Marta Owczarek‐Lipska

581 total citations
29 papers, 384 citations indexed

About

Marta Owczarek‐Lipska is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Marta Owczarek‐Lipska has authored 29 papers receiving a total of 384 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Marta Owczarek‐Lipska's work include Cardiomyopathy and Myosin Studies (6 papers), RNA modifications and cancer (4 papers) and Retinal Development and Disorders (4 papers). Marta Owczarek‐Lipska is often cited by papers focused on Cardiomyopathy and Myosin Studies (6 papers), RNA modifications and cancer (4 papers) and Retinal Development and Disorders (4 papers). Marta Owczarek‐Lipska collaborates with scholars based in Switzerland, Germany and Netherlands. Marta Owczarek‐Lipska's co-authors include Tosso Leeb, John Neidhardt, Cord Drögemüller, Vidhya Jagannathan, Martin Braunschweig, Hannes Lohi, Gaudenz Dolf, Christoph Jüschke, Barbara Glanemann and Peter H Kook and has published in prestigious journals such as PLoS ONE, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Marta Owczarek‐Lipska

29 papers receiving 373 citations

Peers

Marta Owczarek‐Lipska

GENET

CCM

CMN

Marie Abitbol France

Glen R. Monroe Netherlands

Norma Leonard Canada

Julie Vogt United Kingdom

Jerold S. Bell United States

Kaisa Kyöstilä Finland

Mika Asai-Coakwell Canada

Thomas O’Malley United States

Aaron S. Meadows United States

Marta Jones Argentina

Marie Abitbol France

Marta Owczarek‐Lipska

256 ×1.1

99 ×0.7

GENET

103 ×2.2

CCM

90 ×2.2

26 ×0.7

CMN

Citations per year, relative to Marta Owczarek‐Lipska Marta Owczarek‐Lipska (= 1×) peers Marie Abitbol

Countries citing papers authored by Marta Owczarek‐Lipska

Since Specialization

Citations

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

Fields of papers citing papers by Marta Owczarek‐Lipska

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marta Owczarek‐Lipska. 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 Marta Owczarek‐Lipska. The network helps show where Marta Owczarek‐Lipska may publish in the future.

Co-authorship network of co-authors of Marta Owczarek‐Lipska

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

All Works

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20 of 20 papers shown

Owczarek‐Lipska, Marta, et al.. (2022). A TARP Syndrome Phenotype Is Associated with a Novel Splicing Variant in RBM10. Genes. 13(11). 2154–2154. 3 indexed citations

Scholten, Alexander, et al.. (2021). A novel missense variant in the EML1 gene associated with bilateral ribbon-like subcortical heterotopia leads to ciliary defects. Journal of Human Genetics. 66(12). 1159–1167. 5 indexed citations

Jüschke, Christoph, Thomas Klopstock, Claudia B. Catarino, et al.. (2021). Autosomal dominant optic atrophy: A novel treatment for OPA1 splice defects using U1 snRNA adaption. Molecular Therapy — Nucleic Acids. 26. 1186–1197. 15 indexed citations

Gläser, Anne, Markus H. Gräler, Sina M. Coldewey, et al.. (2020). Identification of Brain-Specific Treatment Effects in NPC1 Disease by Focusing on Cellular and Molecular Changes of Sphingosine-1-Phosphate Metabolism. International Journal of Molecular Sciences. 21(12). 4502–4502. 8 indexed citations

Korenke, Georg Christoph, et al.. (2020). A Novel de novo Frameshift Mutation in the BCL11A Gene in a Patient with Intellectual Disability Syndrome and Epilepsy. Molecular Syndromology. 11(3). 135–140. 12 indexed citations

Owczarek‐Lipska, Marta, Lejla Mulahasanovic, Carolin D. Obermaier, et al.. (2019). Novel mutations in the GJC2 gene associated with Pelizaeus–Merzbacher-like disease. Molecular Biology Reports. 46(4). 4507–4516. 10 indexed citations

