Hans van Bokhoven

29.8k citations
243 papers · 13.2k indexed · 3 hit papers · h-index 64
Topics
Genetics and Neurodevelopmental Disorders (79 papers)Genomic variations and chromosomal abnormalities (42 papers)Cancer-related Molecular Pathways (29 papers)

In The Last Decade

Hans van Bokhoven

237 papers receiving 12.9k citations

Hit Papers

Heterozygous Germline Mutations in the p53 Homolog p63 Ar...1990202620022014199920021990100200300400500

Peers

Hans van Bokhoven
Comparison fields: 5 of 151
  • Molecular Biology 9.0k
  • Genetics 4.6k
  • Oncology 1.8k
  • Cell Biology 1.2k
  • Cellular and Molecular Neuroscience 1.1k
Replace Virginia E. Papaioannou with:
Virginia E. Papaioannou United States
Ulrich Rüther Germany
Patrick Tam Australia
André Reis Germany
Andrée Dierich France
Ben C.J. Hamel Netherlands
Hisato Kondoh Japan
C. Geoffrey Woods United Kingdom
Marianne LeMeur France
Shinji Takada Japan
Hans van Bokhoven relative to Virginia E. Papaioannou United States Virginia E. Papaioannou's profile →
Citations per field
00.5×1.5×
Virginia E. Papaioannou · 1×
Citations per year

Countries citing papers authored by Hans van Bokhoven

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 of co-authors of Hans van Bokhoven

This figure shows the co-authorship network connecting the top 25 collaborators of Hans van Bokhoven. A scholar is included among the top collaborators of Hans van Bokhoven based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Hans van Bokhoven. Hans van Bokhoven is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
#WorkIndexed citations
1 1
2 22
3 1
4 37
5 7
6 1
7 82
8 45
9 59
10 12
11 37
12 123
13 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
0
15 68
16 259
17
Haploinsufficiency of the Euchromatin Histone Methyl Transferase1 (Eu-HMTase1) gene causes the 9q subtelomeric deletion syndrome
1
18 65
19 57
20
P63 mutations in the EEC, Hay-Wells, ADULT syndromes and in split hand/foot malformation reveals a genotype-phenotype correlation.
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) and Cancer-related Molecular Pathways (29 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.

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