Wanda Gradowska

1.0k total citations
23 papers, 345 citations indexed

About

Wanda Gradowska is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Wanda Gradowska has authored 23 papers receiving a total of 345 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Clinical Biochemistry, 13 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Wanda Gradowska's work include Metabolism and Genetic Disorders (14 papers), Neonatal Health and Biochemistry (5 papers) and Biochemical and Molecular Research (5 papers). Wanda Gradowska is often cited by papers focused on Metabolism and Genetic Disorders (14 papers), Neonatal Health and Biochemistry (5 papers) and Biochemical and Molecular Research (5 papers). Wanda Gradowska collaborates with scholars based in Poland, Denmark and Sweden. Wanda Gradowska's co-authors include Jolanta Sykut‐Cegielska, Lennart Larsson, H. Krawczyk, Saadet Mercimek‐Mahmutoglu, Sylvia Stöckler‐Ipsiroglu, Anna Tylki‐Szymańska, Ewa Pronicka, Agnieszka Jurecka, Adam Gryff‐Keller and Jakub Krijt and has published in prestigious journals such as Journal of Microbiological Methods, Journal of Pharmaceutical and Biomedical Analysis and Molecular Genetics and Metabolism.

In The Last Decade

Wanda Gradowska

21 papers receiving 330 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wanda Gradowska Poland 11 176 113 52 42 39 23 345
Johannes Penzien Germany 10 309 1.8× 153 1.4× 38 0.7× 109 2.6× 52 1.3× 12 499
L. Sweetman United States 13 272 1.5× 175 1.5× 25 0.5× 35 0.8× 51 1.3× 23 411
Sytske H. Moolenaar Netherlands 10 282 1.6× 129 1.1× 22 0.4× 57 1.4× 11 0.3× 12 458
J. P. Colombo Switzerland 11 116 0.7× 121 1.1× 25 0.5× 43 1.0× 15 0.4× 19 271
Julian C. Williams United States 14 135 0.8× 64 0.6× 38 0.7× 154 3.7× 49 1.3× 23 439
Jeffrey W. Stebbins United States 11 264 1.5× 44 0.4× 21 0.4× 66 1.6× 59 1.5× 17 484
Daniel J. O’Donovan Ireland 10 245 1.4× 40 0.4× 19 0.4× 40 1.0× 26 0.7× 34 420
Jill A. Myers United States 12 434 2.5× 37 0.3× 28 0.5× 23 0.5× 22 0.6× 13 595
C. Vianey‐Liaud France 9 345 2.0× 398 3.5× 20 0.4× 93 2.2× 26 0.7× 19 526
Kittipong Tachampa Thailand 9 332 1.9× 52 0.5× 22 0.4× 17 0.4× 38 1.0× 22 664

