Eeva Therman

4.9k citations
89 papers · 3.3k indexed · 1 hit paper · h-index 30

Impact in

  • Genetics top 0.5%
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders

Papers in

    • Genomic variations and chromosomal abnormalities 20
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 14
    • Chromosomal and Genetic Variations 32
    • Plant Genetic and Mutation Studies 7

Eeva Therman

88 papers receiving 2.8k citations

Hit Papers

MULTIPLE CONGENITAL ANOMALY CAUSED BY AN EXTRA AUTOSOME 1960 · 473 citations
4731960202619822004100200300400

Peers

Eeva Therman
Comparison fields: 5 of 115
  • Developmental Biology 151
  • Genetics 1.9k
  • Pediatrics, Perinatology and Child Health 690
  • Plant Science 949
  • Molecular Biology 1.5k
Replace J. de Grouchy with:
J. de Grouchy France
Catherine G. Palmer United States
C Turleau France
Klaus Pätau United States
Irene A. Uchida Canada
W. Roy Breg United States
H.P. Klinger United States
Maj Hultén United Kingdom
Tadashi Kajii Japan
D.G. Harnden United Kingdom
Eeva Therman relative to J. de Grouchy France J. de Grouchy's profile →
Citations per field
00.5×
J. de Grouchy · 1×
Citations per year

Countries citing papers authored by Eeva Therman

Since Specialization
Citations

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

Fields of papers citing papers by Eeva Therman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

20 of 20 papers shown
#Work
1 20105
2 20106
3 20102
4 20101
5 20090
6 19956
7 199123
8 199079
9 1989137
10 198810
11 19875
12 19876
13 198719
14 19859
15 197911
16
The effect of procarbazine on the chromosomes of normal and malignant mouse cells.
19771
17
Chromosome breakage by 1-methyl-2-benzylhydrazine in mouse cancer cells.
19726
18 1963112
19 1960152
20
MULTIPLE CONGENITAL ANOMALY CAUSED BY AN EXTRA AUTOSOME
Hit paper breakdown →
1960473

About Eeva Therman

Eeva Therman is a scholar working on Genetics, Plant Science, Cancer Research, Molecular Biology and Developmental Biology, having authored 89 papers that have together received 3.3k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (32 papers), Genomic variations and chromosomal abnormalities (20 papers), DNA Repair Mechanisms (15 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (14 papers), Genomics and Chromatin Dynamics (11 papers), Carcinogens and Genotoxicity Assessment (7 papers), Plant Genetic and Mutation Studies (7 papers) and DNA and Nucleic Acid Chemistry (6 papers). The work is most often cited by research in Developmental Biology (151 citations), Genetics (1.9k citations), Pediatrics, Perinatology and Child Health (690 citations), Plant Science (949 citations) and Molecular Biology (1.5k citations). Eeva Therman has collaborated with scholars based in United States, Finland and Brazil. Frequent co-authors include Klaus Pätau, Gloria E. Sarto, Evelyn M. Kuhn, Carter Denniston, Stanley L. Inhorn, David W. Smith, David W. Smith, Robert DeMars, Renata Laxová and Lassi Alvesalo. Their work appears in journals such as Human Genetics, Chromosoma, Hereditas, American Journal of Botany and Physiologia Plantarum.

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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