Klaus Wagner

4.9k citations

62 papers · 2.9k · 1 hit paper · h-index 23

Impact in

Neurology top 2%
- Amyotrophic Lateral Sclerosis Research
- Neurological diseases and metabolism
Cellular and Molecular Neuroscience top 2%
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases

Papers in

Molecular Biology 21
Genetics 20
- Genomic variations and chromosomal abnormalities 13
- Genetics and Neurodevelopmental Disorders 5
- Genetic Syndromes and Imprinting 5

Co-authors: Michaela Auer‐Grumbach (13 shared papers)Vincent Timmerman (8 shared papers)Peter De Jonghe (8 shared papers)Erwin Petek (29 shared papers)Christian Windpassinger (23 shared papers)Wolfram Hörz (1 shared paper)Philip D. Gregory (1 shared paper)Peter M. Kroisel (18 shared papers)
Journals: Human Genetics (3 papers)Clinical Genetics (3 papers)The American Journal of Human Genetics (3 papers)Gene (2 papers)PLoS ONE (2 papers)
Partner nations: Austria Germany United States

In The Last Decade

Klaus Wagner

61 papers receiving 2.9k citations

Klaus Wagner's Hit Papers

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DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4) 2004 · 609 citations

Peers

Countries citing papers authored by Klaus Wagner

Since Specialization

Citations

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

Fields of papers citing papers by Klaus Wagner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Klaus Wagner, 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 Klaus Wagner Line = papers co-authored together Klaus Wagner 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 62 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4) The American Journal of Human Genetics ·Ying-Zhang Chen, Craig L. Bennett, Huy M. Huynh, Ian P. Blair, Imke Puls, Joy Irobi, Ines Dierick, Annette Abel, Marina Kennerson, Bruce A. Rabin, Garth A. Nicholson, Michaela Auer‐Grumbach, Klaus Wagner, Peter De Jonghe, John W. Griffin, Kenneth H. Fischbeck, Vincent Timmerman, David R. Cornblath, Phillip F. Chance Hit paper breakdown →	2004	609
2	Mutations in the Small GTP-ase Late Endosomal Protein RAB7 Cause Charcot-Marie-Tooth Type 2B Neuropathy The American Journal of Human Genetics ·Kristien Verhoeven, Peter De Jonghe, Katrien Coen, Nathalie Verpoorten, Michaela Auer‐Grumbach, Jennifer M. Kwon, David Fitzpatrick, Eric Schmedding, Els De Vriendt, An Jacobs, Veerle Van Gerwen, Klaus Wagner, Hans‐Peter Hartung, Vincent Timmerman	2003	353
3	Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome Nature Genetics ·Christian Windpassinger, Michaela Auer‐Grumbach, Joy Irobi, Heema Patel, Erwin Petek, Gerd Hörl, Roland Malli, Johanna A. Reed, Ines Dierick, Nathalie Verpoorten, Thomas T. Warner, Christos Proukakis, Peter Van den Bergh, Christine Verellen, Lionel Van Maldergem, Luciano Merlini, Peter De Jonghe, Vincent Timmerman, Andrew H. Crosby, Klaus Wagner	2004	280
4	Histone Acetylation and Chromatin Remodeling Experimental Cell Research ·Philip D. Gregory, Klaus Wagner, Wolfram Hörz	2001	217
5	Maternal methylation imprints on human chromosome 15 are established during or after fertilization Nature Genetics ·Osman El‐Maarri, Karin Buiting, Edwin G. Peery, Peter M. Kroisel, Başak Balaban, Klaus Wagner, Bülent Urman, Julia Heyd, Christina Lich, Camilynn I. Brannan, Jörn Walter, Bernhard Horsthemke	2001	159
6	An X-Linked Myopathy with Postural Muscle Atrophy and Generalized Hypertrophy, Termed XMPMA, Is Caused by Mutations in FHL1 The American Journal of Human Genetics ·Christian Windpassinger, Benedikt Schoser, Volker Straub, Sonja Hochmeister, Abdul Noor, Birgit Lohberger, Natalie Farra, Erwin Petek, Thomas Schwarzbraun, Lisa Ofner, Wolfgang N. Löscher, Klaus Wagner, Hanns Lochmüller, John B. Vincent, Stefan Quasthoff	2008	108
7	Membrane topology of the human seipin protein FEBS Letters ·Carolina Lundin, Rickard Nordström, Klaus Wagner, Christian Windpassinger, Helena Andersson, Gunnar von Heijne, IngMarie Nilsson	2006	104
8	Phenotypes of the N88S Berardinelli–Seip congenital lipodystrophy 2 mutation Annals of Neurology ·Michaela Auer‐Grumbach, Beate Schlotter‐Weigel, Hanns Lochmüller, Gertrud Strobl‐Wildemann, Piet Auer‐Grumbach, Renate Fischer, H. Offenbacher, Ernst B. Zwick, Tanja Robl, Gerald Hartl, Hans‐Peter Hartung, Klaus Wagner, Christian Windpassinger, (unknown)	2005	83
9	Surface expression of CC- and CXC-chemokine receptors on leucocyte subsets in inflammatory joint diseases Clinical & Experimental Immunology ·Hilke Brühl, Klaus Wagner, H Kellner, M Schattenkirchner, Detlef Schlöndorff, Matthias Mack	2001	67
