Joanna Kosińska

1.8k total citations
54 papers, 891 citations indexed

About

Joanna Kosińska is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Joanna Kosińska has authored 54 papers receiving a total of 891 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 20 papers in Genetics and 6 papers in Cell Biology. Recurrent topics in Joanna Kosińska's work include Genetics and Neurodevelopmental Disorders (9 papers), Mitochondrial Function and Pathology (8 papers) and Genomics and Rare Diseases (6 papers). Joanna Kosińska is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Mitochondrial Function and Pathology (8 papers) and Genomics and Rare Diseases (6 papers). Joanna Kosińska collaborates with scholars based in Poland, United Kingdom and Germany. Joanna Kosińska's co-authors include Rafał Płoski, Małgorzata Rydzanicz, Piotr Stawiński, Agnieszka Pollak, Ewa Pronicka, Dariusz Rokicki, Elżbieta Ciara, Anna Walczak, Maciej Pronicki and Elżbieta Jurkiewicz and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Scientific Reports.

In The Last Decade

Joanna Kosińska

54 papers receiving 886 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Joanna Kosińska Poland	19	544	188	117	75	75	54	891
Eija H. Seppälä Finland	17	436 0.8×	417 2.2×	108 0.9×	61 0.8×	29 0.4×	34	1.1k
Anthi Drousiotou Cyprus	14	465 0.9×	368 2.0×	109 0.9×	49 0.7×	24 0.3×	47	1.1k
Stefano Castellana Italy	16	616 1.1×	259 1.4×	52 0.4×	41 0.5×	32 0.4×	73	952
Kyriacos Markianos United States	17	546 1.0×	219 1.2×	43 0.4×	131 1.7×	65 0.9×	35	1.6k
Irina R. Tikhonova United States	3	721 1.3×	526 2.8×	27 0.2×	43 0.6×	60 0.8×	3	1.3k
Lifang Gao China	16	556 1.0×	209 1.1×	20 0.2×	25 0.3×	52 0.7×	58	1.2k
Swarnaseetha Adusumalli Singapore	7	624 1.1×	408 2.2×	23 0.2×	24 0.3×	109 1.5×	8	1.1k
Brian R. Keegan United States	13	1.1k 2.1×	151 0.8×	87 0.7×	70 0.9×	30 0.4×	19	1.4k
Sarit Cohen Israel	21	892 1.6×	180 1.0×	90 0.8×	13 0.2×	354 4.7×	26	1.2k
Allerdien Visser Netherlands	19	959 1.8×	145 0.8×	23 0.2×	31 0.4×	55 0.7×	35	1.7k

Countries citing papers authored by Joanna Kosińska

Since Specialization

Citations

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

Fields of papers citing papers by Joanna Kosińska

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joanna Kosińska

This figure shows the co-authorship network connecting the top 25 collaborators of Joanna Kosińska. A scholar is included among the top collaborators of Joanna Kosińska 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 Joanna Kosińska. Joanna Kosińska 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

Lin, Ting‐Yu, Robert Śmigiel, Bożena Kuźniewska, et al.. (2022). Destabilization of mutated human PUS3 protein causes intellectual disability. Human Mutation. 43(12). 2063–2078. 20 indexed citations

Badura‐Stronka, Magdalena, Robert Śmigiel, Krystyna Szymańska, et al.. (2022). FINCA syndrome—Defining neurobehavioral phenotype in survivors into late childhood. Molecular Genetics & Genomic Medicine. 10(4). e1899–e1899. 3 indexed citations

Kosińska, Joanna, Agnieszka Pollak, Małgorzata Rydzanicz, et al.. (2022). A novel de novo FEM1C variant is linked to neurodevelopmental disorder with absent speech, pyramidal signs and limb ataxia. Human Molecular Genetics. 32(7). 1152–1161. 1 indexed citations

Szczałuba, Krzysztof, Małgorzata Rydzanicz, Anna Walczak, et al.. (2021). Brain Tissue Low-Level Mosaicism for MTOR Mutation Causes Smith–Kingsmore Phenotype with Recurrent Hypoglycemia—A Novel Phenotype and a Further Proof for Testing of an Affected Tissue. Diagnostics. 11(7). 1269–1269. 3 indexed citations

Szczałuba, Krzysztof, Hanna Mierzewska, Robert Śmigiel, et al.. (2020). AP4B1-associated hereditary spastic paraplegia: expansion of phenotypic spectrum related to homozygous p.Thr387fs variant. Journal of Applied Genetics. 61(2). 213–218. 7 indexed citations

