Barbara Ryniewicz

800 total citations
56 papers, 553 citations indexed

About

Barbara Ryniewicz is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Barbara Ryniewicz has authored 56 papers receiving a total of 553 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 19 papers in Cellular and Molecular Neuroscience and 15 papers in Genetics. Recurrent topics in Barbara Ryniewicz's work include Hereditary Neurological Disorders (15 papers), Neurogenetic and Muscular Disorders Research (15 papers) and Muscle Physiology and Disorders (12 papers). Barbara Ryniewicz is often cited by papers focused on Hereditary Neurological Disorders (15 papers), Neurogenetic and Muscular Disorders Research (15 papers) and Muscle Physiology and Disorders (12 papers). Barbara Ryniewicz collaborates with scholars based in Poland, United States and Belgium. Barbara Ryniewicz's co-authors include Hubert Kwieciński, Anna Kostera‐Pruszczyk, Anna Fidziańska, I Hausmanowa-Pétrusewicz, Dagmara Kabzińska, Marta Lipowska, Andrzej Kochański, K Rowińska-Marcińska, Maria Jędrzejowska and Beata Szyluk and has published in prestigious journals such as Neurology, Journal of the Neurological Sciences and Muscle & Nerve.

In The Last Decade

Barbara Ryniewicz

54 papers receiving 538 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Barbara Ryniewicz Poland 13 257 222 197 121 107 56 553
Keiji Chida Japan 9 203 0.8× 170 0.8× 92 0.5× 59 0.5× 77 0.7× 23 468
Masakazu Kawajiri Japan 13 176 0.7× 93 0.4× 81 0.4× 28 0.2× 93 0.9× 46 408
Saunder Bernes United States 14 316 1.2× 57 0.3× 109 0.6× 79 0.7× 54 0.5× 16 500
Bum Chun Suh South Korea 12 101 0.4× 194 0.9× 191 1.0× 21 0.2× 40 0.4× 44 451
Coşkun Özdemır Türkiye 9 277 1.1× 199 0.9× 102 0.5× 27 0.2× 203 1.9× 17 502
M. Al-Lozi United States 6 175 0.7× 67 0.3× 67 0.3× 93 0.8× 17 0.2× 10 361
Jochen Schäfer Germany 8 228 0.9× 78 0.4× 73 0.4× 54 0.4× 21 0.2× 21 406
S Riku Japan 12 210 0.8× 186 0.8× 174 0.9× 28 0.2× 16 0.1× 26 431
GABRIEL A. SCHWARZ United States 11 86 0.3× 213 1.0× 193 1.0× 62 0.5× 29 0.3× 20 545
Yoshimitsu Shimatani Japan 13 88 0.3× 282 1.3× 170 0.9× 125 1.0× 12 0.1× 31 434

Countries citing papers authored by Barbara Ryniewicz

Since Specialization
Citations

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

Fields of papers citing papers by Barbara Ryniewicz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Barbara Ryniewicz

