Ralf Werner

2.7k total citations
75 papers, 1.4k citations indexed

About

Ralf Werner is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Ralf Werner has authored 75 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Molecular Biology, 28 papers in Endocrinology, Diabetes and Metabolism and 25 papers in Genetics. Recurrent topics in Ralf Werner's work include Sexual Differentiation and Disorders (45 papers), Hormonal and reproductive studies (26 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (14 papers). Ralf Werner is often cited by papers focused on Sexual Differentiation and Disorders (45 papers), Hormonal and reproductive studies (26 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (14 papers). Ralf Werner collaborates with scholars based in Germany, United States and Brazil. Ralf Werner's co-authors include Olaf Hiort, Paul‐Martin Holterhus, Dagmar Struve, Hans‐Peter Mühlbach, Lutz Wünsch, Susanne Thiele, Ieuan A. Hughes, Dieter Mergenhagen, Trevor Bunch and Felix G. Riepe and has published in prestigious journals such as Nature, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Ralf Werner

75 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ralf Werner Germany 23 1.1k 698 387 219 100 75 1.4k
Bertha Chávez Mexico 19 488 0.4× 395 0.6× 355 0.9× 117 0.5× 13 0.1× 49 824
Yung-Ming Lin Taiwan 17 449 0.4× 345 0.5× 82 0.2× 80 0.4× 62 0.6× 46 1.0k
Emanuela Scarano Italy 25 1.0k 0.9× 454 0.7× 107 0.3× 16 0.1× 101 1.0× 67 1.6k
Kiran Kucheria India 17 633 0.6× 585 0.8× 48 0.1× 94 0.4× 131 1.3× 67 1.1k
Huifen Zhao Canada 21 626 0.6× 551 0.8× 834 2.2× 15 0.1× 22 0.2× 40 1.6k
Miki Yoshiike Japan 20 437 0.4× 316 0.5× 121 0.3× 36 0.2× 81 0.8× 49 1.2k
Paul E. Juniewicz United States 17 305 0.3× 138 0.2× 157 0.4× 97 0.4× 38 0.4× 37 1.1k
Alastair S. H. Goldman United Kingdom 21 1.1k 1.0× 436 0.6× 84 0.2× 19 0.1× 408 4.1× 41 1.5k
Jan Frayne United Kingdom 24 666 0.6× 193 0.3× 76 0.2× 46 0.2× 23 0.2× 56 1.5k
Carolina J. Jorgez United States 21 1.2k 1.1× 548 0.8× 62 0.2× 112 0.5× 33 0.3× 45 2.1k

Countries citing papers authored by Ralf Werner

Since Specialization
Citations

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

Fields of papers citing papers by Ralf Werner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ralf Werner