Bräuer, Anja U., et al.. (2019). Combining Engineered U1 snRNA and Antisense Oligonucleotides to Improve the Treatment of a BBS1 Splice Site Mutation. Molecular Therapy — Nucleic Acids. 18. 123–130. 16 indexed citations

Hytönen, Marjo K., Meharji Arumilli, Anu K. Lappalainen, et al.. (2016). Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes. PLoS Genetics. 12(5). e1006037–e1006037. 28 indexed citations

Reiff, Charlotte, Marta Owczarek‐Lipska, Georg Spital, et al.. (2016). The mutation p.E113K in the Schiff base counterion of rhodopsin is associated with two distinct retinal phenotypes within the same family. Scientific Reports. 6(1). 36208–36208. 11 indexed citations

10.

Frischknecht, Mirjam, Vidhya Jagannathan, Marta Owczarek‐Lipska, et al.. (2013). A COL11A2 Mutation in Labrador Retrievers with Mild Disproportionate Dwarfism. PLoS ONE. 8(3). e60149–e60149. 34 indexed citations

11.

Owczarek‐Lipska, Marta, Vidhya Jagannathan, Cord Drögemüller, et al.. (2013). A Frameshift Mutation in the Cubilin Gene (CUBN) in Border Collies with Imerslund-Gräsbeck Syndrome (Selective Cobalamin Malabsorption). PLoS ONE. 8(4). e61144–e61144. 36 indexed citations

12.

Jagannathan, Vidhya, Jeanette Bannoehr, Philippe Plattet, et al.. (2013). A Mutation in the SUV39H2 Gene in Labrador Retrievers with Hereditary Nasal Parakeratosis (HNPK) Provides Insights into the Epigenetics of Keratinocyte Differentiation. PLoS Genetics. 9(10). e1003848–e1003848. 32 indexed citations

13.

Gendron, Karine, Marta Owczarek‐Lipska, Johann Lang, & Tosso Leeb. (2013). Maine Coon renal screening: ultrasonographical characterisation and preliminary genetic analysis for common genes in cats with renal cysts. Journal of Feline Medicine and Surgery. 15(12). 1079–1085. 5 indexed citations

14.

Owczarek‐Lipska, Marta, Béatrice Lauber, Marcin Kierczak, et al.. (2012). Two Loci on Chromosome 5 Are Associated with Serum IgE Levels in Labrador Retrievers. PLoS ONE. 7(6). e39176–e39176. 17 indexed citations

15.

Wijnberg, Inge D., Marta Owczarek‐Lipska, Roberta Sacchetto, et al.. (2011). A missense mutation in the skeletal muscle chloride channel 1 (CLCN1) as candidate causal mutation for congenital myotonia in a New Forest pony. Neuromuscular Disorders. 22(4). 361–367. 23 indexed citations

16.

Braunschweig, Martin, et al.. (2011). Relationship of porcine IGF2 imprinting status to DNA methylation at the H19 DMD and the IGF2 DMRs 1 and 2. BMC Genetics. 12(1). 47–47. 18 indexed citations

17.

Owczarek‐Lipska, Marta, Philippe Plattet, Ljerka Zipperle, et al.. (2010). A nonsense mutation in the optic atrophy 3 gene (OPA3) causes dilated cardiomyopathy in Red Holstein cattle. Genomics. 97(1). 51–57. 13 indexed citations

18.

Owczarek‐Lipska, Marta, Catherine Denis, Andre A. Eggen, et al.. (2009). The bovine dilated cardiomyopathy locus maps to a 1.0-Mb interval on chromosome 18. Mammalian Genome. 20(3). 187–192. 7 indexed citations

19.

Owczarek‐Lipska, Marta, G. Dolf, Karina E Guziewicz, et al.. (2009). Bovine cardiac troponin I gene (TNNI3) as a candidate gene for bovine dilated cardiomyopathy. Archives animal breeding/Archiv für Tierzucht. 52(2). 113–123. 1 indexed citations

20.

Guziewicz, Karina E, Marta Owczarek‐Lipska, C. Schelling, et al.. (2007). The locus for bovine dilated cardiomyopathy maps to chromosome 18. Animal Genetics. 38(3). 265–269. 8 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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