Countries citing papers authored by Wanda Gradowska

Since Specialization
Citations

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

Fields of papers citing papers by Wanda Gradowska

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wanda Gradowska

This figure shows the co-authorship network connecting the top 25 collaborators of Wanda Gradowska. A scholar is included among the top collaborators of Wanda Gradowska 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 Wanda Gradowska. Wanda Gradowska 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.
Mazur, Artur, Mariusz Ołtarzewski, Jolanta Sykut‐Cegielska, et al.. (2011). An Investigation of the Neurological and Neuropsychiatric Disturbances in Adults with Undiagnosed and/or Untreated Phenylketonuria in Poland. Journal of Applied Research in Intellectual Disabilities. 24(5). 482–488. 1 indexed citations
2.
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
3.
Tylki‐Szymańska, Anna, Wanda Gradowska, Melanie Walter, et al.. (2010). Aminoacylase 1 deficiency associated with autistic behavior. Journal of Inherited Metabolic Disease. 33(S3). 211–214. 16 indexed citations
4.
Jurecka, Agnieszka, Blanka Stibůrková, Jakub Krijt, Wanda Gradowska, & Anna Tylki‐Szymańska. (2010). Xanthine dehydrogenase deficiency with novel sequence variations presenting as rheumatoid arthritis in a 78‐year‐old patient. Journal of Inherited Metabolic Disease. 33(S3). 21–24. 20 indexed citations
5.
Piekutowska‐Abramczuk, Dorota, Rikke Katrine Jentoft Olsen, Jolanta Wierzba, et al.. (2010). A comprehensive HADHA c.1528G>C frequency study reveals high prevalence of long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency in Poland. Journal of Inherited Metabolic Disease. 33(S3). 373–377. 22 indexed citations
6.
Mazur, Artur, et al.. (2009). Evaluation of Somatic Development in Adult Patients with Previously Undiagnosed and/or Untreated Phenylketonuria. Medical Principles and Practice. 19(1). 46–50. 8 indexed citations
7.
Jurecka, Agnieszka, Anna Tylki‐Szymańska, Wanda Gradowska, et al.. (2008). Case report A very rare case of classical xanthinuria (type I). Reumatologia/Rheumatology. 46(2). 95–98.
8.
Jurecka, Agnieszka, Marie Zikánová, Anna Tylki‐Szymańska, et al.. (2008). Clinical, biochemical and molecular findings in seven Polish patients with adenylosuccinate lyase deficiency. Molecular Genetics and Metabolism. 94(4). 435–442. 51 indexed citations
9.
Gradowska, Wanda, et al.. (2008). Investigation of a wide spectrum of inherited metabolic disorders by 13C NMR spectroscopy.. Acta Biochimica Polonica. 55(1). 107–118. 8 indexed citations
10.
Mazur, Artur, Judith Meijer, Lida Zoetekouw, et al.. (2008). Dihydropyrimidine dehydrogenase deficiency presenting with psychomotor retardation in the first Polish patient.. Acta Biochimica Polonica. 55(4). 787–790. 3 indexed citations
11.
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
12.
Gryff‐Keller, Adam, et al.. (2005). Absolute configuration of N‐acetylaspartate in urine from patients with Canavan disease. Journal of Inherited Metabolic Disease. 28(4). 607–609. 3 indexed citations
13.
Sykut‐Cegielska, Jolanta, Wanda Gradowska, Saadet Mercimek‐Mahmutoglu, & Sylvia Stöckler‐Ipsiroglu. (2004). Biochemical and clinical characteristics of creatine deficiency syndromes.. Acta Biochimica Polonica. 51(4). 875–882. 46 indexed citations
14.
Krawczyk, H. & Wanda Gradowska. (2003). Characterisation of the 1H and 13C NMR spectra of N-acetylaspartylglutamate and its detection in urine from patients with Canavan disease. Journal of Pharmaceutical and Biomedical Analysis. 31(3). 455–463. 16 indexed citations
15.
Gradowska, Wanda, et al.. (2002). Determination of the absolute configuration of 2-hydroxyglutaric acid and 5-oxoproline in urine samples by high-resolution NMR spectroscopy in the presence of chiral lanthanide complexes. Journal of Pharmaceutical and Biomedical Analysis. 28(6). 1061–1071. 14 indexed citations
16.
Krawczyk, H., Adam Gryff‐Keller, Wanda Gradowska, Marinus Duran, & Ewa Pronicka. (2001). 13C NMR spectroscopy: a convenient tool for detection of argininosuccinic aciduria. Journal of Pharmaceutical and Biomedical Analysis. 26(3). 401–408. 9 indexed citations
17.
Burlina, Alessandro P., V. Ferrari, P. Divry, et al.. (1999). N-acetylaspartylglutamate in Canavan disease: an adverse effector?. European Journal of Pediatrics. 158(5). 406–409. 32 indexed citations
18.
Krajewska‐Walasek, Małgorzata, et al.. (1999). Further delineation of the classical Smith-Lemli-Opitz syndrome phenotype at different patient ages. Clinical Dysmorphology. 8(1). 29???40–29???40. 14 indexed citations
19.
Mårtensson, Lennart, Wanda Gradowska, & Lennart Larsson. (1997). Use of gas chromatography-mass spectrometry versus the limulus amebocyte lysate test for the determination of airborne endotoxin in confined swine buildings. Aerobiologia. 13(2). 99–107. 5 indexed citations
20.
Gradowska, Wanda & Lennart Larsson. (1994). Determination of absolute configurations of 2- and 3-hydroxy fatty acids in organic dust by gas chromatography-mass spectrometry. Journal of Microbiological Methods. 20(1). 55–67. 29 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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