Michael Peter

2.9k total citations
93 papers, 2.1k citations indexed

About

Michael Peter is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Michael Peter has authored 93 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Endocrinology, Diabetes and Metabolism, 43 papers in Molecular Biology and 17 papers in Clinical Biochemistry. Recurrent topics in Michael Peter's work include Sexual Differentiation and Disorders (30 papers), Hormonal Regulation and Hypertension (29 papers) and Metabolism and Genetic Disorders (17 papers). Michael Peter is often cited by papers focused on Sexual Differentiation and Disorders (30 papers), Hormonal Regulation and Hypertension (29 papers) and Metabolism and Genetic Disorders (17 papers). Michael Peter collaborates with scholars based in Germany, Austria and Netherlands. Michael Peter's co-authors include Wolfgang G. Sippell, Nils Janzen, Johannes Sander, Stefanie Sander, Carl‐Joachim Partsch, Michael Terhardt, Ulrike Steuerwald, W.G. Sippell, Matthias Viemann and Ute Holtkamp and has published in prestigious journals such as The Lancet, The Journal of Clinical Endocrinology & Metabolism and Journal of Lipid Research.

In The Last Decade

Michael Peter

86 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
Michael Peter Germany 26 1.2k 1.1k 429 406 202 93 2.1k
A.C. Roy Singapore 23 595 0.5× 217 0.2× 283 0.7× 140 0.3× 233 1.2× 82 1.8k
Trine Holm Johannsen Denmark 24 774 0.7× 701 0.6× 409 1.0× 51 0.1× 138 0.7× 63 1.6k
Franca Fruzzetti Italy 29 435 0.4× 702 0.6× 242 0.6× 61 0.2× 193 1.0× 106 2.2k
Bon Jeong Ku South Korea 24 1.0k 0.9× 506 0.4× 211 0.5× 49 0.1× 55 0.3× 108 2.6k
Wael Salameh United States 24 607 0.5× 744 0.7× 428 1.0× 20 0.0× 186 0.9× 39 2.5k
Yii‐Der I. Chen United States 25 549 0.5× 629 0.6× 340 0.8× 44 0.1× 105 0.5× 57 2.0k
Fred I. Chasalow United States 20 383 0.3× 411 0.4× 225 0.5× 21 0.1× 138 0.7× 63 1.2k
Leszek Pawełczyk Poland 26 629 0.5× 427 0.4× 256 0.6× 63 0.2× 185 0.9× 130 2.7k
Manubai Nagamani United States 28 481 0.4× 785 0.7× 651 1.5× 17 0.0× 174 0.9× 102 2.7k
John Alcolado United Kingdom 17 562 0.5× 420 0.4× 281 0.7× 217 0.5× 167 0.8× 45 1.5k

Countries citing papers authored by Michael Peter

Since Specialization
Citations

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

Fields of papers citing papers by Michael Peter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michael Peter

