Simone Schuffenhauer
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Craniofacial Disorders and Treatments
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 35
- Genomic variations and chromosomal abnormalities 21
- Genetic Syndromes and Imprinting 8
- Genetics and Neurodevelopmental Disorders 5
- Craniofacial Disorders and Treatments 4
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- Congenital heart defects research 7
- Epigenetics and DNA Methylation 6
- Co-authors
- Thomas Meitinger (14 shared papers)Peter Lichtner (7 shared papers)Jan Murken (11 shared papers)Hilde Van Esch (1 shared paper)Nicholas J Shaw (1 shared paper)Peter Groenen (1 shared paper)J P Fryns (1 shared paper)Rudolf W. Bilous (1 shared paper)
- Journals
- Human Genetics (4 papers)Journal of Medical Genetics (4 papers)Clinical Genetics (4 papers)European Journal of Human Genetics (2 papers)The American Journal of Human Genetics (2 papers)
- Partner nations
- GermanyAustraliaUnited Kingdom
In The Last Decade
Simone Schuffenhauer
42 papers receiving 1.6k citations
Peers
Comparison fields: 5 of 94
- Genetics 964
- Pediatrics, Perinatology and Child Health 308
- Molecular Biology 1.0k
- Sensory Systems 53
- Nephrology 47
Countries citing papers authored by Simone Schuffenhauer
This map shows the geographic impact of Simone Schuffenhauer'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 Simone Schuffenhauer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Simone Schuffenhauer more than expected).
Fields of papers citing papers by Simone Schuffenhauer
This network shows the impact of papers produced by Simone Schuffenhauer. 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 Simone Schuffenhauer. The network helps show where Simone Schuffenhauer may publish in the future.
Co-authors
The 25 scholars most cited alongside Simone Schuffenhauer, 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 42 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 399 | |
| 2 | 1996 | 134 | |
| 3 | 1998 | 73 | |
| 4 | 1999 | 72 | |
| 5 | 1998 | 64 | |
| 6 | 2000 | 61 | |
| 7 | 2000 | 57 | |
| 8 | 2016 | 52 | |
| 9 | 1996 | 52 | |
| 10 | 1996 | 50 | |
| 11 | 2000 | 48 | |
| 12 | 1995 | 46 | |
| 13 | 1993 | 42 | |
| 14 | 1993 | 39 | |
| 15 | 1999 | 39 | |
| 16 | 2002 | 35 | |
| 17 | 1993 | 33 | |
| 18 | 1997 | 33 | |
| 19 | 1997 | 31 | |
| 20 | 1997 | 31 |
About Simone Schuffenhauer
Simone Schuffenhauer is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Pathology and Forensic Medicine, having authored 42 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (21 papers), Prenatal Screening and Diagnostics (11 papers), Genetic Syndromes and Imprinting (8 papers), Congenital heart defects research (7 papers), Epigenetics and DNA Methylation (6 papers), Chromosomal and Genetic Variations (6 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Craniofacial Disorders and Treatments (4 papers). The work is most often cited by research in Genetics (964 citations), Pediatrics, Perinatology and Child Health (308 citations), Molecular Biology (1.0k citations), Sensory Systems (53 citations) and Nephrology (47 citations). Simone Schuffenhauer has collaborated with scholars based in Germany, Australia and United Kingdom. Frequent co-authors include Thomas Meitinger, Peter Lichtner, Jan Murken, Hilde Van Esch, Nicholas J Shaw, Peter Groenen, J P Fryns, Rudolf W. Bilous, I. M. Holdaway and M. Andrew Nesbit. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, Clinical Genetics, European Journal of Human Genetics and The American Journal of Human 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.