Fleur S. van Dijk

1.9k citations

11 papers · 999 indexed · 1 hit paper · h-index 10

Co-authors: David Sillence Gerard Pals Rick R. van Rijn Jan M. Cobben Peter G. J. Nikkels J. M. Cobben Ariana Kariminejad Alessandra Maugeri
Topics: Connective tissue disorders research (8 papers)Bone and Dental Protein Studies (4 papers)Ubiquitin and proteasome pathways (3 papers)
Cited by: Genetics Rheumatology Anatomy
Journals: Genetics in Medicine European Journal of Human Genetics JAMA Dermatology
Partner nations: Netherlands United Kingdom Australia

In The Last Decade

Fleur S. van Dijk

11 papers receiving 956 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Osteogenesis imperfecta: Clinical diagnosis, nomenclature and severity assessment

2014 501 citations Fleur S. van Dijk, David Sillence American Journal of Medical Genetics Part A profile →

Peers

Countries citing papers authored by Fleur S. van Dijk

Since Specialization

Citations

This map shows the geographic impact of Fleur S. van Dijk'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 Fleur S. van Dijk with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fleur S. van Dijk more than expected).

Fields of papers citing papers by Fleur S. van Dijk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fleur S. van Dijk. 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 Fleur S. van Dijk. The network helps show where Fleur S. van Dijk may publish in the future.

Co-authorship network of co-authors of Fleur S. van Dijk

This figure shows the co-authorship network connecting the top 25 collaborators of Fleur S. van Dijk. A scholar is included among the top collaborators of Fleur S. van Dijk 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 Fleur S. van Dijk. Fleur S. van Dijk is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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11 of 11 papers shown

#	Work	Indexed citations
1	Atrophoderma Vermiculatum 2015 ·JAMA Dermatology ·Fleur S. van Dijk,Helen Brittain,Ragna S. Boerma,(unknown),Jan M. Cobben	1
2	Osteogenesis imperfecta: Clinical diagnosis, nomenclature and severity assessmentbreakdown → 2014 ·American Journal of Medical Genetics Part A ·Fleur S. van Dijk,David Sillence	501
3	Pectus excavatum and carinatum 2014 ·European Journal of Medical Genetics ·Jan M. Cobben,Roelof‐Jan Oostra,Fleur S. van Dijk	58
4	A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disability 2014 ·European Journal of Medical Genetics ·Jan-Maarten Cobben,Marjan M. Weiss,Fleur S. van Dijk,(unknown),(unknown),Willem Pondaag,R Hennekam,Helger G. Yntema	31
5	A novel homozygous 5 bp deletion in FKBP10 causes clinically Bruck syndrome in an Indonesian patient 2011 ·European Journal of Medical Genetics ·(unknown),Fleur S. van Dijk,Jan M. Cobben,Rick R. van Rijn,Erik A. Sistermans,Sultana MH Faradz,(unknown),Gerard Pals	23
6	Osteogenesis Imperfecta: A Review with Clinical Examples 2011 ·Molecular Syndromology ·Fleur S. van Dijk,J. M. Cobben,Ariana Kariminejad,Alessandra Maugeri,Peter G. J. Nikkels,Rick R. van Rijn,Gerard Pals	142
7	Complete COL1A1 allele deletions in osteogenesis imperfecta 2010 ·Genetics in Medicine ·Fleur S. van Dijk,(unknown),Ariana Kariminejad,Carlo Marcelis,Astrid S. Plomp,Pauline Terhal,Hanne Meijers‐Heijboer,Marjan M. Weiss,Rick R. van Rijn,Jan M. Cobben,Gerard Pals	33
8	Lethal/Severe Osteogenesis Imperfecta in a Large Family: A Novel Homozygous LEPRE1 Mutation and Bone Histological Findings 2010 ·Pediatric and Developmental Pathology ·Fleur S. van Dijk,Peter G. J. Nikkels,Nicolette S. den Hollander,I. M. Nesbitt,Rick R. van Rijn,Jan M. Cobben,Gerard Pals	16
9	Classification of Osteogenesis Imperfecta revisited 2009 ·European Journal of Medical Genetics ·Fleur S. van Dijk,Gerard Pals,Rick R. van Rijn,Peter G. J. Nikkels,Jan M. Cobben	139
10	CRTAP mutations in lethal and severe osteogenesis imperfecta: the importance of combining biochemical and molecular genetic analysis 2009 ·European Journal of Human Genetics ·Fleur S. van Dijk,I. M. Nesbitt,Peter G. J. Nikkels,Ann Dalton,Ernie M.H.F. Bongers,Jiddeke M. van de Kamp,Yvonne Hilhorst‐Hofstee,Nicolette S. den Hollander,Augusta M.A. Lachmeijer,Carlo Marcelis,Gita Tan-Sindhunata,Rick R. van Rijn,Hanne Meijers‐Heijboer,Jan M. Cobben,Gerard Pals	34
11	Compound-heterozygous Marfan syndrome 2008 ·European Journal of Medical Genetics ·Fleur S. van Dijk,Ben C.J. Hamel,Yvonne Hilhorst‐Hofstee,B. J. M. Mulder,Jean‐Pierre Timmermans,Gerard Pals,J. M. Cobben	21

About Fleur S. van Dijk

Fleur S. van Dijk is a scholar working on Developmental Biology, Genetics and Rheumatology, having authored 11 papers that have together received 999 indexed citations. Recurring topics across this work include Connective tissue disorders research (8 papers), Bone and Dental Protein Studies (4 papers) and Ubiquitin and proteasome pathways (3 papers). The work is most often cited by research in Genetics (846 citations), Rheumatology (370 citations) and Anatomy (16 citations). Fleur S. van Dijk has collaborated with scholars based in Netherlands, United Kingdom and Australia. Frequent co-authors include David Sillence, Gerard Pals, Rick R. van Rijn, Jan M. Cobben, Peter G. J. Nikkels, J. M. Cobben, Ariana Kariminejad, Alessandra Maugeri, Roelof‐Jan Oostra and Marjan M. Weiss. Their work appears in journals such as Genetics in Medicine, European Journal of Human Genetics and JAMA Dermatology.

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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