Tomasz Kmieć

1.8k total citations
50 papers, 865 citations indexed

About

Tomasz Kmieć is a scholar working on Molecular Biology, Clinical Biochemistry and Neurology. According to data from OpenAlex, Tomasz Kmieć has authored 50 papers receiving a total of 865 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 17 papers in Clinical Biochemistry and 16 papers in Neurology. Recurrent topics in Tomasz Kmieć's work include Metabolism and Genetic Disorders (17 papers), Neurological diseases and metabolism (16 papers) and Genetic Neurodegenerative Diseases (7 papers). Tomasz Kmieć is often cited by papers focused on Metabolism and Genetic Disorders (17 papers), Neurological diseases and metabolism (16 papers) and Genetic Neurodegenerative Diseases (7 papers). Tomasz Kmieć collaborates with scholars based in Poland, Germany and Italy. Tomasz Kmieć's co-authors include Elżbieta Jurkiewicz, Sergiusz Jóźwiak, Katarzyna Kotulska, Dariusz Kuczyński, Dariusz Chmielewski, Barbara Łojszczyk, Dorota Dunin-Wąsowicz, Julita Borkowska, Małgorzata Syczewska and Dorota Domańska‐Pakieła and has published in prestigious journals such as PLoS ONE, Brain and Annals of Neurology.

In The Last Decade

Tomasz Kmieć

48 papers receiving 846 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tomasz Kmieć Poland 12 399 301 262 158 157 50 865
Mónica Sánchez-Contreras United States 19 381 1.0× 319 1.1× 194 0.7× 122 0.8× 59 0.4× 27 918
Barry A. Chioza United Kingdom 20 551 1.4× 76 0.3× 147 0.6× 182 1.2× 53 0.3× 39 1.1k
Nobuyoshi Fukuhara Japan 17 693 1.7× 120 0.4× 79 0.3× 205 1.3× 261 1.7× 35 1.1k
Annabelle Chaussenot France 16 634 1.6× 106 0.4× 94 0.4× 140 0.9× 210 1.3× 35 870
Chikahiko Numakura Japan 22 688 1.7× 117 0.4× 184 0.7× 435 2.8× 262 1.7× 60 1.4k
Luc Régal Belgium 15 336 0.8× 195 0.6× 36 0.1× 51 0.3× 84 0.5× 33 689
Elisa Alonso Mexico 15 795 2.0× 100 0.3× 104 0.4× 624 3.9× 36 0.2× 31 1.3k
Serena Ghezzi Italy 17 470 1.2× 135 0.4× 195 0.7× 205 1.3× 16 0.1× 33 944
Sebahattin Çırak Germany 20 538 1.3× 157 0.5× 51 0.2× 106 0.7× 24 0.2× 62 943
Daniel Darvish United States 10 664 1.7× 304 1.0× 182 0.7× 170 1.1× 13 0.1× 16 1.3k

