Katrin Koehler

2.3k total citations
52 papers, 1.3k citations indexed

About

Katrin Koehler is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Katrin Koehler has authored 52 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 10 papers in Genetics and 9 papers in Cell Biology. Recurrent topics in Katrin Koehler's work include Nuclear Structure and Function (21 papers), RNA regulation and disease (14 papers) and Neurogenetic and Muscular Disorders Research (7 papers). Katrin Koehler is often cited by papers focused on Nuclear Structure and Function (21 papers), RNA regulation and disease (14 papers) and Neurogenetic and Muscular Disorders Research (7 papers). Katrin Koehler collaborates with scholars based in Germany, United Kingdom and Croatia. Katrin Koehler's co-authors include Angela Huebner, Manuela Krumbholz, Barbara Kind, Birgit Nickel, Molly Przeworski, David A. Hinds, Susan E. Ptak, Nila Patil, Kelly A. Frazer and Svante Pääbo and has published in prestigious journals such as Nature Genetics, PLoS ONE and Molecular and Cellular Biology.

In The Last Decade

Katrin Koehler

51 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Katrin Koehler Germany 19 873 333 196 193 148 52 1.3k
Andrew Dearlove United Kingdom 13 846 1.0× 223 0.7× 86 0.4× 118 0.6× 218 1.5× 17 1.9k
June Davies United Kingdom 14 770 0.9× 1.3k 3.8× 60 0.3× 609 3.2× 57 0.4× 18 2.1k
Gurbax S. Sekhon United States 17 596 0.7× 522 1.6× 68 0.3× 71 0.4× 68 0.5× 42 1.1k
Mark E. Samuels Canada 21 615 0.7× 412 1.2× 30 0.2× 135 0.7× 98 0.7× 41 1.2k
Idan Cohen Israel 18 669 0.8× 173 0.5× 33 0.2× 58 0.3× 189 1.3× 34 1.0k
Ortal Barel Israel 15 450 0.5× 247 0.7× 68 0.3× 104 0.5× 58 0.4× 63 868
Dorota Monies Saudi Arabia 22 579 0.7× 507 1.5× 25 0.1× 109 0.6× 70 0.5× 48 1.3k
L. A. Sandkuyl Netherlands 18 550 0.6× 297 0.9× 61 0.3× 111 0.6× 56 0.4× 29 1.1k
Carol Saunders United States 22 744 0.9× 635 1.9× 119 0.6× 72 0.4× 95 0.6× 59 1.3k
Louise Tee United Kingdom 18 801 0.9× 781 2.3× 19 0.1× 78 0.4× 83 0.6× 31 1.5k

Countries citing papers authored by Katrin Koehler

Since Specialization
Citations

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

Fields of papers citing papers by Katrin Koehler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katrin Koehler

