Peter Burfeind
Impact in
- Genetics top 1%
- 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
- Genetics and Neurodevelopmental Disorders 8
- Genomics and Rare Diseases 8
- Estrogen and related hormone effects 7
- Co-authors
- Hans‐Ulrich Pauer (9 shared papers)Thomas Renné (4 shared papers)Bernhard Nieswandt (2 shared papers)David Gailani (2 shared papers)Kai Schuh (2 shared papers)Paul Thelen (15 shared papers)Bernhard Hemmerlein (11 shared papers)Sabine Grüner (1 shared paper)
- Journals
- Cytogenetic and Genome Research (10 papers)Biochemical and Biophysical Research Communications (6 papers)International Journal of Oncology (5 papers)Oncotarget (5 papers)Clinical Genetics (5 papers)
- Partner nations
- GermanyUnited StatesPoland
In The Last Decade
Peter Burfeind
102 papers receiving 3.8k citations
Peter Burfeind's Hit Papers
Peers
Comparison fields: 5 of 115
- Genetics 979
- Hematology 841
- Reproductive Medicine 224
- Genetics 720
- Cancer Research 384
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 | 537 |
| 2 | 2006 | 360 | |
| 3 | 1995 | 288 | |
| 4 | 2011 | 200 | |
| 5 | 1996 | 199 | |
| 6 | 2014 | 147 | |
| 7 | 2004 | 103 | |
| 8 | 2004 | 77 | |
| 9 | 1997 | 76 | |
| 10 | 2003 | 72 | |
| 11 | 1991 | 65 | |
| 12 | 1994 | 64 | |
| 13 | 2007 | 64 | |
| 14 | 2010 | 63 | |
| 15 | 2003 | 62 | |
| 16 | 2009 | 59 | |
| 17 | 2005 | 57 | |
| 18 | 2012 | 55 | |
| 19 | 2005 | 55 | |
| 20 | 2003 | 43 |
About Peter Burfeind
Peter Burfeind is a scholar working on Genetics, Molecular Biology, Reproductive Medicine, Surgery and Pulmonary and Respiratory Medicine, having authored 102 papers that have together received 3.9k 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), Genetics and Neurodevelopmental Disorders (8 papers), Genomics and Rare Diseases (8 papers), Estrogen and related hormone effects (7 papers) and Prenatal Screening and Diagnostics (7 papers). The work is most often cited by research in Genetics (979 citations), Hematology (841 citations), Reproductive Medicine (224 citations), Genetics (720 citations) and Cancer Research (384 citations). Peter Burfeind has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include Hans‐Ulrich Pauer, Thomas Renné, Bernhard Nieswandt, David Gailani, Kai Schuh, Paul Thelen, Bernhard Hemmerlein, Sabine Grüner, Miroslava Požgajová and Frauke Rininsland. Their work appears in journals such as Cytogenetic and Genome Research, Biochemical and Biophysical Research Communications, International Journal of Oncology, Oncotarget and Clinical 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.