E. Schwinger

9.9k citations

217 papers · 6.6k · h-index 43

Impact in

Neurology top 1%
- Parkinson's Disease Mechanisms and Treatments
- Neurological disorders and treatments
Cellular and Molecular Neuroscience top 1%
- Genetic Neurodegenerative Diseases

Papers in

Molecular Biology 82
- Mitochondrial Function and Pathology 16
Genetics 71
- Genomic variations and chromosomal abnormalities 23
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 17
- Genetics and Neurodevelopmental Disorders 17
- Genetic Syndromes and Imprinting 12

Co-authors: Andreas Gal (23 shared papers)Christine Zühlke (19 shared papers)Christine Klein (18 shared papers)Yorck Hellenbroich (15 shared papers)Helga Rehder (13 shared papers)Joachim Müller–Quernheim (7 shared papers)Katja Hedrich (14 shared papers)Susanna Bunge (11 shared papers)
Journals: Human Genetics (24 papers)European Journal of Human Genetics (9 papers)Human Mutation (8 papers)Prenatal Diagnosis (8 papers)Clinical Genetics (8 papers)
Partner nations: Germany United States Italy

In The Last Decade

E. Schwinger

202 papers receiving 6.1k 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-authors

The 25 scholars most cited alongside E. Schwinger, 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 E. Schwinger Line = papers co-authored together E. Schwinger 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 217 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutations in the X-Linked Cyclin-Dependent Kinase–Like 5 (CDKL5/STK9) Gene Are Associated with Severe Neurodevelopmental Retardation The American Journal of Human Genetics ·Jiong Tao, Hilde Van Esch, M. Hagedorn-Greiwe, Kirsten Hoffmann, Bettina A. Moser, Martine Raynaud, Jürgen Sperner, Jean‐Pierre Fryns, E. Schwinger, Jozef Gécz, Hans‐Hilger Ropers, Vera M. Kalscheuer	2004	246
2	Disruption of the Serine/Threonine Kinase 9 Gene Causes Severe X-Linked Infantile Spasms and Mental Retardation The American Journal of Human Genetics ·Vera M. Kalscheuer, Jiong Tao, Andrew J. Donnelly, Georgina E. Hollway, E. Schwinger, Sabine Kübart, Corinna Menzel, Maria Hoeltzenbein, Niels Tommerup, Helen J. Eyre, Michael Harbord, Eric Haan, Grant R. Sutherland, Hans‐Hilger Ropers, Jozef Gécz	2003	233
3	Heterozygous missense mutation in the rod cGMP phosphodiesterase β–subunit gene in autosomal dominant stationary night blindness Nature Genetics ·Andreas Gal, Ulrike Orth, Wolfgang Baehr, E. Schwinger, Thomas Rosenberg	1994	192
4	Over-expression of wild-type Rad51 correlates with histological grading of invasive ductal breast cancer International Journal of Cancer ·Heiko Maacke, Sven Opitz, Kirsten Jost, Willem Hamdorf, Wilhelm Henning, Stefan Kr�ger, Alfred C. Feller, A. Lopens, Klaus Diedrich, E. Schwinger, Horst-Werner St�rzbecher	2000	190
5	Distribution, type, and origin of Parkin mutations: Review and case studies Movement Disorders ·Katja Hedrich, Cordula Eskelson, Beth Wilmot, Karen Marder, Juliette Harris, Jennifer Garrels, Helen Meija‐Santana, P. Vieregge, Helfried Jacobs, Susan Bressman, Anthony E. Lang, Martin Kann, Giovanni Abbruzzese, Paolo Martinelli, E. Schwinger, Laurie J. Ozelius, Peter P. Pramstaller, Christine Klein, Patricia Kramer	2004	177
6	Eye tracking dysfunction is a putative phenotypic susceptibility marker of schizophrenia and maps to a locus on chromosome 6p in families with multiple occurrence of the disease American Journal of Medical Genetics ·Volker Arolt, Rebekka Lencer, Achim Nolte, Bertram Müller‐Myhsok, Sabine Purmann, Manfred Schürmann, Jutta Leutelt, Marlene Pinnow, E. Schwinger	1996	163
7	DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease Neurology ·Katja Hedrich, Ana Djarmati, Niklas Schäfer, Robert Hering, Claudia Wellenbrock, Peter H. Weiss, R. Hilker, P. Vieregge, Laurie J. Ozelius, Peter Heutink, Vincenzo Bonifati, E. Schwinger, Anthony E. Lang, J. Noth, Susan Bressman, Peter P. Pramstaller, (unknown), Christine Klein	2004	160
8	Results from a Genome-wide Search for Predisposing Genes in Sarcoidosis American Journal of Respiratory and Critical Care Medicine ·Manfred Schürmann, PHILIPP REICHEL, Bertram Müller‐Myhsok, Max Schlaak, Joachim Müller–Quernheim, E. Schwinger	2001	151
9	Evaluation of 50 probands with early-onset Parkinson’s disease for Parkin mutations Neurology ·Katja Hedrich, Karen Marder, Juliette Harris, Martin Kann, Timothy Lynch, Helen Meija‐Santana, Peter P. Pramstaller, E. Schwinger, Susan Bressman, Stanley Fahn, Christine Klein	2002	123
