Magdalena Pajdowska

715 citations

22 papers · 422 indexed · h-index 11

Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders 12
Molecular Biology
- Mitochondrial Function and Pathology 12
- ATP Synthase and ATPases Research 4
- RNA modifications and cancer 2
Genetics
- Diabetes and associated disorders 2
Sensory Systems
Biochemistry
Pediatrics, Perinatology and Child Health
- Neonatal Health and Biochemistry 2
Cell Biology
- Biotin and Related Studies 2
Neurology
- Alcoholism and Thiamine Deficiency 2

Co-authors: Maciej Pronicki Ewa Pronicka Dorota Piekutowska‐Abramczuk Agnieszka Karkucińska‐Więckowska Elżbieta Ciara Dariusz Rokicki Joanna Trubicka Elżbieta Jurkiewicz
Cited by: Clinical Biochemistry Molecular Biology Genetics
Journals: SHILAP Revista de lepidopterología (1 paper)PLoS ONE (1 paper)Acta Paediatrica (1 paper)
Partner nations: Poland Austria Denmark

In The Last Decade

Magdalena Pajdowska

20 papers receiving 416 citations

Peers

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

The 25 scholars most cited alongside Magdalena Pajdowska, 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 Magdalena Pajdowska Line = papers co-authored together Magdalena Pajdowska links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Case report: Early (molecular) diagnosis is the clue: report on ALDH7A1 deficiency in newborns Frontiers in Genetics ·Patryk Lipiński,Katarzyna Wójcicka-Kowalczyk,Anna Bogdańska,Ewa Ehmke,Magdalena Pajdowska,Katarzyna Skrzypek,Agnieszka Charzewska,Dorota Hoffman‐Zacharska	2024	0
2	Emotional and behavioural functioning in children with tyrosinaemia type 1 Pediatric Endocrinology Diabetes and Metabolism ·Monika Pohorecka,Marcin Biernacki,A. Jakubowska-Winecka,Kinga Leszczynska-Iwanicka,Dariusz Rokicki,Paulina Pokora,Barbara Perkowska,Magdalena Pajdowska,Marta Biernacka	2024	0
3	Early treatment of biotin–thiamine–responsive basal ganglia disease improves the prognosis Molecular Genetics and Metabolism Reports ·Dorota Wesół‐Kucharska,Milena Greczan,Magdalena Kaczor,Magdalena Pajdowska,Dorota Piekutowska‐Abramczuk,Elżbieta Ciara,Paulina Halat-Wolska,Paweł Kowalski,Elżbieta Jurkiewicz,Dariusz Rokicki	2021	6
4	Transferrin isoform analysis from dried blood spots and serum samples by gel isoelectric focusing for screening congenital disorders of glycosylation Acta Biochimica Polonica ·Anna Bogdańska,Dariusz Kozłowski,Magdalena Pajdowska,Patryk Lipiński,Anna Tylki‐Szymańska	2021	2
5	Clinical picture and treatment effects in 5 patients with Methylmalonic aciduria related to MMAA mutations Molecular Genetics and Metabolism Reports ·Dorota Wesół‐Kucharska,Magdalena Kaczor,Magdalena Pajdowska,Ewa Ehmke vel Emczyńska‐Seliga,Anna Bogdańska,Dariusz Kozłowski,Dorota Piekutowska‐Abramczuk,Elżbieta Ciara,Dariusz Rokicki	2020	5
6	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 ·Katarzyna Iwanicka‐Pronicka,Elżbieta Ciara,Dorota Piekutowska‐Abramczuk,Paulina Halat,Magdalena Pajdowska,Maciej Pronicki	2019	6
