E Strengman

2.6k citations
9 papers · 337 · h-index 8

Impact in

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

Papers in

    • Cancer-related gene regulation 2
    • Genetic Associations and Epidemiology 3
    • Genetic Mapping and Diversity in Plants and Animals 2

E Strengman

9 papers receiving 329 citations

Peers

E Strengman
Comparison fields: 5 of 72
  • Genetics 112
  • Neurology 54
  • Genetics 34
  • Endocrinology, Diabetes and Metabolism 39
  • Oncology 55
Replace Ritesh Kaushal with:
Ritesh Kaushal United States
Christine Makowski Germany
Mikołaj Łabuda Canada
Ann V. Griffith United States
Merel W. Boogaard Netherlands
Marwan Nashabat Saudi Arabia
Jean‐Christophe Devedjian France
Likui Lu China
Alix de Becdelièvre France
Galam Khan United States
E Strengman relative to Ritesh Kaushal United States Ritesh Kaushal's profile →
Citations per field
00.5×6.5×
Ritesh Kaushal · 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 201613
8 200312
9 20173

About E Strengman

E Strengman is a scholar working on Molecular Biology, Genetics, Surgery, Endocrine and Autonomic Systems and Pathology and Forensic Medicine, having authored 9 papers that have together received 337 indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (3 papers), Genetic Mapping and Diversity in Plants and Animals (2 papers), Cancer-related gene regulation (2 papers), Circadian rhythm and melatonin (2 papers), Pancreatic function and diabetes (1 paper), Colorectal Cancer Treatments and Studies (1 paper), Cancer Treatment and Pharmacology (1 paper) and Genetic factors in colorectal cancer (1 paper). The work is most often cited by research in Genetics (112 citations), Neurology (54 citations), Genetics (34 citations), Endocrinology, Diabetes and Metabolism (39 citations) and Oncology (55 citations). E Strengman has collaborated with scholars based in Netherlands, United States and Belgium. Frequent co-authors include Timon W. van Haeften, Cisca Wijmenga, Ronit Shiri‐Sverdlov, Jana V. van Vliet‐Ostaptchouk, Alexandra Zhernakova, Marten H. Hofker, Roel A. Ophoff, P. Pearson, Lodewijk A. Sandkuijl and H. van Someren. Their work appears in journals such as Translational Psychiatry, Human Molecular Genetics, Diabetologia, Neurology and Diseases of the Esophagus.

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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