Krystyna Szymańska

939 total citations
48 papers, 485 citations indexed

About

Krystyna Szymańska is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Krystyna Szymańska has authored 48 papers receiving a total of 485 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 13 papers in Genetics and 6 papers in Oncology. Recurrent topics in Krystyna Szymańska's work include Genetics and Neurodevelopmental Disorders (11 papers), Genomics and Rare Diseases (5 papers) and RNA regulation and disease (5 papers). Krystyna Szymańska is often cited by papers focused on Genetics and Neurodevelopmental Disorders (11 papers), Genomics and Rare Diseases (5 papers) and RNA regulation and disease (5 papers). Krystyna Szymańska collaborates with scholars based in Poland, United States and Netherlands. Krystyna Szymańska's co-authors include Krzysztof Szczałuba, Rafał Płoski, Robert Śmigiel, Joanna Kosińska, Monika Bekiesińska‐Figatowska, Małgorzata Rydzanicz, Ewa Obersztyn, Piotr Stawiński, Beata Nowakowska and B Schmidt-Sidor and has published in prestigious journals such as Brain, Neurology and The American Journal of Human Genetics.

In The Last Decade

Krystyna Szymańska

42 papers receiving 474 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Krystyna Szymańska Poland 14 218 177 52 50 49 48 485
Ewa Jamroz Poland 13 241 1.1× 139 0.8× 47 0.9× 50 1.0× 35 0.7× 52 529
Lisa Flint United States 8 199 0.9× 151 0.9× 22 0.4× 96 1.9× 57 1.2× 9 514
Kristina Jülich United States 8 475 2.2× 116 0.7× 57 1.1× 53 1.1× 47 1.0× 14 674
Kinga Hadzsiev Hungary 14 316 1.4× 212 1.2× 19 0.4× 34 0.7× 43 0.9× 73 624
Michelle Demos Canada 13 270 1.2× 145 0.8× 64 1.2× 97 1.9× 26 0.5× 23 482
Raúl Sanz Spain 14 341 1.6× 206 1.2× 26 0.5× 76 1.5× 49 1.0× 45 631
M. Pineda Spain 13 285 1.3× 118 0.7× 59 1.1× 111 2.2× 18 0.4× 26 533
Nicole Créau France 16 397 1.8× 335 1.9× 31 0.6× 44 0.9× 29 0.6× 25 801
Joyce So Canada 13 328 1.5× 438 2.5× 31 0.6× 26 0.5× 38 0.8× 26 643

Countries citing papers authored by Krystyna Szymańska

Since Specialization
Citations

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

Fields of papers citing papers by Krystyna Szymańska

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Krystyna Szymańska

This figure shows the co-authorship network connecting the top 25 collaborators of Krystyna Szymańska. A scholar is included among the top collaborators of Krystyna Szymańska 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 Krystyna Szymańska. Krystyna Szymańska 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.
Nowakowska, Dominika, Pedro Rosa‐Neto, Mateusz Zawadka, et al.. (2025). Visual Function Characteristics in STXBP1 Epileptic Encephalopathy Patients. Journal of Clinical Medicine. 14(19). 6840–6840.
2.
Szczałuba, Krzysztof, Krystyna Szymańska, Małgorzata Rydzanicz, et al.. (2022). A novel KEL c.1414‐1G>T allele in a polish patient with anti‐Ku antibody. Transfusion. 62(9). E43–E44.
3.
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
4.
Rydzanicz, Małgorzata, et al.. (2021). Variants of ATP1A3 in residue 756 cause a separate phenotype of relapsing encephalopathy with cerebellar ataxia (RECA)—Report of two cases and literature review. Molecular Genetics & Genomic Medicine. 9(9). e1772–e1772. 9 indexed citations
5.
Szymańska, Krystyna, et al.. (2021). Kabuki Syndrome—Clinical Review with Molecular Aspects. Genes. 12(4). 468–468. 49 indexed citations
6.
Kostera‐Pruszczyk, Anna, Krystyna Szymańska, Joanna Jędrzejczak, et al.. (2021). Spinal muscular atrophy: epidemiology and health burden in children — a Polish national healthcare database perspective before introduction of SMA-specific treatment. Neurologia i Neurochirurgia Polska. 55(5). 479–484. 3 indexed citations
7.
Tarka, Sylwia, Milena Laure‐Kamionowska, Teresa Wierzba‐Bobrowicz, et al.. (2020). POLG gene mutation. Clinico-neuropathological study. Folia Neuropathologica. 58(4). 386–392. 1 indexed citations
8.
Szczałuba, Krzysztof, Małgorzata Rydzanicz, Krystyna Szymańska, et al.. (2018). Neurodevelopmental phenotype caused by a de novo PTPN4 single nucleotide variant disrupting protein localization in neuronal dendritic spines. Clinical Genetics. 94(6). 581–585. 12 indexed citations
9.
Szczepanik, Elżbieta, et al.. (2018). Autoimmune Neurological Disorder with Anti-Ma2/Ta Antibodies in a Pediatric Patient.. PubMed. 20(10). 653–655. 1 indexed citations
10.
Szymańska, Krystyna, et al.. (2017). Proteomics in the Diagnosis of Inborn Encephalopathies of Unknown Origin: A Myth or Reality. Advances in experimental medicine and biology. 1040. 83–99. 1 indexed citations
11.
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
12.
Rybakowski, Filip, Izabela Chojnicka, Piotr Dziechciarz, et al.. (2016). The role of genetic factors and pre- and perinatal influences in the etiology of autism spectrum disorders – indications for genetic referral. Psychiatria Polska. 50(3). 543–554. 7 indexed citations
13.
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
14.
Szymańska, Krystyna, Krzysztof Szczałuba, Agnieszka Ługowska, et al.. (2014). The Analysis of Genetic Aberrations in Children with Inherited Neurometabolic and Neurodevelopmental Disorders. BioMed Research International. 2014. 1–8. 10 indexed citations
15.
Szymańska, Krystyna, Katarzyna Kuśmierska, Maria Nowacka, Jolanta Sykut‐Cegielska, & Urszula Demkow. (2014). Phenotypic features of children with neurodevelopmental diseases in relation to biogenic amines. Respiratory Physiology & Neurobiology. 209. 124–132. 1 indexed citations
16.
Rybakowski, Filip, Izabela Chojnicka, Piotr Dziechciarz, et al.. (2014). [Autism spectrum disorders - epidemiology, symptoms, comorbidity and diagnosis].. PubMed. 48(4). 653–65. 14 indexed citations
17.
Nowakowska, Beata, Ewa Obersztyn, Krystyna Szymańska, et al.. (2010). Severe mental retardation, seizures, and hypotonia due to deletions of MEF2C. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(5). 1042–1051. 71 indexed citations
18.
Szymańska, Krystyna, Katarzyna Kuśmierska, & Hanna Mierzewska. (2007). Wrodzone zaburzenia metabolizmuamin biogennych i pteryn. 16(31). 41–50. 1 indexed citations
19.
Szymańska, Krystyna, et al.. (1996). Restoration of the continuity of dog ureter after resection of its 5 cm middle segment. British Journal of Urology. 77(3). 342–346. 8 indexed citations
20.
Szymańska, Krystyna, et al.. (1993). Microwave-assisted staining of mucosal mast cells and granulated intra-epithelial lymphocytes after formalin fixation. The Histochemical Journal. 25(12). 854–856. 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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