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Kateřina Pavelcová

Observed names: K Pavelcova, K. Pavelcova, Katerina Pavelcova, PAVELCOVÁ, Kateřina, Pavelcova, Katerina, Pavelcová, Kateřina
Observed institutions: Ministry of Health, Charles University, Institute of Rheumatology, German Rheumatism Research Centre, Monash Health, Institute for Medical Research, Hospital Selayang, Second Hospital of Shanxi Medical University, Charité – Universitätsmedizin Berlin
ORCID: 0000-0002-5379-7282
Observed ORCID: 0000-0002-5379-7282
OpenAlex ID: A5005008108
Functional non-synonymous variants of ABCG2 and gout risk
2017 · Blanka Stiburkova, Katerina Pavelcova, et al. · Rheumatology · 92
The impact of dysfunctional variants of ABCG2 on hyperuricemia and gout in pediatric-onset patients
2019 · Blanka Stiburkova, Katerina Pavelcova, et al. · Arthritis Research & Therapy · 78
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Functional Characterization of Clinically-Relevant Rare Variants in ABCG2 Identified in a Gout and Hyperuricemia Cohort
2019 · Yu Toyoda, Andrea Mančíková, et al. · Cells · 70
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Evaluation of the Influence of Genetic Variants of SLC2A9 (GLUT9) and SLC22A12 (URAT1) on the Development of Hyperuricemia and Gout
2020 · Katerina Pavelcova, Jana Bohata, et al. · Journal of Clinical Medicine · 65
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Novel Somatic UBA1 Variant in a Patient With VEXAS Syndrome
2023 · Blanka Stiburkova, Katerina Pavelcova, et al. · Arthritis & Rheumatology · 53
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Alterations in lipidome profiles distinguish early-onset hyperuricemia, gout, and the effect of urate-lowering treatment
2023 · Aleš Kvasnička, David Friedecký, et al. · Arthritis Research & Therapy · 47
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Identification of Two Dysfunctional Variants in the ABCG2 Urate Transporter Associated with Pediatric-Onset of Familial Hyperuricemia and Early-Onset Gout
2021 · Yu Toyoda, Kateřina Pavelcová, et al. · International Journal of Molecular Sciences · 36
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Functional Characterization of Rare Variants in OAT1/SLC22A6 and OAT3/SLC22A8 Urate Transporters Identified in a Gout and Hyperuricemia Cohort
2022 · Jiří Vávra, Andrea Mančíková, et al. · Cells · 29
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Interaction of the p.Q141K Variant of the ABCG2 Gene with Clinical Data and Cytokine Levels in Primary Hyperuricemia and Gout
2019 · Veronika Horváthová, Jana Bohatá, et al. · Journal of Clinical Medicine · 29
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Familial early-onset hyperuricemia and gout associated with a newly identified dysfunctional variant in urate transporter ABCG2
2019 · Yu Toyoda, Kateřina Pavelcová, et al. · Arthritis Research & Therapy · 27
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Renal Hypouricemia 1: Rare Disorder as Common Disease in Eastern Slovakia Roma Population
2021 · Blanka Stiburkova, Jana Bohatá, et al. · Biomedicines · 20
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Genetic background of uric acid metabolism in a patient with severe chronic tophaceous gout
2016 · Lenka Petru, Katerina Pavelcova, et al. · Clinica Chimica Acta · 19
Thiopurine-induced toxicity is associated with dysfunction variant of the human molybdenum cofactor sulfurase gene (xanthinuria type II)
2018 · Blanka Stiburkova, Katerina Pavelcova, et al. · Toxicology and Applied Pharmacology · 18
Identification of a dysfunctional exon-skipping splice variant in GLUT9/SLC2A9 causal for renal hypouricemia type 2
2023 · Yu Toyoda, Sung Kweon Cho, et al. · Frontiers in Genetics · 12
Examining the Association of Rare Allelic Variants in Urate Transporters SLC22A11, SLC22A13, and SLC17A1 with Hyperuricemia and Gout
2024 · Jiří Vávra, Kateřina Pavelcová, et al. · Disease Markers · 11
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The Examination of a TPMT Gene Before Administration of Azathioprine in Rheumatology Practice and Identification of a Novel Variant p.W29R
2021 · Katerina Pavelcova, Petra Hanova, et al. · JCR Journal of Clinical Rheumatology · 4
A prevalent MOCS2 variant in the Roma population is associated with a novel mild form of molybdenum cofactor deficiency
2025 · Sung Kweon Cho, Guenter Schwarz, et al. · European Journal of Pediatrics · 3
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An Unusual Cause of Exercise-Induced Acute Kidney Injury
2017 · Virginia Quan, Omer Ali, et al. · The American Journal of Medicine · 2
Diagnostic performance of four proposed algorithms for suspected VEXAS syndrome
2025 · Tereza Sychrovská, Blanka Stibůrková, et al. · Rheumatology · 1
Identification of pathogenic variants in the ABCG2 gene in patients with severe familial hyperuricemia and gout
2025 · Yu Toyoda, Katerina Pavelcova, et al. · Molecular and Cellular Biochemistry · 1
Ab1275 Suggested Approach to Uba1 Gene Mutation Testing in Patients With Suspected Vexas Syndrome
2022 · K. Pavelcova, B. Stiburkova, et al. · Annals of the Rheumatic Diseases · 1
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Thu0404 Influence of Urate Transportosome for Hyperuricemia and Gout
2020 · B. Stiburkova, K. Pavelcova, et al. · Annals of the Rheumatic Diseases · 1
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P107 Polymorphisms in SLC2A9 and SLC22A12 genes are related to hyperuricemia, gout and also to hypouricemia
2019 · K Pavelcova, J Bohata, et al. · Annals of the Rheumatic Diseases · 1
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07.05 Detection of polymorphisms in genes associated with azathioprine toxicity
2017 · Katerina Pavelcova, Lenka Petru, et al. · Annals of the Rheumatic Diseases · 1
Selected autoantibodies and cytokines as potential markers of disease activity in systemic lupus erythematosus
2026 · Pavelcova, Katerina, Navratilova, Adela, et al. · German Medical Science (German Research Foundation)
Works count: 50
Citation count: 621
H-index: 13
I10-index: 15
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