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 36
- Genomic variations and chromosomal abnormalities 22
- 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 5
- Co-authors
- Thomas Meitinger (14 shared papers)Peter Lichtner (7 shared papers)Jan Murken (11 shared papers)Rudolf W. Bilous (1 shared paper)Brian Harding (1 shared paper)Wim Van de Ven (1 shared paper)Koenraad Devriendt (1 shared paper)J P Fryns (1 shared paper)
- Journals
- Journal of Medical Genetics (4 papers)Human Genetics (4 papers)Clinical Genetics (4 papers)The American Journal of Human Genetics (2 papers)Genomics (2 papers)
- Partner nations
- GermanyAustraliaUnited Kingdom
In The Last Decade
Simone Schuffenhauer
43 papers receiving 1.7k citations
Peers
Comparison fields: 5 of 93
- Genetics 1.0k
- Pediatrics, Perinatology and Child Health 313
- Molecular Biology 1.0k
- Sensory Systems 54
- Nephrology 74
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 43 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 486 | |
| 2 | 1996 | 165 | |
| 3 | 1998 | 76 | |
| 4 | 1998 | 74 | |
| 5 | 1999 | 72 | |
| 6 | 2000 | 65 | |
| 7 | 2000 | 63 | |
| 8 | 2000 | 61 | |
| 9 | 1996 | 58 | |
| 10 | 2016 | 55 | |
| 11 | 1996 | 51 | |
| 12 | 1995 | 48 | |
| 13 | 1993 | 42 | |
| 14 | 1993 | 41 | |
| 15 | 1999 | 40 | |
| 16 | 2002 | 38 | |
| 17 | 1997 | 37 | |
| 18 | 1997 | 36 | |
| 19 | 1996 | 35 | |
| 20 | 1993 | 34 |
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 43 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (22 papers), Prenatal Screening and Diagnostics (11 papers), Genetic Syndromes and Imprinting (8 papers), Congenital heart defects research (7 papers), Chromosomal and Genetic Variations (6 papers), Genetics and Neurodevelopmental Disorders (5 papers), Epigenetics and DNA Methylation (5 papers) and Craniofacial Disorders and Treatments (4 papers). The work is most often cited by research in Genetics (1.0k citations), Pediatrics, Perinatology and Child Health (313 citations), Molecular Biology (1.0k citations), Sensory Systems (54 citations) and Nephrology (74 citations). Simone Schuffenhauer has collaborated with scholars based in Germany, Australia and United Kingdom. Frequent co-authors include Thomas Meitinger, Peter Lichtner, Jan Murken, Rudolf W. Bilous, Brian Harding, Wim Van de Ven, Koenraad Devriendt, J P Fryns, Rolf Beetz and I. M. Holdaway. Their work appears in journals such as Journal of Medical Genetics, Human Genetics, Clinical Genetics, The American Journal of Human Genetics and Genomics.
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.