Michael Peter - Concepedia

Author

Michael Peter

Also Known As

Andreas Ott, M Peter, M Péter, M. Peter, M. Péter, Mary Beth Peter, Mayer Peter, Merlin Peter, Michael Peter, Peter, Michael

185

Publications

2.9K

Citations

H-Index

104

Concepts

All Affiliations

Christian-Albrechts-Universität zu Kiel Medizinische Hochschule Hannover Hannover Re (Germany)University of Lübeck University Hospitals of the Ruhr-University of Bochum

About

Michael Peter is an author at Christian-Albrechts-Universität zu Kiel specializing in medicine, genetics, and endocrinology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	20	30	1.2K
2	Education	3	3	74
3	Health Sciences	2	2	84
4	Natural Sciences	2	2	66
5	Public Health	1	1	18

Michael Peter

Publications

2.4K

Citations

H-Index

Page 1

	Year	Citations
Newborn Screening for Congenital Adrenal Hyperplasia: Additional Steroid Profile using Liquid Chromatography-Tandem Mass Spectrometry Nils Janzen, Michael Peter, Stefanie Sander, The Journal of Clinical Endocrinology & Metabolism	2007	204
Congenital Adrenal Hypoplasia: Clinical Spectrum, Experience with Hormonal Diagnosis, and Report on New Point Mutations of the DAX-1 Gene Michael Peter, Matthias Viemann, Carl‐Joachim Partsch, The Journal of Clinical Endocrinology & Metabolism GeneticsAdrenal GlandMendelian DisorderAhc PatientsDax-1 Gene	1998	147
CYP11B1 mutations causing congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency. Stephan Geley, Klaus Kapelari, Karin Jöhrer, The Journal of Clinical Endocrinology & Metabolism GeneticsPathologyMolecular GeneticsDisease Gene IdentificationEpigenetics	1996	127
Fast and direct quantification of adrenal steroids by tandem mass spectrometry in serum and dried blood spots Nils Janzen, Stefanie Sander, Michael Terhardt, Journal of Chromatography B Adrenal SteroidsAdrenal GlandMedicineBioanalysisMass Spectrometry	2007	120
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 Anne Marie Moisan, Marie‐Louise Ricketts, Véronique Tardy, The Journal of Clinical Endocrinology & Metabolism	1999	105
A higher rate of hyperandrogenic disorders in female-to-male transsexuals Hartmut A.G. Bosinski, Michael Peter, G. Bonatz, Psychoneuroendocrinology Gender StudiesSexual DysfunctionHigher RateGender TransitionSexual Orientation	1997	91
Neonatal screening for defects of the mitochondrial trifunctional protein Johannes Sander, Stefanie Sander, Ulrike Steuerwald, Molecular Genetics and Metabolism Neonatal ScreeningMitochondrial FunctionGeneticsMolecular BiologyMitochondrial Medicine	2005	66
Follow up of growth and steroids in premature adrenarche A Père, Jaakko Perheentupa, Michael Peter, European Journal of Pediatrics Animal PhysiologyMetabolic SyndromePremature AdrenarcheAdrenal GlandMedicine	1995	66
Elucidating the Underlying Molecular Pathogenesis of<i>NR3C2</i>Mutants Causing Autosomal Dominant Pseudohypoaldosteronism Type 1 Felix G. Riepe, Johannes Finkeldei, Luisa De Sanctis, The Journal of Clinical Endocrinology & Metabolism	2006	65
Rapid steroid hormone quantification for congenital adrenal hyperplasia (CAH) in dried blood spots using UPLC liquid chromatography–tandem mass spectrometry Nils Janzen, Stefanie Sander, Michael Terhardt, Steroids Adrenal GlandCongenital Adrenal HyperplasiaMedicineMass SpectrometryGynecology	2011	63

Page 1