Nerine Gregersen

455 citations
18 papers · 351 · h-index 9

Impact in

  • Pharmacology top 10%
    • Pharmacogenetics and Drug Metabolism
    • Genomics and Rare Diseases
    • Craniofacial Disorders and Treatments
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities

Papers in

    • Genetics and Neurodevelopmental Disorders 4
    • Genomics and Rare Diseases 4
    • Genomic variations and chromosomal abnormalities 3
    • Congenital Ear and Nasal Anomalies 2
    • Craniofacial Disorders and Treatments 2
    • Down syndrome and intellectual disability research 1

Nerine Gregersen

15 papers receiving 337 citations

Peers

Nerine Gregersen
Comparison fields: 5 of 39
  • Pharmacology 48
  • Genetics 122
  • Molecular Medicine 13
  • Public Health, Environmental and Occupational Health 63
  • Pediatrics, Perinatology and Child Health 19
Replace Parvinder Kumar with:
Parvinder Kumar India
Ljubica Boban Croatia
Catherine Lynn T. Silao Philippines
Angélica María Muñoz Contreras Colombia
Ashley R. Gilman Canada
Francisco Javier Martín Carpi Spain
Rona Karahoda Czechia
Concepción Álvarez del Vayo Benito Spain
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Citations per field
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Citations per year

Countries citing papers authored by Nerine Gregersen

Since Specialization
Citations

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

Fields of papers citing papers by Nerine Gregersen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Nerine Gregersen, 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 Nerine Gregersen Line = papers co-authored together Nerine Gregersen links everyone, so they are left out of the graph.

All Works

18 of 18 papers shown
#Work
1 201864
2 201950
3 201148
4 202041
5 201737
6 200431
7 199930
8 201314
9 201512
10 20138
11 20055
12 20133
13 20133
14 20133
15
Birth asphyxia - Presenting the case for' A stitch in time'
19992
16 20190
17 20250
18 20250

About Nerine Gregersen

Nerine Gregersen is a scholar working on Genetics, Genetics, Public Health, Environmental and Occupational Health, Pediatrics, Perinatology and Child Health and Endocrinology, Diabetes and Metabolism, having authored 18 papers that have together received 351 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Congenital Ear and Nasal Anomalies (2 papers), Craniofacial Disorders and Treatments (2 papers), Down syndrome and intellectual disability research (1 paper), Chromatin Remodeling and Cancer (1 paper) and Neonatal and fetal brain pathology (1 paper). The work is most often cited by research in Pharmacology (48 citations), Genetics (122 citations), Molecular Medicine (13 citations), Public Health, Environmental and Occupational Health (63 citations) and Pediatrics, Perinatology and Child Health (19 citations). Nerine Gregersen has collaborated with scholars based in New Zealand, South Africa and Australia. Frequent co-authors include Amanda Krause, Denis Viljoen, Anne von Gottberg, Alice M. George, Donald R. Love, Arnold L. Christianson, Shahida Moosa, Juliet P. Taylor, Ian Hayes and Cynthia M. Sharpe. Their work appears in journals such as Modern Pathology, The Pediatric Infectious Disease Journal, Pharmacogenomics, Genetics in Medicine and Circulation.

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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