Katharina Löhner

868 total citations
5 papers, 137 citations indexed

About

Katharina Löhner is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Katharina Löhner has authored 5 papers receiving a total of 137 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 2 papers in Oncology and 2 papers in Genetics. Recurrent topics in Katharina Löhner's work include RNA modifications and cancer (2 papers), Peptidase Inhibition and Analysis (2 papers) and Protein Tyrosine Phosphatases (1 paper). Katharina Löhner is often cited by papers focused on RNA modifications and cancer (2 papers), Peptidase Inhibition and Analysis (2 papers) and Protein Tyrosine Phosphatases (1 paper). Katharina Löhner collaborates with scholars based in Netherlands, United States and Denmark. Katharina Löhner's co-authors include Patrick Rump, Wilhelmina S. Kerstjens‐Frederikse, Conny M.A. van Ravenswaaij‐Arts, Klasien A. Bergman, Cleo C. van Diemen, Irene M. van Langen, Jan D.H. Jongbloed, Cisca Wijmenga, Morris A. Swertz and Birgit Sikkema‐Raddatz and has published in prestigious journals such as PEDIATRICS, The American Journal of Human Genetics and European Journal of Human Genetics.

In The Last Decade

Katharina Löhner

4 papers receiving 136 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Katharina Löhner Netherlands	4	87	59	28	19	17	5	137
Sara Caylor United States	4	109 1.3×	44 0.7×	34 1.2×	22 1.2×	16 0.9×	4	139
Joanna Lazier Canada	8	67 0.8×	46 0.8×	55 2.0×	10 0.5×	9 0.5×	19	126
Helen Dolling United Kingdom	2	130 1.5×	52 0.9×	32 1.1×	28 1.5×	26 1.5×	3	159
David Tilstra United States	5	55 0.6×	31 0.5×	19 0.7×	16 0.8×	11 0.6×	6	95
Laura Konczal United States	6	119 1.4×	77 1.3×	13 0.5×	34 1.8×	30 1.8×	13	185
Michelle Steinraths Canada	8	104 1.2×	60 1.0×	60 2.1×	23 1.2×	3 0.2×	12	168
Myrthe van den Born Netherlands	7	38 0.4×	29 0.5×	30 1.1×	16 0.8×	8 0.5×	12	160
Kelly Watkins United States	3	83 1.0×	27 0.5×	14 0.5×	19 1.0×	7 0.4×	4	99
Charlotte Pöe France	5	56 0.6×	41 0.7×	15 0.5×	11 0.6×	4 0.2×	6	86
Jasmine Lee Fong Fung China	7	122 1.4×	49 0.8×	48 1.7×	15 0.8×	2 0.1×	15	167

Countries citing papers authored by Katharina Löhner

Since Specialization

Citations

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

Fields of papers citing papers by Katharina Löhner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katharina Löhner

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

All Works

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5 of 5 papers shown

1.

Zhang, Kejia, Katharina Löhner, Henny H. Lemmink, et al.. (2024). Epileptic encephalopathy linked to a DALRD3 missense variant that impairs tRNA modification. Human Genetics and Genomics Advances. 6(1). 100377–100377.

2.

Leenders, Erika, Pauline Terhal, Katharina Löhner, et al.. (2021). TAB2 deletions and variants cause a highly recognisable syndrome with mitral valve disease, cardiomyopathy, short stature and hypermobility. European Journal of Human Genetics. 29(11). 1669–1676. 15 indexed citations

3.

Muir, Alison M., Jennifer L. Cohen, Sarah E. Sheppard, et al.. (2020). Bi-allelic Loss-of-Function Variants in NUP188 Cause a Recognizable Syndrome Characterized by Neurologic, Ocular, and Cardiac Abnormalities. The American Journal of Human Genetics. 106(5). 623–631. 19 indexed citations

4.

Bergman, Jorieke E. H., Katharina Löhner, Corry K. van der Sluis, Patrick Rump, & Hermien E. K. de Walle. (2020). Etiological diagnosis in limb reduction defects and the number of affected limbs: A population‐based study in the Northern Netherlands. American Journal of Medical Genetics Part A. 182(12). 2909–2918. 14 indexed citations

5.

Diemen, Cleo C. van, Wilhelmina S. Kerstjens‐Frederikse, Klasien A. Bergman, et al.. (2017). Rapid Targeted Genomics in Critically Ill Newborns. PEDIATRICS. 140(4). 89 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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