Nicole Van Regemorter

3.1k citations
57 papers · 2.0k indexed · 1 hit paper · h-index 24
Topics
Prenatal Screening and Diagnostics (10 papers)RNA regulation and disease (7 papers)Genomic variations and chromosomal abnormalities (7 papers)

In The Last Decade

Nicole Van Regemorter

57 papers receiving 1.9k citations

Hit Papers

A human homologue of the Drosophila eyes absent gene unde...19972026200620161997100200300400

Peers

Nicole Van Regemorter
Comparison fields: 5 of 94
  • Molecular Biology 1.2k
  • Genetics 532
  • Pediatrics, Perinatology and Child Health 380
  • Cellular and Molecular Neuroscience 344
  • Surgery 297
Replace Elizabeth Ives with:
Elizabeth Ives Canada
Zoha Kibar Canada
Andreas Winterpacht Germany
Mohnish Suri United Kingdom
Dvorah Abeliovich Israel
Peter Wieacker Germany
Anna Pelet France
Hubert Journel France
J P Fryns Belgium
Pierre Bitoun France
Nicole Van Regemorter relative to Elizabeth Ives Canada Elizabeth Ives's profile →
Citations per field
00.5×2.8×
Elizabeth Ives · 1×
Citations per year

Countries citing papers authored by Nicole Van Regemorter

Since Specialization
Citations

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

Fields of papers citing papers by Nicole Van Regemorter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nicole Van Regemorter. 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 Nicole Van Regemorter. The network helps show where Nicole Van Regemorter may publish in the future.

Co-authorship network of co-authors of Nicole Van Regemorter

This figure shows the co-authorship network connecting the top 25 collaborators of Nicole Van Regemorter. A scholar is included among the top collaborators of Nicole Van Regemorter 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 Nicole Van Regemorter. Nicole Van Regemorter 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 50
2 110
3 1
4 29
5 66
6 45
7
A comprehensive survey of spectrum of mutations in the OPA1 gene in patients with optic atrophy
1
8
OPA1 gene mutations cluster in functional protein domains in ADOA patients and reveal a founder allele in the Danish population.
1
9 10
10 30
11 2
12 24
13 126
14 4
15 76
16 32
17 9
18 5
19 41
20
[Auditory deficiency and genetic counseling].
1

About Nicole Van Regemorter

Nicole Van Regemorter is a scholar working on Pediatrics, Perinatology and Child Health, Developmental Biology and Genetics, having authored 57 papers that have together received 2.0k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (10 papers), RNA regulation and disease (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). The work is most often cited by research in Sensory Systems (100 citations), Pediatrics, Perinatology and Child Health (380 citations) and Genetics (532 citations). Nicole Van Regemorter has collaborated with scholars based in Belgium, United Kingdom and France. Frequent co-authors include F Rodesch, Françoise Meire, Marc Abramowicz, Christine Van Broeckhoven, Jean‐Jacques Martin, Dominique Weil, Sonia Abdelhak, Iman Sahly, Delphine Samson and Jean Weissenbach. Their work appears in journals such as Nature Genetics, Radiology and The American 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.

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