7	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 ·Ewa Pronicka,Mariola Ropacka‐Lesiak,Joanna Trubicka,Magdalena Pajdowska,Markus Linke,Elsebet Østergaard,Carol Saunders,Sandra Horsch,Clara van Karnebeek,Joy Yaplito‐Lee,Felix Distelmaier,Katrin Õunap,Shamima Rahman,Martin Castelle,John F. Kelleher,Safa Barış,Katarzyna Iwanicka‐Pronicka,Colin G. Steward,Elżbieta Ciara,Saskia B. Wortmann,(unknown)	2017	20
8	Neuropathological characteristics of the brain in two patients with SLC19A3 mutations related to the biotin-thiamine-responsive basal ganglia disease Folia Neuropathologica ·Maciej Pronicki,Dorota Piekutowska‐Abramczuk,Elżbieta Jurkiewicz,Dariusz Rokicki,Elżbieta Ciara,Joanna Trubicka,Katarzyna Iwanicka‐Pronicka,Magdalena Pajdowska,Marek Migdał,Wiesława Grajkowska	2017	4
9	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 ·Elżbieta Ciara,Dariusz Rokicki,Paulina Halat,Agnieszka Karkucińska‐Więckowska,Dorota Piekutowska‐Abramczuk,Johannes A. Mayr,Joanna Trubicka,Tamara Szymańska-Dębińska,Maciej Pronicki,Magdalena Pajdowska,Magdalena Dudzińska,Maria Giżewska,Małgorzata Krajewska‐Walasek,Janusz Książyk,Wolfgang Sperl,Rafał Płoski,Ewa Pronicka	2016	14
10	New perspective in diagnostics of mitochondrial disorders: two years’ experience with whole-exome sequencing at a national paediatric centre Journal of Translational Medicine ·Ewa Pronicka,Dorota Piekutowska‐Abramczuk,Elżbieta Ciara,Joanna Trubicka,Dariusz Rokicki,Agnieszka Karkucińska‐Więckowska,Magdalena Pajdowska,Elżbieta Jurkiewicz,Paulina Halat,Joanna Kosińska,Agnieszka Pollak,Małgorzata Rydzanicz,Piotr Stawiński,Maciej Pronicki,Małgorzata Krajewska‐Walasek,Rafał Płoski	2016	159
11	Outcomes of oral biotin treatment in patients with biotinidase deficiency — Twenty years follow-up SHILAP Revista de lepidopterología ·Edyta Szymańska,Małgorzata Średzińska,Agnieszka Ługowska,Magdalena Pajdowska,Dariusz Rokicki,Anna Tylki‐Szymańska	2015	12
12	“Drop attacks” as first clinical symptoms in a child carrying MTTK m.8344A>G mutation Folia Neuropathologica ·Piotr Buda,Dorota Piekutowska‐Abramczuk,Agnieszka Karkucińska‐Więckowska,Elżbieta Jurkiewicz,Sylwia Chełstowska,Magdalena Pajdowska,Marek Migdał,Janusz Książyk,Katarzyna Kotulska,Ewa Pronicka	2013	8
13	Left ventricular noncompaction (LVNC) and low mitochondrial membrane potential are specific for Barth syndrome Journal of Inherited Metabolic Disease ·Agnieszka Karkucińska‐Więckowska,Joanna Trubicka,Bożena Werner,Katarzyna Kokoszyńska,Magdalena Pajdowska,Maciej Pronicki,E. Czarnowska,Magdalena Lebiedzińska,Jolanta Sykut‐Cegielska,Lidia Ziółkowska,Weronika Jaron,Anna Dobrzańska,Elżbieta Ciara,Mariusz R. Wiȩckowski,Ewa Pronicka	2013	20
14	Postlingual Hearing Loss as a Mitochondrial 3243A>G Mutation Phenotype PLoS ONE ·Katarzyna Iwanicka‐Pronicka,Agnieszka Pollak,Agata Skórka,Urszula Lechowicz,Magdalena Pajdowska,Mariusz Furmanek,Maciej Rzeski,L Korniszewski,Henryk Skarżyńśki,Rafał Płoski	2012	16
15	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 ·Agnieszka Karkucińska‐Więckowska,Magdalena Lebiedzińska,Elżbieta Jurkiewicz,Magdalena Pajdowska,Joanna Trubicka,Tamara Szymańska-Dębińska,Jan M. Suski,Paolo Pinton,Jerzy Duszyński,Maciej Pronicki,Mariusz R. Wiȩckowski,Ewa Pronicka	2011	16