This figure shows the co-authorship network connecting the top 25 collaborators of Ralf Werner. A scholar is included among the top collaborators of Ralf Werner 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 Ralf Werner. Ralf Werner 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.
Mazzola, Taís Nitsch, Maricilda Palandi de Mello, Sofia Helena Valente de Lemos‐Marini, et al.. (2023). DHX37 and NR5A1 Variants Identified in Patients with 46,XY Partial Gonadal Dysgenesis. Life. 13(5). 1093–1093. 12 indexed citations
2.
Knerr, Julian, Ralf Werner, Carsten Schwan, et al.. (2023). Formin-mediated nuclear actin at androgen receptors promotes transcription. Nature. 617(7961). 616–622. 28 indexed citations
3.
Fabbri‐Scallet, Helena, Ralf Werner, Juliana Gabriel Ribeiro de Andrade, et al.. (2022). Can Non-Coding NR5A1 Gene Variants Explain Phenotypes of Disorders of Sex Development?. Sexual Development. 16(4). 252–260. 7 indexed citations
4.
Hornig, Nadine, Eva Maria Murga Penas, Almuth Caliebe, et al.. (2019). Reduced Androgen Receptor Expression in Genital Skin Fibroblasts From Patients With 45,X/46,XY Mosaicism. The Journal of Clinical Endocrinology & Metabolism. 104(10). 4630–4638. 4 indexed citations
5.
Andrade, Juliana Gabriel Ribeiro de, Helena Fabbri‐Scallet, Ana Paula Santos, et al.. (2019). Clinical Findings and Follow-Up of 46,XY and 45,X/46,XY Testicular Dysgenesis. Sexual Development. 13(4). 171–177. 17 indexed citations
6.
Kumar, Anil, Rajni Sharma, Mohammed Faruq, et al.. (2019). Spectrum of Pathogenic Variants in <b><i>SRD5A2</i></b> in Indian Children with 46,XY Disorders of Sex Development and Clinically Suspected Steroid 5α-Reductase 2 Deficiency. Sexual Development. 13(5-6). 228–239. 9 indexed citations
7.
Hornig, Nadine, Helmuth G. Dörr, Nina C. Hubner, et al.. (2018). Epigenetic Repression of Androgen Receptor Transcription in Mutation-Negative Androgen Insensitivity Syndrome (AIS Type II). The Journal of Clinical Endocrinology & Metabolism. 103(12). 4617–4627. 22 indexed citations
8.
Hiort, Olaf, Louise Marshall, Wiebke Birnbaum, et al.. (2016). Pubertal Development in
17Beta-Hydroxysteroid Dehydrogenase Type 3 Deficiency. Hormone Research in Paediatrics. 87(5). 354–358. 12 indexed citations
9.
Ellaithi, Mona, Ralf Werner, Felix G. Riepe, et al.. (2014). 46,XY Disorder of Sex Development in a Sudanese Patient Caused by a Novel Mutation in the <b><i>HSD17B3</i></b> Gene. Sexual Development. 8(4). 151–155. 8 indexed citations
10.
Werner, Ralf & Paul‐Martin Holterhus. (2014). Androgen Action. Endocrine development. 27. 28–40. 17 indexed citations
11.
Hiort, Olaf, Wiebke Birnbaum, Louise Marshall, et al.. (2014). Management of disorders of sex development. Nature Reviews Endocrinology. 10(9). 520–529. 83 indexed citations
12.
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
13.
Ammerpohl, Ole, Susanne Bens, Mahesh Appari, et al.. (2013). Androgen Receptor Function Links Human Sexual Dimorphism to DNA Methylation. PLoS ONE. 8(9). e73288–e73288. 25 indexed citations
14.
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
15.
16.
Bens, Susanne, Ole Ammerpohl, José I. Martı́n-Subero, et al.. (2011). Androgen Receptor Mutations Are Associated with Altered Epigenomic Programming as Evidenced by <i>HOXA5</i> Methylation. Sexual Development. 5(2). 70–76. 9 indexed citations
17.
Werner, Ralf, et al.. (2009). Selective Deficiency of Gsα and the Possible Role of Alternative Gene Products of GNAS in Albright Hereditary Osteodystrophy and Pseudohypoparathyroidism Type Ia. Experimental and Clinical Endocrinology & Diabetes. 118(2). 127–132. 7 indexed citations
18.
Appari, Mahesh, Ralf Werner, Lutz Wünsch, et al.. (2009). Apolipoprotein D (APOD) is a putative biomarker of androgen receptor function in androgen insensitivity syndrome. Journal of Molecular Medicine. 87(6). 623–632. 30 indexed citations
19.
Thiele, Susanne, Ralf Werner, Wiebke Ahrens, et al.. (2007). A Disruptive Mutation in Exon 3 of the GNAS Gene with Albright Hereditary Osteodystrophy, Normocalcemic Pseudohypoparathyroidism, and Selective Long Transcript Variant Gsα-L Deficiency. The Journal of Clinical Endocrinology & Metabolism. 92(5). 1764–1768. 16 indexed citations
20.
Holterhus, Paul‐Martin, et al.. (2005). Transactivation Properties of Wild-Type and Mutant Androgen Receptors in Transiently Transfected Primary Human Fibroblasts. Hormone Research in Paediatrics. 63(3). 152–158. 2 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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