David Sillence

14.4k citations
120 papers · 8.4k · 5 hit papers · h-index 43

Impact in

  • Genetics top 0.1%
    • Connective tissue disorders research
    • Dermatological and Skeletal Disorders
    • Neurogenetic and Muscular Disorders Research
  • Rheumatology top 0.2%
    • Bone and Dental Protein Studies

Papers in

    • Connective tissue disorders research 63
    • Neurogenetic and Muscular Disorders Research 8
    • Dermatological and Skeletal Disorders 8
    • Craniofacial Disorders and Treatments 7
    • Bone and Dental Protein Studies 11

David Sillence

119 papers receiving 8.1k citations

David Sillence's Hit Papers

Nosology and classification of genetic skeletal disorders: 2019 revision 2019 · 389 citations
3890+15+31Years since publication50010001.5k

Peers

David Sillence
Comparison fields: 5 of 125
  • Genetics 5.3k
  • Rheumatology 2.0k
  • Immunology and Allergy 258
  • Anatomy 56
  • Genetics 388
Replace Anne De Paepe with:
Anne De Paepe Belgium
Shiro Ikegawa Japan
Deborah Krakow United States
Gen Nishimura Japan
Clair A. Francomano United States
Jürgen W. Spranger Germany
Valérie Cormier‐Daire France
Anthony Celeste United States
Fransiska Malfait Belgium
Ravi Savarirayan Australia
David Sillence relative to Anne De Paepe Belgium Anne De Paepe's profile →
Citations per field
00.5×3.3×
Anne De Paepe · 1×
Citations per year

Countries citing papers authored by David Sillence

Since Specialization
Citations

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

Fields of papers citing papers by David Sillence

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David Sillence. 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 David Sillence. The network helps show where David Sillence may publish in the future.

Co-authors

The 25 scholars most cited alongside David Sillence, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with David Sillence Line = papers co-authored together David Sillence links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 120 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Genetic heterogeneity in osteogenesis imperfecta.
Hit paper breakdown →
19791648
2
Osteogenesis imperfecta: Clinical diagnosis, nomenclature and severity assessment
Hit paper breakdown →
2014516
3
Nosology and classification of genetic skeletal disorders: 2010 revision
Hit paper breakdown →
2011452
4
Nosology and classification of genetic skeletal disorders: 2019 revision
Hit paper breakdown →
2019389
5
Nosology and classification of genetic skeletal disorders: 2015 revision
Hit paper breakdown →
2015372
6 2003314
7 2007267
8 1981267
9 2009239
10 1998202
11 1986153
12 1999145
13
Clinical variability in osteogenesis imperfecta-variable expressivity or genetic heterogeneity.
1979126
14 2004120
15 1984118
16 2008117
17 1995115
18 1995106
19 2005101
20 199792

About David Sillence

David Sillence is a scholar working on Genetics, Rheumatology, Molecular Biology, Physiology and Pathology and Forensic Medicine, having authored 120 papers that have together received 8.4k indexed citations. Recurring topics across this work include Connective tissue disorders research (63 papers), Lysosomal Storage Disorders Research (15 papers), Bone and Dental Protein Studies (11 papers), Neurogenetic and Muscular Disorders Research (8 papers), Dermatological and Skeletal Disorders (8 papers), Craniofacial Disorders and Treatments (7 papers), Bone fractures and treatments (6 papers) and Bone health and treatments (6 papers). The work is most often cited by research in Genetics (5.3k citations), Rheumatology (2.0k citations), Immunology and Allergy (258 citations), Anatomy (56 citations) and Genetics (388 citations). David Sillence has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include D. M. Danks, Fleur S. van Dijk, Ravi Savarirayan, Stefan Mundlos, Geert Mortier, Valérie Cormier‐Daire, Matthew L. Warman, Sheila Unger, Christine M Hall and Gen Nishimura. Their work appears in journals such as Journal of Medical Genetics, The American Journal of Human Genetics, Journal of Clinical Investigation, Skeletal Radiology and Journal of Biological Chemistry.

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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