E. Schwinger

9.9k total citations
210 papers, 6.0k citations indexed

About

E. Schwinger is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, E. Schwinger has authored 210 papers receiving a total of 6.0k indexed citations (citations by other indexed papers that have themselves been cited), including 84 papers in Molecular Biology, 71 papers in Genetics and 41 papers in Cellular and Molecular Neuroscience. Recurrent topics in E. Schwinger's work include Prenatal Screening and Diagnostics (37 papers), Genetic Neurodegenerative Diseases (23 papers) and Genomic variations and chromosomal abnormalities (22 papers). E. Schwinger is often cited by papers focused on Prenatal Screening and Diagnostics (37 papers), Genetic Neurodegenerative Diseases (23 papers) and Genomic variations and chromosomal abnormalities (22 papers). E. Schwinger collaborates with scholars based in Germany, United States and Italy. E. Schwinger's co-authors include Andreas Gal, Christine Zühlke, Christine Klein, Yorck Hellenbroich, U. Froster‐Iskenius, Helga Rehder, Katja Hedrich, Susanna Bunge, Joachim Müller‐Quernheim and Peter P. Pramstaller and has published in prestigious journals such as The Lancet, Nature Genetics and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

E. Schwinger

199 papers receiving 5.8k citations

Peers

Countries citing papers authored by E. Schwinger

Since Specialization

Citations

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

Fields of papers citing papers by E. Schwinger

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E. Schwinger

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Exome sequencing in a family with restless legs syndrome 2012 ·Movement Disorders ·Anne Weißbach, (unknown), Norbert Brüggemann, Alexander Schmidt, Meike Kasten, Irene Pichler, Hiltrud Muhle, Ebba Lohmann, Thora Lohnau, E. Schwinger, Johann Hagenah, Ulrich Stephani, Peter P. Pramstaller, Christine Klein, Katja Lohmann	17
2	Study of C-C Chemokine Receptor 2 Alleles in Sarcoidosis, with Emphasis on Family-based Analysis 2005 ·American Journal of Respiratory and Critical Care Medicine ·Ruta Valentonyte, Jochen Hampe, Peter J.P. Croucher, Joachim Müller‐Quernheim, E. Schwinger, Stefan Schreiber, Manfred Schürmann	37
3	Spinocerebellar ataxia type 4 (SCA4): Initial pathoanatomical study reveals widespread cerebellar and brainstem degeneration 2005 ·Journal of Neural Transmission ·Yorck Hellenbroich, K. Gierga, E. Reusche, E. Schwinger, Thomas Deller, Rob A. I. de Vos, Christine Zühlke, Udo Rüb	27
4	Mutations in the X-Linked Cyclin-Dependent Kinase–Like 5 (CDKL5/STK9) Gene Are Associated with Severe Neurodevelopmental Retardation 2004 ·The American Journal of Human Genetics ·Jiong Tao, Hilde Van Esch, (unknown), Kirsten Hoffmann, Bettina A. Moser, Martine Raynaud, Jürgen Sperner, Jean‐Pierre Fryns, E. Schwinger, Jozef Gécz, Hans‐Hilger Ropers, Vera M. Kalscheuer	236
5	Extension of the mutation spectrum in Friedreich's ataxia: detection of an exon deletion and novel missense mutations 2004 ·European Journal of Human Genetics ·Christine Zühlke, Andreas Dalski, (unknown), Korinna Straube, Katja Hedrich, Maria Hoeltzenbein, (unknown), Yorck Hellenbroich, E. Schwinger	33
6	Evidence That Paternal Expression of the ε-Sarcoglycan Gene Accounts for Reduced Penetrance in Myoclonus-Dystonia 2002 ·The American Journal of Human Genetics ·B. Müller, Katja Hedrich, Norman Kock, Nataša Dragašević, Marina Svetel, Jennifer Garrels, Olfert Landt, Matthias Nitschke, Peter P. Pramstaller, Wolf Reik, E. Schwinger, Jürgen Sperner, Laurie J. Ozelius, Vladimir Kostić, Christine Klein	102
