E Strengman

2.6k citations
9 papers · 338 · h-index 8

Impact in

    • Amyotrophic Lateral Sclerosis Research
    • Genetic Associations and Epidemiology
    • Neurogenetic and Muscular Disorders Research
    • Genetics and Neurodevelopmental Disorders
    • Diabetes and associated disorders

Papers in

    • Cancer-related gene regulation 2
    • Peroxisome Proliferator-Activated Receptors 1
    • Bioinformatics and Genomic Networks 1
    • Genetic Associations and Epidemiology 3
    • Genetic Mapping and Diversity in Plants and Animals 2

E Strengman

9 papers receiving 330 citations

Peers

E Strengman
Comparison fields: 5 of 62
  • Neurology 54
  • Genetics 84
  • Genetics 28
  • Oncology 51
  • Neurology 14
Replace Fang Cui with:
Fang Cui China
Ann V. Griffith United States
Alix de Becdelièvre France
Donatella Bardelli Italy
Astrid Edland Norway
Elisa J. Cops Australia
Lianting Ma China
Likui Lu China
L Kádasi Slovakia
E Strengman relative to Fang Cui China Fang Cui's profile →
Citations per field
00.5×2.7×
Fang Cui · 1×
Citations per year

Countries citing papers authored by E Strengman

Since Specialization
Citations

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

Fields of papers citing papers by E Strengman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

9 of 9 papers shown
#Work
1 200694
2 200959
3 201756
4 200345
5 201430
6 201325
7 201614
8 200312
9 20173

About E Strengman

E Strengman is a scholar working on Molecular Biology, Genetics, Endocrine and Autonomic Systems, Surgery and Cellular and Molecular Neuroscience, having authored 9 papers that have together received 338 indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (3 papers), Circadian rhythm and melatonin (2 papers), Genetic Mapping and Diversity in Plants and Animals (2 papers), Cancer-related gene regulation (2 papers), Peroxisome Proliferator-Activated Receptors (1 paper), Behavioral Health and Interventions (1 paper), Amyotrophic Lateral Sclerosis Research (1 paper) and Bioinformatics and Genomic Networks (1 paper). The work is most often cited by research in Neurology (54 citations), Genetics (84 citations), Genetics (28 citations), Oncology (51 citations) and Neurology (14 citations). E Strengman has collaborated with scholars based in Netherlands, United States and Belgium. Frequent co-authors include Timon W. van Haeften, Cisca Wijmenga, Jana V. van Vliet‐Ostaptchouk, Alexandra Zhernakova, Marten H. Hofker, Ronit Shiri‐Sverdlov, Roel A. Ophoff, P. Pearson, Lodewijk A. Sandkuijl and H. van Someren. Their work appears in journals such as Translational Psychiatry, European Journal of Clinical Investigation, Neurology, Annals of Oncology and The Journal of Clinical Endocrinology & Metabolism.

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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