Hans Scheffer
Impact in
- Genetics top 0.5%
- Genomics and Rare Diseases
- Neurogenetic and Muscular Disorders Research
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
-
- Genetic Neurodegenerative Diseases
Papers in
-
- RNA modifications and cancer 15
- Mitochondrial Function and Pathology 11
- Genetics 33
- Neurogenetic and Muscular Disorders Research 20
- Genomics and Rare Diseases 15
- Genomic variations and chromosomal abnormalities 12
- Co-authors
- Helger G. Yntema (7 shared papers)Joris A. Veltman (7 shared papers)Christian Gilissen (6 shared papers)Charles H.C.M. Buys (35 shared papers)Alexander Hoischen (4 shared papers)Petra de Vries (3 shared papers)Lisenka E.L.M. Vissers (3 shared papers)Barbara Franke (20 shared papers)
- Journals
- European Journal of Human Genetics (21 papers)Human Genetics (19 papers)Human Mutation (11 papers)Journal of Medical Genetics (5 papers)Nucleic Acids Research (5 papers)
- Partner nations
- NetherlandsUnited StatesGermany
In The Last Decade
Hans Scheffer
187 papers receiving 8.0k citations
Hans Scheffer's Hit Papers
Peers
Comparison fields: 5 of 143
- Genetics 1.0k
- Genetics 2.5k
- Cellular and Molecular Neuroscience 1.2k
- Clinical Biochemistry 341
- Molecular Biology 3.4k
Countries citing papers authored by Hans Scheffer
This map shows the geographic impact of Hans Scheffer'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 Hans Scheffer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hans Scheffer more than expected).
Fields of papers citing papers by Hans Scheffer
This network shows the impact of papers produced by Hans Scheffer. 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 Hans Scheffer. The network helps show where Hans Scheffer may publish in the future.
Co-authors
The 25 scholars most cited alongside Hans Scheffer, 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 190 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability Hit paper breakdown → | 2012 | 1037 |
| 2 | 2015 | 358 | |
| 3 | Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics. | 2013 | 282 |
| 4 | 2013 | 279 | |
| 5 | 1997 | 202 | |
| 6 | Deletions of the survival motor neuron gene in unaffected siblings of patients with spinal muscular atrophy. | 1995 | 179 |
| 7 | 2002 | 178 | |
| 8 | 2010 | 177 | |
| 9 | 2008 | 172 | |
| 10 | 2011 | 153 | |
| 11 | 2013 | 144 | |
| 12 | 1996 | 136 | |
| 13 | 1995 | 134 | |
| 14 | 2005 | 120 | |
| 15 | 2008 | 116 | |
| 16 | 2004 | 115 | |
| 17 | 2012 | 114 | |
| 18 | 2013 | 100 | |
| 19 | 2008 | 99 | |
| 20 | 2015 | 98 |
About Hans Scheffer
Hans Scheffer is a scholar working on Molecular Biology, Genetics, Genetics, Cellular and Molecular Neuroscience and Pulmonary and Respiratory Medicine, having authored 190 papers that have together received 8.4k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (20 papers), Genetic Neurodegenerative Diseases (20 papers), Cystic Fibrosis Research Advances (19 papers), Skin and Cellular Biology Research (19 papers), Genomics and Rare Diseases (15 papers), RNA modifications and cancer (15 papers), Genomic variations and chromosomal abnormalities (12 papers) and Mitochondrial Function and Pathology (11 papers). The work is most often cited by research in Genetics (1.0k citations), Genetics (2.5k citations), Cellular and Molecular Neuroscience (1.2k citations), Clinical Biochemistry (341 citations) and Molecular Biology (3.4k citations). Hans Scheffer has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Helger G. Yntema, Joris A. Veltman, Christian Gilissen, Charles H.C.M. Buys, Alexander Hoischen, Petra de Vries, Lisenka E.L.M. Vissers, Barbara Franke, Joep de Ligt and Han G. Brunner. Their work appears in journals such as European Journal of Human Genetics, Human Genetics, Human Mutation, Journal of Medical Genetics and Nucleic Acids 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.