Kutkowska‐Kaźmierczak, Anna, Paweł Gawliński, Wojciech Wiszniewski, et al.. (2020). The MED13L haploinsufficiency syndrome associated with de novo nonsense variant (p.Gln1981*). PubMed. 24(3). 32–36. 2 indexed citations

Kosińska, Joanna, et al.. (2020). Progressive External Ophthalmoplegia in Polish Patients—From Clinical Evaluation to Genetic Confirmation. Genes. 12(1). 54–54. 2 indexed citations

Zatoński, Tomasz, Małgorzata Rydzanicz, Anna Rozensztrauch, et al.. (2020). Single median maxillary central incisor syndrome and variant in SMO gene associated with SHH pathway. International Journal of Pediatric Otorhinolaryngology. 134. 110038–110038. 2 indexed citations

Pienkowski, Victor Murcia, Szymon Ziętkiewicz, Małgorzata Rydzanicz, et al.. (2019). Syndromic chorioretinal coloboma associated with heterozygous de novo RARA mutation affecting an amino acid critical for retinoic acid interaction. Clinical Genetics. 96(4). 371–375. 7 indexed citations

10.

Kroc, Magdalena, Grzegorz Koczyk, Paweł Krajewski, et al.. (2019). Transcriptome-derived investigation of biosynthesis of quinolizidine alkaloids in narrow-leafed lupin (Lupinus angustifolius L.) highlights candidate genes linked to iucundus locus. Scientific Reports. 9(1). 33 indexed citations

11.

Śmigiel, Robert, Victor Murcia Pienkowski, Elżbieta Szmida, et al.. (2018). Novel de novo mutation affecting two adjacent aminoacids in the EED gene in a patient with Weaver syndrome. Journal of Human Genetics. 63(4). 517–520. 15 indexed citations

12.

Ciara, Elżbieta, Dariusz Rokicki, Michał Łaźniewski, et al.. (2018). Clinical and molecular characteristics of newly reported mitochondrial disease entity caused by biallelic PARS2 mutations. Journal of Human Genetics. 63(4). 473–485. 18 indexed citations

13.

Szczałuba, Krzysztof, Krystyna Szymańska, Piotr Gasperowicz, et al.. (2017). Novel GNB1 de novo mutation in a patient with neurodevelopmental disorder and cutaneous mastocytosis: Clinical report and literature review. European Journal of Medical Genetics. 61(3). 157–160. 21 indexed citations

14.

Szczałuba, Krzysztof, Krystyna Szymańska, Joanna Kosińska, et al.. (2017). Isolated Hearing Impairment Caused by SPATA5 Mutations in a Family with Variable Phenotypic Expression. Advances in experimental medicine and biology. 980. 59–66. 8 indexed citations

15.

Płoski, Rafał, Małgorzata Rydzanicz, Maria Franaszczyk, et al.. (2016). Evidence for troponin C (TNNC1) as a gene for autosomal recessive restrictive cardiomyopathy with fatal outcome in infancy. American Journal of Medical Genetics Part A. 170(12). 3241–3248. 42 indexed citations

16.

Śmigiel, Robert, Grażyna Kostrzewa, Joanna Kosińska, et al.. (2016). Further evidence for GRIN2B mutation as the cause of severe epileptic encephalopathy. American Journal of Medical Genetics Part A. 170(12). 3265–3270. 22 indexed citations

17.

Rydzanicz, Małgorzata, Mateusz Jagła, Joanna Kosińska, et al.. (2016). KIF5A de novo mutation associated with myoclonic seizures and neonatal onset progressive leukoencephalopathy. Clinical Genetics. 91(5). 769–773. 27 indexed citations

18.

Bukowska‐Ośko, Iwona, Karol Perlejewski, Shota Nakamura, et al.. (2016). Sensitivity of Next-Generation Sequencing Metagenomic Analysis for Detection of RNA and DNA Viruses in Cerebrospinal Fluid: The Confounding Effect of Background Contamination. Advances in experimental medicine and biology. 53–62. 49 indexed citations

19.

Pronicka, Ewa, Dorota Piekutowska‐Abramczuk, Elżbieta Ciara, et al.. (2016). New perspective in diagnostics of mitochondrial disorders: two years’ experience with whole-exome sequencing at a national paediatric centre. Journal of Translational Medicine. 14(1). 174–174. 159 indexed citations

20.

Skórkowska‐Telichowska, Katarzyna, et al.. (2012). Comparison and assessment of thyroid morphology and function in inhabitants of Lower Silesia before and after administration of a single dose of iodine-containing contrast agent during cardiac intervention procedure.. PubMed. 63(4). 294–9. 10 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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