Peter M. Kroisel
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Molecular Biology top 10%
- Epigenetics and DNA Methylation
- CRISPR and Genetic Engineering
- Genomics and Chromatin Dynamics
Papers in
- Genetics 19
- Genomic variations and chromosomal abnormalities 9
- Genetics and Neurodevelopmental Disorders 5
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- Hedgehog Signaling Pathway Studies 4
- RNA and protein synthesis mechanisms 3
- Congenital heart defects research 2
- Co-authors
- Jeffrey Garnes (1 shared paper)Pieter J. de Jong (2 shared papers)Hiroaki Shizuya (1 shared paper)Chris T. Amemiya (1 shared paper)Mark A. Batzer (1 shared paper)Klaus Wagner (18 shared papers)Erwin Petek (20 shared papers)Christian Windpassinger (13 shared papers)
- Journals
- Nature Genetics (2 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2 papers)Prenatal Diagnosis (2 papers)Clinical Genetics (2 papers)Journal of the Neurological Sciences (1 paper)
- Partner nations
- AustriaUnited StatesCanada
In The Last Decade
Peter M. Kroisel
39 papers receiving 1.5k citations
Peter M. Kroisel's Hit Papers
Peers
Comparison fields: 5 of 95
- Genetics 681
- Molecular Biology 948
- Genetics 108
- Pediatrics, Perinatology and Child Health 143
- Immunology 122
Countries citing papers authored by Peter M. Kroisel
This map shows the geographic impact of Peter M. Kroisel'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 M. Kroisel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter M. Kroisel more than expected).
Fields of papers citing papers by Peter M. Kroisel
This network shows the impact of papers produced by Peter M. Kroisel. 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 M. Kroisel. The network helps show where Peter M. Kroisel may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter M. Kroisel, 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 40 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A new bacteriophage P1–derived vector for the propagation of large human DNA fragments Hit paper breakdown → | 1994 | 719 |
| 2 | 2001 | 169 | |
| 3 | 1994 | 77 | |
| 4 | 1984 | 60 | |
| 5 | 2002 | 53 | |
| 6 | 2006 | 50 | |
| 7 | 2011 | 49 | |
| 8 | 2001 | 40 | |
| 9 | 2001 | 39 | |
| 10 | 2016 | 37 | |
| 11 | 1991 | 23 | |
| 12 | 2011 | 22 | |
| 13 | 2004 | 20 | |
| 14 | 2002 | 20 | |
| 15 | 2020 | 20 | |
| 16 | 2022 | 17 | |
| 17 | 2000 | 16 | |
| 18 | 2000 | 14 | |
| 19 | 1997 | 14 | |
| 20 | 2003 | 13 |
About Peter M. Kroisel
Peter M. Kroisel is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Pulmonary and Respiratory Medicine and Cognitive Neuroscience, having authored 40 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (5 papers), Autism Spectrum Disorder Research (4 papers), Hedgehog Signaling Pathway Studies (4 papers), Prenatal Screening and Diagnostics (3 papers), RNA and protein synthesis mechanisms (3 papers), Congenital heart defects research (2 papers) and Fetal and Pediatric Neurological Disorders (2 papers). The work is most often cited by research in Genetics (681 citations), Molecular Biology (948 citations), Genetics (108 citations), Pediatrics, Perinatology and Child Health (143 citations) and Immunology (122 citations). Peter M. Kroisel has collaborated with scholars based in Austria, United States and Canada. Frequent co-authors include Jeffrey Garnes, Pieter J. de Jong, Hiroaki Shizuya, Chris T. Amemiya, Mark A. Batzer, Klaus Wagner, Erwin Petek, Christian Windpassinger, George Polgar and M Zach. Their work appears in journals such as Nature Genetics, American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Prenatal Diagnosis, Clinical Genetics and Journal of the Neurological Sciences.
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.