H. U. Tietze

648 total citations
21 papers, 475 citations indexed

About

H. U. Tietze is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, H. U. Tietze has authored 21 papers receiving a total of 475 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in H. U. Tietze's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Electrolyte and hormonal disorders (3 papers) and Chromosomal and Genetic Variations (3 papers). H. U. Tietze is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Electrolyte and hormonal disorders (3 papers) and Chromosomal and Genetic Variations (3 papers). H. U. Tietze collaborates with scholars based in Germany, United States and Belgium. H. U. Tietze's co-authors include Anita Rauch, G. Buheitel, Helmuth-Guenther Doerr, R. Rauch, Wolfram Kreß, André Reis, Michael Hofbeck, Martin Zenker, Rainer Koenig and H. Singer and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Scientific Reports and The Journal of Pediatrics.

In The Last Decade

H. U. Tietze

21 papers receiving 458 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
H. U. Tietze Germany 10 318 156 144 88 56 21 475
Mario Saare Estonia 13 234 0.7× 314 2.0× 138 1.0× 190 2.2× 25 0.4× 17 626
Shinichi Igarashi Japan 11 131 0.4× 292 1.9× 66 0.5× 25 0.3× 34 0.6× 22 668
Walter Zumkeller Germany 11 228 0.7× 24 0.2× 218 1.5× 192 2.2× 25 0.4× 17 497
Maria Kalina Poland 9 174 0.5× 39 0.3× 90 0.6× 113 1.3× 15 0.3× 26 370
Stacey Jamieson Australia 9 266 0.8× 32 0.2× 147 1.0× 27 0.3× 21 0.4× 10 510
Jacques Leclère France 10 222 0.7× 86 0.6× 122 0.8× 372 4.2× 25 0.4× 15 614
Luca Mariani Italy 11 155 0.5× 44 0.3× 104 0.7× 48 0.5× 49 0.9× 28 396
Johji Inazawa Japan 10 308 1.0× 50 0.3× 54 0.4× 11 0.1× 57 1.0× 16 452
Svetlana Pidasheva Canada 7 179 0.6× 80 0.5× 89 0.6× 19 0.2× 58 1.0× 9 429
Feng-Tao Shi China 14 422 1.3× 94 0.6× 66 0.5× 13 0.1× 23 0.4× 18 633

Countries citing papers authored by H. U. Tietze

Since Specialization
Citations

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

Fields of papers citing papers by H. U. Tietze

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H. U. Tietze

This figure shows the co-authorship network connecting the top 25 collaborators of H. U. Tietze. A scholar is included among the top collaborators of H. U. Tietze 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 H. U. Tietze. H. U. Tietze 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.
Tietze, H. U., et al.. (2025). Identification of a binding pocket of letermovir in the terminase subunit pUL56 of human cytomegalovirus. Scientific Reports. 15(1). 10334–10334. 3 indexed citations
2.
Meyer, Jörg, et al.. (2024). Experimental and numerical investigation of droplet–fiber interaction on mechanically excited fiber. Physics of Fluids. 36(3). 3 indexed citations
3.
Hüffmeier, Ulrike, H. U. Tietze, & Anita Rauch. (2007). Severe skeletal dysplasia caused by undiagnosed hypothyroidism. European Journal of Medical Genetics. 50(3). 209–215. 20 indexed citations
4.
Zenker, Martin, G. Buheitel, R. Rauch, et al.. (2004). Genotype-phenotype correlations in Noonan syndrome. The Journal of Pediatrics. 144(3). 368–374. 177 indexed citations
5.
Dötsch, Jörg, et al.. (2003). Verlauf, Therapie und Komorbidität bei Hashimoto-Thyreoiditis im Kindesalter. Monatsschrift Kinderheilkunde. 151(5). 528–531. 2 indexed citations
6.
Wirth, Jutta, Thomas Wagner, Jobst Meyer, et al.. (1996). Translocation breakpoints in three patients with campomelic dysplasia and autosomal sex reversal map more than 130 kb from SOX9. Human Genetics. 97(2). 186–193. 82 indexed citations
7.
Trautmann, Udo, et al.. (1993). Simultaneous de novo interstitial deletion of 16q21 and intercalary duplication of 19q in a retarded infant with minor dysmorphic features.. Journal of Medical Genetics. 30(4). 330–331. 5 indexed citations
8.
Seemanová, E, et al.. (1992). Das Syndrom von Zimmermann-Laband. Klinische Pädiatrie. 204(1). 1–5. 14 indexed citations
9.
Attanasio, Andrea, et al.. (1992). Prevalence of Autoantibodies to Endocrine Organs in Girls with Ullrich-Turner Syndrome Aged 5-14 Years. Hormone Research. 38(3-4). 114–119. 18 indexed citations
10.
Kuhnle, Ursula, Meta Damkjær Nielsen, H. U. Tietze, et al.. (1990). Pseudohypoaldosteronism in Eight Families: Different Forms of Inheritance Are Evidence for Various Genetic Defects. The Journal of Clinical Endocrinology & Metabolism. 70(3). 638–641. 46 indexed citations
11.
Chen, Theresa L., Margaret Hirst, Charlotte M. Cone, et al.. (1984). 1,25-Dihydroxyvitamin D Resistance, Rickets, and Alopecia: Analysis of Receptors and Bioresponse in Cultured Fibroblasts from Patients and Parents*. The Journal of Clinical Endocrinology & Metabolism. 59(3). 383–388. 57 indexed citations
12.
Schwanitz, Gesa, et al.. (1983). Gonadendysgenesie - Variationsbreite klinischer, hormoneller, zytogenetischer und histologischer Befunde. Klinische Pädiatrie. 195(6). 422–429. 1 indexed citations
13.
Pfeiffer, R. A., et al.. (1983). Extremer Gewebe-Mosaizismus bei Trisomie 8-Syndrom - Trisomie 8 in Fibroblasten bei normalem Karyotyp in Lymphozyten. Klinische Pädiatrie. 195(5). 365–368. 5 indexed citations
14.
Schwanitz, Gesa, et al.. (1977). Duplication Deficiency of an X-Chromosome with and Without 45,X Mosaicism in Three Girls — Cytogenetic, Clinical, and Hormonal Findings. Acta geneticae medicae et gemellologiae. 26(3-4). 277–281. 9 indexed citations
15.
Oetliker, O, J Simon, & H. U. Tietze. (1974). DIAGNOSTIC VALUE OF MANNITOL‐INDUCED DIURESIS IN CHILDREN. Acta Paediatrica. 63(1). 113–121. 5 indexed citations
16.
17.
Dhom, G., et al.. (1970). AUTORADIOGRAPHIC STUDIES ON NUCLEAR DNA AND RNA SYNTHESIS IN THE ADENOHYPOPHYSIS OF CASTRATED RATS. European Journal of Endocrinology. 64(2). 324–338. 9 indexed citations
18.
Tietze, H. U., et al.. (1969). DNA- AND RNA-SYNTHESIS IN THE ANTERIOR PITUITARY OF CASTRATED RATS. European Journal of Endocrinology. 61(1_Suppl). S199–S199. 2 indexed citations
19.
Tietze, H. U., et al.. (1969). H�molytisch-ur�misches Syndrom. European Journal of Pediatrics. 106(4). 249–259. 1 indexed citations
20.
Dhom, G., et al.. (1962). ?Thyreoidektomiezellen? im Hypophysenvorderlappen der Ratte nach Nebennierenblockade. Cell and Tissue Research. 57(5). 679–691. 11 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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