Anna Kamińska

7.7k total citations
177 papers, 3.7k citations indexed

About

Anna Kamińska is a scholar working on Psychiatry and Mental health, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Anna Kamińska has authored 177 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 65 papers in Psychiatry and Mental health, 47 papers in Pediatrics, Perinatology and Child Health and 35 papers in Molecular Biology. Recurrent topics in Anna Kamińska's work include Epilepsy research and treatment (59 papers), Neonatal and fetal brain pathology (31 papers) and Metabolism and Genetic Disorders (19 papers). Anna Kamińska is often cited by papers focused on Epilepsy research and treatment (59 papers), Neonatal and fetal brain pathology (31 papers) and Metabolism and Genetic Disorders (19 papers). Anna Kamińska collaborates with scholars based in France, Poland and United States. Anna Kamińska's co-authors include Olivier Dulac, Catherine Chiron, Rima Nabbout, Mathieu Milh, Renzo Guerrini, Roustem Khazipov, Anna Belmonte, Pierre Genton, Charlotte Dravet and Nathalie Boddaert and has published in prestigious journals such as Neuron, Nature Genetics and Journal of Clinical Oncology.

In The Last Decade

Anna Kamińska

165 papers receiving 3.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anna Kamińska France 30 1.5k 982 964 953 859 177 3.7k
Yushi Inoue Japan 35 2.5k 1.6× 1.3k 1.3× 1.5k 1.5× 1.0k 1.1× 689 0.8× 222 4.3k
Lionel Carmant Canada 37 2.5k 1.7× 1.4k 1.5× 1.7k 1.7× 969 1.0× 735 0.9× 156 5.1k
Martha Feucht Austria 35 2.0k 1.3× 909 0.9× 836 0.9× 729 0.8× 533 0.6× 136 4.0k
Bruria Ben‐Zeev Israel 33 892 0.6× 514 0.5× 737 0.8× 1.3k 1.4× 994 1.2× 105 3.4k
Thomas Bast Germany 41 2.5k 1.6× 1.6k 1.6× 1.1k 1.1× 567 0.6× 414 0.5× 134 4.2k
Aristea S. Galanopoulou United States 39 1.9k 1.2× 1.0k 1.0× 2.1k 2.1× 1.1k 1.1× 658 0.8× 129 4.1k
Hirokazu Oguni Japan 35 2.5k 1.7× 1.4k 1.4× 1.1k 1.2× 796 0.8× 748 0.9× 144 3.6k
Anne Lortie Canada 27 1.2k 0.8× 579 0.6× 776 0.8× 736 0.8× 585 0.7× 59 2.5k
W.O. Renier Netherlands 32 1.4k 1.0× 1.2k 1.2× 858 0.9× 1.1k 1.1× 472 0.5× 116 3.5k
Norimichi Higurashi Japan 15 2.6k 1.7× 1.4k 1.4× 1.0k 1.1× 437 0.5× 488 0.6× 40 3.4k

