Dagmar Struve

585 total citations
17 papers, 411 citations indexed

About

Dagmar Struve is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Dagmar Struve has authored 17 papers receiving a total of 411 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 13 papers in Endocrinology, Diabetes and Metabolism and 5 papers in Genetics. Recurrent topics in Dagmar Struve's work include Sexual Differentiation and Disorders (14 papers), Hormonal and reproductive studies (12 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Dagmar Struve is often cited by papers focused on Sexual Differentiation and Disorders (14 papers), Hormonal and reproductive studies (12 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Dagmar Struve collaborates with scholars based in Germany, Brazil and Portugal. Dagmar Struve's co-authors include Olaf Hiort, Ralf Werner, Paul‐Martin Holterhus, Gernot H.G. Sinnecker, Christine Marschke, Olaf Hellwinkel, Carl‐Joachim Partsch, Felix G. Riepe, U. Hoppe and John C. Achermann and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Human Molecular Genetics and Molecular and Cellular Endocrinology.

In The Last Decade

Dagmar Struve

17 papers receiving 405 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dagmar Struve Germany 12 341 211 206 52 42 17 411
Anna Wai-Fun Cheng China 8 331 1.0× 181 0.9× 201 1.0× 95 1.8× 16 0.4× 12 426
Christine Marschke Germany 7 216 0.6× 111 0.5× 144 0.7× 25 0.5× 17 0.4× 7 267
Kyosuke Imasaki Japan 8 200 0.6× 201 1.0× 131 0.6× 23 0.4× 31 0.7× 12 375
Michael J McPhaul United States 6 144 0.4× 126 0.6× 131 0.6× 38 0.7× 84 2.0× 9 353
C Lecointre France 10 336 1.0× 155 0.7× 203 1.0× 58 1.1× 35 0.8× 15 506
Kristina Lundin Sweden 9 234 0.7× 131 0.6× 124 0.6× 51 1.0× 36 0.9× 16 364
Lilia Baldazzi Italy 15 546 1.6× 393 1.9× 280 1.4× 99 1.9× 11 0.3× 28 669
Laurence Michel‐Calemard France 9 325 1.0× 49 0.2× 295 1.4× 76 1.5× 31 0.7× 22 438
T E Romer Poland 12 202 0.6× 170 0.8× 107 0.5× 32 0.6× 5 0.1× 22 366
B.D. Brown United Kingdom 9 283 0.8× 94 0.4× 76 0.4× 16 0.3× 72 1.7× 15 381

Countries citing papers authored by Dagmar Struve

Since Specialization
Citations

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

Fields of papers citing papers by Dagmar Struve

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dagmar Struve

This figure shows the co-authorship network connecting the top 25 collaborators of Dagmar Struve. A scholar is included among the top collaborators of Dagmar Struve 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 Dagmar Struve. Dagmar Struve is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Hiort, Olaf, Dagmar Struve, Julia Gesing, et al.. (2017). Functional Impact of Novel Androgen Receptor Mutations on the Clinical Manifestation of Androgen Insensitivity Syndrome. Sexual Development. 11(5-6). 238–247. 10 indexed citations
2.
Fabbri‐Scallet, Helena, Maricilda Palandi de Mello, Gil Guerra‐Júnior, et al.. (2017). Functional characterization of fiveNR5A1gene mutations found in patients with 46,XY disorders of sex development. Human Mutation. 39(1). 114–123. 13 indexed citations
3.
Hiort, Olaf, Dagmar Struve, Andréa Trevas Maciel‐Guerra, et al.. (2014). Preserved Fertility in a Patient with Gynecomastia Associated with the p.Pro695Ser Mutation in the Androgen Receptor. Sexual Development. 8(6). 350–355. 9 indexed citations
4.
Thiele, Susanne, Ralf Werner, Joachim Grötzinger, et al.. (2014). A positive genotype–phenotype correlation in a large cohort of patients with Pseudohypoparathyroidism Type Ia and Pseudo‐pseudohypoparathyroidism and 33 newly identified mutations in the GNAS gene. Molecular Genetics & Genomic Medicine. 3(2). 111–120. 39 indexed citations
5.
6.
Grötsch, Helga, Katrin A. Mooslehner, Zhigang Gao, et al.. (2012). RWDD1 interacts with the ligand binding domain of the androgen receptor and acts as a coactivator of androgen-dependent transactivation. Molecular and Cellular Endocrinology. 358(1). 53–62. 9 indexed citations
7.
Werner, Ralf, Jianying Zhan, Julia Gesing, Dagmar Struve, & Olaf Hiort. (2008). In-vitro Characterization of Androgen Receptor Mutations Associated with Complete Androgen Insensitivity Syndrome Reveals Distinct Functional Deficits. Sexual Development. 2(2). 73–83. 10 indexed citations
8.
Werner, Ralf, Paul‐Martin Holterhus, Gerhard Binder, et al.. (2006). The A645D Mutation in the Hinge Region of the Human Androgen Receptor (AR) Gene Modulates AR Activity, Depending on the Context of the Polymorphic Glutamine and Glycine Repeats. The Journal of Clinical Endocrinology & Metabolism. 91(9). 3515–3520. 38 indexed citations
9.
Werner, Ralf, et al.. (2005). Mutations in the Amino-Terminal Domain of the Human Androgen Receptor may be Associated with Partial Androgen Insensitivity and Impaired Transactivation in vitro. Experimental and Clinical Endocrinology & Diabetes. 113(8). 457–463. 6 indexed citations
10.
Hiort, Olaf, Paul‐Martin Holterhus, Ralf Werner, et al.. (2005). Homozygous Disruption of P450 Side-Chain Cleavage (CYP11A1) Is Associated with Prematurity, Complete 46,XY Sex Reversal, and Severe Adrenal Failure. The Journal of Clinical Endocrinology & Metabolism. 90(1). 538–541. 75 indexed citations
11.
Hiort, Olaf, et al.. (2002). A novel homozygous disruptive mutation in the SRD5A2‐gene in a partially virilized patient with 5α‐reductase deficiency. International Journal of Andrology. 25(1). 55–58. 18 indexed citations
12.
Hellwinkel, Olaf, et al.. (2001). A Unique Exonic Splicing Mutation in the Human Androgen Receptor Gene Indicates a Physiologic Relevance of Regular Androgen Receptor Transcript Variants1. The Journal of Clinical Endocrinology & Metabolism. 86(6). 2569–2575. 26 indexed citations
13.
Müller, Andreas, et al.. (2000). Influence of androgens and age on androgen receptor and 5 alpha-reductase II transcription. European Journal of Endocrinology. 143(2). 217–225. 11 indexed citations
14.
Holterhus, Paul‐Martin, Gernot H.G. Sinnecker, H. A. Wollmann, et al.. (1999). Expression of two functionally different androgen receptors in a patient with androgen insensitivity. European Journal of Pediatrics. 158(9). 702–706. 12 indexed citations
15.
16.
Hiort, Olaf, et al.. (1996). Nonisotopic single strand conformation analysis of the 5 alpha-reductase type 2 gene for the diagnosis of 5 alpha-reductase deficiency.. The Journal of Clinical Endocrinology & Metabolism. 81(9). 3415–3418. 28 indexed citations
17.
Hiort, Olaf, et al.. (1994). Detection of point mutations in the androgen receptor gene using non-isotopic single strand conformation polymorphism analysis. Human Molecular Genetics. 3(7). 1163–1166. 68 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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