Gudrun Schreiber

1.3k total citations
17 papers, 549 citations indexed

About

Gudrun Schreiber is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Gudrun Schreiber has authored 17 papers receiving a total of 549 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Cell Biology and 3 papers in Genetics. Recurrent topics in Gudrun Schreiber's work include Muscle Physiology and Disorders (7 papers), Skin and Cellular Biology Research (3 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Gudrun Schreiber is often cited by papers focused on Muscle Physiology and Disorders (7 papers), Skin and Cellular Biology Research (3 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Gudrun Schreiber collaborates with scholars based in Germany, United States and United Kingdom. Gudrun Schreiber's co-authors include Carsten G. Bönnemann, F. Hanefeld, Ana Ferreiro, Knut Brockmann, Yaqun Zou, Pascale Richard, Michel Fardeau, Chantal Ceuterick‐de Groote, Pascale Guicheney and Hans H. Goebel and has published in prestigious journals such as Annals of Neurology, Human Molecular Genetics and Human Mutation.

In The Last Decade

Gudrun Schreiber

15 papers receiving 537 citations

Peers

Gudrun Schreiber

GENET

CCM

GENET

C. Sewry United Kingdom

R. Mein United Kingdom

Ermelinda Ceco United States

Daniel Natera‐de Benito Spain

Takahito Niiyama Japan

Justin L. Chen Australia

Alex Hennebry New Zealand

Kitipong Uaesoontrachoon United States

Brian K. Buckley United States

Anne Rochat France

C. Sewry United Kingdom

Gudrun Schreiber

382 ×1.2

67 ×0.6

32 ×0.3

GENET

122 ×1.4

CCM

69 ×0.9

GENET

Citations per year, relative to Gudrun Schreiber Gudrun Schreiber (= 1×) peers C. Sewry

Countries citing papers authored by Gudrun Schreiber

Since Specialization

Citations

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

Fields of papers citing papers by Gudrun Schreiber

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gudrun Schreiber

This figure shows the co-authorship network connecting the top 25 collaborators of Gudrun Schreiber. A scholar is included among the top collaborators of Gudrun Schreiber 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 Gudrun Schreiber. Gudrun Schreiber 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:

17 of 17 papers shown

Schreiber, Gudrun, et al.. (2023). Early Development of Spinal Deformities in Children Severely Affected with Spinal Muscular Atrophy after Gene Therapy with Onasemnogene Abeparvovec—Preliminary Results. Children. 10(6). 998–998. 12 indexed citations

Hopkinson, Mark, Juliane Heilig, Thomas Imhof, et al.. (2023). Ablation of collagen XII disturbs joint extracellular matrix organization and causes patellar subluxation. iScience. 26(7). 107225–107225. 4 indexed citations

Schmidt, Julia, Gudrun Schreiber, Janine Altmüller, et al.. (2021). Familial cleft tongue caused by a unique translation initiation codon variant in TP63. European Journal of Human Genetics. 30(2). 211–218. 5 indexed citations

Polster, Tilman, et al.. (2021). Gait Disturbance in 10-Year-Old Boy with Dravet Dyndrome, Stiripentol-associated Myopathy. Neuropediatrics.

Zou, Yaqun, Daniela Zwolanek, Yayoi Izu, et al.. (2013). Recessive and dominant mutations in COL12A1 cause a novel EDS/myopathy overlap syndrome in humans and mice. Human Molecular Genetics. 23(9). 2339–2352. 99 indexed citations

Zou, Yaqun, Daniela Zwolanek, Yanjia Hu, et al.. (2013). O.2 Collagen type XII: A new congenital matrix and muscle disease. Neuromuscular Disorders. 23(9-10). 739–740. 1 indexed citations

Schara, Ulrike, H.‐J. Christen, Hacer Durmuş, et al.. (2009). Long-term follow-up in patients with congenital myasthenic syndrome due to CHAT mutations. European Journal of Paediatric Neurology. 14(4). 326–333. 40 indexed citations

Lampe, Anne Katrin, Yaqun Zou, Kirsty O’Brien, et al.. (2008). Exon skipping mutations in collagen VI are common and are predictive for severity and inheritance. Human Mutation. 29(6). 809–822. 68 indexed citations

Schara, Ulrike, Wolfram Kreß, Carsten G. Bönnemann, et al.. (2008). The phenotype and long-term follow-up in 11 patients with juvenile selenoprotein N1-related myopathy. European Journal of Paediatric Neurology. 12(3). 224–230. 46 indexed citations

10.

Schessl, Joachim, Gudrun Schreiber, Ulrike Schara, et al.. (2008). Phenotypic variability in siblings with calpainopathy (LGMD2A).. PubMed. 27. 54–8. 12 indexed citations

11.

Schara, Ulrike, Marja Hietala, Carmelo Rodolico, et al.. (2007). G.P.10.01 Long-term follow-up in patients with congenital myasthenic syndrome due to CHAT mutations. Neuromuscular Disorders. 17(9-10). 818–818. 2 indexed citations

12.

Zou, Yaqun, Joachim Schessl, Ying Hu, et al.. (2007). C.P.2.04 Skipping of exon 16 in COL6A3 is a recurrent mutation causing severe congenital muscular dystrophy type Ullrich. Neuromuscular Disorders. 17(9-10). 844–844. 1 indexed citations

13.

Brockmann, Knut, P. E. Becker, Gudrun Schreiber, et al.. (2007). Sensitivity and specificity of qualitative muscle ultrasound in assessment of suspected neuromuscular disease in childhood. Neuromuscular Disorders. 17(7). 517–523. 54 indexed citations

14.

Brockmann, Knut, Peter Dechent, Carsten G. Bönnemann, et al.. (2006). Quantitative proton MRS of cerebral metabolites in laminin α2 chain deficiency. Brain and Development. 29(6). 357–364. 7 indexed citations

15.

Kirschner, Janbernd, Ingrid Haußer, Yaqun Zou, et al.. (2004). Ullrich congenital muscular dystrophy: Connective tissue abnormalities in the skin support overlap with Ehlers–Danlos syndromes. American Journal of Medical Genetics Part A. 132A(3). 296–301. 64 indexed citations

16.

Ferreiro, Ana, Chantal Ceuterick‐de Groote, Nathalie Goemans, et al.. (2004). Desmin‐related myopathy with mallory body–like inclusions is caused by mutations of the selenoprotein N gene. Annals of Neurology. 55(5). 676–686. 134 indexed citations

17.

Schreiber, Gudrun. (1959). [The genetics of resistance to insecticides].. PubMed. 11. 707–14.

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