Darina Behúlová

491 total citations
30 papers, 325 citations indexed

About

Darina Behúlová is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Darina Behúlová has authored 30 papers receiving a total of 325 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 12 papers in Clinical Biochemistry and 9 papers in Physiology. Recurrent topics in Darina Behúlová's work include Metabolism and Genetic Disorders (12 papers), Diet and metabolism studies (4 papers) and Glycogen Storage Diseases and Myoclonus (3 papers). Darina Behúlová is often cited by papers focused on Metabolism and Genetic Disorders (12 papers), Diet and metabolism studies (4 papers) and Glycogen Storage Diseases and Myoclonus (3 papers). Darina Behúlová collaborates with scholars based in Slovakia, Czechia and Italy. Darina Behúlová's co-authors include Steve Kitchen, Sverre Sandberg, Joris Delanghe, Mario Plebani, Nora Nikolac, Stephen Church, Kjell Grankvist, Matthias Nauck, Kathleen Becan-McBride and Giuseppe Lippi and has published in prestigious journals such as Journal of Chromatography A, Clinical Biochemistry and Clinical Chemistry and Laboratory Medicine (CCLM).

In The Last Decade

Darina Behúlová

30 papers receiving 300 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Darina Behúlová Slovakia	7	144	93	69	62	39	30	325
Haijian Zhao China	12	190 1.3×	175 1.9×	47 0.7×	66 1.1×	44 1.1×	78	500
David J. Hassemer United States	14	159 1.1×	42 0.5×	57 0.8×	58 0.9×	42 1.1×	26	688
María Antonia Llopis Spain	12	220 1.5×	53 0.6×	24 0.3×	117 1.9×	31 0.8×	23	371
Solveig Linko Finland	11	93 0.6×	39 0.4×	20 0.3×	50 0.8×	51 1.3×	18	279
Oswald Sonntag Germany	9	155 1.1×	32 0.3×	27 0.4×	76 1.2×	28 0.7×	33	291
P M Broughton United Kingdom	13	127 0.9×	75 0.8×	22 0.3×	51 0.8×	13 0.3×	28	415
Marta Stahl Denmark	12	152 1.1×	43 0.5×	17 0.2×	81 1.3×	11 0.3×	20	353
C G Fraser United Kingdom	9	257 1.8×	38 0.4×	20 0.3×	122 2.0×	16 0.4×	16	447
Athena K. Petrides United States	12	52 0.4×	49 0.5×	12 0.2×	15 0.2×	39 1.0×	29	339
Timothy C. Hardman United Kingdom	14	112 0.8×	155 1.7×	20 0.3×	14 0.2×	62 1.6×	60	621

Countries citing papers authored by Darina Behúlová

Since Specialization

Citations

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

Fields of papers citing papers by Darina Behúlová

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Darina Behúlová

This figure shows the co-authorship network connecting the top 25 collaborators of Darina Behúlová. A scholar is included among the top collaborators of Darina Behúlová 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 Darina Behúlová. Darina Behúlová 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

Behúlová, Darina, et al.. (2018). An unusually high frequency of SCAD deficiency caused by two pathogenic variants in the ACADS gene and its relationship to the ethnic structure in Slovakia. BMC Medical Genetics. 19(1). 64–64. 18 indexed citations

Matulová, Mária, et al.. (2018). Case study: monitoring of Glc4 tetrasaccharide in the urine of Pompe patients, use of MALDI-TOF MS, and 1H NMR. Chemical Papers. 73(3). 701–711. 6 indexed citations

Urbanová, D, et al.. (2017). GAI – distinct genotype and phenotype characteristics in reported Slovak patients. Bratislavské lekárske listy/Bratislava medical journal. 117(11). 631–638. 2 indexed citations

Górová, Renáta, et al.. (2016). The state of treatment approach and diagnostics in Canavan disease with focus on the determination of N-acetylasparic acid. Chemical Papers. 71(1). 29–40. 2 indexed citations

Behúlová, Darina, et al.. (2015). Amount of folic acid in different types of nutrition used in the neonatal period. Bratislavské lekárske listy/Bratislava medical journal. 116(6). 349–353. 3 indexed citations

Demlová, Regina, Jaroslav Štěrba, Jan Starý, et al.. (2014). Augmenting Clinical Interpretability of Thiopurine Methyltransferase Laboratory Evaluation. Oncology. 86(3). 152–158. 5 indexed citations

Behúlová, Darina, et al.. (2014). The thirteen new cases of isolated ATP synthase deficiency due to TMEM70 mutation in Slovakia: Clinical and biochemical findings. Clinical Biochemistry. 47(9). 769–769. 1 indexed citations

Lippi, Giuseppe, Kathleen Becan-McBride, Darina Behúlová, et al.. (2012). Preanalytical quality improvement: in quality we trust. Clinical Chemistry and Laboratory Medicine (CCLM). 51(1). 229–241. 157 indexed citations

Blaško, Jaroslav, L. Soják, Renáta Górová, et al.. (2011). Determination of sevoflurane and its metabolite hexafluoroisopropanol by direct injection of human plasma into gas chromatography–tandem mass spectrometry. Journal of Chromatography A. 1219. 173–176. 4 indexed citations

10.

Janečková, Hana, Karel Hron, David Friedecký, et al.. (2011). Targeted metabolomic analysis of plasma samples for the diagnosis of inherited metabolic disorders. Journal of Chromatography A. 1226. 11–17. 41 indexed citations

11.

Kolníková, Miriam, Peter Sýkora, & Darina Behúlová. (2011). P05.1 Efficacy and tolerability of miglustat in patients with Niemann – Pick C disease. European Journal of Paediatric Neurology. 15. S49–S49. 1 indexed citations

12.

Behúlová, Darina, et al.. (2010). Newborn with neonatal form of molybdenum cofactor deficiency - the first patient in the Slovak Republic.. PubMed. 31 Suppl 2. 5–7. 2 indexed citations

13.

Behúlová, Darina, et al.. (2009). Conjugated hyperbilirubinaemia as the first manifestation of mevalonic aciduria in a term newborn.. PubMed. 30 Suppl 1. 29–31. 2 indexed citations

14.

Sýkora, Peter, et al.. (2008). Glucose transporter type 1 (GLUT-1) deficiency.. PubMed. 109(10). 245–2. 1 indexed citations

15.

Behúlová, Darina, et al.. (2003). Serum free carnitine in medium chain acyl-CoA dehydrogenase deficiency.. PubMed. 104(12). 405–7. 4 indexed citations

16.

Bzdúch, Vladimı́r, et al.. (2001). Metabolic cause of Reye-like syndrome.. PubMed. 102(9). 427–9. 8 indexed citations

17.

Bzdúch, Vladimı́r, et al.. (2000). Smith–Lemli–Opitz syndrome with extremely low plasma cholesterol. Journal of Inherited Metabolic Disease. 23(6). 638–639. 3 indexed citations

18.

Behúlová, Darina, et al.. (2000). Serum lipids and apolipoproteins in children with the Smith–Lemli–Opitz syndrome. Journal of Inherited Metabolic Disease. 23(4). 413–415. 7 indexed citations

19.

Behúlová, Darina, et al.. (1993). [Electrophoresis of alkaline phosphatase isoenzymes--the key to rapid diagnosis in transient hyperphosphatemia].. PubMed. 48(4). 193–5. 1 indexed citations

20.

Behúlová, Darina, et al.. (1992). [Increased acid phosphatase in isolated transitory hyperphosphatasemia].. PubMed. 131(9). 271–2. 1 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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