Klaus Wagner

4.8k total citations · 1 hit paper
61 papers, 2.9k citations indexed

About

Klaus Wagner is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Klaus Wagner has authored 61 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 19 papers in Genetics and 13 papers in Cellular and Molecular Neuroscience. Recurrent topics in Klaus Wagner's work include Genomic variations and chromosomal abnormalities (13 papers), Hereditary Neurological Disorders (12 papers) and Cellular transport and secretion (7 papers). Klaus Wagner is often cited by papers focused on Genomic variations and chromosomal abnormalities (13 papers), Hereditary Neurological Disorders (12 papers) and Cellular transport and secretion (7 papers). Klaus Wagner collaborates with scholars based in Austria, Germany and United States. Klaus Wagner's 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 and has published in prestigious journals such as The Lancet, Nucleic Acids Research and Nature Genetics.

In The Last Decade

Klaus Wagner

61 papers receiving 2.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

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

2004 602 citations Marina Kennerson, Garth A. Nicholson et al. profile →

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-authorship network of co-authors of Klaus Wagner

This figure shows the co-authorship network connecting the top 25 collaborators of Klaus Wagner. A scholar is included among the top collaborators of Klaus Wagner 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 Klaus Wagner. Klaus Wagner 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	Association of BRCA1/2 mutations with FMR1 genotypes: Effects on menarcheal and menopausal age 2013 ·Maturitas ·Muy‐Kheng M. Tea, Andrea Weghofer, Klaus Wagner, Christian F. Singer	12
2	Four and a Half LIM Protein 1C (FHL1C): A Binding Partner for Voltage-Gated Potassium Channel Kv1.5 2011 ·PLoS ONE ·(unknown), Wolfgang Schreibmayer, Benedikt Schoser, Gernot Desoyé, (unknown), (unknown), Sonja Hochmeister, Josepha Binder, Stefan Quasthoff, Klaus Wagner, Christian Windpassinger, Ernst Malle	10
3	Nijmegen breakage syndrome (NBS) due to maternal isodisomy of chromosome 8 2006 ·American Journal of Medical Genetics Part A ·Raymonda Varon, (unknown), Klaus Wagner, (unknown), (unknown), (unknown), Erwin Petek, Holger Tönnies, (unknown), Karl Sperling, Peter M. Kroisel	7
4	Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome 2006 ·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	46
5	Phenotypic and molecular characterisation of a de novo 5q deletion that includes the APC gene 2005 ·Journal of Human Genetics ·(unknown), Jochen Raedle, Christian Windpassinger, Thomas Schwarzbraun, Peter M. Kroisel, Klaus Wagner, Erwin Petek	10
6	Cloning, genomic structure, and expression profiles of TULIP1 (GARNL1), a brain-expressed candidate gene for 14q13-linked neurological phenotypes, and its murine homologue 2004 ·Genomics ·Thomas Schwarzbraun, John B. Vincent, Axel Schumacher, Daniel H. Geschwind, João Ricardo Mendes de Oliveira, Christian Windpassinger, (unknown), (unknown), Peter M. Kroisel, Klaus Wagner, Erwin Petek	20
7	Refinement of the "Silver syndrome locus" on chromosome 11q12-q14 in four families and exclusion of eight candidate genes 2003 ·Human Genetics ·Christian Windpassinger, Klaus Wagner, Erwin Petek, Renate Fischer, Michaela Auer‐Grumbach	31
8	Autosomal Dominant Inherited Neuropathies With Prominent Sensory Loss and Mutilations 2003 ·Archives of Neurology ·Michaela Auer‐Grumbach, Peter De Jonghe, Kristien Verhoeven, Vincent Timmerman, Klaus Wagner, Hans‐Peter Hartung, Garth A. Nicholson	62
9	Exclusion of serine palmitoyltransferase long chain base subunit 2 (SPTLC2) as a common cause for hereditary sensory neuropathy 2002 ·Neuromuscular Disorders ·Jennifer L. Dawkins, Sonal Brahmbhatt, Michaela Auer‐Grumbach, Klaus Wagner, Hans-Peter Hartung, Kristien Verhoeven, Vincent Timmerman, Peter De Jonghe, Marina Kennerson, Éric Leguern, Garth A. Nicholson	19
10	The human γ-aminobutyric acid A receptor delta (GABRD) gene: molecular characterisation and tissue-specific expression 2002 ·Gene ·Christian Windpassinger, Peter M. Kroisel, Klaus Wagner, Erwin Petek	53
11	Chronic myeloid leukemia with a rare variant Philadelphia translocation 2001 ·Cancer Genetics and Cytogenetics ·(unknown), A. Behmel, (unknown), H. L. Seewann, Erwin Petek, Peter M. Kroisel, Klaus Wagner	10
12	Histone Acetylation and Chromatin Remodeling 2001 ·Experimental Cell Research ·Philip D. Gregory, Klaus Wagner, Wolfram Hörz	216
13	Maternal methylation imprints on human chromosome 15 are established during or after fertilization 2001 ·Nature Genetics ·Osman El‐Maarri, Karin Buiting, (unknown), Peter M. Kroisel, Başak Balaban, Klaus Wagner, Bülent Urman, (unknown), Christina Lich, Camilynn I. Brannan, Jörn Walter, Bernhard Horsthemke	159
14	Identification of New Regulatory Sequences Far Upstream of the Mouse Monocyte Chemoattractant Protein-1 Gene 2001 ·Genomics ·Klaus Wagner, U Dendorfer, Silvia Chilla, Detlef Schlöndorff, Bruno Luckow	8
15	Clinical predominance of proximal upper limb weakness in CMT1A syndrome 2000 ·Muscle & Nerve ·Michaela Auer‐Grumbach, Klaus Wagner, Siegrid Strasser‐Fuchs, (unknown), Franz Fazekas, Michael Millner, Hans-Peter Hartung	13
16	Prenatal diagnosis of partial trisomy 4q26-qter and monosomy for the Wolf-Hirschhorn critical region in a fetus with split hand malformation 2000 ·Prenatal Diagnosis ·Erwin Petek, Klaus Wagner, H. Steiner, (unknown), Peter M. Kroisel	14
17	A rapid and efficient PCR approach for the generation of direct-labeled DNA probes for FISH analysis 1999 ·Erwin Petek, Klaus Wagner	1
18	Roussy–Lévy syndrome is a phenotypic variant of Charcot–Marie–Tooth syndrome IA associated with a duplication on chromosome 17p11.2 1998 ·Journal of the Neurological Sciences ·Michaela Auer‐Grumbach, Siegrid Strasser‐Fuchs, Klaus Wagner, (unknown), Franz Fazekas	21
19	A Taql RFLP detected by the probe TN157 (D7S145) at the human chromosome region 7p13 – 14.2 1991 ·Nucleic Acids Research ·Klaus Wagner, Peter M. Kroisel, W Rosenkranz	3
20	The human pregnancy-specific glycoprotein genes are tightly linked on the long arm of chromosome 19 and are coordinately expressed 1990 ·Biochemical and Biophysical Research Communications ·John R. Thompson, (unknown), Klaus Wagner, Sabine Barnert, (unknown), Heinrich Schrewe, Wolfgang Zimmermann, (unknown), W. Schempp, (unknown), (unknown), Norman Hardman	52

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