Wioletta Krysa

1.2k total citations
20 papers, 271 citations indexed

About

Wioletta Krysa is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Wioletta Krysa has authored 20 papers receiving a total of 271 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Cellular and Molecular Neuroscience, 10 papers in Molecular Biology and 9 papers in Neurology. Recurrent topics in Wioletta Krysa's work include Genetic Neurodegenerative Diseases (16 papers), Mitochondrial Function and Pathology (7 papers) and Neurological diseases and metabolism (4 papers). Wioletta Krysa is often cited by papers focused on Genetic Neurodegenerative Diseases (16 papers), Mitochondrial Function and Pathology (7 papers) and Neurological diseases and metabolism (4 papers). Wioletta Krysa collaborates with scholars based in Poland, Germany and Sweden. Wioletta Krysa's co-authors include Anna Sułek, Jacek Zaremba, Maria Rakowicz, Elżbieta Zdzienicka, Iwona Stępniak, Ralf Reilmann, Anna Sobańska, Emilia J. Sitek, Piotr Robowski and Anna Łusakowska and has published in prestigious journals such as Journal of the Neurological Sciences, Muscle & Nerve and Journal of the International Neuropsychological Society.

In The Last Decade

Wioletta Krysa

20 papers receiving 266 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wioletta Krysa Poland 10 197 112 95 81 52 20 271
Jason Hehir United Kingdom 4 109 0.6× 79 0.7× 195 2.1× 69 0.9× 39 0.8× 5 252
Haitian Nan China 8 86 0.4× 88 0.8× 44 0.5× 58 0.7× 21 0.4× 43 233
Gian Maria Fabrizi Italy 6 301 1.5× 65 0.6× 164 1.7× 94 1.2× 27 0.5× 8 351
Xiaohui Duan China 8 108 0.5× 64 0.6× 56 0.6× 45 0.6× 16 0.3× 22 204
Hatice Karasoy Türkiye 10 88 0.4× 147 1.3× 131 1.4× 52 0.6× 48 0.9× 26 332
Mario Cornejo‐Olivas Peru 12 239 1.2× 195 1.7× 172 1.8× 40 0.5× 14 0.3× 58 394
Mariangela Lo Giudice Italy 8 94 0.5× 117 1.0× 38 0.4× 44 0.5× 29 0.6× 18 283
Emilia K. Bijlsma Netherlands 10 295 1.5× 273 2.4× 141 1.5× 17 0.2× 22 0.4× 15 395
Monia Ginevrino Italy 10 81 0.4× 78 0.7× 180 1.9× 54 0.7× 9 0.2× 27 303
Yanetza González-Zaldívar Cuba 13 301 1.5× 242 2.2× 159 1.7× 64 0.8× 15 0.3× 29 413

Countries citing papers authored by Wioletta Krysa

Since Specialization
Citations

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

Fields of papers citing papers by Wioletta Krysa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wioletta Krysa

