Hans Scheffer
- Genetics top 0.5%
- Neurogenetic and Muscular Disorders Research 22
- Genomics and Rare Diseases 16
- Genomic variations and chromosomal abnormalities 13
- Genetics top 0.5%
- Neurogenetic and Muscular Disorders Research 22
- Genomics and Rare Diseases 16
- Genomic variations and chromosomal abnormalities 13
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- Genetic Neurodegenerative Diseases 20
- Neurology top 2%
- Molecular Biology top 2%
- RNA modifications and cancer 17
- Mitochondrial Function and Pathology 14
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- Cystic Fibrosis Research Advances 20
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- Skin and Cellular Biology Research 19
- Co-authors
- Helger G. YntemaJoris A. VeltmanChristian GilissenCharles H.C.M. BuysAlexander HoischenPetra de VriesBarbara FrankeLisenka E.L.M. Vissers
- Journals
- European Journal of Human Genetics (21 papers)Human Genetics (19 papers)Human Mutation (11 papers)
- Partner nations
- NetherlandsUnited StatesUnited Kingdom
In The Last Decade
Hans Scheffer
188 papers receiving 7.7k citations
Hit Papers
Peers
Comparison fields: 5 of 145
- Genetics 1.1k
- Genetics 2.7k
- Cellular and Molecular Neuroscience 1.2k
- Neurology 471
- Molecular Biology 3.7k
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-authorship network
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
| # | Work | ||
|---|---|---|---|
| 1 | 2024 | 4 | |
| 2 | 2019 | 9 | |
| 3 | EuroGentest guidelines for diagnostic next generation sequencing | 2014 | 3 |
| 4 | 2013 | 256 | |
| 5 | 2012 | 7 | |
| 6 | 2011 | 146 | |
| 7 | 2010 | 37 | |
| 8 | 2009 | 72 | |
| 9 | 2009 | 3 | |
| 10 | 2008 | 6 | |
| 11 | 2002 | 48 | |
| 12 | A new family with a mutation in exon 2 of COL2A1 and Stickler syndrome without systemic manifestations. | 2001 | 1 |
| 13 | [From gene to disease; 'survival' motor neuron protein and hereditary proximal spinal muscle atrophy]. | 2001 | 8 |
| 14 | 2000 | 32 | |
| 15 | 1997 | 21 | |
| 16 | RECOMBINATION FREQUENCY OVER THE GENOMIC SEQUENCE OF RB1 | 1993 | 2 |
| 17 | 1993 | 8 | |
| 18 | 1992 | 6 | |
| 19 | LINKAGE ANALYSIS IN FAMILIES WITH PROXIMAL SPINAL MUSCULAR-ATROPHY FROM THE NETHERLANDS | 1991 | 22 |
| 20 | 1989 | 1 |
About Hans Scheffer
Hans Scheffer is a scholar working on Genetics, Cellular and Molecular Neuroscience and Genetics, having authored 191 papers that have together received 7.9k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (22 papers), Genetic Neurodegenerative Diseases (20 papers), Cystic Fibrosis Research Advances (20 papers), Skin and Cellular Biology Research (19 papers), RNA modifications and cancer (17 papers), Genomics and Rare Diseases (16 papers), Mitochondrial Function and Pathology (14 papers) and Genomic variations and chromosomal abnormalities (13 papers). The work is most often cited by research in Genetics (1.1k citations), Genetics (2.7k citations) and Cellular and Molecular Neuroscience (1.2k citations). Hans Scheffer has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Helger G. Yntema, Joris A. Veltman, Christian Gilissen, Charles H.C.M. Buys, Alexander Hoischen, Petra de Vries, Barbara Franke, Lisenka E.L.M. Vissers, Han G. Brunner and Joep de Ligt. Their work appears in journals such as European Journal of Human Genetics, Human Genetics, Human Mutation, Nucleic Acids Research and Journal of Medical 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.