10	Autosomal Dominant Inherited Neuropathies With Prominent Sensory Loss and Mutilations Archives of Neurology ·Michaela Auer‐Grumbach, Peter De Jonghe, Kristien Verhoeven, Vincent Timmerman, Klaus Wagner, Hans‐Peter Hartung, Garth A. Nicholson	2003	62
11	Tetraploid partial hydatidiform moles: two cases with a triple paternal contribution and a 92,XXXY karyotype Human Genetics ·Urvashi Surti, Aron E. Szulman, Klaus Wagner, Mark Leppert, Stephen J. O’Brien	1986	61
12	Autosomal dominant juvenile amyotrophic lateral sclerosis and distal hereditary motor neuronopathy with pyramidal tract signs: synonyms for the same disorder? Brain ·Peter De Jonghe, Michaela Auer‐Grumbach, Joy Irobi, Klaus Wagner, Barbara Plecko, Marina Kennerson, Danqing Zhu, Els De Vriendt, Veerle Van Gerwen, Garth A. Nicholson, Hans‐Peter Hartung, Vincent Timmerman	2002	58
13	The human γ-aminobutyric acid A receptor delta (GABRD) gene: molecular characterisation and tissue-specific expression Gene ·Christian Windpassinger, Peter M. Kroisel, Klaus Wagner, Erwin Petek	2002	53
14	The human pregnancy-specific glycoprotein genes are tightly linked on the long arm of chromosome 19 and are coordinately expressed Biochemical and Biophysical Research Communications ·John R. Thompson, Rosa Koumari, Klaus Wagner, Sabine Barnert, Cathrin Schleussner, Heinrich Schrewe, Wolfgang Zimmermann, Gaby Müller, W. Schempp, Daniela Zaninetta, Domenico Ammaturo, Norman Hardman	1990	52
15	Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome Molecular Genetics and Genomics ·Erwin Petek, Thomas Schwarzbraun, Abdul Noor, Megha Patel, Kazuhiko Nakabayashi, Sanaa Choufani, Christian Windpassinger, M. Stamenković, Mary M. Robertson, H.N. Aschauer, Hugh Gurling, Peter M. Kroisel, Klaus Wagner, Stephen W. Scherer, John B. Vincent	2006	46
16	Phenotype–genotype correlations in a CMT2B family with refined 3q13-q22 locus Neurology ·Michaela Auer‐Grumbach, Peter De Jonghe, Klaus Wagner, K. Verhoeven, Hans‐Peter Hartung, Vincent Timmerman	2000	38
17	Candidate region for Gilles de la Tourette syndrome at 7q31 American Journal of Medical Genetics ·Peter M. Kroisel, Erwin Petek, Werner Emberger, Christian Windpassinger, Wolfgang Wladika, Klaus Wagner	2001	34
18	Refinement of the "Silver syndrome locus" on chromosome 11q12-q14 in four families and exclusion of eight candidate genes Human Genetics ·Christian Windpassinger, Klaus Wagner, Erwin Petek, Renate Fischer, Michaela Auer‐Grumbach	2003	31
19	Ulcero-mutilating neuropathy in an Austrian kinship without linkage to hereditary motor and sensory neuropathy IIB and hereditary sensory neuropathy I loci Neurology ·Michaela Auer‐Grumbach, Klaus Wagner, Vincent Timmerman, Peter De Jonghe, Hans‐Peter Hartung	2000	31
20	Screening of patients with hereditary spastic paraplegia reveals seven novel mutations in theSPG4 (Spastin) gene Human Mutation ·Christos Proukakis, Michaela Auer‐Grumbach, Klaus Wagner, P.A. Wilkinson, Evan Reid, M A Patton, Thomas T. Warner, Andrew H. Crosby	2003	25

About Klaus Wagner

Klaus Wagner is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Pediatrics, Perinatology and Child Health and Cell Biology, having authored 62 papers that have together received 2.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Hereditary Neurological Disorders (12 papers), Prenatal Screening and Diagnostics (8 papers), Cellular transport and secretion (7 papers), Cystic Fibrosis Research Advances (6 papers), Genetics and Neurodevelopmental Disorders (5 papers), Genetic Syndromes and Imprinting (5 papers) and Neurological diseases and metabolism (4 papers). The work is most often cited by research in Neurology (368 citations), Cellular and Molecular Neuroscience (827 citations), Neurology (575 citations), Genetics (404 citations) and Cell Biology (479 citations). Klaus Wagner has collaborated with scholars based in Austria, Germany and United States. Frequent co-authors include Michaela Auer‐Grumbach, Vincent Timmerman, Peter De Jonghe, Erwin Petek, Christian Windpassinger, Wolfram Hörz, Philip D. Gregory, Peter M. Kroisel, Hans‐Peter Hartung and Joy Irobi. Their work appears in journals such as Human Genetics, Clinical Genetics, The American Journal of Human Genetics, Gene and PLoS ONE.

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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