This figure shows the co-authorship network connecting the top 25 collaborators of Katrin Koehler. A scholar is included among the top collaborators of Katrin Koehler 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 Katrin Koehler. Katrin Koehler 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.
Schubert, Tina, Ronald Naumann, Ilka Reichardt, et al.. (2024). A Humanized and Viable Animal Model for Congenital Adrenal Hyperplasia–CYP21A2-R484Q Mutant Mouse. International Journal of Molecular Sciences. 25(10). 5062–5062. 2 indexed citations
2.
Heinrichs, Claudine, Katrin Koehler, Angela Huebner, et al.. (2024). Fertility and sexual activity in patients with Triple A syndrome. Frontiers in Endocrinology. 15. 1357084–1357084. 1 indexed citations
3.
Mitrović, Katarina, Rade Vuković, Tatjana Milenković, et al.. (2024). Very early and severe presentation of Triple A syndrome – case report and review of the literature. Frontiers in Endocrinology. 15. 1431383–1431383.
4.
Schubert, Tina, Nicole Reisch, Ronald Naumann, et al.. (2022). CYP21A2 Gene Expression in a Humanized 21-Hydroxylase Mouse Model Does Not Affect Adrenocortical Morphology and Function. Journal of the Endocrine Society. 6(6). bvac062–bvac062. 5 indexed citations
5.
Jühlen, Ramona, et al.. (2018). Compensation for chronic oxidative stress in ALADIN null mice. Biology Open. 7(1). 3 indexed citations
6.
Stevense, Michelle, Katrin Koehler, Ronald Naumann, et al.. (2017). ALADIN is required for the production of fertile mouse oocytes. Molecular Biology of the Cell. 28(19). 2470–2478. 12 indexed citations
7.
Jühlen, Ramona, et al.. (2016). Identification of a novel putative interaction partner of the nucleoporin ALADIN. Biology Open. 5(11). 1697–1705. 17 indexed citations
8.
Canaud, Bernard, Katrin Koehler, Sudhir K. Bowry, & Stefano Stuard. (2016). What Is the Optimal Target Convective Volume in On-Line Hemodiafiltration Therapy?. Contributions to nephrology. 189. 9–16. 22 indexed citations
9.
Dumić, Miroslav, Nataša Rojnić Putarek, Vesna Kuŝec, et al.. (2015). Low bone mineral density for age/osteoporosis in triple A syndrome—an overlooked symptom of unexplained etiology. Osteoporosis International. 27(2). 521–526. 6 indexed citations
10.
Kind, Barbara, et al.. (2010). Intracellular ROS level is increased in fibroblasts of triple A syndrome patients. Journal of Molecular Medicine. 88(12). 1233–1242. 24 indexed citations
11.
Milenković, Tatjana, Dragan Zdravković, Sladjana Todorovic, et al.. (2010). Triple A syndrome: 32 years experience of a single centre (1977–2008). European Journal of Pediatrics. 169(11). 1323–1328. 42 indexed citations
12.
Koehler, Katrin, et al.. (2010). Two Patients with an Identical Novel Mutation in the AAAS Gene and Similar Phenotype of Triple A (Allgrove) Syndrome. Experimental and Clinical Endocrinology & Diabetes. 118(8). 530–536. 6 indexed citations
13.
Kind, Barbara, Katrin Koehler, Mike Lorenz, & Angela Huebner. (2009). The nuclear pore complex protein ALADIN is anchored via NDC1 but not via POM121 and GP210 in the nuclear envelope. Biochemical and Biophysical Research Communications. 390(2). 205–210. 36 indexed citations
14.
Toromanović, Alma, Husref Tahirović, Tatjana Milenković, et al.. (2008). Clinical and molecular genetic findings in a 6-year-old Bosnian boy with triple A syndrome. European Journal of Pediatrics. 168(3). 317–320. 11 indexed citations
15.
Mazur, Artur, et al.. (2008). Familial Glucocorticoid Deficiency Type 1 due to a Novel Compound Heterozygous <i>MC2R</i> Mutation. Hormone Research in Paediatrics. 69(6). 363–368. 8 indexed citations
16.
Keegan, Catherine E., Janna Hutz, Katrin Koehler, et al.. (2007). Novel polymorphisms and lack of mutations in the ACD gene in patients with ACTH resistance syndromes. Clinical Endocrinology. 67(2). 168–174. 2 indexed citations
17.
Hagen, Maja von der, et al.. (2005). Limb girdle muscular dystrophy type 2I caused by a novel missense mutation in the FKRP gene presenting as acute virus-associated myositis in infancy. European Journal of Pediatrics. 165(1). 62–63. 7 indexed citations
18.
Hagen, Maja von der, Angela M. Kaindl, Katrin Koehler, et al.. (2005). Facing the genetic heterogeneity in neuromuscular disorders: Linkage analysis as an economic diagnostic approach towards the molecular diagnosis. Neuromuscular Disorders. 16(1). 4–13. 16 indexed citations
19.
Kaindl, Angela M., Sibylle Jakubiczka, Thomas Lücke, et al.. (2005). Homozygous microdeletion of chromosome 4q11-q12 causes severe limb-girdle muscular dystrophy type 2E with joint hyperlaxity and contractures. Human Mutation. 26(3). 279–280. 13 indexed citations
20.
Huebner, Angela, Angela M. Kaindl, Klaus‐Peter Knobeloch, et al.. (2004). The Triple A Syndrome Is Due to Mutations in ALADIN, a Novel Member of the Nuclear Pore Complex. Endocrine Research. 30(4). 891–899. 52 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Andrew Dearlove Breakdown of academic impact, for papers by June Davies Breakdown of academic impact, for papers by Gurbax S. Sekhon Breakdown of academic impact, for papers by Mark E. Samuels Breakdown of academic impact, for papers by Idan Cohen Breakdown of academic impact, for papers by Ortal Barel Breakdown of academic impact, for papers by Dorota Monies Breakdown of academic impact, for papers by L. A. Sandkuyl Breakdown of academic impact, for papers by Carol Saunders Breakdown of academic impact, for papers by Louise Tee
Rankless by CCL
2026