Cornelia Köhler

624 total citations
19 papers, 184 citations indexed

About

Cornelia Köhler is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Cornelia Köhler has authored 19 papers receiving a total of 184 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 5 papers in Genetics and 5 papers in Genetics. Recurrent topics in Cornelia Köhler's work include RNA modifications and cancer (6 papers), Muscle Physiology and Disorders (5 papers) and Neurogenetic and Muscular Disorders Research (5 papers). Cornelia Köhler is often cited by papers focused on RNA modifications and cancer (6 papers), Muscle Physiology and Disorders (5 papers) and Neurogenetic and Muscular Disorders Research (5 papers). Cornelia Köhler collaborates with scholars based in Germany, Austria and United Kingdom. Cornelia Köhler's co-authors include Thomas Lücke, Ulrike Schara, Matthias Vorgerd, Sabine Hoffjan, Christoph M. Heyer, Charlotte Thiels, Arslan Arinc Kayacelebi, Eberhard Varenhorst, Oliver Schwartz and Wolfgang Müller‐Felber and has published in prestigious journals such as International Journal of Molecular Sciences, Amino Acids and Viruses.

In The Last Decade

Cornelia Köhler

18 papers receiving 181 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cornelia Köhler Germany 9 108 44 41 34 22 19 184
Pouria Mashouri Canada 6 118 1.1× 16 0.4× 85 2.1× 15 0.4× 12 0.5× 10 201
Cristina Curcio Italy 9 135 1.3× 45 1.0× 79 1.9× 17 0.5× 8 0.4× 25 300
Jing-Jing Ji China 9 93 0.9× 12 0.3× 13 0.3× 17 0.5× 18 0.8× 15 204
Shakti Sagar India 9 177 1.6× 11 0.3× 9 0.2× 11 0.3× 14 0.6× 16 277
Norman Barker United States 7 127 1.2× 27 0.6× 18 0.4× 16 0.5× 36 1.6× 14 249
Michele Zerah United States 10 152 1.4× 25 0.6× 100 2.4× 115 3.4× 7 0.3× 13 322
Alexandra Quezada United States 6 116 1.1× 7 0.2× 15 0.4× 28 0.8× 19 0.9× 9 302
Sarah Groves United Kingdom 4 250 2.3× 8 0.2× 55 1.3× 15 0.4× 42 1.9× 8 334
Carole Kubjak Belgium 6 95 0.9× 7 0.2× 11 0.3× 33 1.0× 25 1.1× 8 344
Ignacio Ramírez‐Pardo Spain 7 153 1.4× 20 0.5× 11 0.3× 14 0.4× 4 0.2× 8 238

Countries citing papers authored by Cornelia Köhler

Since Specialization
Citations

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

Fields of papers citing papers by Cornelia Köhler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cornelia Köhler

