Peter J. Oefner
Impact in
- Genetics top 0.2%
- Forensic and Genetic Research
- Genetic diversity and population structure
- Race, Genetics, and Society
- Genetic Mapping and Diversity in Plants and Animals
- Archeology top 0.2%
- Forensic Anthropology and Bioarchaeology Studies
Papers in
- Genetics 39
- Forensic and Genetic Research 21
- Genetic diversity and population structure 13
- Race, Genetics, and Society 8
- BRCA gene mutations in cancer 7
- Genetic Associations and Epidemiology 6
- Co-authors
- Peter A. Underhill (17 shared papers)Peidong Shen (17 shared papers)Luca L. Cavalli-Sforza (4 shared papers)P. A. Underhill (5 shared papers)Harvey W. Mohrenweiser (1 shared paper)Monique N. Vergouwe (1 shared paper)Dennis E. Bulman (1 shared paper)Marten H. Hofker (1 shared paper)
- Journals
- Proceedings of the National Academy of Sciences (10 papers)The American Journal of Human Genetics (6 papers)Human Mutation (4 papers)Electrophoresis (4 papers)Human Genetics (2 papers)
- Partner nations
- United StatesGermanyAustria
In The Last Decade
Peter J. Oefner
85 papers receiving 9.2k citations
Peter J. Oefner's Hit Papers
Peers
Comparison fields: 5 of 188
- Genetics 4.4k
- Archeology 846
- Psychiatry and Mental health 1.0k
- Paleontology 348
- Molecular Biology 3.0k
Countries citing papers authored by Peter J. Oefner
This map shows the geographic impact of Peter J. Oefner'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 J. Oefner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter J. Oefner more than expected).
Fields of papers citing papers by Peter J. Oefner
This network shows the impact of papers produced by Peter J. Oefner. 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 J. Oefner. The network helps show where Peter J. Oefner may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter J. Oefner, 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 85 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4 Hit paper breakdown → | 1996 | 1927 |
| 2 | 2001 | 606 | |
| 3 | The Genetic Legacy of Paleolithic Homo sapiens sapiens in Extant Europeans: A Y Chromosome Perspective Hit paper breakdown → | 2000 | 599 |
| 4 | 2002 | 412 | |
| 5 | 2002 | 379 | |
| 6 | 2004 | 313 | |
| 7 | 1996 | 297 | |
| 8 | 2004 | 296 | |
| 9 | 1998 | 283 | |
| 10 | 2002 | 281 | |
| 11 | 2000 | 265 | |
| 12 | 1999 | 240 | |
| 13 | 2001 | 208 | |
| 14 | 2000 | 201 | |
| 15 | 2002 | 179 | |
| 16 | 2007 | 171 | |
| 17 | 2011 | 166 | |
| 18 | 2000 | 143 | |
| 19 | 2003 | 141 | |
| 20 | 2005 | 140 |
About Peter J. Oefner
Peter J. Oefner is a scholar working on Genetics, Molecular Biology, Biochemistry, Clinical Biochemistry and Biomedical Engineering, having authored 85 papers that have together received 9.8k indexed citations. Recurring topics across this work include Forensic and Genetic Research (21 papers), Genetic diversity and population structure (13 papers), Microfluidic and Capillary Electrophoresis Applications (9 papers), Race, Genetics, and Society (8 papers), BRCA gene mutations in cancer (7 papers), Genetic Associations and Epidemiology (6 papers), Analytical Chemistry and Chromatography (4 papers) and Metabolism and Genetic Disorders (4 papers). The work is most often cited by research in Genetics (4.4k citations), Archeology (846 citations), Psychiatry and Mental health (1.0k citations), Paleontology (348 citations) and Molecular Biology (3.0k citations). Peter J. Oefner has collaborated with scholars based in United States, Germany and Austria. Frequent co-authors include Peter A. Underhill, Peidong Shen, Luca L. Cavalli-Sforza, P. A. Underhill, Harvey W. Mohrenweiser, Monique N. Vergouwe, Dennis E. Bulman, Marten H. Hofker, Gert‐Jan B. van Ommen and Michel D. Ferrari. Their work appears in journals such as Proceedings of the National Academy of Sciences, The American Journal of Human Genetics, Human Mutation, Electrophoresis 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.