Michael Peter

2.9k citations

93 papers · 2.1k indexed · h-index 26

Impact in

Endocrinology, Diabetes and Metabolism top 1%
- Hormonal Regulation and Hypertension
- Hormonal and reproductive studies
- Adrenal Hormones and Disorders
- Growth Hormone and Insulin-like Growth Factors
Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders

Papers in ⓘ

Endocrinology, Diabetes and Metabolism 48
- Hormonal Regulation and Hypertension 29
- Hormonal and reproductive studies 17
- Adrenal Hormones and Disorders 13
Molecular Biology 43
- Sexual Differentiation and Disorders 30
- Ion Transport and Channel Regulation 7

Co-authors: Wolfgang G. Sippell (31 shared papers)Nils Janzen (14 shared papers)Johannes Sander (14 shared papers)Stefanie Sander (12 shared papers)Carl‐Joachim Partsch (13 shared papers)Michael Terhardt (8 shared papers)Ulrike Steuerwald (9 shared papers)W.G. Sippell (7 shared papers)
Journals: The Journal of Clinical Endocrinology & Metabolism (17 papers)Hormone Research in Paediatrics (6 papers)European Journal of Endocrinology (4 papers)Pediatric Research (4 papers)European Journal of Pediatrics (4 papers)
Partner nations: Germany Austria Netherlands

