Daniela Steinberger

3.2k total citations
43 papers, 1.3k citations indexed

About

Daniela Steinberger is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Daniela Steinberger has authored 43 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 17 papers in Molecular Biology and 11 papers in Cellular and Molecular Neuroscience. Recurrent topics in Daniela Steinberger's work include Craniofacial Disorders and Treatments (14 papers), Cleft Lip and Palate Research (14 papers) and Genetic Neurodegenerative Diseases (11 papers). Daniela Steinberger is often cited by papers focused on Craniofacial Disorders and Treatments (14 papers), Cleft Lip and Palate Research (14 papers) and Genetic Neurodegenerative Diseases (11 papers). Daniela Steinberger collaborates with scholars based in Germany, United States and United Kingdom. Daniela Steinberger's co-authors include Ulrich Müller, John B. Mulliken, Ronald E. Carr, Donald C. Hood, Robert Ritch, Vivienne C. Greenstein, Ulrich M�ller, Helge Topka, Andrea H. Németh and U. Müller and has published in prestigious journals such as Journal of Neuroscience, PLoS ONE and Neurology.

In The Last Decade

Daniela Steinberger

43 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daniela Steinberger Germany 24 541 539 279 211 170 43 1.3k
Sophie Nicole France 25 1.4k 2.5× 391 0.7× 440 1.6× 267 1.3× 70 0.4× 60 2.2k
Birgit Assmann Germany 23 870 1.6× 299 0.6× 304 1.1× 342 1.6× 789 4.6× 51 1.7k
Judith Conroy Ireland 16 473 0.9× 404 0.7× 160 0.6× 37 0.2× 59 0.3× 31 1.0k
S. Merin Israel 21 387 0.7× 135 0.3× 51 0.2× 47 0.2× 37 0.2× 52 1.1k
Denise Cassandrini Italy 23 735 1.4× 176 0.3× 222 0.8× 106 0.5× 228 1.3× 62 1.3k
K. Tada Japan 24 889 1.6× 145 0.3× 91 0.3× 55 0.3× 939 5.5× 102 1.6k
Lejin Wang China 11 808 1.5× 221 0.4× 315 1.1× 53 0.3× 30 0.2× 18 1.2k
Katsuro Iwase Japan 16 406 0.8× 79 0.1× 108 0.4× 27 0.1× 59 0.3× 33 883
Fei Xiao China 18 562 1.0× 133 0.2× 301 1.1× 81 0.4× 28 0.2× 82 1.2k
Guy M. Lenk United States 23 616 1.1× 191 0.4× 339 1.2× 220 1.0× 27 0.2× 38 1.7k

Countries citing papers authored by Daniela Steinberger

Since Specialization
Citations

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

Fields of papers citing papers by Daniela Steinberger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniela Steinberger

