L Kádasi

1.2k total citations
18 papers, 416 citations indexed

About

L Kádasi is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, L Kádasi has authored 18 papers receiving a total of 416 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Clinical Biochemistry and 5 papers in Genetics. Recurrent topics in L Kádasi's work include Metabolism and Genetic Disorders (6 papers), Amino Acid Enzymes and Metabolism (2 papers) and Neurological diseases and metabolism (2 papers). L Kádasi is often cited by papers focused on Metabolism and Genetic Disorders (6 papers), Amino Acid Enzymes and Metabolism (2 papers) and Neurological diseases and metabolism (2 papers). L Kádasi collaborates with scholars based in Slovakia, Spain and United States. L Kádasi's co-authors include Eva Feráková, V. Ferák, Martina Plášilová, Ivaylo Stoilov, Mansoor Sarfarazi, H Poláková, Andrea Zaťková, Santiago Rodrı́guez de Córdoba, Daniel Beltrán Valero de Bernabé and Jürg Ott and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Journal of Medical Genetics.

In The Last Decade

L Kádasi

18 papers receiving 403 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
L Kádasi Slovakia	9	207	139	98	79	67	18	416
JJ Mullins United Kingdom	8	180 0.9×	125 0.9×	14 0.1×	59 0.7×	55 0.8×	16	409
Masatoshi Murata Japan	12	159 0.8×	136 1.0×	48 0.5×	116 1.5×	19 0.3×	18	371
David P. Bingaman United States	9	209 1.0×	455 3.3×	45 0.5×	238 3.0×	9 0.1×	13	634
Jiexi Zeng China	10	182 0.9×	243 1.7×	10 0.1×	134 1.7×	20 0.3×	14	455
Aurora Mazzeo Italy	12	210 1.0×	119 0.9×	24 0.2×	39 0.5×	4 0.1×	18	389
Loresa Kriaučiūnienė Lithuania	10	90 0.4×	124 0.9×	13 0.1×	52 0.7×	18 0.3×	69	314
Amirfarbod Yazdanyar United States	10	141 0.7×	91 0.7×	14 0.1×	65 0.8×	12 0.2×	17	298
Jiping Cai China	12	168 0.8×	99 0.7×	30 0.3×	43 0.5×	5 0.1×	22	338
Dalia Žaliūnienė Lithuania	10	82 0.4×	187 1.3×	13 0.1×	103 1.3×	11 0.2×	54	351
Thomas Fredrick United States	9	244 1.2×	226 1.6×	10 0.1×	110 1.4×	33 0.5×	15	459

Countries citing papers authored by L Kádasi

Since Specialization

Citations

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

Fields of papers citing papers by L Kádasi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of L Kádasi

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

All Works

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18 of 18 papers shown

Zaťková, Andrea, L. Ranganath, & L Kádasi. (2020). Alkaptonuria: Current Perspectives. SHILAP Revista de lepidopterología. 4 indexed citations

Radvánszky, Ján, Eckhard Fiedler, L Kádasi, et al.. (2016). Complex phenotypes blur conventional borders between Say–Barber–Biesecker–Young–Simpson syndrome and genitopatellar syndrome. Clinical Genetics. 91(2). 339–343. 23 indexed citations

Baldovič, Marián, et al.. (2013). Analysis of Leucine-rich repeat kinase 2 (LRRK2) and Parkinson protein 2 (parkin, PARK2) genes mutations in Slovak Parkinson disease patients. General Physiology and Biophysics. 32(1). 55–66. 5 indexed citations

Némethová, Miroslava, Andrea Zaťková, L Kádasi, et al.. (2013). Clustering of mutations in the 5’ tertile of the NF1 gene in Slovakia patients with optic pathway glioma. Neoplasma. 60(6). 655–665. 29 indexed citations

Kovács, László, et al.. (2010). Elevated immunoglobulin D levels in children with PFAPA syndrome.. PubMed. 31(6). 743–6. 11 indexed citations

Poláková, H, Gabriel Minárik, Eva Feráková, et al.. (2007). Detection of His1069Gln mutation in Wilson disease by bidirectional PCR amplification of specific alleles (BI-PASA) test.. PubMed. 26(2). 91–6. 8 indexed citations

Brunetti‐Pierri, Nicola, et al.. (2003). Identification of three novel SEDL mutations, including mutation in the rare, non‐canonical splice site of exon 4. Clinical Genetics. 64(3). 235–242. 35 indexed citations

Zaťková, Andrea, Daniel Beltrán Valero de Bernabé, H Poláková, et al.. (2000). High Frequency of Alkaptonuria in Slovakia: Evidence for the Appearance of Multiple Mutations in HGO Involving Different Mutational Hot Spots. The American Journal of Human Genetics. 67(5). 1333–1339. 67 indexed citations

Zaťková, Andrea, Eric Hahnen, Brunhilde Wirth, & L Kádasi. (2000). Analysis of the SMN and NAIP Genes in Slovak Spinal Muscular Atrophy Patients. Human Heredity. 50(3). 171–174. 6 indexed citations

10.

Zaťková, Andrea, Daniel Beltrán Valero de Bernabé, H Poláková, et al.. (2000). High Frequency of Alkaptonuria in Slovakia: Evidence for the Appearance of Multiple Mutations inHGOInvolving Different Mutational Hot Spots. The American Journal of Human Genetics. 67(5). 1333–1339. 25 indexed citations

11.

Plášilová, Martina, Ivaylo Stoilov, Mansoor Sarfarazi, et al.. (1999). Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma. Journal of Medical Genetics. 36(4). 290–294. 143 indexed citations

12.

Plášilová, Martina, Eva Feráková, L Kádasi, et al.. (1998). Linkage of Autosomal Recessive Primary Congenital Glaucoma to the GLC3A Locus in Roms (Gypsies) from Slovakia. Human Heredity. 48(1). 30–33. 43 indexed citations

13.

Poláková, H, et al.. (1998). [Analysis of inversion in intron 22 of the factor F VIII:C gene in patients with hemophilia A in the Slovak population].. PubMed. 99(10). 538–42. 3 indexed citations

14.

Kádasi, L, et al.. (1998). [The spectrum of mutations in the CFTR gene in patients with cystic fibrosis in Slovakia].. PubMed. 99(1). 33–6. 2 indexed citations

15.

Kádasi, L, H Poláková, Eva Feráková, et al.. (1995). PKU in Slovakia: mutation screening and haplotype analysis. Human Genetics. 95(1). 112–114. 4 indexed citations

16.

Kádasi, L, et al.. (1994). Distribution of ApoBII, MCT118 (D1S80), YNZ22 (D17S30), and COL2A1 Amp-FLPs (amplified fragment length polymorphisms) in Caucasoid population of Slovakia.. PubMed. 8(2). 121–7. 3 indexed citations

17.

Feráková, Eva, et al.. (1992). A unique RFLP haplotype at the phenylalanine hydroxylase locus in Czechoslovak Gypsies with phenylketonuria.. PubMed. 2(2). 139–40. 3 indexed citations

18.

Kádasi, L, et al.. (1991). Frequency and distribution of deletions in dystrophin gene in Duchenne muscular dystrophy patients from an east-European Slavonic population.. PubMed. 5(3). 137–40. 2 indexed citations

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