16	Drug-resistant epilepsia and fulminant valproate liver toxicity. Alpers-Huttenlocher syndrome in two children confirmed post mortem by identification of p.W748S mutation in POLG gene Medical Science Monitor ·Ewa Pronicka,Anna Węglewska-Jurkiewicz,Maciej Pronicki,Jolanta Sykut‐Cegielska,Paweł Kowalski,Magdalena Pajdowska,Irena Jankowska,Katarzyna Kotulska,Piotr Kaliciński,Joanna Jakóbkiewicz‐Banecka,Grzegorz Węgrzyn	2011	28
17	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 ·Ewa Pronicka,Anna Węglewska-Jurkiewicz,Joanna Taybert,Maciej Pronicki,Tamara Szymańska-Dębińska,Agnieszka Karkucińska‐Więckowska,Joanna Jakóbkiewicz‐Banecka,Paweł Kowalski,Dorota Piekutowska‐Abramczuk,Magdalena Pajdowska,Piotr Socha,Jolanta Sykut‐Cegielska,Grzegorz Węgrzyn	2010	36
18	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 ·Jolanta Sykut‐Cegielska,Wanda Gradowska,Dorota Piekutowska‐Abramczuk,Brage Storstein Andresen,Rikke Katrine Jentoft Olsen,Mariusz Ołtarzewski,Maciej Pronicki,Magdalena Pajdowska,Anna Bogdańska,Ewa Jabłońska,Barbara Radomyska,Katarzyna Kuśmierska,Małgorzata Krajewska‐Walasek,Niels Gregersen,Ewa Pronicka	2010	32
19	A homozygous mutation in the SCO2 gene causes a spinal muscular atrophy like presentation with stridor and respiratory insufficiency European Journal of Paediatric Neurology ·Maciej Pronicki,Paweł Kowalski,Dorota Piekutowska‐Abramczuk,Joanna Taybert,Agnieszka Karkucińska‐Więckowska,Tamara Szymańska-Dębińska,Elżbieta Karczmarewicz,Magdalena Pajdowska,Marek Migdał,B Milewska-Bobula,Jolanta Sykut‐Cegielska,Ewa Popowska	2009	21
20	Trial of erythropoietin treatment in a boy with glutathione synthetase deficiency Journal of Inherited Metabolic Disease ·Jolanta Sykut‐Cegielska,Agnieszka Jurecka,Joanna Taybert,Wanda Gradowska,Magdalena Pajdowska,Ewa Pronicka	2005	3

About Magdalena Pajdowska

Magdalena Pajdowska is a scholar working on Clinical Biochemistry, Biochemistry and Sensory Systems, having authored 22 papers that have together received 422 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (12 papers), Metabolism and Genetic Disorders (12 papers), ATP Synthase and ATPases Research (4 papers), Neonatal Health and Biochemistry (2 papers), Biotin and Related Studies (2 papers), Alcoholism and Thiamine Deficiency (2 papers), RNA modifications and cancer (2 papers) and Diabetes and associated disorders (2 papers). The work is most often cited by research in Clinical Biochemistry (209 citations), Molecular Biology (316 citations) and Genetics (76 citations). Magdalena Pajdowska has collaborated with scholars based in Poland, Austria and Denmark. Frequent co-authors include Maciej Pronicki, Ewa Pronicka, Dorota Piekutowska‐Abramczuk, Agnieszka Karkucińska‐Więckowska, Elżbieta Ciara, Dariusz Rokicki, Joanna Trubicka, Elżbieta Jurkiewicz, Małgorzata Krajewska‐Walasek and Paulina Halat. Their work appears in journals such as SHILAP Revista de lepidopterología, PLoS ONE and Acta Paediatrica.

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