U Theile

769 citations
23 papers · 243 · h-index 9

Impact in

    • Genetic Syndromes and Imprinting
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases
    • Genetics and Neurodevelopmental Disorders
    • Skin and Cellular Biology Research

Papers in

    • Genomic variations and chromosomal abnormalities 2
    • Sexual Differentiation and Disorders 3
    • RNA modifications and cancer 3
    • Molecular Biology Techniques and Applications 2

U Theile

22 papers receiving 232 citations

Peers

U Theile
Comparison fields: 5 of 51
  • Genetics 144
  • Cell Biology 36
  • Molecular Biology 132
  • Pediatrics, Perinatology and Child Health 31
  • Developmental Biology 3
Replace Mira Kyttälä with:
Mira Kyttälä Finland
M. Tuchman United States
C. R. Greenberg Canada
Franklin L. DeBusk United States
Shane C. Quinonez United States
Katalin Szakszon Hungary
Ariella Weinberg‐Shukron Israel
Erina Inoue Japan
H. Heilbronner Germany
Shiga Hasuike Japan
U Theile relative to Mira Kyttälä Finland Mira Kyttälä's profile →
Citations per field
00.5×
Mira Kyttälä · 1×
Citations per year

Countries citing papers authored by U Theile

Since Specialization
Citations

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

Fields of papers citing papers by U Theile

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 23 papers — load more, or switch the sort, to bring in the rest.

#Work
1 199962
2 197439
3 200323
4 199718
5 196316
6 199616
7 200410
8 200010
9 200010
10
[FAMILIAL STUDIES ON GAMMA GLOBULIN GROUPS; GM (A), GM (B), GM (X) AND GM (R)].
19636
11 20005
12 19744
13 19634
14 19974
15 19733
16 19743
17 19783
18
[Effect of heredity and environment in immune diseases. Presentation of twin data].
19942
19 20042
20
[Cardiac findings in Noonan syndrome].
19861

About U Theile

U Theile is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Plant Science and Clinical Biochemistry, having authored 23 papers that have together received 243 indexed citations. Recurring topics across this work include Sexual Differentiation and Disorders (3 papers), Chromosomal and Genetic Variations (3 papers), RNA modifications and cancer (3 papers), Metabolism and Genetic Disorders (2 papers), Hormonal and reproductive studies (2 papers), Tumors and Oncological Cases (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Molecular Biology Techniques and Applications (2 papers). The work is most often cited by research in Genetics (144 citations), Cell Biology (36 citations), Molecular Biology (132 citations), Pediatrics, Perinatology and Child Health (31 citations) and Developmental Biology (3 citations). U Theile has collaborated with scholars based in Germany, Estonia and France. Frequent co-authors include G. G. Wendt, Stephanie Demuth, Hannelore Thiele, Christina Lich, Gabriele Gillessen‐Kaesbach, Bernhard Horsthemke, M. Rister, Peter Wieacker, Vera Beyer and Sabine Scherer. Their work appears in journals such as Human Genetics, Prenatal Diagnosis, Human Mutation, European Journal of Human Genetics and Human Heredity.

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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