Barbara Leube

3.5k total citations
27 papers, 989 citations indexed

About

Barbara Leube is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Barbara Leube has authored 27 papers receiving a total of 989 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Cellular and Molecular Neuroscience, 12 papers in Neurology and 9 papers in Molecular Biology. Recurrent topics in Barbara Leube's work include Genetic Neurodegenerative Diseases (12 papers), Neurological disorders and treatments (9 papers) and Hereditary Neurological Disorders (4 papers). Barbara Leube is often cited by papers focused on Genetic Neurodegenerative Diseases (12 papers), Neurological disorders and treatments (9 papers) and Hereditary Neurological Disorders (4 papers). Barbara Leube collaborates with scholars based in Germany, United States and United Kingdom. Barbara Leube's co-authors include Georg Auburger, Elisabeth Falkenstein, Martin Wehling, Dirk Gerdes, Kirn R. Kessler, Brigitte Royer‐Pokora, R. Benecke, R. Benecke, Timm O. Goecke and R. Benecke and has published in prestigious journals such as PLoS ONE, Annals of Neurology and Human Molecular Genetics.

In The Last Decade

Barbara Leube

26 papers receiving 961 citations

Peers

Barbara Leube
Vı́ctor Volpini Spain
Pieter J.L.M. Snijders Netherlands
Robyn Labrum United Kingdom
Hidetoshi Date Japan
Barry A. Chioza United Kingdom
Hiroyuki Morino Japan
Laura Davis Keppen United States
Martin Kann Germany
Francesca Madia Italy
Norman Kock Germany
Vı́ctor Volpini Spain
Barbara Leube
Citations per year, relative to Barbara Leube Barbara Leube (= 1×) peers Vı́ctor Volpini

Countries citing papers authored by Barbara Leube

Since Specialization
Citations

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

Fields of papers citing papers by Barbara Leube

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Barbara Leube

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

All Works

20 of 20 papers shown
1.
Beier, Manfred, Barbara Leube, Carmen de Torres, et al.. (2016). Establishment of a Conditionally Immortalized Wilms Tumor Cell Line with a Homozygous WT1 Deletion within a Heterozygous 11p13 Deletion and UPD Limited to 11p15. PLoS ONE. 11(5). e0155561–e0155561. 6 indexed citations
2.
Kummer, Sebastian, et al.. (2013). Synergistic mutations in SLC3A1 and SLC7A9 leading to heterogeneous cystinuria phenotypes: pitfalls in the diagnostic workup. Pediatric Nephrology. 29(1). 155–159. 4 indexed citations
3.
Xiao, Jianfeng, Ryan J. Uitti, Yu Zhao, et al.. (2012). Mutations in CIZ1 cause adult onset primary cervical dystonia. Annals of Neurology. 71(4). 458–469. 96 indexed citations
4.
Winter, Pia, Christoph Kamm, Saskia Biskup, et al.. (2012). DYT7 gene locus for cervical dystonia on chromosome 18p is questionable. Movement Disorders. 27(14). 1820–1822. 13 indexed citations
5.
Engels, Hartmut, Herdit M. Schüler, Alexander M. Zink, et al.. (2012). A phenotype map for 14q32.3 terminal deletions. American Journal of Medical Genetics Part A. 158A(4). 695–706. 24 indexed citations
6.
Leube, Barbara, Karin Hardt, Bettina Westhoff, et al.. (2008). Ulna/Height Ratio as Clinical Parameter Separating EXT1 from EXT2 Families?. Genetic Testing. 12(1). 129–133. 5 indexed citations
7.
Jäger, Markus, Bettina Westhoff, Barbara Leube, et al.. (2007). Clinical outcome and genotype in patients with hereditary multiple exostoses. Journal of Orthopaedic Research®. 25(12). 1541–1551. 35 indexed citations
8.
Steinberger, Daniela, et al.. (2006). Utility of MLPA in deletion analysis of GCH1 in dopa-responsive dystonia. Neurogenetics. 8(1). 51–55. 21 indexed citations
9.
Leube, Barbara, Frank Majewski, Matthias Drechsler, & Brigitte Royer‐Pokora. (2003). Unbalanced cryptic translocation der(14)t(9;14)(q34.3;q32.33) identified by subtelomeric FISH. Clinical Dysmorphology. 12(4). 261–265. 5 indexed citations
10.
Leube, Barbara, et al.. (2003). Clinical, cytogenetic, and molecular observations in a patient with Pallister‐Killian‐syndrome with an unusual karyotype. American Journal of Medical Genetics Part A. 123A(3). 296–300. 19 indexed citations
11.
Leube, Barbara, Matthias Drechsler, Reinhold Schäfer, et al.. (2002). Refined mapping of allele loss at chromosome 10q23‐26 in prostate cancer. The Prostate. 50(3). 135–144. 31 indexed citations
12.
Voït, Thomas, Barbara Leube, Eva Neuen-Jacob, et al.. (2001). Autosomal dominant distal myopathy: further evidence of a chromosome 14 locus. Neuromuscular Disorders. 11(1). 11–19. 39 indexed citations
13.
Leube, Barbara, Kirn R. Kessler, A. Ferbert, et al.. (1999). Phenotypic variability of the DYT1 mutation in German dystonia patients. Acta Neurologica Scandinavica. 99(4). 248–251. 33 indexed citations
14.
Jarman, Paul, N. Del Grosso, Enza Maria Valente, et al.. (1999). Primary torsion dystonia: the search for genes is not over. Journal of Neurology Neurosurgery & Psychiatry. 67(3). 395–397. 34 indexed citations
15.
Gerdes, Dirk, Martin Wehling, Barbara Leube, & Elisabeth Falkenstein. (1998). Short Communication. Biological Chemistry. 379(7). 907–930. 166 indexed citations
16.
Leube, Barbara, Kirn R. Kessler, Timm O. Goecke, Georg Auburger, & R. Benecke. (1997). Frequency of familial inheritance among 488 index patients with idiopathic focal dystonia and clinical variability in a large family. Movement Disorders. 12(6). 1000–1006. 63 indexed citations
17.
Leube, Barbara, et al.. (1997). Evidence for DYT7 being a common cause of cervical dystonia (torticollis) in Central Europe. American Journal of Medical Genetics. 74(5). 529–532. 35 indexed citations
18.
Leube, Barbara, et al.. (1997). Sporadic focal dystonia in Northwest Germany: Molecular basis on chromosome 18p. Annals of Neurology. 42(1). 111–114. 39 indexed citations
19.
20.

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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