Gabriele Dekomien

1.7k total citations
65 papers, 1.1k citations indexed

About

Gabriele Dekomien is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Gabriele Dekomien has authored 65 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 13 papers in Genetics and 12 papers in Cellular and Molecular Neuroscience. Recurrent topics in Gabriele Dekomien's work include Retinal Development and Disorders (16 papers), Neurological diseases and metabolism (8 papers) and Muscle Physiology and Disorders (7 papers). Gabriele Dekomien is often cited by papers focused on Retinal Development and Disorders (16 papers), Neurological diseases and metabolism (8 papers) and Muscle Physiology and Disorders (7 papers). Gabriele Dekomien collaborates with scholars based in Germany, Norway and United Kingdom. Gabriele Dekomien's co-authors include Jörg T. Epplen, Sabine Hoffjan, Wanda M. Gerding, Maren Runte, Denis A. Akkad, Martin Kurz, Jan Larsen, Elisabeth Petrasch‐Parwez, Dag Aarsland and Volker Straub and has published in prestigious journals such as PLoS ONE, Neurology and Pain.

In The Last Decade

Gabriele Dekomien

65 papers receiving 1.0k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Gabriele Dekomien Germany 21 586 301 186 134 119 65 1.1k
Isabelle Schrauwen United States 25 690 1.2× 336 1.1× 92 0.5× 94 0.7× 75 0.6× 105 1.8k
Hossein Darvish Iran 18 609 1.0× 332 1.1× 270 1.5× 208 1.6× 259 2.2× 96 1.3k
Dominique Baas France 22 871 1.5× 450 1.5× 168 0.9× 153 1.1× 36 0.3× 36 1.5k
Janine Davis United States 17 959 1.6× 245 0.8× 270 1.5× 114 0.9× 68 0.6× 23 1.6k
Benjamin K. August United States 19 717 1.2× 138 0.5× 153 0.8× 164 1.2× 32 0.3× 40 1.5k
Tarja Joensuu Finland 19 670 1.1× 344 1.1× 158 0.8× 261 1.9× 141 1.2× 31 1.3k
Jacquie Greenberg South Africa 18 927 1.6× 187 0.6× 575 3.1× 135 1.0× 244 2.1× 44 1.3k
Karl B. Shpargel United States 23 1.9k 3.2× 332 1.1× 116 0.6× 87 0.6× 71 0.6× 28 2.6k
Tomohide Goto Japan 18 602 1.0× 165 0.5× 328 1.8× 159 1.2× 101 0.8× 67 1.3k
Rick A. Friedman United States 25 661 1.1× 109 0.4× 127 0.7× 102 0.8× 137 1.2× 53 1.7k

