Felix G. Riepe

3.7k total citations
91 papers, 2.1k citations indexed

About

Felix G. Riepe is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Felix G. Riepe has authored 91 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 69 papers in Molecular Biology, 62 papers in Endocrinology, Diabetes and Metabolism and 21 papers in Genetics. Recurrent topics in Felix G. Riepe's work include Sexual Differentiation and Disorders (51 papers), Hormonal and reproductive studies (35 papers) and Hormonal Regulation and Hypertension (21 papers). Felix G. Riepe is often cited by papers focused on Sexual Differentiation and Disorders (51 papers), Hormonal and reproductive studies (35 papers) and Hormonal Regulation and Hypertension (21 papers). Felix G. Riepe collaborates with scholars based in Germany, United Kingdom and United States. Felix G. Riepe's co-authors include Wolfgang G. Sippell, Paul‐Martin Holterhus, Carl‐Joachim Partsch, Nils Krone, Alexandra Kulle, Olaf Hiort, Joachim Grötzinger, D. Melchior, Michael Peter and Ralf Werner and has published in prestigious journals such as Genes & Development, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Felix G. Riepe

89 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Felix G. Riepe Germany 26 1.4k 1.3k 528 197 171 91 2.1k
W L Miller United States 15 912 0.6× 817 0.6× 478 0.9× 113 0.6× 139 0.8× 17 2.0k
Nicole Reisch Germany 29 1.4k 1.0× 1.7k 1.3× 439 0.8× 245 1.2× 601 3.5× 147 2.6k
Jean‐Marie Villette France 20 441 0.3× 523 0.4× 174 0.3× 49 0.2× 116 0.7× 38 1.4k
Walter R. Eberlein United States 27 624 0.4× 937 0.7× 317 0.6× 106 0.5× 168 1.0× 65 1.8k
Juilee Rege United States 21 578 0.4× 1.0k 0.8× 264 0.5× 29 0.1× 245 1.4× 45 1.4k
Ζ. Josefsberg Israel 16 529 0.4× 712 0.5× 278 0.5× 42 0.2× 364 2.1× 60 1.4k
J. Homoki Germany 16 408 0.3× 521 0.4× 250 0.5× 81 0.4× 71 0.4× 63 964
Allen S. Goldman United States 20 389 0.3× 411 0.3× 255 0.5× 73 0.4× 178 1.0× 52 1.3k
Randall W. Whitcomb United States 22 950 0.7× 1.1k 0.8× 451 0.9× 70 0.4× 130 0.8× 38 2.7k
Ichiro Yokota Japan 24 716 0.5× 235 0.2× 245 0.5× 675 3.4× 204 1.2× 92 2.0k

Countries citing papers authored by Felix G. Riepe

Since Specialization
Citations

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

Fields of papers citing papers by Felix G. Riepe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Felix G. Riepe. 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 Felix G. Riepe. The network helps show where Felix G. Riepe may publish in the future.

