Author

Michael Peter

Observed names: M Peter, M. Peter

Institution: Fraunhofer Institute for Telecommunications, Heinrich Hertz Institute

Observed institutions: University of Geneva, Centre National de la Recherche Scientifique, Innsbruck Medical University, University of Veterinary Medicine Hannover, Foundation, Universität Innsbruck, University of Münster, Fraunhofer Institute for Telecommunications, Heinrich Hertz Institute, Christian-Albrechts-Universität zu Kiel, Medizinische Hochschule Hannover, Endocrinology Research Center, University Hospital of Geneva, University Hospital Schleswig-Holstein, Institut de Pharmacologie Moléculaire et Cellulaire, Martin Luther University Halle-Wittenberg, Freie Universität Berlin, Leipzig University

OpenAlex ID: A5110159969

Newborn Screening for Congenital Adrenal Hyperplasia: Additional Steroid Profile using Liquid Chromatography-Tandem Mass Spectrometry

2007 · N. Janzen, M. Peter, et al. · The Journal of Clinical Endocrinology & Metabolism · 211

Congenital Adrenal Hypoplasia: Clinical Spectrum, Experience with Hormonal Diagnosis, and Report on New Point Mutations of the DAX-1 Gene

1998 · Michael Peter, Matthias Viemann, et al. · The Journal of Clinical Endocrinology & Metabolism · 155

CYP11B1 mutations causing congenital adrenal hyperplasia due to 11 beta- hydroxylase deficiency

1996 · S Geley, K Kapelari, et al. · The Journal of Clinical Endocrinology & Metabolism · 134

Fast and direct quantification of adrenal steroids by tandem mass spectrometry in serum and dried blood spots

2007 · Nils Janzen, Stefanie Sander, et al. · Journal of Chromatography B · 119

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

1999 · Anne Marie Moisan, Marie Louise Ricketts, et al. · The Journal of Clinical Endocrinology & Metabolism · 107

A higher rate of hyperandrogenic disorders in female-to-male transsexuals

1997 · Hartmut A.G. Bosinski, Michael Peter, et al. · Psychoneuroendocrinology · 91

Neonatal screening for defects of the mitochondrial trifunctional protein

2005 · Johannes Sander, Stefanie Sander, et al. · Molecular Genetics and Metabolism · 68

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

2001 · Matthias Viemann, Michael Peter, et al. · The Journal of Clinical Endocrinology & Metabolism · 67

Follow up of growth and steroids in premature adrenarche

1995 · A. Pere, J. Perheentupa, et al. · European Journal of Pediatrics · 67

Rapid steroid hormone quantification for congenital adrenal hyperplasia (CAH) in dried blood spots using UPLC liquid chromatography–tandem mass spectrometry

2011 · Nils Janzen, Stefanie Sander, et al. · Steroids · 66

Elucidating the Underlying Molecular Pathogenesis ofNR3C2Mutants Causing Autosomal Dominant Pseudohypoaldosteronism Type 1

2006 · Felix G. Riepe, Johannes Finkeldei, et al. · The Journal of Clinical Endocrinology & Metabolism · 65

Multiplex Minisequencing of the 21-Hydroxylase Gene as a Rapid Strategy to Confirm Congenital Adrenal Hyperplasia

2002 · Nils Krone, Andreas Braun, et al. · Clinical Chemistry · 64

Newborn Screening for Hepatorenal Tyrosinemia: Tandem Mass Spectrometric Quantification of Succinylacetone

2006 · Johannes Sander, Nils Janzen, et al. · Clinical Chemistry · 62

Congenital Adrenal Hyperplasia: 11β-Hydroxylase Deficiency

2002 · Michael Peter · Seminars in Reproductive Medicine · 62

Disorders of the Aldosterone Synthase and Steroid 11β-Hydroxylase Deficiencies

1999 · M. Peter, J.-M. Dubuis, et al. · Hormone Research in Paediatrics · 62

Congenital Adrenal Hyperplasia Due to 11-Hydroxylase Deficiency: Functional Characterization of Two Novel Point Mutations and a Three-Base Pair Deletion in theCYP11B1Gene

2005 · Nils Krone, Felix G. Riepe, et al. · The Journal of Clinical Endocrinology & Metabolism · 58

Gonadal Histology with Testicular Carcinoma in Situ in a 15-Year-Old 46,XY Female Patient with a Premature Termination in the Steroidogenic Acute Regulatory Protein Causing Congenital Lipoid Adrenal Hyperplasia

1999 · Eckhard Korsch, Michael Peter, et al. · The Journal of Clinical Endocrinology & Metabolism · 53

Relevance of Major Histocompatibility Complex Class II Expression as a Hallmark for the Cellular Differentiation in the Human Adrenal Cortex1

1997 · Christian Marx, Stefan R. Bornstein, et al. · The Journal of Clinical Endocrinology & Metabolism · 51

A New Insight Into the Molecular Basis of 3β-Hydroxysteroid Dehydrogenase Deficiency

2000 · Jacques Simard, Marie Louise Ricketts, et al. · Endocrine Research · 48

Amino acid substitution R384P in aldosterone synthase causes corticosterone methyloxidase type I deficiency

1995 · S Geley, K Jöhrer, et al. · The Journal of Clinical Endocrinology & Metabolism · 48

The Influence of Mode of Delivery on Hematologic Values in the Umbilical Vein

2010 · Werner Nikischin, Michael Peter, et al. · Gynecologic and Obstetric Investigation · 47

Improved test to identify heterozygotes for congenital adrenal hyperplasia without index case examination

1990 · M. Peter, W.G. Sippell, et al. · The Lancet · 41

Comparison of Complete and Incomplete Suppression of Pituitary-Gonadal Activity in Girls with Central Precocious Puberty: Influence on Growth and Predicted Final Height

2008 · C.J. Partsch, R. Hümmelink, et al. · Hormone Research · 40

Hereditary Defect in Biosynthesis of Aldosterone: Aldosterone Synthase Deficiency 1964–19971

1997 · Michael Peter, Lubna Fawaz, et al. · The Journal of Clinical Endocrinology & Metabolism · 40

Neonatal Screening: Identification of Children with 11β-Hydroxylase Deficiency by Second-Tier Testing

2012 · Nils Janzen, Felix G. Riepe, et al. · Hormone Research in Paediatrics · 37

Works count: 92

Citation count: 2,717

H-index: 32

I10-index: 60