Randi Koll

711 total citations
13 papers, 346 citations indexed

About

Randi Koll is a scholar working on Molecular Biology, Epidemiology and Pathology and Forensic Medicine. According to data from OpenAlex, Randi Koll has authored 13 papers receiving a total of 346 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 4 papers in Epidemiology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Randi Koll's work include Muscle Physiology and Disorders (3 papers), Inflammatory Myopathies and Dermatomyositis (3 papers) and Congenital limb and hand anomalies (2 papers). Randi Koll is often cited by papers focused on Muscle Physiology and Disorders (3 papers), Inflammatory Myopathies and Dermatomyositis (3 papers) and Congenital limb and hand anomalies (2 papers). Randi Koll collaborates with scholars based in Germany, United Kingdom and France. Randi Koll's co-authors include Eva Klopocki, Stefan Mundlos, Petra Seemann, Katarina Dathe, Marc Trimborn, Denise Horn, Pablo Villavicencio‐Lorini, Josefine Radke, Olaf Hiort and Thomy de Ravel and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and The American Journal of Human Genetics.

In The Last Decade

Randi Koll

13 papers receiving 327 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Randi Koll Germany 9 206 152 65 46 44 13 346
Philip N. Mowrey United States 11 162 0.8× 232 1.5× 56 0.9× 35 0.8× 17 0.4× 22 436
A Baxová Czechia 10 243 1.2× 246 1.6× 26 0.4× 29 0.6× 16 0.4× 40 416
Alper Gezdirici Türkiye 9 209 1.0× 129 0.8× 25 0.4× 21 0.5× 17 0.4× 55 337
Gökhan Yigit Germany 11 207 1.0× 132 0.9× 33 0.5× 40 0.9× 19 0.4× 24 355
Josef Davidsson Sweden 11 191 0.9× 165 1.1× 55 0.8× 49 1.1× 14 0.3× 16 442
Güven Toksoy Türkiye 12 185 0.9× 116 0.8× 22 0.3× 39 0.8× 15 0.3× 51 353
Vanesa López‐González Spain 15 264 1.3× 311 2.0× 36 0.6× 45 1.0× 26 0.6× 24 532
Eri Imagawa Japan 13 250 1.2× 170 1.1× 20 0.3× 13 0.3× 24 0.5× 30 418
D. Sillence Australia 10 181 0.9× 310 2.0× 22 0.3× 80 1.7× 43 1.0× 22 451
Wolfram Heinritz Germany 12 175 0.8× 104 0.7× 10 0.2× 53 1.2× 46 1.0× 28 380

Countries citing papers authored by Randi Koll

Since Specialization
Citations

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

Fields of papers citing papers by Randi Koll

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Randi Koll

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

All Works

13 of 13 papers shown
1.
Roos, Andreas, Martin Häusler, Laxmikanth Kollipara, et al.. (2024). HNRNPA1 de novo Variant Associated with Early Childhood Onset, Rapidly Progressive Generalized Myopathy. Journal of Neuromuscular Diseases. 11(5). 1131–1137. 2 indexed citations
2.
Corman, Victor M., Corinna Preuße, Olivier Benvéniste, et al.. (2023). Deep RNA sequencing of muscle tissue reveals absence of viral signatures in dermatomyositis. SHILAP Revista de lepidopterología. 5. 1–1. 1 indexed citations
3.
Radke, Josefine, Elisa Schumann, Julia Onken, et al.. (2022). Decoding molecular programs in melanoma brain metastases. Nature Communications. 13(1). 7304–7304. 13 indexed citations
4.
Preuße, Corinna, Pascale Eede, Kiara Freitag, et al.. (2021). NanoString technology distinguishes anti‐TIF‐1γ+ from anti‐Mi‐2+ dermatomyositis patients. Brain Pathology. 31(3). e12957–e12957. 13 indexed citations
5.
Radke, Josefine, Arend Koch, Elisa Schumann, et al.. (2019). Predictive MGMT status in a homogeneous cohort of IDH wildtype glioblastoma patients. Acta Neuropathologica Communications. 7(1). 89–89. 51 indexed citations
6.
Radke, Josefine, Randi Koll, Esther Gill, et al.. (2018). Autophagic vacuolar myopathy is a common feature of CLN3 disease. Annals of Clinical and Translational Neurology. 5(11). 1385–1393. 11 indexed citations
7.
Radke, Josefine, Randi Koll, Corinna Preuße, et al.. (2018). Architectural B-cell organization in skeletal muscle identifies subtypes of dermatomyositis. Neurology Neuroimmunology & Neuroinflammation. 5(3). e451–e451. 19 indexed citations
8.
Graul‐Neumann, Luitgard, Ulrike Wille, Naseebullah Kakar, et al.. (2013). Homozygous missense and nonsense mutations in BMPR1B cause acromesomelic chondrodysplasia-type Grebe. European Journal of Human Genetics. 22(6). 726–733. 19 indexed citations
9.
Villavicencio‐Lorini, Pablo, Eva Klopocki, Marc Trimborn, et al.. (2012). Phenotypic variant of Brachydactyly-mental retardation syndrome in a family with an inherited interstitial 2q37.3 microdeletion including HDAC4. European Journal of Human Genetics. 21(7). 743–748. 52 indexed citations
10.
Klopocki, Eva, Bianca P. Hennig, Katarina Dathe, et al.. (2010). Deletion and Point Mutations of PTHLH Cause Brachydactyly Type E. The American Journal of Human Genetics. 86(3). 434–439. 93 indexed citations
11.
Klopocki, Eva, Silke B. Lohan, Francesco Brancati, et al.. (2010). Copy-Number Variations Involving the IHH Locus Are Associated with Syndactyly and Craniosynostosis. The American Journal of Human Genetics. 88(1). 70–75. 67 indexed citations
12.
Koll, Randi, et al.. (1985). Mastitis non-puerperalis - eine Erkrankung mit zunehmender klinischer Relevanz?. Geburtshilfe und Frauenheilkunde. 45(1). 29–35. 4 indexed citations
13.
Koll, Randi. (1980). Report on 69 Uterine Sarcomas Treated at the University Hospital for Women Hamburg-Eppendorf during 1953–1977. Pathology - Research and Practice. 169(2). 185–191. 1 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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