U Theile

768 total citations
23 papers, 242 citations indexed

About

U Theile is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, U Theile has authored 23 papers receiving a total of 242 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 10 papers in Molecular Biology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in U Theile's work include Sexual Differentiation and Disorders (3 papers), RNA modifications and cancer (3 papers) and Chromosomal and Genetic Variations (3 papers). U Theile is often cited by papers focused on Sexual Differentiation and Disorders (3 papers), RNA modifications and cancer (3 papers) and Chromosomal and Genetic Variations (3 papers). U Theile collaborates with scholars based in Germany, Estonia and United Kingdom. U Theile's co-authors include G. G. Wendt, Hannelore Thiele, Christina Lich, Gabriele Gillessen‐Kaesbach, Stephanie Demuth, Bernhard Horsthemke, M. Rister, Peter Wieacker, Vera Beyer and Sabine Scherer and has published in prestigious journals such as Human Mutation, Human Genetics and European Journal of Human Genetics.

In The Last Decade

U Theile

22 papers receiving 231 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
U Theile Germany 9 147 144 36 36 19 23 242
C. R. Greenberg Canada 8 88 0.6× 72 0.5× 31 0.9× 20 0.6× 23 1.2× 13 218
Erina Inoue Japan 10 90 0.6× 298 2.1× 33 0.9× 24 0.7× 17 0.9× 14 394
S Jansen South Africa 6 65 0.4× 159 1.1× 8 0.2× 16 0.4× 12 0.6× 14 216
Katalin Szakszon Hungary 10 103 0.7× 178 1.2× 16 0.4× 30 0.8× 17 0.9× 29 276
Ariella Weinberg‐Shukron Israel 9 173 1.2× 229 1.6× 55 1.5× 20 0.6× 16 0.8× 15 377
Shane C. Quinonez United States 11 172 1.2× 221 1.5× 56 1.6× 17 0.5× 11 0.6× 29 396
Bai-Lin Wu United States 6 163 1.1× 142 1.0× 51 1.4× 6 0.2× 11 0.6× 7 228
Nadiya Sosonkina United States 8 70 0.5× 115 0.8× 41 1.1× 13 0.4× 12 0.6× 14 212
Osamu Miyoshi Japan 11 116 0.8× 176 1.2× 74 2.1× 16 0.4× 8 0.4× 22 278
N.J. Barton United Kingdom 7 303 2.1× 264 1.8× 51 1.4× 19 0.5× 15 0.8× 10 453

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-authorship network of co-authors of U Theile

This figure shows the co-authorship network connecting the top 25 collaborators of U Theile. A scholar is included among the top collaborators of U Theile based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with U Theile. U Theile is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Theile, U, et al.. (2004). Geschwisterpaar mit neonatalem progeroidem Syndrom (Wiedemann-Rautenstrauch). Klinische Pädiatrie. 216(2). 70–71. 10 indexed citations
2.
3.
Scherer, Sabine, et al.. (2003). Patient with Kabuki syndrome and acute leukemia. American Journal of Medical Genetics Part A. 122A(1). 76–79. 22 indexed citations
4.
Hallermann, Christian, Nicolai Kohlschmidt, R. A. Schumacher, et al.. (2000). Syndrome of autosomal recessive polycystic kidneys with skeletal and facial anomalies is not linked to the ARPKD gene locus on chromosome 6p. American Journal of Medical Genetics. 90(2). 115–119. 10 indexed citations
5.
Haußer, Ingrid, et al.. (2000). Das neonatale progeroide Syndrom (Wiedemann-Rautenstrauch-Syndrom): Kasuistik und Literaturübersicht. Klinische Pädiatrie. 212(2). 71–204. 5 indexed citations
6.
Stümm, Markus, et al.. (2000). Deletion of the Dm-Domain Gene Cluster in a Fetus with Ring Chromosome 9 and Sex Reversal. Pediatric Pathology & Molecular Medicine. 19(6). 415–423. 10 indexed citations
7.
Gillessen‐Kaesbach, Gabriele, Stephanie Demuth, Hannelore Thiele, et al.. (1999). A previously unrecognised phenotype characterised by obesity, muscular hypotonia, and ability to speak in patients with Angelman syndrome caused by an imprinting defect. European Journal of Human Genetics. 7(6). 638–644. 62 indexed citations
8.
Jakubiczka, Sibylle, et al.. (1997). Mutations of the androgen receptor gene in patients with complete androgen insensitivity. Human Mutation. 9(1). 57–61. 18 indexed citations
9.
10.
11.
Theile, U, et al.. (1994). [Effect of heredity and environment in immune diseases. Presentation of twin data].. PubMed. 89(6). 312–8. 2 indexed citations
12.
Theile, U. (1986). [Cardiac findings in Noonan syndrome].. PubMed. 81(14). 481–5. 1 indexed citations
13.
Theile, U, et al.. (1974). Tricho-rhino-phalangeal syndrome ? a seldom constitutional disorder. Case report. Human Genetics. 22(3). 4 indexed citations
14.
Wendt, G. G. & U Theile. (1974). A pilot scheme for a genetic clinic. Human Genetics. 21(2). 145–151. 3 indexed citations
15.
Theile, U. (1974). Sjögren-Larsson Syndrome. PubMed. 22(2). 91–118. 39 indexed citations
16.
Theile, U, et al.. (1973). The Sj�gren-Larsson syndrome. Human Genetics. 17(2). 155–5. 3 indexed citations
17.
Theile, U, et al.. (1972). [Diagnostic problems in malignant thymoma with skeletal metastasizing].. PubMed. 23(46). 1685–8. 1 indexed citations
18.
Deicher, H., et al.. (1963). Familienuntersuchungen über die Gammaglobulingruppen Gm (a), Gm (b), Gm (x) und Gm (r). Human Heredity. 13(2). 124–131. 4 indexed citations
19.
Deicher, H., et al.. (1963). [FAMILIAL STUDIES ON GAMMA GLOBULIN GROUPS; GM (A), GM (B), GM (X) AND GM (R)].. PubMed. 13. 124–31. 6 indexed citations
20.
Wendt, G. G. & U Theile. (1963). Untersuchungen über den Gc-Faktor. DMW - Deutsche Medizinische Wochenschrift. 88(14). 696–701. 16 indexed citations

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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