Magdalena Pajdowska

715 total citations
22 papers, 422 citations indexed

About

Magdalena Pajdowska is a scholar working on Molecular Biology, Clinical Biochemistry and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Magdalena Pajdowska has authored 22 papers receiving a total of 422 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 12 papers in Clinical Biochemistry and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Magdalena Pajdowska's work include Mitochondrial Function and Pathology (12 papers), Metabolism and Genetic Disorders (12 papers) and ATP Synthase and ATPases Research (4 papers). Magdalena Pajdowska is often cited by papers focused on Mitochondrial Function and Pathology (12 papers), Metabolism and Genetic Disorders (12 papers) and ATP Synthase and ATPases Research (4 papers). Magdalena Pajdowska collaborates with scholars based in Poland, France and Austria. Magdalena Pajdowska's co-authors include Maciej Pronicki, Ewa Pronicka, Dorota Piekutowska‐Abramczuk, Agnieszka Karkucińska‐Więckowska, Elżbieta Ciara, Joanna Trubicka, Dariusz Rokicki, Małgorzata Krajewska‐Walasek, Elżbieta Jurkiewicz and Rafał Płoski and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Acta Paediatrica.

In The Last Decade

Magdalena Pajdowska

20 papers receiving 416 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Magdalena Pajdowska Poland	11	316	209	76	34	27	22	422
Heiko Brennenstuhl Germany	11	180 0.6×	99 0.5×	74 1.0×	16 0.5×	30 1.1×	25	315
Sarah Macklin United States	9	176 0.6×	121 0.6×	183 2.4×	25 0.7×	54 2.0×	21	423
Yoichi Wada Japan	13	209 0.7×	113 0.5×	39 0.5×	41 1.2×	43 1.6×	27	372
Emma Glamuzina New Zealand	11	148 0.5×	149 0.7×	62 0.8×	61 1.8×	68 2.5×	30	323
Anke Schumann Germany	11	179 0.6×	149 0.7×	64 0.8×	37 1.1×	75 2.8×	32	379
M.T. García‐Silva Spain	10	378 1.2×	170 0.8×	62 0.8×	18 0.5×	86 3.2×	16	515
Magalie Barth France	12	274 0.9×	171 0.8×	35 0.5×	27 0.8×	92 3.4×	32	378
M. DiRocco Italy	8	353 1.1×	244 1.2×	45 0.6×	19 0.6×	78 2.9×	11	497
Colleen Muraresku United States	10	263 0.8×	175 0.8×	41 0.5×	18 0.5×	30 1.1×	19	313
T. M. Wardell United Kingdom	7	620 2.0×	402 1.9×	44 0.6×	15 0.4×	22 0.8×	10	669

Countries citing papers authored by Magdalena Pajdowska

Since Specialization

Citations

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

Fields of papers citing papers by Magdalena Pajdowska

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Magdalena Pajdowska

This figure shows the co-authorship network connecting the top 25 collaborators of Magdalena Pajdowska. A scholar is included among the top collaborators of Magdalena Pajdowska 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 Magdalena Pajdowska. Magdalena Pajdowska is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Rokicki, Dariusz, et al.. (2024). Emotional and behavioural functioning in children with tyrosinaemia type 1. Pediatric Endocrinology Diabetes and Metabolism. 30(1). 8–13.

Lipiński, Patryk, et al.. (2024). Case report: Early (molecular) diagnosis is the clue: report on ALDH7A1 deficiency in newborns. Frontiers in Genetics. 15. 1464556–1464556.

Pajdowska, Magdalena, et al.. (2021). Early treatment of biotin–thiamine–responsive basal ganglia disease improves the prognosis. Molecular Genetics and Metabolism Reports. 29. 100801–100801. 6 indexed citations

Pajdowska, Magdalena, et al.. (2021). Transferrin isoform analysis from dried blood spots and serum samples by gel isoelectric focusing for screening congenital disorders of glycosylation. Acta Biochimica Polonica. 68(1). 139–142. 2 indexed citations

Pajdowska, Magdalena, et al.. (2020). Clinical picture and treatment effects in 5 patients with Methylmalonic aciduria related to MMAA mutations. Molecular Genetics and Metabolism Reports. 22. 100559–100559. 5 indexed citations

Szymańska, Edyta, Aleksandra Jezela‐Stanek, Dariusz Rokicki, et al.. (2020). Long Term Follow-Up of Polish Patients with Isovaleric Aciduria. Clinical and Molecular Delineation of Isovaleric Aciduria. Diagnostics. 10(10). 738–738. 8 indexed citations