This figure shows the co-authorship network connecting the top 25 collaborators of Wioletta Krysa. A scholar is included among the top collaborators of Wioletta Krysa 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 Wioletta Krysa. Wioletta Krysa 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.
Nojszewska, Monika, Anna Łusakowska, Małgorzata Gaweł, et al.. (2019). The needle EMG findings in myotonia congenita. Journal of Electromyography and Kinesiology. 49. 102362–102362. 4 indexed citations
2.
Stępniak, Iwona, Wioletta Krysa, Maria Rakowicz, et al.. (2019). Next-generation sequencing study reveals the broader variant spectrum of hereditary spastic paraplegia and related phenotypes. Neurogenetics. 20(1). 27–38. 33 indexed citations
3.
Rakowicz, Maria, Iwona Stępniak, Grzegorz Witkowski, et al.. (2019). Clinical evaluation of the effectiveness of teleneuroforma – A home rehabilitation tool for patients with Huntington's disease. Journal of the Neurological Sciences. 405. 357–358. 1 indexed citations
4.
Sułek, Anna, Anna Łusakowska, Wioletta Krysa, et al.. (2018). Evidence for a relatively high proportion of DM2 mutations in a large group of Polish patients. Neurologia i Neurochirurgia Polska. 52(6). 736–742. 1 indexed citations
5.
Krysa, Wioletta, et al.. (2016). High relative frequency of SCA1 in Poland reflecting a potential founder effect. Neurological Sciences. 37(8). 1319–1325. 17 indexed citations
6.
Stępniak, Iwona, Wioletta Krysa, Maria Rakowicz, et al.. (2015). Molecular spectrum of the SPAST, ATL1 and REEP1 gene mutations associated with the most common hereditary spastic paraplegias in a group of Polish patients. Journal of the Neurological Sciences. 359(1-2). 35–39. 25 indexed citations
7.
Nojszewska, Monika, Anna Łusakowska, Elżbieta Szmidt-Sałkowska, et al.. (2015). Peripheral nerve involvement in myotonic dystrophy type 2 – similar or different than in myotonic dystrophy type 1?. Neurologia i Neurochirurgia Polska. 49(3). 164–170. 8 indexed citations
8.
Szmidt-Sałkowska, Elżbieta, Małgorzata Gaweł, Anna Łusakowska, et al.. (2014). Does quantitative EMG differ myotonic dystrophy type 2 and type 1?. Journal of Electromyography and Kinesiology. 24(5). 755–761. 6 indexed citations
9.
Eatough, Virginia, Christine Eiser, Wioletta Krysa, et al.. (2013). The personal experience of parenting a child with Juvenile Huntington’s Disease: perceptions across Europe. European Journal of Human Genetics. 21(10). 1042–1048. 18 indexed citations
10.
Gaweł, Małgorzata, Elżbieta Szmidt-Sałkowska, Anna Łusakowska, et al.. (2013). Value of short exercise and short exercise with cooling tests in the diagnosis of myotonic dystrophies (DM1 AND DM2). Muscle & Nerve. 49(2). 277–283. 6 indexed citations
11.
Zimowski, Janusz, J Kulczycki, Wanda Łojkowska, et al.. (2012). Hereditary form of prion disease in Poland. Neurologia i Neurochirurgia Polska. 46(6). 509–518. 3 indexed citations
12.
Krysa, Wioletta, et al.. (2012). Rapid detection of large expansions in progressive myoclonus epilepsy type 1, myotonic dystrophy type 2 and spinocerebellar ataxia type 8. Neurologia i Neurochirurgia Polska. 46(2). 113–120. 10 indexed citations
13.
Sułek, Anna, et al.. (2011). A molecular and cytogenetic investigation of FMR1 gene premutations in Polish patients with primary ovarian insufficiency. European Journal of Obstetrics & Gynecology and Reproductive Biology. 155(2). 176–179. 3 indexed citations
14.
Sitek, Emilia J., Witold Sołtan, Dariusz Wieczorek, et al.. (2011). Self-awareness of Motor Dysfunction in Patients with Huntington's Disease in Comparison to Parkinson's Disease and Cervical Dystonia. Journal of the International Neuropsychological Society. 17(5). 788–795. 50 indexed citations
15.
16.
Nadaj‐Pakleza, Aleksandra, Anna Łusakowska, Anna Sułek, et al.. (2011). Muscle pathology in myotonic dystrophy: light and electron microscopic investigation in eighteen patients.. PubMed. 70(2). 121–9. 15 indexed citations
17.
Sułek, Anna, et al.. (2010). The occurrence of spinocerebellar ataxias caused by dynamic mutations in Polish patients. Neurologia i Neurochirurgia Polska. 44(3). 238–245. 19 indexed citations
18.
Sułek, Anna, et al.. (2009). Screening for premutation in the FMR1 gene in male patients suspected of spinocerebellar ataxia.. PubMed. 42(6). 497–504. 9 indexed citations
19.
Sułek, Anna, Wioletta Krysa, Elżbieta Zdzienicka, et al.. (2008). Searching for mutation in the JPH3, ATN1 and TBP genes in Polish patients suspected of Huntington's disease and without mutation in the IT15 gene.. PubMed. 42(3). 203–9. 11 indexed citations
20.
Sułek, Anna, et al.. (2005). CAG repeat polymorphism in the androgen receptor (AR) gene of SBMA patients and a control group.. PubMed. 46(2). 237–9. 7 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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