The neurofibromatosis type 1 gene encodes a protein related to GAP Hit paper breakdown → | 1990 | 965 |
| 3 | A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations Hit paper breakdown → | 1990 | 942 |
| 4 | Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus Hit paper breakdown → | 1990 | 918 |
| 5 | The GAP-related domain of the neurofibromatosis type 1 gene product interacts with ras p21 Hit paper breakdown → | 1990 | 856 |
| 6 | Gene expression profiling for the prediction of therapeutic response to docetaxel in patients with breast cancer Hit paper breakdown → | 2003 | 712 |
| 7 | The Gene for Familial Polyposis Coli Maps to the Long Arm of Chromosome 5 Hit paper breakdown → | 1987 | 576 |
| 8 | Gene for von Recklinghausen Neurofibromatosis Is in the Pericentromeric Region of Chromosome 17 Hit paper breakdown → | 1987 | 571 |
| 9 | 1993 | 455 | |
| 10 | A closely linked genetic marker for cystic fibrosis Hit paper breakdown → | 1985 | 402 |
| 11 | 1994 | 377 | |
| 12 | 1998 | 291 | |
| 13 | 1998 | 291 | |
| 14 | 1999 | 289 | |
| 15 | 2008 | 231 | |
| 16 | 1999 | 220 | |
| 17 | 1990 | 220 | |
| 18 | A hypersensitive estrogen receptor-alpha mutation in premalignant breast lesions. | 2000 | 203 |
| 19 | Precise localization of NF1 to 17q11.2 by balanced translocation. | 1989 | 181 |
| 20 | 2002 | 169 |
About Peter O'Connell
Peter O'Connell is a scholar working on Genetics, Molecular Biology, Neurology, Pulmonary and Respiratory Medicine and Pathology and Forensic Medicine, having authored 248 papers that have together received 17.0k indexed citations. Recurring topics across this work include DNA and Nucleic Acid Chemistry (44 papers), Genomic variations and chromosomal abnormalities (37 papers), DNA Repair Mechanisms (27 papers), Neurofibromatosis and Schwannoma Cases (25 papers), Genomics and Chromatin Dynamics (18 papers), Neuroblastoma Research and Treatments (13 papers), CRISPR and Genetic Engineering (11 papers) and Genetic factors in colorectal cancer (11 papers). The work is most often cited by research in Neurology (4.0k citations), Cancer Research (2.0k citations), Genetics (3.8k citations), Pathology and Forensic Medicine (1.7k citations) and Molecular Biology (6.7k citations). Peter O'Connell has collaborated with scholars based in United States, Ireland and United Kingdom. Frequent co-authors include Ray L. White, Richard Cawthon, Melanie Culver, David H. Viskochil, Mark Leppert, Yusuke Nakamura, Donald Craig Allred, Gregory Mark Lathrop, Gangfeng Xu and Roger K. Wolff. Their work appears in journals such as Nucleic Acids Research, Genomics, Breast Cancer Research and Treatment, Cell and Science.
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.