C E de Die-Smulders

1.4k citations
21 papers · 516 indexed · h-index 13
Topics
Genetic Neurodegenerative Diseases (5 papers)Mitochondrial Function and Pathology (4 papers)Genomic variations and chromosomal abnormalities (4 papers)
Partner nations
NetherlandsGermanyFrance

In The Last Decade

C E de Die-Smulders

21 papers receiving 498 citations

Peers

C E de Die-Smulders
Comparison fields: 5 of 56
  • Molecular Biology 272
  • Genetics 266
  • Pediatrics, Perinatology and Child Health 90
  • Cellular and Molecular Neuroscience 89
  • Public Health, Environmental and Occupational Health 66
Replace Sarah Vergult with:
Sarah Vergult Belgium
Thomas A. Maher United States
Tiia Reimand Estonia
Tadeusz Mazurczak Poland
Karin Writzl Slovenia
C. J. Partsch Germany
LaDonna Immken United States
Linda Meredith United Kingdom
Vanna Pecile Italy
C E de Die-Smulders relative to Sarah Vergult Belgium Sarah Vergult's profile →
Citations per field
00.5×4.4×
Sarah Vergult · 1×
Citations per year

Countries citing papers authored by C E de Die-Smulders

Since Specialization
Citations

This map shows the geographic impact of C E de Die-Smulders'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 C E de Die-Smulders with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C E de Die-Smulders more than expected).

Fields of papers citing papers by C E de Die-Smulders

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by C E de Die-Smulders. 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 C E de Die-Smulders. The network helps show where C E de Die-Smulders may publish in the future.

Co-authorship network of co-authors of C E de Die-Smulders

This figure shows the co-authorship network connecting the top 25 collaborators of C E de Die-Smulders. A scholar is included among the top collaborators of C E de Die-Smulders 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 C E de Die-Smulders. C E de Die-Smulders 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 31
2 5
3 18
4 35
5 59
6 16
7 36
8 61
9 6
10
Lateral facial clefts: a case report.
5
11 2
12 7
13
Lethal hypophosphatasia, spur type: case report and fetopathological study.
5
14 26
15
Instability of the CGG repeat and expression of the FMR1 protein in a male fragile X patient with a lung tumor.
49
16
Coffin-Lowry syndrome: clinical aspects at different ages and symptoms in female carriers.
16
17 9
18 17
19 3
20 39

About C E de Die-Smulders

C E de Die-Smulders is a scholar working on Pediatrics, Perinatology and Child Health, Clinical Biochemistry and Genetics, having authored 21 papers that have together received 516 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (5 papers), Mitochondrial Function and Pathology (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). The work is most often cited by research in Genetics (266 citations), Reproductive Medicine (51 citations) and Clinical Biochemistry (36 citations). C E de Die-Smulders has collaborated with scholars based in Netherlands, Germany and France. Frequent co-authors include J.J.M. Engelen, S. B. van der Meer, Rob Willemsen, Esther de Graaff, Nanbert Zhong, B. A. Oostra, W. Ted Brown, Marinus J. Blok, Marjolein Visser and Alexandra T.M. Hendrickx. Their work appears in journals such as Human Reproduction, Journal of Medical Genetics and European Journal of Human 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026