Countries citing papers authored by Gabriele Dekomien

Since Specialization
Citations

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

Fields of papers citing papers by Gabriele Dekomien

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gabriele Dekomien

This figure shows the co-authorship network connecting the top 25 collaborators of Gabriele Dekomien. A scholar is included among the top collaborators of Gabriele Dekomien 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 Gabriele Dekomien. Gabriele Dekomien 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.
2.
Hoffjan, Sabine, et al.. (2016). WDR45 mutations in Rett (-like) syndrome and developmental delay: Case report and an appraisal of the literature. Molecular and Cellular Probes. 30(1). 44–49. 30 indexed citations
3.
Prejbisz, Aleksander, Lorenz Sellin, Magdalena Woznowski, et al.. (2015). Smaller caliber renal arteries are a novel feature of uromodulin-associated kidney disease. Kidney International. 88(1). 160–166. 4 indexed citations
4.
Hoffjan, Sabine, et al.. (2015). Mutational analysis of the CYP7B1, PNPLA6 and C19orf12 genes in autosomal recessive hereditary spastic paraplegia. Molecular and Cellular Probes. 30(1). 53–55. 2 indexed citations
5.
Dekomien, Gabriele, et al.. (2015). Analysis of the C19orf12 and WDR45 genes in patients with neurodegeneration with brain iron accumulation. Journal of the Neurological Sciences. 349(1-2). 105–109. 24 indexed citations
6.
Dekomien, Gabriele, Kristl G. Claeys, Maja von der Hagen, et al.. (2015). Two novel nebulin variants in an adult patient with congenital nemaline myopathy. Neuromuscular Disorders. 25(5). 392–396. 3 indexed citations
7.
Hoffjan, Sabine, et al.. (2014). Point mutation frequency in the FMR1 gene as revealed by fragile X syndrome screening. Molecular and Cellular Probes. 28(5-6). 279–283. 35 indexed citations
8.
Gerding, Wanda M., Andreia Marques, Jenny Atorf, et al.. (2011). Ccdc66 null mutation causes retinal degeneration and dysfunction. Human Molecular Genetics. 20(18). 3620–3631. 32 indexed citations
9.
Gerding, Wanda M., S. Schreiber, Gabriele Dekomien, & Jörg T. Epplen. (2010). Tracing the origin of ‘blue Weimaraner’ dogs by molecular genetics. Journal of Animal Breeding and Genetics. 128(2). 153–160. 2 indexed citations
10.
Streitberger, Konrad, et al.. (2010). On ancestors of dog breeds with focus on Weimaraner hunting dogs. Journal of Animal Breeding and Genetics. 128(1). 64–72. 8 indexed citations
11.
Dekomien, Gabriele, et al.. (2008). Detecting copy number variations in autosomal recessive limb-girdle muscular dystrophies using a multiplex ligation-dependent probe amplification (MLPA) assay. Molecular and Cellular Probes. 23(1). 55–59. 14 indexed citations
12.
Klinge, Lars, Gabriele Dekomien, Richard Charlton, et al.. (2008). Sarcoglycanopathies: Can muscle immunoanalysis predict the genotype?. Neuromuscular Disorders. 18(12). 934–941. 42 indexed citations
13.
Kurz, Martin, Anna Melissa Schlitter, Thomas Mueller, et al.. (2007). FMR1 Alleles in Parkinson's Disease: Relation to Cognitive Decline and Hallucinations, A Longitudinal Study. Journal of Geriatric Psychiatry and Neurology. 20(2). 89–92. 32 indexed citations
14.
Vonend, Oliver, Nikolaus Büchner, Gabriele Dekomien, et al.. (2007). A German family with glucocorticoid-remediable aldosteronism. Nephrology Dialysis Transplantation. 22(4). 1123–1130. 14 indexed citations
15.
Rommel, O., Rudolf A. Kley, Gabriele Dekomien, et al.. (2006). Muscle pain in myophosphorylase deficiency (McArdle’s disease): The role of gender, genotype, and pain-related coping. Pain. 124(3). 295–304. 23 indexed citations
16.
Felderbauer, Peter, Wolfram Klein, Kerem Bulut, et al.. (2005). Mutations in the calcium-sensing receptor: A new genetic risk factor for chronic pancreatitis?. Scandinavian Journal of Gastroenterology. 41(3). 343–348. 51 indexed citations
17.
Dekomien, Gabriele, Beate Schlotter‐Weigel, Peter Reilich, et al.. (2004). Respiratory insufficiency as a presenting symptom of LGMD2D in adulthood.. PubMed. 23(1). 1–5. 13 indexed citations
18.
Dekomien, Gabriele & Jörg T. Epplen. (2002). Screening of the arrestin gene in dogs afflicted with generalized progressive retinal atrophy. BMC Genetics. 3(1). 12–12. 2 indexed citations
19.
Dekomien, Gabriele, et al.. (2000). Generalized progressive retinal atrophy of Sloughi dogs is due to an 8-bp insertion in exon 21 of the PDE6B gene. Cytogenetic and Genome Research. 90(3-4). 261–267. 56 indexed citations
20.
Klein, Wolfram, Gabriele Dekomien, N. G. Holmes, & Jörg T. Epplen. (1998). Evaluation of ROM1 as a candidate gene in generalised progressive retinal atrophy in dogs. Animal Genetics. 29(4). 316–318. 3 indexed citations

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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