Esther Janson

1.3k citations
11 papers · 826 · h-index 10

Impact in

  • Genetics top 10%
    • Genetic Syndromes and Imprinting
    • Genetic Associations and Epidemiology
    • Genetics and Neurodevelopmental Disorders

Papers in

    • Epigenetics and DNA Methylation 2
    • Ubiquitin and proteasome pathways 1
    • Gene expression and cancer classification 1
    • Genetics and Neurodevelopmental Disorders 2
    • Genetic Mapping and Diversity in Plants and Animals 2
    • Genomic variations and chromosomal abnormalities 2
    • Genetic Associations and Epidemiology 2
    • Genetic Syndromes and Imprinting 1

Esther Janson

11 papers receiving 818 citations

Peers

Esther Janson
Comparison fields: 5 of 100
  • Biological Psychiatry 40
  • Genetics 241
  • Molecular Biology 484
  • Immunology 110
  • Aging 7
Replace Srilaxmi Nerella with:
Srilaxmi Nerella United States
Maša Umićević Mirkov Netherlands
H.H.H. Göring United States
Hua Chang United States
Cathérine Dupont Netherlands
Jiewei Liu China
Andy Madrid United States
Xiang Zhao United States
Anne O’Donnell‐Luria United States
Laura Crisponi Italy
Esther Janson relative to Srilaxmi Nerella United States Srilaxmi Nerella's profile →
Citations per field
00.5×1.6×
Srilaxmi Nerella · 1×
Citations per year

Countries citing papers authored by Esther Janson

Since Specialization
Citations

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

Fields of papers citing papers by Esther Janson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

11 of 11 papers shown
#Work
1 2009280
2 2012162
3 2012114
4 201397
5 201251
6 201245
7 201133
8 201016
9 201110
10 201210
11 20128

About Esther Janson

Esther Janson is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Oncology and Neurology, having authored 11 papers that have together received 826 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (2 papers), Epigenetics and DNA Methylation (2 papers), Genetic Mapping and Diversity in Plants and Animals (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Genetic Associations and Epidemiology (2 papers), Ubiquitin and proteasome pathways (1 paper), Gene expression and cancer classification (1 paper) and Genetic Syndromes and Imprinting (1 paper). The work is most often cited by research in Biological Psychiatry (40 citations), Genetics (241 citations), Molecular Biology (484 citations), Immunology (110 citations) and Aging (7 citations). Esther Janson has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Roel A. Ophoff, Marco P. Boks, René S. Kahn, Eske M. Derks, Iris E. Sommer, Daniel J. Weisenberger, Simone de Jong, Eric Strengman, Leonard H. van den Berg and Jan H. Veldink. Their work appears in journals such as PLoS ONE, BMC Genomics, Psychiatric Genetics, Journal of Allergy and Clinical Immunology and NeuroImage Clinical.

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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