Peter M. Kroisel
Impact in
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- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 18
- Genomic variations and chromosomal abnormalities 12
- Genetic Syndromes and Imprinting 5
- Genetics and Neurodevelopmental Disorders 4
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
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- Hedgehog Signaling Pathway Studies 4
- Epigenetics and DNA Methylation 2
- Co-authors
- Barbara Pertl (3 shared papers)Susanne Kopp (2 shared papers)Jon Sherlock (2 shared papers)Lucia Tului (1 shared paper)B. Brambati (1 shared paper)W Rosenkranz (3 shared papers)Klaus Wagner (4 shared papers)Matteo Adinolfí (1 shared paper)
- Journals
- Genomics (2 papers)Human Genetics (2 papers)European Journal of Human Genetics (2 papers)Mammalian Genome (1 paper)Cytogenetic and Genome Research (1 paper)
- Partner nations
- AustriaGermanyUnited Kingdom
In The Last Decade
Peter M. Kroisel
18 papers receiving 498 citations
Peers
Comparison fields: 5 of 45
- Pediatrics, Perinatology and Child Health 249
- Genetics 352
- Developmental Biology 12
- Molecular Biology 212
- Reproductive Medicine 12
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
| # | Work | ||
|---|---|---|---|
| 1 | 1999 | 102 | |
| 2 | 1996 | 68 | |
| 3 | 2000 | 58 | |
| 4 | 1997 | 54 | |
| 5 | 2004 | 43 | |
| 6 | 2007 | 39 | |
| 7 | 1990 | 26 | |
| 8 | 1999 | 26 | |
| 9 | 2011 | 24 | |
| 10 | 2000 | 23 | |
| 11 | 2003 | 19 | |
| 12 | 2010 | 18 | |
| 13 | 2021 | 18 | |
| 14 | 1991 | 16 | |
| 15 | 2006 | 7 | |
| 16 | 2006 | 6 | |
| 17 | 1992 | 4 | |
| 18 | 2005 | 1 | |
| 19 | 2025 | 0 |
About Peter M. Kroisel
Peter M. Kroisel is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Surgery, having authored 19 papers that have together received 552 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Genetic Syndromes and Imprinting (5 papers), Prenatal Screening and Diagnostics (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Chromosomal and Genetic Variations (4 papers), Hedgehog Signaling Pathway Studies (4 papers), Epigenetics and DNA Methylation (2 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (249 citations), Genetics (352 citations), Developmental Biology (12 citations), Molecular Biology (212 citations) and Reproductive Medicine (12 citations). Peter M. Kroisel has collaborated with scholars based in Austria, Germany and United Kingdom. Frequent co-authors include Barbara Pertl, Susanne Kopp, Jon Sherlock, Lucia Tului, B. Brambati, W Rosenkranz, Klaus Wagner, Matteo Adinolfí, Erwin Petek and Klaus W. Wagner. Their work appears in journals such as Genomics, Human Genetics, European Journal of Human Genetics, Mammalian Genome and Cytogenetic and Genome Research.
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.