Iwanicka‐Pronicka, Katarzyna, Elżbieta Ciara, Dorota Piekutowska‐Abramczuk, et al.. (2019). Congenital cochlear deafness in mitochondrial diseases related to RRM2B and SERAC1 gene defects. A study of the mitochondrial patients of the CMHI hospital in Warsaw, Poland. International Journal of Pediatric Otorhinolaryngology. 121. 143–149. 6 indexed citations

Książyk, Janusz, et al.. (2018). Nutritional therapy complications in children with ultra‐short bowel syndrome include growth deficiency but not cholestasis. Acta Paediatrica. 107(6). 1088–1093. 6 indexed citations

Pronicki, Maciej, Dorota Piekutowska‐Abramczuk, Elżbieta Jurkiewicz, et al.. (2017). Neuropathological characteristics of the brain in two patients with SLC19A3 mutations related to the biotin-thiamine-responsive basal ganglia disease. Folia Neuropathologica. 2(2). 146–153. 4 indexed citations

10.

Pronicka, Ewa, Mariola Ropacka‐Lesiak, Joanna Trubicka, et al.. (2017). A scoring system predicting the clinical course of CLPB defect based on the foetal and neonatal presentation of 31 patients. Journal of Inherited Metabolic Disease. 40(6). 853–860. 20 indexed citations

11.

Ciara, Elżbieta, Dariusz Rokicki, Paulina Halat, et al.. (2016). Difficulties in recognition of pyruvate dehydrogenase complex deficiency on the basis of clinical and biochemical features. The role of next-generation sequencing. Molecular Genetics and Metabolism Reports. 7. 70–76. 14 indexed citations

12.

Pronicka, Ewa, Dorota Piekutowska‐Abramczuk, Elżbieta Ciara, et al.. (2016). New perspective in diagnostics of mitochondrial disorders: two years’ experience with whole-exome sequencing at a national paediatric centre. Journal of Translational Medicine. 14(1). 174–174. 159 indexed citations

13.

Szymańska, Edyta, et al.. (2015). Outcomes of oral biotin treatment in patients with biotinidase deficiency — Twenty years follow-up. SHILAP Revista de lepidopterología. 5. 33–35. 12 indexed citations

14.

Piekutowska‐Abramczuk, Dorota, Agnieszka Karkucińska‐Więckowska, Elżbieta Jurkiewicz, et al.. (2013). “Drop attacks” as first clinical symptoms in a child carrying MTTK m.8344A>G mutation. Folia Neuropathologica. 4(4). 347–354. 8 indexed citations

15.

Iwanicka‐Pronicka, Katarzyna, Agnieszka Pollak, Agata Skórka, et al.. (2012). Postlingual Hearing Loss as a Mitochondrial 3243A>G Mutation Phenotype. PLoS ONE. 7(10). e44054–e44054. 16 indexed citations

16.

Karkucińska‐Więckowska, Agnieszka, Magdalena Lebiedzińska, Elżbieta Jurkiewicz, et al.. (2011). Increased reactive oxygen species (ROS) production and low catalase level in fibroblasts of a girl with MEGDEL association (Leigh syndrome, deafness, 3-methylglutaconic aciduria).. PubMed. 49(1). 56–63. 16 indexed citations

17.

Pronicka, Ewa, Joanna Taybert, Maciej Pronicki, et al.. (2010). Post mortem identification of deoxyguanosine kinase (DGUOK) gene mutations combined with impaired glucose homeostasis and iron overload features in four infants with severe progressive liver failure. Journal of Applied Genetics. 52(1). 61–66. 36 indexed citations

18.

Sykut‐Cegielska, Jolanta, Wanda Gradowska, Dorota Piekutowska‐Abramczuk, et al.. (2010). Urgent metabolic service improves survival in long‐chain 3‐hydroxyacyl‐CoA dehydrogenase (LCHAD) deficiency detected by symptomatic identification and pilot newborn screening. Journal of Inherited Metabolic Disease. 34(1). 185–195. 32 indexed citations

19.

Pronicki, Maciej, Dorota Piekutowska‐Abramczuk, Joanna Taybert, et al.. (2009). A homozygous mutation in the SCO2 gene causes a spinal muscular atrophy like presentation with stridor and respiratory insufficiency. European Journal of Paediatric Neurology. 14(3). 253–260. 21 indexed citations

20.

Sykut‐Cegielska, Jolanta, Agnieszka Jurecka, Joanna Taybert, et al.. (2005). Trial of erythropoietin treatment in a boy with glutathione synthetase deficiency. Journal of Inherited Metabolic Disease. 28(6). 1153–1154. 3 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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