In The Last Decade

Michael Peter

86 papers receiving 2.0k citations

Peers

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-authors

The 25 scholars most cited alongside Michael Peter, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Michael Peter Line = papers co-authored together Michael Peter links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 93 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Newborn Screening for Congenital Adrenal Hyperplasia: Additional Steroid Profile using Liquid Chromatography-Tandem Mass Spectrometry The Journal of Clinical Endocrinology & Metabolism ·Nils Janzen, Michael Peter, Stefanie Sander, Ulrike Steuerwald, Michael Terhardt, Ute Holtkamp, Johannes Sander	2007	164
2	CYP11B1 mutations causing congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency. The Journal of Clinical Endocrinology & Metabolism ·Stephan Geley, Klaus Kapelari, Karin Jöhrer, Michael Peter, J Glatzl, H Vierhapper, S. Schwarz, Arno Helmberg, Wolfgang G. Sippell, Perrin C. White, Reinhard Kofler	1996	99
3	Congenital Adrenal Hypoplasia: Clinical Spectrum, Experience with Hormonal Diagnosis, and Report on New Point Mutations of the DAX-1 Gene The Journal of Clinical Endocrinology & Metabolism ·Michael Peter, Matthias Viemann, Carl‐Joachim Partsch, Wolfgang G. Sippell	1998	97
4	Fast and direct quantification of adrenal steroids by tandem mass spectrometry in serum and dried blood spots Journal of Chromatography B ·Nils Janzen, Stefanie Sander, Michael Terhardt, Michael Peter, Johannes Sander	2007	94
5	New Insight into the Molecular Basis of 3β-Hydroxysteroid Dehydrogenase Deficiency: Identification of Eight Mutations in the HSD3B2 Gene in Eleven Patients from Seven New Families and Comparison of the Functional Properties of Twenty-Five Mutant Enzymes1 The Journal of Clinical Endocrinology & Metabolism ·Anne Marie Moisan, Marie‐Louise Ricketts, Véronique Tardy, Marc Desrochers, Farida Mébarki, Jean‐Louis Chaussain, Sylvie Cabrol, Marie Charles Raux-Demay, Maguelone G. Forest, Wolfgang G. Sippell, Michael Peter, Yves Morel, Jacques Simard	1999	75
6	A higher rate of hyperandrogenic disorders in female-to-male transsexuals Psychoneuroendocrinology ·Hartmut A.G. Bosinski, Michael Peter, G. Bonatz, R Arndt, Maren Heidenreich, Wolfgang G. Sippell, R. Wille	1997	63
7	Follow up of growth and steroids in premature adrenarche European Journal of Pediatrics ·A Père, Jaakko Perheentupa, Michael Peter, Raimo Voutilainen	1995	57
8	Multiplex Minisequencing of the 21-Hydroxylase Gene as a Rapid Strategy to Confirm Congenital Adrenal Hyperplasia Clinical Chemistry ·Nils Krone, Andreas Braun, Stefanie Weinert, Michael Peter, Adelbert A. Roscher, Carl‐Joachim Partsch, Wolfgang G. Sippell	2002	57
9	Neonatal screening for defects of the mitochondrial trifunctional protein Molecular Genetics and Metabolism ·Johannes Sander, Stefanie Sander, Ulrike Steuerwald, Nils Janzen, Michael Peter, Ronald J. A. Wanders, Iris Marquardt, Georg Christoph Korenke, Anibh M. Das	2005	56
10	Rapid steroid hormone quantification for congenital adrenal hyperplasia (CAH) in dried blood spots using UPLC liquid chromatography–tandem mass spectrometry Steroids ·Nils Janzen, Stefanie Sander, Michael Terhardt, Ulrike Steuerwald, Michael Peter, Anibh M. Das, Johannes Sander	2011	46
11	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 ·Nils Krone, Felix G. Riepe, Dorothea Götze, Eckhard Korsch, M. Rister, Jens Commentz, Carl‐Joachim Partsch, Joachim Grötzinger, Michael Peter, Wolfgang G. Sippell	2005	44
12	Disorders of the Aldosterone Synthase and Steroid 11β-Hydroxylase Deficiencies Hormone Research in Paediatrics ·Michael Peter, J.-M. Dubuis, W.G. Sippell	1999	43
13	Evidence for Genetic Heterogeneity of Pseudohypoaldosteronism Type 1: Identification of a Novel Mutation in the Human Mineralocorticoid Receptor in one Sporadic Case and No Mutations in Two Autosomal Dominant Kindreds The Journal of Clinical Endocrinology & Metabolism ·Matthias Viemann, Michael Peter, Juan Pedro López-Siguero, Gunter Ŝimić-Schleicher, Wolfgang G. Sippell	2001	42
14	Elucidating the Underlying Molecular Pathogenesis ofNR3C2Mutants Causing Autosomal Dominant Pseudohypoaldosteronism Type 1 The Journal of Clinical Endocrinology & Metabolism ·Felix G. Riepe, Johannes Finkeldei, Luisa De Sanctis, Silvia Einaudi, Alberto Testa, Beate Karges, Michael Peter, Matthias Viemann, Joachim Grötzinger, Wolfgang G. Sippell, Géza Fejes‐Tóth, Nils Krone	2006	42
15	Newborn Screening for Hepatorenal Tyrosinemia: Tandem Mass Spectrometric Quantification of Succinylacetone Clinical Chemistry ·Johannes Sander, Nils Janzen, Michael Peter, Stefanie Sander, Ulrike Steuerwald, Ute Holtkamp, Bernd Schwahn, Ertan Mayatepek, Friedrich K. Trefz, Anibh M. Das	2006	40
16	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 ·Christian Marx, Stefan R. Bornstein, Gernot W. Wolkersdörfer, Michael Peter, Wolfgang G. Sippell, Werner A. Scherbaum	1997	39
17	Comparison of Complete and Incomplete Suppression of Pituitary-Gonadal Activity in Girls with Central Precocious Puberty: Influence on Growth and Predicted Final Height Hormone Research ·C. J. Partsch, R. H uuml mmelink, Michael Peter, Wolfgang G. Sippell, Wilma Oostdijk, Roelof J. Odink, S.L.S. Drop	1993	35
18	Amino acid substitution R384P in aldosterone synthase causes corticosterone methyloxidase type I deficiency. The Journal of Clinical Endocrinology & Metabolism ·Stephan Geley, Karin Jöhrer, Michael Peter, Karsten Denner, Rita Bernhardt, Wolfgang G. Sippell, Reinhard Kofler	1995	34
19	Congenital Adrenal Hyperplasia: 11β-Hydroxylase Deficiency Seminars in Reproductive Medicine ·Michael Peter	2002	33
20	The Influence of Mode of Delivery on Hematologic Values in the Umbilical Vein Gynecologic and Obstetric Investigation ·Werner Nikischin, Michael Peter, Hans Dieter Oldigs	1997	31

About Michael Peter

Michael Peter is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology, Clinical Biochemistry, Pediatrics, Perinatology and Child Health and Pharmacology, having authored 93 papers that have together received 2.1k indexed citations. Recurring topics across this work include Sexual Differentiation and Disorders (30 papers), Hormonal Regulation and Hypertension (29 papers), Metabolism and Genetic Disorders (17 papers), Hormonal and reproductive studies (17 papers), Adrenal Hormones and Disorders (13 papers), Pharmacogenetics and Drug Metabolism (11 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers) and Ion Transport and Channel Regulation (7 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (1.1k citations), Clinical Biochemistry (406 citations), Reproductive Medicine (202 citations), Molecular Biology (1.2k citations) and Pharmacology (144 citations). Michael Peter has collaborated with scholars based in Germany, Austria and Netherlands. Frequent 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. Their work appears in journals such as The Journal of Clinical Endocrinology & Metabolism, Hormone Research in Paediatrics, European Journal of Endocrinology, Pediatric Research and European Journal of Pediatrics.

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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