10	Evidence That Paternal Expression of the ε-Sarcoglycan Gene Accounts for Reduced Penetrance in Myoclonus-Dystonia 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	2002	117
11	Molecular basis of mucopolysaccharidosis type II: Mutations in the iduronate-2-sulphatase gene Human Mutation ·John J. Hopwood, Susanna Bunge, C. Phillip Morris, Peter J. Wilson, Cordula Steglich, Michael Beck, E. Schwinger, Andreas Gal	1993	116
12	Role of parkin mutations in 111 community‐based patients with early‐onset parkinsonism Annals of Neurology ·Martin Kann, Helfried Jacobs, K. Mohrmann, Kirsten Schumacher, Katja Hedrich, Jennifer Garrels, Karin Wiegers, E. Schwinger, Peter P. Pramstaller, Xandra O. Breakefield, Laurie J. Ozelius, P. Vieregge, Christine Klein	2002	115
13	Retinal Dystrophy Due to Paternal Isodisomy for Chromosome 1 or Chromosome 2, with Homoallelism for Mutations in RPE65 or MERTK, Respectively 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	2002	115
14	Mucopolysaccharidosis type I: identification of 8 novel mutations and determination of the frequency of the two common α-L-iduronidase mutations (W402X and Q70X) among European patients Human Molecular Genetics ·Susanna Bunge, Wim J. Kleijer, Cordula Steglich, Michael Beck, Cornelia Zuther, C. Phillip Morris, E. Schwinger, John J. Hopwood, Hamish S. Scott, Andreas Gal	1994	98
15	Different types of repeat expansion in the TATA-binding protein gene are associated with a new form of inherited ataxia European Journal of Human Genetics ·Christine Zühlke, Yorck Hellenbroich, Andreas Dalski, Johann Hagenah, P. Vieregge, Olaf Rieß, Christine Klein, E. Schwinger	2001	96
16	Familial Sarcoidosis is Linked to the Major Histocompatibility Complex Region American Journal of Respiratory and Critical Care Medicine ·Manfred Schürmann, Penny Lympany, PHILIPP REICHEL, Bertram Müller‐Myhsok, Karl Wurm, Max Schlaak, Joachim Müller–Quernheim, RON M. du BOIS, E. Schwinger	2000	95
17	Assisted reproductive technologies do not enhance the variability of DNA methylation imprints in human Journal of Medical Genetics ·Sascha Tierling, N. Y. Souren, Jasmin Gries, Christina LoPorto, Marco Groth, Pavlo Lutsik, Heidemarie Neitzel, I. Utz-Billing, Gabriele Gillessen‐Kaesbach, Heribert Kentenich, Georg Griesinger, Karl Sperling, E. Schwinger, Joern Walter	2009	92
18	Down's syndrome in the male. Reproductive pathology and meiotic studies Human Genetics ·R. Johannisson, A. Gropp, Heinz Winking, Wiltrud Coerdt, Helga Rehder, E. Schwinger	1983	90
19	Molecular Analysis and Genetic Mapping of the Rhodopsin Gene in Families with Autosomal Dominant Retinitis Pigmentosa Genomics ·Susanna Bunge, Heike Wedemann, D. David, D.J. Terwilliger, L.I. van den Born, C. Aulehla‐Scholz, C. Samanns, M Horn, J. Ott, E. Schwinger, Albert Schinzel, M. J. Denton, Andreas Gal	1993	83
20	Mutation analysis in the fibroblast growth factor 14 gene: frameshift mutation and polymorphisms in patients with inherited ataxias European Journal of Human Genetics ·Andreas Dalski, Jassemien Atici, Friedmar R. Kreuz, Yorck Hellenbroich, E. Schwinger, Christine Zühlke	2004	81

About E. Schwinger

E. Schwinger is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Cellular and Molecular Neuroscience and Physiology, having authored 217 papers that have together received 6.6k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (39 papers), Genomic variations and chromosomal abnormalities (23 papers), Genetic Neurodegenerative Diseases (22 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (17 papers), Genetics and Neurodevelopmental Disorders (17 papers), Mitochondrial Function and Pathology (16 papers), Genetic Syndromes and Imprinting (12 papers) and Chromosomal and Genetic Variations (12 papers). The work is most often cited by research in Neurology (1.0k citations), Cellular and Molecular Neuroscience (1.3k citations), Genetics (2.0k citations), Pediatrics, Perinatology and Child Health (757 citations) and Physiology (1.0k citations). E. Schwinger has collaborated with scholars based in Germany, United States and Italy. Frequent co-authors include Andreas Gal, Christine Zühlke, Christine Klein, Yorck Hellenbroich, Helga Rehder, Joachim Müller–Quernheim, Katja Hedrich, Susanna Bunge, U. Froster‐Iskenius and Peter P. Pramstaller. Their work appears in journals such as Human Genetics, European Journal of Human Genetics, Human Mutation, Prenatal Diagnosis and Clinical Genetics.

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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E. Schwinger

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