Countries citing papers authored by Anna Kamińska

Since Specialization
Citations

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

Fields of papers citing papers by Anna Kamińska

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Kamińska

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Kamińska. A scholar is included among the top collaborators of Anna Kamińska 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 Anna Kamińska. Anna Kamińska 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.
Semeraro, Michaëla, Fabienne Marquant, Laurence Robel, et al.. (2025). Allopurinol Treatment Improves Cognitive Skills, Adaptive Behavior, and Biochemical Markers in Young Patients With Adenylosuccinate Lyase Deficiency. Journal of Inherited Metabolic Disease. 48(6). e70092–e70092. 1 indexed citations
2.
Guillou, Julien, Joan Duprez, Rima Nabbout, et al.. (2024). Interhemispheric coherence of EEG rhythms in children: Maturation and differentiation in corpus callosum dysgenesis. Neurophysiologie Clinique. 54(3). 102981–102981.
3.
Kamińska, Anna, et al.. (2024). Density of smooth functions in Musielak–Orlicz–Sobolev spaces Wk,Φ(Ω)$W^{k,\Phi }(\Omega)$. Mathematische Nachrichten. 297(6). 2006–2035. 1 indexed citations
4.
Grévent, D., Mélodie Aubart, Manoëlle Kossorotoff, et al.. (2023). Clinical and radiological description of 120 pediatric stroke‐like episodes. European Journal of Neurology. 30(7). 2051–2061. 2 indexed citations
5.
Kamińska, Anna, et al.. (2023). Clinical and functional assessment of Acrysof Alcon Vivity extended depth of focus intraocular lenses. SHILAP Revista de lepidopterología. 126(1). 23–26. 1 indexed citations
7.
Łusakowska, Anna, Maria Jędrzejowska, Anna Kamińska, et al.. (2021). Observation of the natural course of type 3 spinal muscular atrophy: data from the polish registry of spinal muscular atrophy. Orphanet Journal of Rare Diseases. 16(1). 150–150. 26 indexed citations
8.
Chiron, Catherine, Anna Kamińska, Cécile Laroche, et al.. (2018). Do children with Dravet syndrome continue to benefit from stiripentol for long through adulthood?. Epilepsia. 59(9). 1705–1717. 42 indexed citations
9.
Brassier, Anaïs, Vassili Valayannopoulos, Nadia Bahi‐Buisson, et al.. (2015). Two new cases of serine deficiency disorders treated with l-serine. European Journal of Paediatric Neurology. 20(1). 53–60. 29 indexed citations
10.
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
11.
Pac, Małgorzata, Jacinta Bustamante, Maja Klaudel‐Dreszler, et al.. (2013). Clinical immunology<br>Disseminated <i>Mycobacterium tuberculosis</i>complex infection in a girl with partialdominant IFN-γ receptor 1 deficiency. Central European Journal of Immunology. 37(4). 378–381. 3 indexed citations
12.
Chipaux, Mathilde, Laurent Vercueil, Anna Kamińska, Séverine Mahon, & Stéphane Charpier. (2013). Persistence of Cortical Sensory Processing during Absence Seizures in Human and an Animal Model: Evidence from EEG and Intracellular Recordings. PLoS ONE. 8(3). e58180–e58180. 31 indexed citations
13.
Kamińska, Anna, et al.. (2011). Diabetes insipidus in the diagnosis of polyuria. Via Medica Journals. 10. 111–114.
14.
Turska‐Kmieć, Anna, Lidia Ziółkowska, Wanda Kawalec, et al.. (2011). Modern concepts on the etiology of the „idiopathic” ventricular arrhythmias in children. Postępy Nauk Medycznych. 1 indexed citations
15.
Kamińska, Anna, et al.. (2010). The assessment of the implementation of the Polish Diabetes Association recommendations in the scope of metabolic control in patients with diabetes treated in endocrinological-diabetological outpatient clinic. Clinical Diabetology. 11(5). 160–166. 2 indexed citations
16.
Pintaudi, Maria, Monika Eisermann, Dorothée Ville, et al.. (2007). Can fever treat epileptic encephalopathies?. Epilepsy Research. 77(1). 44–61. 5 indexed citations
17.
Kamińska, Anna & Perrine Plouin. (2006). Apport de l’EEG dans le diagnostic et le suivi des épilepsies de l’enfant. MTP. Médecine thérapeutique pédiatrie. 9(5). 279–292.
18.
Bronisz, Agata, et al.. (2005). [Assessment of selected factors influencing birthweight in pregnant women with gestational diabetes mellitus].. PubMed. 76(12). 949–54. 3 indexed citations
19.
Dalakas, Marinos C., et al.. (2002). Desmin myopathy: Distinct filamentopathy caused by mutations in the desmin gene. Oxford University Research Archive (ORA) (University of Oxford). 4 indexed citations
20.
Bienvenu, Thierry, Isabelle Souville, Karine Poirier, et al.. (2001). Five novel frameshift mutations in exon 3 and 4 of the MECP2 gene identified in Rett patients: Consequences for the molecular diagnosis strategy. Human Mutation. 18(3). 251–252. 8 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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