Eckhard Korsch

1.3k total citations
28 papers, 756 citations indexed

About

Eckhard Korsch is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Physiology. According to data from OpenAlex, Eckhard Korsch has authored 28 papers receiving a total of 756 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 8 papers in Endocrinology, Diabetes and Metabolism and 6 papers in Physiology. Recurrent topics in Eckhard Korsch's work include Sexual Differentiation and Disorders (6 papers), Glycosylation and Glycoproteins Research (4 papers) and Neonatal Respiratory Health Research (3 papers). Eckhard Korsch is often cited by papers focused on Sexual Differentiation and Disorders (6 papers), Glycosylation and Glycoproteins Research (4 papers) and Neonatal Respiratory Health Research (3 papers). Eckhard Korsch collaborates with scholars based in Germany, Netherlands and France. Eckhard Korsch's co-authors include Michael Peter, Dirk J. Lefeber, F Bläker, Ron A. Wevers, Éva Morava, Olaf Hiort, R. Cremer, Bettina Gohlke, Joachim Woelfle and Felix G. Riepe and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, The American Journal of Human Genetics and Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease.

In The Last Decade

Eckhard Korsch

27 papers receiving 723 citations

Peers

Countries citing papers authored by Eckhard Korsch

Since Specialization

Citations

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

Fields of papers citing papers by Eckhard Korsch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eckhard Korsch