This figure shows the co-authorship network connecting the top 25 collaborators of Michael Peter. A scholar is included among the top collaborators of Michael Peter 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 Michael Peter. Michael Peter 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.
Peter, Michael, et al.. (2025). Real-Time Demonstration of Integrated Sensing and Communication in the Sub-Terahertz D-Band. 1–2. 1 indexed citations
2.
Mazeh, Haggi, Daniel J. Weiss, Michael Peter, et al.. (2023). Deliberate Compensated Vasoplegia–A Novel Pharmaceutical Approach for Controlling Blood Pressure During Surgery for Pheochromocytoma. World Journal of Surgery. 47(4). 985–994.
3.
Nguyen, Sinh Le Hong, J. Medbo, Michael Peter, et al.. (2018). On the frequency dependency of radio Channel's delay spread. Aaltodoc (Aalto University). 16 indexed citations
4.
Janzen, Nils, Michael Terhardt, Stefanie Sander, et al.. (2013). Towards newborn screening for ornithine transcarbamylase deficiency: Fast non-chromatographic orotic acid quantification from dried blood spots by tandem mass spectrometry. Clinica Chimica Acta. 430. 28–32. 14 indexed citations
5.
Sander, Johannes, Nils Janzen, Michael Terhardt, et al.. (2010). Monitoring tyrosinaemia type I: Blood spot test for nitisinone (NTBC). Clinica Chimica Acta. 412(1-2). 134–138. 23 indexed citations
6.
Janzen, Nils, Stefanie Sander, Michael Terhardt, et al.. (2010). Rapid quantification of conjugated and unconjugated bile acids and C27 precursors in dried blood spots and small volumes of serum. Journal of Lipid Research. 51(6). 1591–1598. 21 indexed citations
7.
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
8.
Janzen, Nils, Stefanie Sander, Michael Terhardt, Michael Peter, & Johannes Sander. (2007). Fast and direct quantification of adrenal steroids by tandem mass spectrometry in serum and dried blood spots. Journal of Chromatography B. 861(1). 117–122. 94 indexed citations
9.
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
10.
Krone, Nils, Felix G. Riepe, Helmuth‐Günther Dörr, et al.. (2005). Thirteen novel mutations in theNR0B1(DAX1) gene as cause of adrenal hypoplasia congenita. Human Mutation. 25(5). 502–502. 16 indexed citations
11.
Peter, Michael & Jean-Michel Dubuis. (2000). Transcription factors as regulators of steroidogenic P‐450 enzymes. European Journal of Clinical Investigation. 30(s3). 14–20. 21 indexed citations
12.
López‐Siguero, Juan Pedro, Emilio García García, Michael Peter, & Wolfgang G. Sippell. (1999). Aldosterone Synthase Deficiency Type I: Hormonal and Genetic Analyses of Two Cases. Hormone Research in Paediatrics. 52(6). 298–300. 5 indexed citations
13.
Peter, Michael, et al.. (1999). Disorders of the Aldosterone Synthase and Steroid 11β-Hydroxylase Deficiencies. Hormone Research in Paediatrics. 51(5). 211–222. 43 indexed citations
14.
Peter, Michael, et al.. (1998). Molecular genetic study in two patients with congenital hypoaldosteronism (types I and II) in relation to previously published hormonal studies. European Journal of Endocrinology. 139(1). 96–100. 18 indexed citations
15.
Bosinski, Hartmut A.G., et al.. (1997). Anthropometrical Measurements and Androgen Levels in Males, Females, and Hormonally Untreated Female-To-Male Transsexuals. Archives of Sexual Behavior. 26(2). 143–157. 21 indexed citations
16.
Nikischin, Werner, et al.. (1997). The Influence of Mode of Delivery on Hematologic Values in the Umbilical Vein. Gynecologic and Obstetric Investigation. 43(2). 104–107. 31 indexed citations
17.
Peter, Michael & Wolfgang G. Sippell. (1997). Evidence for Endocrinological Abnormalities in Heterozygotes for Adrenal 11β-Hydroxylase Deficiency of a Family with the R448H Mutation in the CYP11B1 Gene1. The Journal of Clinical Endocrinology & Metabolism. 82(10). 3506–3508. 8 indexed citations
18.
Marx, Christian, Stefan R. Bornstein, Gernot W. Wolkersdörfer, et al.. (1997). Relevance of Major Histocompatibility Complex Class II Expression as a Hallmark for the Cellular Differentiation in the Human Adrenal Cortex1. The Journal of Clinical Endocrinology & Metabolism. 82(9). 3136–3140. 39 indexed citations
19.
Père, A, Jaakko Perheentupa, Michael Peter, & Raimo Voutilainen. (1995). Follow up of growth and steroids in premature adrenarche. European Journal of Pediatrics. 154(5). 346–352. 57 indexed citations
20.
Peter, Michael, Wolfgang G. Sippell, & H. Wernze. (1993). Diagnosis and treatment of 17-hydroxylase deficiency. The Journal of Steroid Biochemistry and Molecular Biology. 45(1-3). 107–116. 19 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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