This figure shows the co-authorship network connecting the top 25 collaborators of Barbara Ryniewicz. A scholar is included among the top collaborators of Barbara Ryniewicz 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 Barbara Ryniewicz. Barbara Ryniewicz 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.
Frączek, Anna, Anna Potulska‐Chromik, Małgorzata Bednarska‐Makaruk, et al.. (2020). Spinal muscular atrophy with an overlapping syndrome — “double trouble” or a potentially better outcome?. Neurologia i Neurochirurgia Polska. 54(5). 475–477. 1 indexed citations
2.
Dorobek, Małgorzata, Barbara Ryniewicz, Dagmara Kabzińska, et al.. (2015). The Frequency of c.550delA Mutation of the CANP3 Gene in the Polish LGMD2A Population. Genetic Testing and Molecular Biomarkers. 19(11). 637–640. 13 indexed citations
3.
Potulska‐Chromik, Anna, Barbara Ryniewicz, Dagmara Kabzińska, et al.. (2015). Are electrophysiological criteria useful in distinguishing childhood demyelinating neuropathies?. Journal of the Peripheral Nervous System. 21(1). 22–26. 11 indexed citations
4.
Gaweł, Małgorzata, Anna Kostera‐Pruszczyk, Anna Łusakowska, et al.. (2014). Motor unit loss estimation by the multipoint incremental MUNE method in children with spinal muscular atrophy – A preliminary study. Neuromuscular Disorders. 25(3). 216–221. 20 indexed citations
5.
Jędrzejowska, Maria, Monika Goś, Janusz Zimowski, et al.. (2014). Novel point mutations in survival motor neuron 1 gene expand the spectrum of phenotypes observed in spinal muscular atrophy patients. Neuromuscular Disorders. 24(7). 617–623. 23 indexed citations
6.
Nadaj‐Pakleza, Aleksandra, et al.. (2013). Muscle pathology in 31 patients with calpain 3 gene mutations. Neurologia i Neurochirurgia Polska. 47(3). 214–222. 6 indexed citations
7.
Kostera‐Pruszczyk, Anna, et al.. (2008). Lambert–Eaton myasthenic syndrome in childhood. European Journal of Paediatric Neurology. 13(2). 194–196. 9 indexed citations
8.
Kabzińska, Dagmara, Raül Pérez‐Ollé, H Drac, et al.. (2006). Is a novel I214M substitution in the NEFL gene a cause of Charcot‐Marie‐Tooth disease? Functional analysis using cell culture models. Journal of the Peripheral Nervous System. 11(3). 225–231. 8 indexed citations
9.
Kabzińska, Dagmara, Andrzej Kochański, H Drac, et al.. (2005). Autosomal Recessive Axonal Form of Charcot-Marie-Tooth Disease Caused by Compound Heterozygous 3′-Splice Site and Ser130Cys Mutation in theGDAP1Gene. Neuropediatrics. 36(3). 206–209. 10 indexed citations
10.
Fidziańska, Anna, et al.. (2005). IBM-type inclusions in a patient with slow-channel syndrome caused by a mutation in the AChR epsilon subunit. Neuromuscular Disorders. 15(11). 753–759. 9 indexed citations
11.
Kabzińska, Dagmara, Andrzej Kochański, H Drac, et al.. (2005). A novel Met116Thr mutation in the GDAP1 gene in a Polish family with the axonal recessive Charcot–Marie–Tooth type 4 disease. Journal of the Neurological Sciences. 241(1-2). 7–11. 7 indexed citations
12.
Fidziańska, Anna, Anna Kamińska, & Barbara Ryniewicz. (2005). Congenital Myopathy with Tubular Aggregates and Tubulofilamentous IBM-Type Inclusions. Neuropediatrics. 36(1). 35–39. 6 indexed citations
13.
Jędrzejowska, Maria, Wojciech Wiszniewski, Janusz Zimowski, et al.. (2005). Application of a rapid non-invasive technique in the molecular diagnosis of spinal muscular atrophy (SMA).. PubMed. 39(2). 89–94. 5 indexed citations
14.
Kochański, Andrzej, Dagmara Kabzińska, H Drac, et al.. (2004). Early onset Charcot-Marie-Tooth type 1B disease caused by a novel Leu190fs mutation in the myelin protein zero gene. European Journal of Paediatric Neurology. 8(4). 221–224. 3 indexed citations
15.
Chrzanowski, Łukasz, Jarosław D. Kasprzak, Ewa Trzos, et al.. (2003). Different expressions of X-linked cardiomyopathy in monozygotic triplets with Becker's dystrophy. International journal of cardiac imaging. 19(5). 377–380. 3 indexed citations
16.
Kochański, Andrzej, A. Löfgren, H Jedrzejowska, et al.. (2001). A novel connexin 32 missense mutation (E208G) causing Charcot-Marie-Tooth disease. Human Mutation. 17(2). 157–157. 2 indexed citations
17.
Fidziańska, Anna, Barbara Ryniewicz, Maria Barcikowska, & Hans H. Goebel. (1995). A new familial congenital myopathy in children with desmin and dystrophin reacting plaques. Journal of the Neurological Sciences. 131(1). 88–95. 22 indexed citations
18.
Fidziańska, Anna, Amelia Morrone, Elena Pegoraro, et al.. (1995). An X:Autosome Translocation Stabilizes Truncated Dystrophin: Implications for Lack of Truncated Dystrophins in Duchenne Muscular Dystrophy. Neuropediatrics. 26(3). 163–168. 4 indexed citations
19.
Ryniewicz, Barbara, et al.. (1992). Immunosuppressive treatment for juvenile myasthenia gravis. European Journal of Pediatrics. 151(3). 215–217. 14 indexed citations
20.
Kwieciński, Hubert, et al.. (1992). Treatment of myotonia with antiarrhythmic drugs. Acta Neurologica Scandinavica. 86(4). 371–375. 80 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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