Peter Pecháň
Impact in
- Genetics top 2%
- Virus-based gene therapy research
- Developmental Neuroscience top 10%
Papers in
-
- RNA Interference and Gene Delivery 8
- Retinal Development and Disorders 6
- Viral Infectious Diseases and Gene Expression in Insects 5
- CRISPR and Genetic Engineering 3
- Genetics 23
- Virus-based gene therapy research 18
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
- Co-authors
- Xandra O. Breakefield (6 shared papers)Ulrich Herrlinger (7 shared papers)Miguel Sena‐Esteves (5 shared papers)Faith H. Barnett (4 shared papers)Nikolai G. Rainov (6 shared papers)W. Seifert (2 shared papers)Alice K. Jacobs (4 shared papers)Maureen Chase (4 shared papers)
- Journals
- Human Gene Therapy (8 papers)Neuroreport (4 papers)Molecular Therapy (3 papers)Differentiation (2 papers)Gene Therapy (2 papers)
- Partner nations
- United StatesGermanySwitzerland
In The Last Decade
Peter Pecháň
35 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 87
- Genetics 781
- Developmental Neuroscience 67
- Ophthalmology 130
- Molecular Biology 786
- Biotechnology 80
Countries citing papers authored by Peter Pecháň
This map shows the geographic impact of Peter Pecháň'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 Pecháň with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Pecháň more than expected).
Fields of papers citing papers by Peter Pecháň
This network shows the impact of papers produced by Peter Pecháň. 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 Pecháň. The network helps show where Peter Pecháň may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter Pecháň, 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 36 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1997 | 145 | |
| 2 | Positron emission tomography-based imaging of transgene expression mediated by replication-conditional, oncolytic herpes simplex virus type 1 mutant vectors in vivo. | 2001 | 124 |
| 3 | 1997 | 108 | |
| 4 | 1995 | 88 | |
| 5 | 2008 | 83 | |
| 6 | 1992 | 68 | |
| 7 | 1999 | 68 | |
| 8 | 2010 | 67 | |
| 9 | 1995 | 66 | |
| 10 | 1996 | 53 | |
| 11 | 1997 | 44 | |
| 12 | 1999 | 43 | |
| 13 | 1992 | 38 | |
| 14 | 1979 | 36 | |
| 15 | 1996 | 28 | |
| 16 | 1996 | 28 | |
| 17 | 1997 | 22 | |
| 18 | 1998 | 21 | |
| 19 | 2011 | 20 | |
| 20 | 2021 | 20 |
About Peter Pecháň
Peter Pecháň is a scholar working on Molecular Biology, Genetics, Epidemiology, Ophthalmology and Oncology, having authored 36 papers that have together received 1.3k indexed citations. Recurring topics across this work include Virus-based gene therapy research (18 papers), Herpesvirus Infections and Treatments (10 papers), RNA Interference and Gene Delivery (8 papers), Retinal Development and Disorders (6 papers), Retinal Diseases and Treatments (5 papers), Viral Infectious Diseases and Gene Expression in Insects (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers) and CRISPR and Genetic Engineering (3 papers). The work is most often cited by research in Genetics (781 citations), Developmental Neuroscience (67 citations), Ophthalmology (130 citations), Molecular Biology (786 citations) and Biotechnology (80 citations). Peter Pecháň has collaborated with scholars based in United States, Germany and Switzerland. Frequent co-authors include Xandra O. Breakefield, Ulrich Herrlinger, Miguel Sena‐Esteves, Faith H. Barnett, Nikolai G. Rainov, W. Seifert, Alice K. Jacobs, Maureen Chase, E. Antonio Chiocca and Kamal Chowdhury. Their work appears in journals such as Human Gene Therapy, Neuroreport, Molecular Therapy, Differentiation and Gene Therapy.
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.