7	Retinal Dystrophy Due to Paternal Isodisomy for Chromosome 1 or Chromosome 2, with Homoallelism for Mutations in RPE65 or MERTK, Respectively 2002 ·The American Journal of Human Genetics ·Debra A. Thompson, Christina L. McHenry, Yun Li, Julia E. Richards, Mohammad Othman, E. Schwinger, Douglas Vollrath, Samuel G. Jacobson, Andreas Gal	103
8	Results from a Genome-wide Search for Predisposing Genes in Sarcoidosis 2001 ·American Journal of Respiratory and Critical Care Medicine ·Manfred Schürmann, (unknown), Bertram Müller‐Myhsok, Max Schlaak, Joachim Müller‐Quernheim, E. Schwinger	141
9	Angiotensin‐converting enzyme (ACE) gene polymorphisms and familial occurrence of sarcoidosis 2001 ·Journal of Internal Medicine ·Martin Schürmann, (unknown), Bertram Müller‐Myhsok, (unknown), Karl Wurm, Max Schlaak, Joachim Müller‐Quernheim, E. Schwinger	39
10	Familial Sarcoidosis is Linked to the Major Histocompatibility Complex Region 2000 ·American Journal of Respiratory and Critical Care Medicine ·Manfred Schürmann, Penny Lympany, (unknown), Bertram Müller‐Myhsok, Karl Wurm, Max Schlaak, Joachim Müller‐Quernheim, (unknown), E. Schwinger	85
11	Assignment of transcription factor NFAT5 to human chromosome 16q22.1, murine chromosome 8D and porcine chromosome 6p1.4 and comparison of the polyglutamine domains 2000 ·Cytogenetic and Genome Research ·(unknown), Andreas Dalski, Hartmut Engel, Marie‐Geneviève Mattéi, Rachel Hawken, E. Schwinger, (unknown)	9
12	Quantitative PCR analysis of different splice forms of NFAT5 revealed specific gene expression in fetal and adult brain 2000 ·Molecular Brain Research ·Andreas Dalski, Hans‐Joachim Wagner, E. Schwinger, Christine Zühlke	13
13	HLA-DQB1 and HLA-DPB1 genotypes in familial sarcoidosis 1998 ·Respiratory Medicine ·Martin Schürmann, Gregor Bein, D Kirsten, Max Schlaak, Joachim Müller‐Quernheim, E. Schwinger	22
14	VACTERL with hydrocephalus and branchial arch defects: Prenatal, clinical, and autopsy findings in two brothers 1996 ·American Journal of Medical Genetics ·Ursula G. Froster, (unknown), E. Reusche, E. Schwinger, Helga Rehder	22
15	Mapping of the Autosomal Dominant Exudative Vitreoretinopathy Locus (EVR1) by Multipoint Linkage Analysis in Four Families 1994 ·Genomics ·(unknown), Ulrike Orth, C. E. van Nouhuys, (unknown), (unknown), E. Schwinger, H. Laqua, Andreas Gal	18
16	X-linked dominant Charcot — Marie — Tooth neuropathy: valine-38-methionine substitution of connexin32 1994 ·Human Molecular Genetics ·Ulrike Orth, (unknown), (unknown), E. Schwinger, Andreas Gal	34
17	Molecular analysis in patients with mucopolysaccharidosis type II suggests that DXS466 maps within the Hunter gene 1993 ·Human Genetics ·Cordula Steglich, Susanna Bunge, Theo J.M. Hulsebos, Michael Beck, (unknown), E. Schwinger, (unknown), (unknown)	7
18	The effect of restriction enzyme digestion of human metaphase chromosomes on C-band variants of chromosomes 1 and 9 1988 ·Genome ·(unknown), Martin Schürmann, E. Schwinger	3
19	Four DNA Polymorphisms on the Short Arm of the X Chromosome: Allele Frequencies in a German and in a Turkish Population 1987 ·Human Heredity ·(unknown), (unknown), E. Schwinger	11
20	[How reliable is sex determination in traces of blood?]. 1977 ·Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·E. Schwinger, H. Troger	1

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.

Explore authors with similar magnitude of impact