Hans Scheffer
Impact in
Papers in
- Genetics 42
- Genomics and Rare Diseases 20
- Neurogenetic and Muscular Disorders Research 17
- Genomic variations and chromosomal abnormalities 7
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- Hereditary Neurological Disorders 12
- Genetic Neurodegenerative Diseases 10
- Co-authors
- Han G. Brunner (8 shared papers)Helger G. Yntema (7 shared papers)Jan M. Cobben (11 shared papers)Joris Andre Veltman (7 shared papers)Christian Gilissen (6 shared papers)Gerrit van der Steege (12 shared papers)Charles H.C.M. Buys (35 shared papers)Alexander Hoischen (4 shared papers)
- Journals
- European Journal of Human Genetics (27 papers)Human Genetics (19 papers)Human Mutation (13 papers)Journal of Medical Genetics (8 papers)The American Journal of Human Genetics (6 papers)
- Partner nations
- NetherlandsGermanyUnited Kingdom
In The Last Decade
Hans Scheffer
222 papers receiving 13.4k citations
Hans Scheffer's Hit Papers
Peers
Comparison fields: 5 of 94
- Genetics 833
- Genetics 2.4k
- Neurology 1.2k
- Cellular and Molecular Neuroscience 947
- Cell Biology 572
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 224 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 | 1282 |
| 2 | Guidelines for diagnostic next-generation sequencing Hit paper breakdown → | 2015 | 403 |
| 3 | 2005 | 355 | |
| 4 | Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy Hit paper breakdown → | 2016 | 355 |
| 5 | Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease Hit paper breakdown → | 2017 | 351 |
| 6 | 2010 | 323 | |
| 7 | 2014 | 314 | |
| 8 | 2013 | 310 | |
| 9 | Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics. | 2013 | 310 |
| 10 | 1995 | 309 | |
| 11 | 2013 | 284 | |
| 12 | 2012 | 253 | |
| 13 | 1997 | 214 | |
| 14 | 2002 | 191 | |
| 15 | 2008 | 191 | |
| 16 | 2012 | 184 | |
| 17 | 2010 | 182 | |
| 18 | Deletions of the survival motor neuron gene in unaffected siblings of patients with spinal muscular atrophy. | 1995 | 179 |
| 19 | 2013 | 179 | |
| 20 | 2011 | 172 |
About Hans Scheffer
Hans Scheffer is a scholar working on Genetics, Cellular and Molecular Neuroscience, Genetics, Cell Biology and Rheumatology, having authored 224 papers that have together received 14.0k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (20 papers), Neurogenetic and Muscular Disorders Research (17 papers), Skin and Cellular Biology Research (16 papers), Cystic Fibrosis Research Advances (16 papers), Hereditary Neurological Disorders (12 papers), Genetic Neurodegenerative Diseases (10 papers), Rheumatoid Arthritis Research and Therapies (8 papers) and Genomic variations and chromosomal abnormalities (7 papers). The work is most often cited by research in Genetics (833 citations), Genetics (2.4k citations), Neurology (1.2k citations), Cellular and Molecular Neuroscience (947 citations) and Cell Biology (572 citations). Hans Scheffer has collaborated with scholars based in Netherlands, Germany and United Kingdom. Frequent co-authors include Han G. Brunner, Helger G. Yntema, Jan M. Cobben, Joris Andre Veltman, Christian Gilissen, Gerrit van der Steege, Charles H.C.M. Buys, Alexander Hoischen, Charles H. C. M. Buys and Petra de Vries. Their work appears in journals such as European Journal of Human Genetics, Human Genetics, Human Mutation, Journal of Medical 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.