W Hoepffner

831 total citations
39 papers, 516 citations indexed

About

W Hoepffner is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Reproductive Medicine. According to data from OpenAlex, W Hoepffner has authored 39 papers receiving a total of 516 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 19 papers in Endocrinology, Diabetes and Metabolism and 10 papers in Reproductive Medicine. Recurrent topics in W Hoepffner's work include Sexual Differentiation and Disorders (21 papers), Hormonal and reproductive studies (10 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). W Hoepffner is often cited by papers focused on Sexual Differentiation and Disorders (21 papers), Hormonal and reproductive studies (10 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). W Hoepffner collaborates with scholars based in Germany, Switzerland and Czechia. W Hoepffner's co-authors include Eberhard Keller, H Willgerodt, J Bennek, U. Heinrich, Norbert Albers, Olaf Hiort, Gernot H.G. Sinnecker, Helmuth G. Dörr, K. Kruse and Dirk Schnabel and has published in prestigious journals such as The Journal of Urology, Fertility and Sterility and Clinical Endocrinology.

In The Last Decade

W Hoepffner

37 papers receiving 502 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
W Hoepffner Germany 12 403 266 170 136 56 39 516
Saroj Nimkarn United States 19 598 1.5× 461 1.7× 249 1.5× 146 1.1× 78 1.4× 38 801
Gerry Conway United Kingdom 5 500 1.2× 386 1.5× 132 0.8× 101 0.7× 19 0.3× 7 597
H.J. van der Kamp Netherlands 11 334 0.8× 253 1.0× 149 0.9× 70 0.5× 47 0.8× 23 519
Mercedes Maceiras Argentina 12 231 0.6× 253 1.0× 157 0.9× 49 0.4× 55 1.0× 24 469
D. E. BU'LOCK United Kingdom 11 126 0.3× 166 0.6× 62 0.4× 65 0.5× 50 0.9× 20 380
A. B. Arthur United States 9 159 0.4× 154 0.6× 120 0.7× 57 0.4× 47 0.8× 9 354
PM Holterhus Germany 9 128 0.3× 204 0.8× 149 0.9× 58 0.4× 89 1.6× 13 335
Maud Bidet France 11 367 0.9× 281 1.1× 201 1.2× 53 0.4× 23 0.4× 23 678
D. Melchior Germany 7 103 0.3× 116 0.4× 33 0.2× 76 0.6× 107 1.9× 19 299
Charalambos Hadjiathanasiou Greece 10 261 0.6× 140 0.5× 217 1.3× 53 0.4× 47 0.8× 16 488

Countries citing papers authored by W Hoepffner

Since Specialization
Citations

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

Fields of papers citing papers by W Hoepffner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of W Hoepffner

