Peter Burfeind
Impact in
- Genetics top 0.5%
- Coagulation, Bradykinin, Polyphosphates, and Angioedema
- Genomic variations and chromosomal abnormalities
- Hematology top 1%
- Blood Coagulation and Thrombosis Mechanisms
Papers in
- Genetics 49
- Genomic variations and chromosomal abnormalities 18
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 11
- Estrogen and related hormone effects 7
- Genetics and Neurodevelopmental Disorders 7
- Animal Genetics and Reproduction 7
- Genomics and Rare Diseases 7
- Co-authors
- Hans‐Ulrich Pauer (9 shared papers)Thomas Renné (4 shared papers)Kai Schuh (2 shared papers)Bernhard Nieswandt (2 shared papers)David Gailani (2 shared papers)Paul Thelen (15 shared papers)Bernhard Hemmerlein (11 shared papers)Miroslava Požgajová (1 shared paper)
- Journals
- Cytogenetic and Genome Research (9 papers)Biochemical and Biophysical Research Communications (6 papers)Oncotarget (5 papers)Clinical Genetics (5 papers)International Journal of Oncology (5 papers)
- Partner nations
- GermanyUnited StatesPoland
In The Last Decade
Peter Burfeind
102 papers receiving 3.9k citations
Peter Burfeind's Hit Papers
Peers
Comparison fields: 5 of 115
- Genetics 951
- Hematology 744
- Reproductive Medicine 216
- Genetics 684
- Cancer Research 341
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 102 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Defective thrombus formation in mice lacking coagulation factor XII Hit paper breakdown → | 2005 | 560 |
| 2 | 2006 | 374 | |
| 3 | 1995 | 299 | |
| 4 | 2011 | 210 | |
| 5 | 1996 | 204 | |
| 6 | 2014 | 150 | |
| 7 | 2004 | 104 | |
| 8 | 1997 | 84 | |
| 9 | 2004 | 79 | |
| 10 | 2003 | 75 | |
| 11 | 1991 | 69 | |
| 12 | 2010 | 67 | |
| 13 | 2007 | 66 | |
| 14 | 1994 | 66 | |
| 15 | 2003 | 64 | |
| 16 | 2009 | 62 | |
| 17 | 2005 | 60 | |
| 18 | 2005 | 59 | |
| 19 | 2012 | 55 | |
| 20 | 2003 | 46 |
About Peter Burfeind
Peter Burfeind is a scholar working on Genetics, Molecular Biology, Reproductive Medicine, Cancer Research and Genetics, having authored 102 papers that have together received 4.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (18 papers), Sperm and Testicular Function (13 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers), Chromosomal and Genetic Variations (9 papers), Estrogen and related hormone effects (7 papers), Genetics and Neurodevelopmental Disorders (7 papers), Animal Genetics and Reproduction (7 papers) and Genomics and Rare Diseases (7 papers). The work is most often cited by research in Genetics (951 citations), Hematology (744 citations), Reproductive Medicine (216 citations), Genetics (684 citations) and Cancer Research (341 citations). Peter Burfeind has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include Hans‐Ulrich Pauer, Thomas Renné, Kai Schuh, Bernhard Nieswandt, David Gailani, Paul Thelen, Bernhard Hemmerlein, Miroslava Požgajová, Sabine Grüner and Frauke Rininsland. Their work appears in journals such as Cytogenetic and Genome Research, Biochemical and Biophysical Research Communications, Oncotarget, Clinical Genetics and International Journal of Oncology.
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.