Countries citing papers authored by Tomasz Kmieć

Since Specialization
Citations

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

Fields of papers citing papers by Tomasz Kmieć

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tomasz Kmieć

This figure shows the co-authorship network connecting the top 25 collaborators of Tomasz Kmieć. A scholar is included among the top collaborators of Tomasz Kmieć 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 Tomasz Kmieć. Tomasz Kmieć 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.
Kmieć, Tomasz, et al.. (2022). Deterioration of visual quality and acuity as the first sign of ceroid lipofuscinosis type 3 (CLN3), a rare neurometabolic disease. Metabolic Brain Disease. 38(2). 709–715. 2 indexed citations
2.
Sobstyl, Michał, et al.. (2019). Deep brain stimulation hardware-related complications and their management: A single-center retrospective analysis of 65 patients with various dystonic conditions. Journal of the Neurological Sciences. 407. 116513–116513. 5 indexed citations
3.
Skowrońska, Marta, Tomasz Kmieć, Anna Członkowska, & Iwona Kurkowska‐Jastrzębska. (2017). Transcranial Sonography in Mitochondrial Membrane Protein-Associated Neurodegeneration. Clinical Neuroradiology. 28(3). 385–392. 6 indexed citations
4.
Hogarth, Penelope, Manju A. Kurian, Allison Gregory, et al.. (2016). Consensus clinical management guideline for pantothenate kinase-associated neurodegeneration (PKAN). Molecular Genetics and Metabolism. 120(3). 278–287. 58 indexed citations
5.
Skowrońska, Marta, et al.. (2016). Retinal and optic nerve abnormalities in neurodegeneration associated with mutations in C19orf12 (MPAN). Journal of the Neurological Sciences. 370. 237–240. 9 indexed citations
6.
Gregory, Allison, Monika Hartig, Holger Prokisch, et al.. (2014). Mitochondrial Membrane Protein-Associated Neurodegeneration. 14 indexed citations
7.
Skowrońska, Marta, et al.. (2014). Mitochondrial protein associated neurodegeneration – Case report. Neurologia i Neurochirurgia Polska. 48(1). 81–84. 7 indexed citations
8.
Ługowska, Agnieszka, et al.. (2013). Apolipoprotein E genotype and LRP1 polymorphisms in patients with different clinical types of metachromatic leukodystrophy. Gene. 526(2). 176–181. 4 indexed citations
9.
Kotulska, Katarzyna, Dariusz Chmielewski, Julita Borkowska, et al.. (2013). Long-term effect of everolimus on epilepsy and growth in children under 3 years of age treated for subependymal giant cell astrocytoma associated with tuberous sclerosis complex. European Journal of Paediatric Neurology. 17(5). 479–485. 81 indexed citations
10.
Hoffman‐Zacharska, Dorota, Tomasz Kmieć, Jarosław Poznański, Marta Jurek, & Jerzy Bal. (2012). Mutations in the PLP1 gene residue p. Gly198 as the molecular basis of Pelizeaus–Merzbacher phenotype. Brain and Development. 35(9). 877–880. 1 indexed citations
11.
Jurkiewicz, Elżbieta, Dorota Domańska‐Pakieła, Małgorzata Syczewska, et al.. (2011). Cerebral tuber count and its impact on mental outcome of patients with tuberous sclerosis complex. Epilepsia. 52(1). 22–27. 55 indexed citations
12.
Jóźwiak, Sergiusz, Aleksandra Habich, Katarzyna Kotulska, et al.. (2010). Intracerebroventricular Transplantation of Cord Blood-Derived Neural Progenitors in a Child with Severe Global Brain Ischemic Injury. PubMed. 1(2). 71–80. 36 indexed citations
13.
Piekutowska‐Abramczuk, Dorota, Martin Magner, Ewa Popowska, et al.. (2009). SURF1 missense mutations promote a mild Leigh phenotype. Clinical Genetics. 76(2). 195–204. 29 indexed citations
14.
Madej‐Pilarczyk, Agnieszka, Tomasz Kmieć, Anna Fidziańska, et al.. (2008). Progeria caused by a rare LMNA mutation p.S143F associated with mild myopathy and atrial fibrillation. European Journal of Paediatric Neurology. 12(5). 427–430. 13 indexed citations
15.
Pietrucha, Barbara, Edyta Heropolitańska–Pliszka, Tomasz Kmieć, et al.. (2008). Ataxia–telangiectasia: guidelines for diagnosis and comprehensive care. European Journal of Paediatric Neurology. 12. S16–S16. 7 indexed citations
16.
Pronicki, Maciej, Ewa Matyja, Dorota Piekutowska‐Abramczuk, et al.. (2007). Light and electron microscopy characteristics of the muscle of patients with SURF1 gene mutations associated with Leigh disease. Journal of Clinical Pathology. 61(4). 460–466. 23 indexed citations
17.
Kmieć, Tomasz, et al.. (2007). [Juvenile form of Alexander's disease - a case confirmed by detection of mutation in GFAP gene].. PubMed. 41(3). 267–71.
18.
Nachulewicz, Paweł, Artur Kamiński, Piotr Kaliciński, et al.. (2006). Analysis of Neurological Complications in Children Transplanted Due to Fulminant Liver Failure. Transplantation Proceedings. 38(1). 253–254. 3 indexed citations
19.
Bekiesińska‐Figatowska, Monika, et al.. (2005). Miejsce rezonansu magnetycznego w łańcuchu diagnostycznym wrodzonych chorób istoty białej i innych zwyrodnieniowych chorób ośrodkowego układu nerwowego u dzieci. 14(27). 37–46.
20.
Michałowicz, R, et al.. (1985). [Clinical symptomatology and diagnostic criteria in Rud's syndrome].. PubMed. 40(49). 1374–5. 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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