This figure shows the co-authorship network connecting the top 25 collaborators of W Hoepffner. A scholar is included among the top collaborators of W Hoepffner 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 W Hoepffner. W Hoepffner 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.
Hoepffner, W, Roland Pfäffle, Ruth Gausche, Christof Meigen, & Eberhard Keller. (2011). Early Detection of Growth Disorders With the CrescNet System at the Leipzig Treatment Center. Deutsches Ärzteblatt international. 108(8). 123–8. 15 indexed citations
2.
Hoepffner, W, et al.. (2008). Patients with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency Can Achieve Their Target Height: The Leipzig Experience. Hormone Research in Paediatrics. 70(1). 42–50. 29 indexed citations
3.
Küry, Sébastien, et al.. (2006). Acrodermatitis enteropathica (AE) wird durch Mutationen im Zink-Transportergen SLC39A4 verursacht. Klinische Pädiatrie. 218(4). 221–223. 7 indexed citations
4.
Hoepffner, W, Alexander Herrmann, H Willgerodt, & Eberhard Keller. (2006). Blood Pressure in Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency. Journal of Pediatric Endocrinology and Metabolism. 19(5). 705–11. 23 indexed citations
5.
Hoepffner, W, et al.. (2005). Gonadoblastomas in 5 Patients with 46,XY Gonadal Dysgenesis. Experimental and Clinical Endocrinology & Diabetes. 113(4). 231–235. 12 indexed citations
6.
Hoepffner, W, Egbert Schulze, J Bennek, Eberhard Keller, & H Willgerodt. (2004). Pregnancies in patients with congenital adrenal hyperplasia with complete or almost complete impairment of 21-hydroxylase activity. Fertility and Sterility. 81(5). 1314–1321. 49 indexed citations
7.
Tröbs, Ralf‐Bodo, W Hoepffner, U. Bühligen, et al.. (2004). Video-Assisted Gonadectomy in Children with Ullrich Turner Syndrome or 46,XY Gonadal Dysgenesis. European Journal of Pediatric Surgery. 14(3). 179–184. 10 indexed citations
8.
Müller, Gerd A., Amélie Keller, Adam Reich, et al.. (2004). Priming with Testosterone Enhances Stimulated Growth Hormone Secretion in Boys with Delayed Puberty. Journal of Pediatric Endocrinology and Metabolism. 17(1). 77–83. 18 indexed citations
9.
Hoepffner, W, et al.. (2003). Verlaufsbeobachtung von Zöliakiepatienten im Kindes- und jungen Erwachsenenalter: latente oder transiente Zöliakie?. Klinische Pädiatrie. 215(2). 76–81. 6 indexed citations
10.
Woelfle, Joachim, W Hoepffner, W.G. Sippell, et al.. (2002). Complete virilization in congenital adrenal hyperplasia: clinical course, medical management and disease‐related complications. Clinical Endocrinology. 56(2). 231–238. 41 indexed citations
11.
Kratzsch, Jüergen, E Keller, W Hoepffner, et al.. (2001). The DSL analog free testosterone assay: serum levels are not related to sex hormone-binding globulin in normative data throughout childhood and adolescence.. PubMed. 47(1-2). 73–7. 9 indexed citations
12.
Tröbs, Ralf‐Bodo, W Hoepffner, Thomas Friedrich, & J Bennek. (2001). Growth-arrest and inhomogenous echotexture of the affected testis after tumor enucleation for unilateral Leydig cell tumor. Journal of Pediatric Surgery. 36(9). 20–21. 3 indexed citations
13.
Schoof, Ellen, et al.. (2000). Anorexia nervosa in congenital adrenal hyperplasia: long-term follow-up of 4 cases. Experimental and Clinical Endocrinology & Diabetes. 108(6). 430–435. 1 indexed citations
14.
Hoepffner, W, et al.. (2000). Prediction of Height Velocity of Prepubertal Children with Growth Hormone Deficiency in the First Year of Treatment with Recombinant Human Growth Hormone. Journal of Pediatric Endocrinology and Metabolism. 13(7). 893–7. 6 indexed citations
15.
Schier, Felix, et al.. (1999). Laparoscopic Bilateral Adrenalectomy in a Child. European Journal of Pediatric Surgery. 9(6). 420–421. 8 indexed citations
16.
Sinnecker, Gernot H.G., Olaf Hiort, L. Dibbelt, et al.. (1996). Phenotypic classification of male pseudohermaphroditism due to steroid 5α-reductase 2 deficiency. American Journal of Medical Genetics. 63(1). 223–230. 137 indexed citations
17.
Schulze, E, Gunter Scharer, Lutz Priebe, et al.. (1995). Divergence between genotype and phenotype in relatives of patients with the intron 2 mutation of steroid-21-hydroxylase. Endocrine Research. 21(1-2). 359–364. 43 indexed citations
18.
Amendt, Peter, et al.. (1986). [Current problems in pediatric endocrinology].. PubMed. 80(20). 839–47.
19.
Hoepffner, W, et al.. (1985). Digestion and Absorption Rates of Lactose, Glucose, Galactose, and Fructose in Three Infants with Congenital Glucose‐Galactose Malabsorption. Journal of Pediatric Gastroenterology and Nutrition. 4(6). 887–892. 1 indexed citations
20.
Hoepffner, W & J Bennek. (1984). [Indications and timing of genital operations in children with male and female pseudohermaphroditism].. PubMed. 109(15). 1011–4. 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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