This figure shows the co-authorship network connecting the top 25 collaborators of Daniela Steinberger. A scholar is included among the top collaborators of Daniela Steinberger 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 Daniela Steinberger. Daniela Steinberger 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.
Brivio, Eleonora, Serena Oliveri, Francesca Spinella, et al.. (2022). Genetic testing users in Italy and Germany: Health orientation, health‐related habits, and psychological profile. Molecular Genetics & Genomic Medicine. 10(3). e1851–e1851. 6 indexed citations
2.
Wöhlke, Sabine, Serena Oliveri, Ilaria Cutica, et al.. (2020). German and Italian Users of Web-Accessed Genetic Data: Attitudes on Personal Utility and Personal Sharing Preferences. Results of a Comparative Survey (n=192). Frontiers in Genetics. 11. 102–102. 7 indexed citations
3.
Zirn, Birgit, Luitgard Graul‐Neumann, M. Suckfüll, et al.. (2013). Spectrum of novel mutations found in Waardenburg syndrome types 1 and 2: implications for molecular genetic diagnostics. BMJ Open. 3(3). e001917–e001917. 38 indexed citations
4.
Michaelis, Martin, Stefan Barth, Rainer Breitling, et al.. (2012). Selection of a highly invasive neuroblastoma cell population through long-term human cytomegalovirus infection. Oncogenesis. 1(4). e10–e10. 5 indexed citations
5.
Wildhardt, G., et al.. (2009). A monoallelic double mutation as a cause for TNF receptor-associated periodic fever syndrome. Rheumatology International. 30(6). 805–809. 3 indexed citations
6.
Wildhardt, G., Zeyan Zhong, Rebecca Roth, et al.. (2009). Enhancer deletions of the SHOX gene as a frequent cause of short stature: the essential role of a 250 kb downstream regulatory domain. Journal of Medical Genetics. 46(12). 834–839. 103 indexed citations
7.
Tzschach, Andreas, Christian Ramel, Christian Wüster, et al.. (2007). Hypergonadotropic hypogonadism in a patient with inv ins (2;4). International Journal of Andrology. 32(3). 226–230. 2 indexed citations
8.
Zirn, Birgit, Daniela Steinberger, Christian Troidl, et al.. (2007). Frequency of GCH1 deletions in Dopa-responsive dystonia. Journal of Neurology Neurosurgery & Psychiatry. 79(2). 183–186. 27 indexed citations
9.
Steinberger, Daniela, et al.. (2006). Utility of MLPA in deletion analysis of GCH1 in dopa-responsive dystonia. Neurogenetics. 8(1). 51–55. 21 indexed citations
10.
11.
Steinberger, Daniela, et al.. (2004). Heterozygous mutation in 5?-untranslated region of sepiapterin reductase gene (SPR) in a patient with dopa-responsive dystonia. Neurogenetics. 5(3). 187–190. 41 indexed citations
12.
Mulliken, John B., Karen W. Gripp, Catherine A. Stolle, Daniela Steinberger, & Ulrich Müller. (2004). Molecular Analysis of Patients with Synostotic Frontal Plagiocephaly (Unilateral Coronal Synostosis). Plastic & Reconstructive Surgery. 113(7). 1899–1909. 38 indexed citations
13.
Roth, Christian, B. Hinney, Michael Peter, Daniela Steinberger, & M. Lakomek. (2000). Features of Antley-Bixler syndrome in an infant born to a mother with pregnancy luteoma. European Journal of Pediatrics. 159(3). 189–192. 24 indexed citations
14.
Niemann, Stephan, Daniela Steinberger, & U. Müller. (1999). PGL3 , a third, not maternally imprinted locus in autosomal dominant paraganglioma. Neurogenetics. 2(3). 167–170. 42 indexed citations
15.
Müller, Ulrich, Daniela Steinberger, & Andrea H. Németh. (1998). Clinical and molecular genetics of primary dystonias. Neurogenetics. 1(3). 165–177. 59 indexed citations
16.
Steinberger, Daniela, et al.. (1998). MEHMO (mental retardation, epileptic seizures, hypogonadism and -genitalism, microcephaly, obesity), a novel syndrome: assignment of disease locus to Xp21.1–p22.13. European Journal of Human Genetics. 6(3). 201–206. 38 indexed citations
17.
Steinberger, Daniela, et al.. (1997). Two previously unrecognized splicing mutations of GCH1 in Dopa-responsive dystonia: exon skipping and one base insertion. Neurogenetics. 1(2). 125–127. 14 indexed citations
18.
Steinberger, Daniela, John B. Mulliken, & Ulrich Müller. (1996). Crouzon syndrome: Previously unrecognized deletion, duplication, and point mutation within FGFR2 gene. Human Mutation. 8(4). 386–390. 26 indexed citations
19.
Steinberger, Daniela, et al.. (1996). FGFR2 mutation in clinically nonclassifiable autosomal dominant craniosynostosis with pronounced phenotypic variation. American Journal of Medical Genetics. 66(1). 81–86. 41 indexed citations
20.
Steinberger, Daniela, John B. Mulliken, & Ulrich M�ller. (1995). Predisposition for cysteine substitutions in the immunoglobulin-like chain of FGFR2 in Crouzon syndrome. Human Genetics. 96(1). 113–115. 46 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Sophie Nicole Breakdown of academic impact, for papers by Birgit Assmann Breakdown of academic impact, for papers by Judith Conroy Breakdown of academic impact, for papers by S. Merin Breakdown of academic impact, for papers by Denise Cassandrini Breakdown of academic impact, for papers by K. Tada Breakdown of academic impact, for papers by Lejin Wang Breakdown of academic impact, for papers by Katsuro Iwase Breakdown of academic impact, for papers by Fei Xiao Breakdown of academic impact, for papers by Guy M. Lenk
Rankless by CCL
2026