Maria Rakowicz

6.3k total citations
32 papers, 646 citations indexed

About

Maria Rakowicz is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Maria Rakowicz has authored 32 papers receiving a total of 646 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Cellular and Molecular Neuroscience, 15 papers in Molecular Biology and 14 papers in Neurology. Recurrent topics in Maria Rakowicz's work include Genetic Neurodegenerative Diseases (19 papers), Mitochondrial Function and Pathology (12 papers) and Neurological disorders and treatments (6 papers). Maria Rakowicz is often cited by papers focused on Genetic Neurodegenerative Diseases (19 papers), Mitochondrial Function and Pathology (12 papers) and Neurological disorders and treatments (6 papers). Maria Rakowicz collaborates with scholars based in Poland, Germany and Netherlands. Maria Rakowicz's co-authors include Thomas Klockgether, Dagmar Timmann, Caterina Mariotti, Alexandra Dürr, Tanja Schmitz‐Hübsch, Bart P.C. van de Warrenburg, Lüdger Schöls, Wioletta Krysa, Peter Bauer and Romana Bogusławska and has published in prestigious journals such as NeuroImage, Brain and Movement Disorders.

In The Last Decade

Maria Rakowicz

30 papers receiving 634 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maria Rakowicz Poland 14 482 371 296 140 54 32 646
V. Fetoni Italy 16 360 0.7× 198 0.5× 564 1.9× 112 0.8× 22 0.4× 25 821
Tomoo Mano Japan 14 256 0.5× 253 0.7× 216 0.7× 143 1.0× 60 1.1× 65 678
Bart van de Warrenburg Netherlands 13 328 0.7× 246 0.7× 211 0.7× 96 0.7× 30 0.6× 30 508
Vera Tadić Germany 18 327 0.7× 190 0.5× 556 1.9× 153 1.1× 23 0.4× 43 833
Anita Fletcher‐Turner United States 10 370 0.8× 215 0.6× 249 0.8× 66 0.5× 15 0.3× 12 689
Jesús Calleja Spain 15 632 1.3× 141 0.4× 469 1.6× 212 1.5× 25 0.5× 30 875
Anne D. Sperfeld Germany 10 199 0.4× 176 0.5× 346 1.2× 95 0.7× 59 1.1× 12 608
Pichet Termsarasab United States 14 167 0.3× 114 0.3× 381 1.3× 61 0.4× 52 1.0× 42 636
Daniel Ecker Germany 10 342 0.7× 185 0.5× 360 1.2× 44 0.3× 60 1.1× 11 640
Adolfo Mínguez‐Castellanos Spain 16 234 0.5× 126 0.3× 498 1.7× 92 0.7× 20 0.4× 47 749

Countries citing papers authored by Maria Rakowicz

Since Specialization
Citations

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

Fields of papers citing papers by Maria Rakowicz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maria Rakowicz

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Rakowicz. A scholar is included among the top collaborators of Maria Rakowicz 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 Maria Rakowicz. Maria Rakowicz 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.
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.
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
4.
5.
Antczak, Jakub, et al.. (2017). The influence of the repetitive transcranial magnetic stimulation on sleep quality in depression. Psychiatria Polska. 51(5). 845–857. 18 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.
Linnemann, Christoph, Sophie Tézenas du Montcel, Maria Rakowicz, et al.. (2015). Peripheral Neuropathy in Spinocerebellar Ataxia Type 1, 2, 3, and 6. The Cerebellum. 15(2). 165–173. 53 indexed citations
8.
Reetz, Kathrin, Ana Sofia Costa, Shahram Mirzazade, et al.. (2013). Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6. Brain. 136(3). 905–917. 109 indexed citations
9.
Derejko, Mirosława, et al.. (2013). Corticomotor excitability in drug-naive patients with Parkinson disease. Neurologia i Neurochirurgia Polska. 47(2). 109–115. 5 indexed citations
10.
Antczak, Jakub, et al.. (2013). Negative influence of L-dopa on subjectively assessed sleep but not on nocturnal polysomnography in Parkinson's disease. Pharmacological Reports. 65(3). 614–623. 18 indexed citations
11.
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
12.
Robertson, Lisa, Kirsty O’Donovan, Ferdinando Squitieri, et al.. (2012). Current Pharmacological Management in Juvenile Huntington’s Disease. PLoS Currents. 4. RRN1304–RRN1304. 11 indexed citations
13.
Derejko, Mirosława, Paweł Derejko, Andrzej Przybylski, et al.. (2011). Safety of nerve conduction studies in patients with implantable cardioverter–defibrillators. Clinical Neurophysiology. 123(1). 211–213. 3 indexed citations
14.
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
15.
Banach, Marta & Maria Rakowicz. (2010). [Electrophysiological diagnosis of arnyotrophic lateral sclerosis].. PubMed. 67(9). 736–40. 1 indexed citations
16.
Schulz, Jörg B., Stefanie Wolf, Tanja Schmitz‐Hübsch, et al.. (2009). Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6. NeuroImage. 49(1). 158–168. 131 indexed citations
17.
Globas, Christoph, Sophie Tézenas du Montcel, Sylvia Boesch, et al.. (2008). Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6. Movement Disorders. 23(15). 2232–2238. 98 indexed citations
18.
Kulczycki, J, et al.. (2002). Impairment of the Peripheral Nervous System in Creutzfeldt-Jakob Disease. Archives of Neurology. 59(9). 1430–6. 20 indexed citations
19.
Zdzienicka, Elżbieta, Maria Rakowicz, Hanna Mierzewska, et al.. (2002). [Clinical and genetic study of juvenile form of Huntington's disease].. PubMed. 36(2). 245–58. 1 indexed citations
20.
Kukwa, Andrzej, et al.. (1994). Reanimation of the face after facial nerve palsy resulting from resection of a cerebellopontine angle tumour. British Journal of Neurosurgery. 8(3). 327–332. 23 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by V. Fetoni Breakdown of academic impact, for papers by Tomoo Mano Breakdown of academic impact, for papers by Bart van de Warrenburg Breakdown of academic impact, for papers by Vera Tadić Breakdown of academic impact, for papers by Anita Fletcher‐Turner Breakdown of academic impact, for papers by Jesús Calleja Breakdown of academic impact, for papers by Anne D. Sperfeld Breakdown of academic impact, for papers by Pichet Termsarasab Breakdown of academic impact, for papers by Daniel Ecker Breakdown of academic impact, for papers by Adolfo Mínguez‐Castellanos
Rankless by CCL
2026