This figure shows the co-authorship network connecting the top 25 collaborators of Eckhard Korsch. A scholar is included among the top collaborators of Eckhard Korsch 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 Eckhard Korsch. Eckhard Korsch is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	An expanded clinical spectrum of hypoinsulinaemic hypoketotic hypoglycaemia 2023 ·Orphanet Journal of Rare Diseases ·Alena Welters, (unknown), Nadine Bachmann, Carsten Bergmann, (unknown), Eckhard Korsch, Thomas Meißner, Felicity Payne, Rachel M. Williams, Khalid Hussain, Robert K. Semple, Sebastian Kummer	0
2	„Crazy bitch!“ – Erlebte Aggression und Gewalt im Klinikalltag von Kinderärzten 2020 ·Monatsschrift Kinderheilkunde ·Antje Dresen, Susan Lee, Holger Pfaff, Michael D. Weiss, Eckhard Korsch	1
3	Skin conductance in neonates suffering from abstinence syndrome and unexposed newborns 2016 ·European Journal of Pediatrics ·(unknown), Katrin Mehler, Bernhard Roth, Eckhard Korsch, (unknown), Dominique Singer, A von der Wense, András Treszl, Christoph Hünseler	15
4	Comprehensive review of the duplication 3q syndrome and report of a patient with Currarino syndrome and de novo duplication 3q26.32‐q27.2 2016 ·Clinical Genetics ·Gabriel C. Dworschak, Célia Cretolle, Alina C. Hilger, Hartmut Engels, Eckhard Korsch, Heiko Reutter, Michael Ludwig	32
5	<b><i>MKRN3</i></b> Mutations in Familial Central Precocious Puberty 2014 ·Hormone Research in Paediatrics ·Felix Schreiner, Bettina Gohlke, (unknown), Eckhard Korsch, Joachim Woelfle	50
6	Perinatal and early infantile symptoms in congenital disorders of glycosylation 2013 ·American Journal of Medical Genetics Part A ·Simone Funke, Thatjana Gardeitchik, (unknown), (unknown), Saskia B. Wortmann, Eckhard Korsch, Maciej Adamowicz, Lihadh Al‐Gazali, Ron A. Wevers, (unknown), Dirk J. Lefeber, Éva Morava	30
7	Neonatal Screening: Identification of Children with 11β-Hydroxylase Deficiency by Second-Tier Testing 2012 ·Hormone Research in Paediatrics ·Nils Janzen, Felix G. Riepe, Michael Peter, Stefanie Sander, Ulrike Steuerwald, Eckhard Korsch, Friedrich Krull, Hermann L. Müller, Sabine Heger, Christoph Brack, Johannes Sander	23
8	Clinical and diagnostic approach in unsolved CDG patients with a type 2 transferrin pattern 2011 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Miski Mohamed, Maïlys Guillard, (unknown), Sebahattin Çirak, (unknown), Helen Michelakakis, Eckhard Korsch, Michael S. Adamowicz, Berthold Koletzko, F. J. van Spronsen, Klary E. Niezen‐Koning, Gert Matthijs, Thatjana Gardeitchik, (unknown), Byung Chan Lim, Renate Zeevaert, Ron A. Wevers, Dirk J. Lefeber, Éva Morava	19
9	A Case of 11β-Hydroxylase Deficiency Detected in a Newborn Screening Program by Second-Tier LC-MS/MS 2008 ·Hormone Research in Paediatrics ·Michael Peter, Nils Janzen, Stefanie Sander, Eckhard Korsch, Felix G. Riepe, Johannes Sander	19
10	Congenital hypothyroidism caused by new mutations in the thyroid oxidase 2 (THOX2) gene 2006 ·Clinical Endocrinology ·Nicole Pfarr, Eckhard Korsch, Stefan Kaspers, Antje Herbst, (unknown), (unknown), Joachim Pohlenz	39
11	Congenital Adrenal Hyperplasia Due to 11-Hydroxylase Deficiency: Functional Characterization of Two Novel Point Mutations and a Three-Base Pair Deletion in theCYP11B1Gene 2005 ·The Journal of Clinical Endocrinology & Metabolism ·Nils Krone, Felix G. Riepe, (unknown), Eckhard Korsch, M. Rister, (unknown), Carl‐Joachim Partsch, Joachim Grötzinger, Michael Peter, Wolfgang G. Sippell	44
12	Mosaic tetrasomy 14pter‐q13 due to a supernumerary isodicentric derivate of proximal chromosome 14q 2005 ·American Journal of Medical Genetics Part A ·Thomas Eggermann, Ulrike Gamerdinger, Kristin Bosse, (unknown), (unknown), Esther Meyer, (unknown), Herdit M. Schüler, Eckhard Korsch, Gesa Schwanitz	7
13	Novel insertion frameshift mutation of the LH receptor gene: problematic clinical distinction of Leydig cell hypoplasia from enzyme defects primarily affecting testosterone biosynthesis 2005 ·European Journal of Endocrinology ·Annette Richter-Unruh, Eckhard Korsch, Olaf Hiort, Paul‐Martin Holterhus, Axel P. N. Themmen, Stefan A. Wudy	20
14	Molecular features and clinical phenotypes in androgen insensitivity syndrome in the absence and presence of androgen receptor gene mutations 2005 ·Journal of Molecular Medicine ·Paul‐Martin Holterhus, Ralf Werner, U. Hoppe, (unknown), Eckhard Korsch, Michael B. Ranke, Helmuth G. Dörr, Olaf Hiort	26
15	Childhood asthma knowledge among first year nursing students in three european cities 2004 ·Allergologia et Immunopathologia ·Luis García‐Marcos, Zahir Mughal, Eckhard Korsch, (unknown), Jean Abbott, (unknown), (unknown)	6
16	Four New Cases of Congenital Secondary Hypothyroidism due to a Splice Site Mutation in the Thyrotropin-β Gene: Phenotypic Variability and Founder Effect 2004 ·The Journal of Clinical Endocrinology & Metabolism ·Guntram Borck, A. Kemal Topaloğlu, Eckhard Korsch, Ursula Martiné, (unknown), Neslihan Önenli Mungan, Bilgin Yüksel, (unknown), (unknown), (unknown), Roland Pfäffle, Neal H. Scherberg, Samuel Refetoff, Joachim Pohlenz	18
17	Neurological Phenotype in Waardenburg Syndrome Type 4 Correlates with Novel SOX10 Truncating Mutations and Expression in Developing Brain 2000 ·The American Journal of Human Genetics ·Renaud Touraine, Tania Attié‐Bitach, E. Manceau, Eckhard Korsch, Pierre Sarda, Véronique Pingault, Férechté Encha‐Razavi, Anna Pelet, Joëlle Augé, A Nivelon‐Chevallier, A. M. Holschneider, Marc Munnes, (unknown), Michel Goossens, Arnold Munnich, (unknown), Stanislas Lyonnet	124
18	Gonadal Histology with Testicular Carcinomain Situin a 15-Year-Old 46,XY Female Patient with a Premature Termination in the Steroidogenic Acute Regulatory Protein Causing Congenital Lipoid Adrenal Hyperplasia 1999 ·The Journal of Clinical Endocrinology & Metabolism ·Eckhard Korsch, Michael Peter, Olaf Hiort, Wolfgang G. Sippell, Benno Ure, Berthold P. Hauffa, Martin Bergmann	28
19	Natural rubber latex allergy: prevalence and risk factors in patients with spina bifida compared with atopic children and controls 1998 ·European Journal of Pediatrics ·R. Cremer, (unknown), Eckhard Korsch, (unknown), F Bläker	56
20	[Familial manifestation of idiopathic atrial flutter]. 1992 ·PubMed ·(unknown), Eckhard Korsch	7

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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