Simone Schuffenhauer
Impact in
- Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Craniofacial Disorders and Treatments
- Nephrology top 5%
- Parathyroid Disorders and Treatments
Papers in
- Genetics 35
- Genomic variations and chromosomal abnormalities 20
- Genetic Syndromes and Imprinting 8
- Craniofacial Disorders and Treatments 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Genetic and rare skin diseases. 2
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- Immunodeficiency and Autoimmune Disorders 5
- Co-authors
- Peter Lichtner (7 shared papers)Thomas Meitinger (12 shared papers)Jan D. Murken (10 shared papers)Rudolf W. Bilous (1 shared paper)Nicholas J Shaw (1 shared paper)Hilde Van Esch (1 shared paper)Rajesh V. Thakker (1 shared paper)Peter M. A. Groenen (1 shared paper)
- Journals
- Journal of Medical Genetics (5 papers)Clinical Genetics (4 papers)Human Genetics (4 papers)The American Journal of Human Genetics (2 papers)Genomics (2 papers)
- Partner nations
- GermanyAustraliaUnited Kingdom
In The Last Decade
Simone Schuffenhauer
44 papers receiving 2.8k citations
Simone Schuffenhauer's Hit Papers
Peers
Comparison fields: 5 of 97
- Genetics 1.6k
- Nephrology 213
- Developmental Biology 46
- Sensory Systems 83
- Pediatrics, Perinatology and Child Health 196
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 44 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study. Hit paper breakdown → | 1997 | 956 |
| 2 | 2000 | 501 | |
| 3 | 1996 | 185 | |
| 4 | 2011 | 77 | |
| 5 | 1998 | 76 | |
| 6 | 1998 | 75 | |
| 7 | 1999 | 74 | |
| 8 | 2016 | 71 | |
| 9 | 2000 | 67 | |
| 10 | 2000 | 67 | |
| 11 | 2000 | 62 | |
| 12 | 1996 | 58 | |
| 13 | 1996 | 56 | |
| 14 | 1995 | 49 | |
| 15 | 1993 | 47 | |
| 16 | 1993 | 44 | |
| 17 | 1999 | 44 | |
| 18 | 1993 | 43 | |
| 19 | 2002 | 39 | |
| 20 | 1997 | 38 |
About Simone Schuffenhauer
Simone Schuffenhauer is a scholar working on Genetics, Immunology, Molecular Biology, Information Systems and Cell Biology, having authored 44 papers that have together received 3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (20 papers), Genetic Syndromes and Imprinting (8 papers), Immunodeficiency and Autoimmune Disorders (5 papers), Research Data Management Practices (3 papers), Craniofacial Disorders and Treatments (3 papers), Schizophrenia research and treatment (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers) and Genetic and rare skin diseases. (2 papers). The work is most often cited by research in Genetics (1.6k citations), Nephrology (213 citations), Developmental Biology (46 citations), Sensory Systems (83 citations) and Pediatrics, Perinatology and Child Health (196 citations). Simone Schuffenhauer has collaborated with scholars based in Germany, Australia and United Kingdom. Frequent co-authors include Peter Lichtner, Thomas Meitinger, Jan D. Murken, Rudolf W. Bilous, Nicholas J Shaw, Hilde Van Esch, Rajesh V. Thakker, Peter M. A. Groenen, Wim Van de Ven and J P Fryns. Their work appears in journals such as Journal of Medical Genetics, Clinical Genetics, Human 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.