Anna Sułek

2.4k citations
53 papers · 403 · h-index 13

Impact in

    • Genetic Neurodegenerative Diseases
    • Hereditary Neurological Disorders
  • Neurology top 10%
    • Neurological diseases and metabolism
    • Neurological disorders and treatments
    • Parkinson's Disease Mechanisms and Treatments

Papers in

Anna Sułek

50 papers receiving 396 citations

Peers

Anna Sułek
Comparison fields: 5 of 54
  • Cellular and Molecular Neuroscience 228
  • Neurology 68
  • Neurology 81
  • Genetics 53
  • Nephrology 28
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Countries citing papers authored by Anna Sułek

Since Specialization
Citations

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

Fields of papers citing papers by Anna Sułek

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Anna Sułek, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Anna Sułek Line = papers co-authored together Anna Sułek links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 53 papers — load more, or switch the sort, to bring in the rest.

#Work
1 201933
2 200631
3 201125
4 201525
5 202223
6 201019
7 201617
8
X-linked hypophosphatemia in Polish patients. 2. Analysis of clinical features and genotype-phenotype correlation.
200116
9
Muscle pathology in myotonic dystrophy: light and electron microscopic investigation in eighteen patients.
201115
10
X-linked hypophosphatemia in Polish patients. 1. Mutations in the PHEX gene.
200014
11 200613
12 201613
13 202012
14
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.
200811
15 201610
16
Screening for premutation in the FMR1 gene in male patients suspected of spinocerebellar ataxia.
20099
17
[Spinocerebellar ataxias type 1 and 2: comparison of clinical, electrophysiological and magnetic resonance evaluation].
20068
18 20158
19 20098
20
Polymorphism of trinucleotide repeats in non-translated regions of SCA8 and SCA12 genes: allele distribution in a Polish control group.
20048

About Anna Sułek

Anna Sułek is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Neurology, Genetics and Genetics, having authored 53 papers that have together received 403 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (28 papers), Hereditary Neurological Disorders (8 papers), Mitochondrial Function and Pathology (8 papers), Neurological diseases and metabolism (6 papers), Neurogenetic and Muscular Disorders Research (5 papers), Muscle Physiology and Disorders (5 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Parkinson's Disease Mechanisms and Treatments (3 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (228 citations), Neurology (68 citations), Neurology (81 citations), Genetics (53 citations) and Nephrology (28 citations). Anna Sułek has collaborated with scholars based in Poland, Germany and United States. Frequent co-authors include Wioletta Krysa, Jacek Zaremba, Maria Rakowicz, Iwona Stępniak, Elżbieta Zdzienicka, Małgorzata Chalimoniuk, Dorota Hoffman‐Zacharska, Jarosław Marusiak, Anna Sobańska and Anna Łusakowska. Their work appears in journals such as Parkinsonism & Related Disorders, Neurogenetics, Neurological Sciences, International Journal of Molecular Sciences and Journal of the Neurological Sciences.

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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