Hans van Bokhoven
- Genetics top 0.1%
- Genetics and Neurodevelopmental Disorders 79
- Genomic variations and chromosomal abnormalities 42
- Molecular Biology top 0.5%
- Epigenetics and DNA Methylation 25
- Hedgehog Signaling Pathway Studies 24
- Muscle Physiology and Disorders 19
- RNA modifications and cancer 17
- Developmental Biology top 1%
- Cell Biology top 0.5%
- Oncology top 1%
- Cancer-related Molecular Pathways 29
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- Autism Spectrum Disorder Research 17
- Co-authors
- Han G. BrunnerBen C.J. HamelHuiqing ZhouTjitske KleefstraTuula RinneJacopo CelliEllen van BeusekomHans‐Hilger Ropers
- Partner nations
- NetherlandsUnited StatesGermany
In The Last Decade
Hans van Bokhoven
237 papers receiving 12.9k citations
Hit Papers
Peers
Comparison fields: 5 of 151
- Genetics 4.6k
- Molecular Biology 9.0k
- Developmental Biology 209
- Cell Biology 1.2k
- Oncology 1.8k
Countries citing papers authored by Hans van Bokhoven
This map shows the geographic impact of Hans van Bokhoven'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 van Bokhoven with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hans van Bokhoven more than expected).
Fields of papers citing papers by Hans van Bokhoven
This network shows the impact of papers produced by Hans van Bokhoven. 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 van Bokhoven. The network helps show where Hans van Bokhoven may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Hans van Bokhoven, 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 | 1 | |
| 2 | 2023 | 22 | |
| 3 | 2023 | 1 | |
| 4 | 2022 | 37 | |
| 5 | 2020 | 7 | |
| 6 | 2019 | 1 | |
| 7 | 2019 | 82 | |
| 8 | 2015 | 45 | |
| 9 | 2015 | 59 | |
| 10 | 2014 | 12 | |
| 11 | 2013 | 37 | |
| 12 | 2010 | 123 | |
| 13 | 2009 | 17 | |
| 14 | Mutations in the a2-subunit of the v-type H+-ATPase impair Golgi function and cause a novel congenital disorder of glycosylation with cutix laxa | 2008 | 0 |
| 15 | 2008 | 68 | |
| 16 | 2007 | 259 | |
| 17 | Haploinsufficiency of the Euchromatin Histone Methyl Transferase1 (Eu-HMTase1) gene causes the 9q subtelomeric deletion syndrome | 2006 | 1 |
| 18 | 2003 | 65 | |
| 19 | 2003 | 57 | |
| 20 | P63 mutations in the EEC, Hay-Wells, ADULT syndromes and in split hand/foot malformation reveals a genotype-phenotype correlation. | 2000 | 6 |
About Hans van Bokhoven
Hans van Bokhoven is a scholar working on Developmental Biology, Genetics and Molecular Biology, having authored 243 papers that have together received 13.2k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (79 papers), Genomic variations and chromosomal abnormalities (42 papers), Cancer-related Molecular Pathways (29 papers), Epigenetics and DNA Methylation (25 papers), Hedgehog Signaling Pathway Studies (24 papers), Muscle Physiology and Disorders (19 papers), RNA modifications and cancer (17 papers) and Autism Spectrum Disorder Research (17 papers). The work is most often cited by research in Genetics (4.6k citations), Molecular Biology (9.0k citations) and Developmental Biology (209 citations). Hans van Bokhoven has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Han G. Brunner, Ben C.J. Hamel, Huiqing Zhou, Tjitske Kleefstra, Tuula Rinne, Jacopo Celli, Ellen van Beusekom, Hans‐Hilger Ropers, Nael Nadif Kasri and Jamie M. Kramer. Their work appears in journals such as Science, Cell and Proceedings of the National Academy of Sciences.
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.