Co-authorship network of co-authors of Felix G. Riepe

This figure shows the co-authorship network connecting the top 25 collaborators of Felix G. Riepe. A scholar is included among the top collaborators of Felix G. Riepe 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 Felix G. Riepe. Felix G. Riepe 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.
Bonfig, Walter, Stefan Riedl, H. G. Dörr, et al.. (2015). Blood Pressure in a Large Cohort of Children and Adolescents With Classic Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase Deficiency. American Journal of Hypertension. 29(2). 266–272. 41 indexed citations
2.
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
3.
Şimşek, Yasin, Felix G. Riepe, Halit Diri, et al.. (2014). 17-Alpha Hydroxylase Deficiency: A Rare Case of Primary Amenorrhea and Hypertension. SHILAP Revista de lepidopterología. 18(4). 137–139.
4.
Wudy, Stefan A., Felix G. Riepe, Paul‐Martin Holterhus, et al.. (2014). 17α-Hydroxylase Deficiency Diagnosed in Early Infancy Caused by a Novel Mutation of the <b><i>CYP17A1</i></b> Gene. Hormone Research in Paediatrics. 81(5). 350–355. 4 indexed citations
5.
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
6.
Riepe, Felix G.. (2013). Pseudohypoaldosteronism. Endocrine development. 24. 86–95. 36 indexed citations
7.
Barbaro, Michela, Susanne Bens, Andrea Haake, et al.. (2012). Multiplex Ligation-Dependent Probe Amplification Analysis of the <i>NR0B1</i><i>(DAX1)</i> Locus Enables Explanation of Phenotypic Differences in Patients with X-Linked Congenital Adrenal Hypoplasia. Hormone Research in Paediatrics. 77(2). 100–107. 5 indexed citations
8.
Kulle, Alexandra, Felix G. Riepe, Thomas Blatt, et al.. (2012). Age and skin site related differences in steroid metabolism in male skin point to a key role of sebocytes in cutaneous hormone metabolism. Dermato-Endocrinology. 4(1). 58–64. 7 indexed citations
9.
Güran, Tülay, et al.. (2011). Critical Points in the Management of Pseudohypoaldosteronism Type 1 - Case Report. Journal of Clinical Research in Pediatric Endocrinology. 3(2). 98–100. 18 indexed citations
10.
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
11.
Muhle, Hiltrud, Andreas van Baalen, Felix G. Riepe, Axel Rohr, & Ulrich Stephani. (2009). Hashimoto Encephalopathy in a 15-Year-Old-Girl: EEG Findings and Follow-Up. Pediatric Neurology. 41(4). 301–304. 13 indexed citations
12.
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
13.
Peter, Michael, Nils Janzen, Stefanie Sander, et al.. (2008). A Case of 11β-Hydroxylase Deficiency Detected in a Newborn Screening Program by Second-Tier LC-MS/MS. Hormone Research in Paediatrics. 69(4). 253–256. 19 indexed citations
14.
Riepe, Felix G.. (2007). Molecular pathogenesis of renal pseudohypoaldosteronism type 1. Expert Review of Endocrinology & Metabolism. 2(3). 407–419. 1 indexed citations
15.
Riepe, Felix G. & Wolfgang G. Sippell. (2007). Recent advances in diagnosis, treatment, and outcome of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Reviews in Endocrine and Metabolic Disorders. 8(4). 349–363. 59 indexed citations
16.
Holterhus, Paul‐Martin, Ralf Werner, Annette Richter-Unruh, et al.. (2007). Intrinsic androgen-dependent gene expression patterns revealed by comparison of genital fibroblasts from normal males and individuals with complete and partial androgen insensitivity syndrome. BMC Genomics. 8(1). 376–376. 22 indexed citations
17.
Balsamo, Antonio, Alessandro Cicognani, Monia Gennari, et al.. (2007). Functional characterization of naturally occurring NR3C2 gene mutations in Italian patients suffering from pseudohypoaldosteronism type 1. European Journal of Endocrinology. 156(2). 249–256. 14 indexed citations
18.
Riepe, Felix G., et al.. (2005). Congenital Adrenal Hyperplasia: The Molecular Basis of 21-Hydroxylase Deficiency in H-2aw18 Mice. Endocrinology. 146(6). 2563–2574. 24 indexed citations
19.
Krone, Nils, Felix G. Riepe, Eckhard Korsch, et al.. (2005). Congenital Adrenal Hyperplasia Due to 11-Hydroxylase Deficiency: Functional Characterization of Two Novel Point Mutations and a Three-Base Pair Deletion in theCYP11B1Gene. The Journal of Clinical Endocrinology & Metabolism. 90(6). 3724–3730. 44 indexed citations
20.
Brune, Thomas, et al.. (2002). Differentiation of single populations in a bidirectional mixed lymphocyte culture using X and Y chromosome-specific FiSH markers. Journal of Immunological Methods. 266(1-2). 105–110. 4 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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