Peter Burfeind
Impact in
- Genetics top 1%
- Coagulation, Bradykinin, Polyphosphates, and Angioedema
- Genomic variations and chromosomal abnormalities
- Hematology top 2%
- Blood Coagulation and Thrombosis Mechanisms
- Platelet Disorders and Treatments
Papers in
- Genetics 34
- Genomic variations and chromosomal abnormalities 20
- Genomics and Rare Diseases 7
- Genetics and Neurodevelopmental Disorders 7
- Coagulation, Bradykinin, Polyphosphates, and Angioedema 5
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- Sperm and Testicular Function 18
- Co-authors
- Hans‐Ulrich Pauer (8 shared papers)Thomas Renné (4 shared papers)Bernhard Nieswandt (2 shared papers)Kai Schuh (2 shared papers)David Gailani (2 shared papers)Paul Thelen (14 shared papers)Silke Kaulfuß (16 shared papers)Sabine Grüner (1 shared paper)
- Journals
- Cytogenetic and Genome Research (11 papers)International Journal of Oncology (6 papers)Clinical Genetics (6 papers)Biochemical and Biophysical Research Communications (6 papers)Oncotarget (5 papers)
- Partner nations
- GermanyUnited StatesSwitzerland
In The Last Decade
Peter Burfeind
112 papers receiving 4.6k citations
Peers
Comparison fields: 5 of 102
- Genetics 881
- Hematology 603
- Reproductive Medicine 309
- Genetics 688
- Developmental Biology 51
Countries citing papers authored by Peter Burfeind
This map shows the geographic impact of Peter Burfeind'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 Burfeind with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Burfeind more than expected).
Fields of papers citing papers by Peter Burfeind
This network shows the impact of papers produced by Peter Burfeind. 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 Burfeind. The network helps show where Peter Burfeind may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter Burfeind, 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 112 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 584 | |
| 2 | 2006 | 394 | |
| 3 | 1995 | 298 | |
| 4 | 2011 | 222 | |
| 5 | 1996 | 203 | |
| 6 | 2018 | 170 | |
| 7 | 2014 | 155 | |
| 8 | 1999 | 136 | |
| 9 | 2004 | 113 | |
| 10 | 1999 | 106 | |
| 11 | 1997 | 85 | |
| 12 | 2004 | 78 | |
| 13 | 2003 | 76 | |
| 14 | 1991 | 69 | |
| 15 | 1994 | 69 | |
| 16 | 2007 | 67 | |
| 17 | 2010 | 67 | |
| 18 | 2003 | 64 | |
| 19 | 2009 | 63 | |
| 20 | 2005 | 62 |
About Peter Burfeind
Peter Burfeind is a scholar working on Genetics, Reproductive Medicine, Genetics, Pulmonary and Respiratory Medicine and Molecular Biology, having authored 112 papers that have together received 4.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (20 papers), Sperm and Testicular Function (18 papers), Prostate Cancer Treatment and Research (11 papers), Genomics and Rare Diseases (7 papers), Genetics and Neurodevelopmental Disorders (7 papers), Coagulation, Bradykinin, Polyphosphates, and Angioedema (5 papers), Developmental Biology and Gene Regulation (5 papers) and Blood Coagulation and Thrombosis Mechanisms (4 papers). The work is most often cited by research in Genetics (881 citations), Hematology (603 citations), Reproductive Medicine (309 citations), Genetics (688 citations) and Developmental Biology (51 citations). Peter Burfeind has collaborated with scholars based in Germany, United States and Switzerland. Frequent co-authors include Hans‐Ulrich Pauer, Thomas Renné, Bernhard Nieswandt, Kai Schuh, David Gailani, Paul Thelen, Silke Kaulfuß, Sabine Grüner, Miroslava Požgajová and Bernhard Hemmerlein. Their work appears in journals such as Cytogenetic and Genome Research, International Journal of Oncology, Clinical Genetics, Biochemical and Biophysical Research Communications and Oncotarget.
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.