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

All Works

19 of 19 papers shown
1.
Trollmann, Regina, Jessika Johannsen, Katharina Vill, et al.. (2024). Postnatal management of preterm infants with spinal muscular atrophy: experience from German newborn screening. Orphanet Journal of Rare Diseases. 19(1). 353–353. 2 indexed citations
2.
3.
Hoffjan, Sabine, Wanda M. Gerding, Kristina Döring, et al.. (2023). Exome Sequencing and Optical Genome Mapping in Molecularly Unsolved Cases of Duchenne Muscular Dystrophy: Identification of a Causative X-Chromosomal Inversion Disrupting the DMD Gene. International Journal of Molecular Sciences. 24(19). 14716–14716. 9 indexed citations
4.
Hoffjan, Sabine, Cornelia Köhler, Thomas Lücke, et al.. (2022). Homozygous Inversion on Chromosome 13 Involving SGCG Detected by Short Read Whole Genome Sequencing in a Patient Suffering from Limb-Girdle Muscular Dystrophy. Genes. 13(10). 1752–1752. 3 indexed citations
5.
Wang, Xiaoyan, Wenli Zhang, Cornelia Köhler, et al.. (2022). Seroprevalence of Binding and Neutralizing Antibodies against 39 Human Adenovirus Types in Patients with Neuromuscular Disorders. Viruses. 15(1). 79–79. 8 indexed citations
6.
Blaschek, Astrid, Heike Kölbel, Oliver Schwartz, et al.. (2022). Newborn Screening for SMA – Can a Wait-and-See Strategy be Responsibly Justified in Patients With Four SMN2 Copies?. Journal of Neuromuscular Diseases. 9(5). 597–605. 20 indexed citations
7.
Ziegler, Andreas, Ekkehard Wilichowski, Ulrike Schara, et al.. (2020). Handlungsempfehlungen zur Gentherapie der spinalen Muskelatrophie mit Onasemnogene Abeparvovec – AVXS-101. Der Nervenarzt. 91(6). 518–529. 19 indexed citations
8.
Hahn, Andreas, Cornelia Köhler, Sascha Meyer, et al.. (2020). Expertenempfehlung: Therapie nichtgehfähiger Patienten mit Muskeldystrophie Duchenne. Der Nervenarzt. 92(4). 359–366. 4 indexed citations
9.
10.
Köhler, Cornelia, et al.. (2019). Videos for embryology teaching, power and weakness of an innovative tool. Morphologie. 103(341). 72–79. 6 indexed citations
11.
Dekomien, Gabriele, Thomas Lücke, Matthias Vorgerd, et al.. (2018). Novel Nonsense Mutation in SLC39A13 Initially Presenting as Myopathy: Case Report and Review of the Literature. Molecular Syndromology. 9(2). 100–109. 14 indexed citations
12.
Yoon, Moon Soo, et al.. (2017). Plasmapheresis as at Treatment Option in Anti-MOG–Related Neurological Disorders with Fulminant Progress. Neuropediatrics. 48(S 01). S1–S45. 1 indexed citations
13.
Grigull, Lorenz, Susanne Petri, Katja Kollewe, et al.. (2016). Diagnostic support for selected neuromuscular diseases using answer-pattern recognition and data mining techniques: a proof of concept multicenter prospective trial. BMC Medical Informatics and Decision Making. 16(1). 31–31. 17 indexed citations
14.
Köhler, Cornelia, Christoph M. Heyer, Sabine Hoffjan, et al.. (2015). Early-onset leukoencephalopathy due to a homozygous missense mutation in the DARS2 gene. Molecular and Cellular Probes. 29(5). 319–322. 14 indexed citations
15.
Chobanyan-Jürgens, Kristine, Cornelia Köhler, Ulrike Schara, et al.. (2015). The l-arginine/NO pathway and homoarginine are altered in Duchenne muscular dystrophy and improved by glucocorticoids. Amino Acids. 47(9). 1853–1863. 34 indexed citations
16.
Köhler, Cornelia, Charlotte Thiels, Sabine Hoffjan, et al.. (2015). Infantile Manifestation of a Mitochondriopathy due to a Homozygous Mutation in DARS2 Gene. Neuropediatrics. 46(S 01). 1 indexed citations
17.
Thiels, Charlotte, Cornelia Köhler, Matthias Vorgerd, et al.. (2014). Long Survival in Leigh Syndrome: New Cases and Review of Literature. Neuropediatrics. 45(6). 346–353. 18 indexed citations
18.
Peters, Sören, Cornelia Köhler, Ulrike Schara, et al.. (2008). Myopathien im Kindesalter - Evaluation mittels Kernspintomografie der Muskulatur. Klinische Pädiatrie. 220(1). 37–46. 8 indexed citations
19.
Köhler, Cornelia & Eberhard Varenhorst. (1999). [Microscopic hematuria in adults--a diagnostic dilemma. Scientific guidelines for management are not available according to a review of the literature].. PubMed. 96(45). 4911–6. 5 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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