Nicole Van Regemorter
- Sensory Systems top 5%
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- Prenatal Screening and Diagnostics 10
- Fetal and Pediatric Neurological Disorders 6
- Genetics top 5%
- Genomic variations and chromosomal abnormalities 7
- Connective tissue disorders research 4
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- Genetic Neurodegenerative Diseases 6
- Molecular Biology top 10%
- RNA regulation and disease 7
- Mitochondrial Function and Pathology 6
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- Congenital Anomalies and Fetal Surgery 5
Nicole Van Regemorter
57 papers receiving 1.9k citations
Hit Papers
Peers
Comparison fields: 5 of 94
- Sensory Systems 100
- Pediatrics, Perinatology and Child Health 380
- Genetics 532
- Cellular and Molecular Neuroscience 344
- Molecular Biology 1.2k
Countries citing papers authored by Nicole Van Regemorter
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
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
The 25 scholars most cited alongside Nicole Van Regemorter, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 50 | |
| 2 | 2010 | 110 | |
| 3 | 2009 | 1 | |
| 4 | 2009 | 29 | |
| 5 | 2007 | 66 | |
| 6 | 2005 | 45 | |
| 7 | A comprehensive survey of spectrum of mutations in the OPA1 gene in patients with optic atrophy | 2002 | 1 |
| 8 | OPA1 gene mutations cluster in functional protein domains in ADOA patients and reveal a founder allele in the Danish population. | 2001 | 1 |
| 9 | 1998 | 10 | |
| 10 | 1996 | 30 | |
| 11 | 1996 | 2 | |
| 12 | 1996 | 24 | |
| 13 | 1995 | 126 | |
| 14 | 1995 | 4 | |
| 15 | 1994 | 76 | |
| 16 | 1993 | 32 | |
| 17 | 1989 | 9 | |
| 18 | 1986 | 5 | |
| 19 | 1984 | 41 | |
| 20 | [Auditory deficiency and genetic counseling]. | 1977 | 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), Genomic variations and chromosomal abnormalities (7 papers), Mitochondrial Function and Pathology (6 papers), Genetic Neurodegenerative Diseases (6 papers), Fetal and Pediatric Neurological Disorders (6 papers), Congenital Anomalies and Fetal Surgery (5 papers) and Connective tissue disorders research (4 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.