Sonja de Munnik

747 citations
6 papers · 184 · h-index 4

Impact in

    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases

Papers in

    • Genomics and Chromatin Dynamics 1
    • Epigenetics and DNA Methylation 1
    • DNA Repair Mechanisms 1
    • Cancer-related gene regulation 1
    • RNA modifications and cancer 1
    • Genetics and Neurodevelopmental Disorders 2
    • Genomic variations and chromosomal abnormalities 2

Sonja de Munnik

5 papers receiving 181 citations

Peers

Sonja de Munnik
Comparison fields: 5 of 43
  • Genetics 92
  • Aging 3
  • Molecular Biology 112
  • Developmental Biology 3
  • Cognitive Neuroscience 18
Replace María J. Guillen Sacoto with:
María J. Guillen Sacoto United States
Arjan PM de Brouwer Netherlands
Jianhong Hu United States
Yiping Shen China
Connie T. R. M. Stumpel Netherlands
Alice Bailey United States
Antonio Federico Martínez‐Monseny Spain
Kathleen H. Wood United States
Donald Freed United States
Holly Feret United States
Sonja de Munnik relative to María J. Guillen Sacoto United States María J. Guillen Sacoto's profile →
Citations per field
00.5×1.6×
María J. Guillen Sacoto · 1×
Citations per year

Countries citing papers authored by Sonja de Munnik

Since Specialization
Citations

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

Fields of papers citing papers by Sonja de Munnik

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sonja de Munnik. 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 Sonja de Munnik. The network helps show where Sonja de Munnik may publish in the future.

Co-authors

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

All Works

6 of 6 papers shown
#Work
1 2017107
2 201444
3 201818
4 202114
5 20191
6 20250

About Sonja de Munnik

Sonja de Munnik is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Epidemiology and Infectious Diseases, having authored 6 papers that have together received 184 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Genomics and Chromatin Dynamics (1 paper), Epigenetics and DNA Methylation (1 paper), DNA Repair Mechanisms (1 paper), Cancer-related gene regulation (1 paper), Prenatal Screening and Diagnostics (1 paper) and RNA modifications and cancer (1 paper). The work is most often cited by research in Genetics (92 citations), Aging (3 citations), Molecular Biology (112 citations), Developmental Biology (3 citations) and Cognitive Neuroscience (18 citations). Sonja de Munnik has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Connie T. R. M. Stumpel, Jamie M. Kramer, Rolph Pfundt, Tjitske Kleefstra, Hans van Bokhoven, Marjolein H. Willemsen, Margarita Sáenz, Levinus A. Bok, Alexander P.A. Stegmann and Huiqing Zhou. Their work appears in journals such as HemaSphere, PLoS Genetics, European Journal of Human Genetics, American Journal of Medical Genetics Part A and Molecular Genetics & Genomic Medicine.

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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