Ladislav Kuchař

932 total citations
25 papers, 376 citations indexed

About

Ladislav Kuchař is a scholar working on Physiology, Molecular Biology and Organic Chemistry. According to data from OpenAlex, Ladislav Kuchař has authored 25 papers receiving a total of 376 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Physiology, 13 papers in Molecular Biology and 6 papers in Organic Chemistry. Recurrent topics in Ladislav Kuchař's work include Lysosomal Storage Disorders Research (16 papers), Sphingolipid Metabolism and Signaling (7 papers) and Carbohydrate Chemistry and Synthesis (6 papers). Ladislav Kuchař is often cited by papers focused on Lysosomal Storage Disorders Research (16 papers), Sphingolipid Metabolism and Signaling (7 papers) and Carbohydrate Chemistry and Synthesis (6 papers). Ladislav Kuchař collaborates with scholars based in Czechia, United States and Russia. Ladislav Kuchař's co-authors include J. Ledvinová, Befekadu Asfaw, Jakub Sikora, Agnieszka Ługowska, Helena Poupětová, Helena Jahnová, Vĕra Malinová, Maria Gulinello, Meirong Bai and Michal Holčapek and has published in prestigious journals such as Nature Communications, The Journal of Immunology and Analytical Biochemistry.

In The Last Decade

Ladislav Kuchař

25 papers receiving 375 citations

Peers

Countries citing papers authored by Ladislav Kuchař

Since Specialization

Citations

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

Fields of papers citing papers by Ladislav Kuchař

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ladislav Kuchař

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

#	Work	Indexed citations
1	Deciphering pathophysiological mechanisms underlying cystathionine beta-synthase-deficient homocystinuria using targeted metabolomics, liver proteomics, sphingolipidomics and analysis of mitochondrial function 2024 ·Redox Biology ·Tomáš Majtán, Thomas Olsén, Jitka Sokolová, Jakub Krijt, (unknown), Tomoaki Ida, Tamás Ditrói, Hana Hansíková, (unknown), Jir̆ı́ Petrák, Ladislav Kuchař, Warren D. Kruger, Péter Nagy, Takaaki Akaike, Viktor Kožich	6
2	Simultaneous deletion of ORMDL1 and ORMDL3 proteins disrupts immune cell homeostasis 2024 ·Frontiers in Immunology ·(unknown), (unknown), (unknown), Ladislav Kuchař, (unknown), Meritxell Alberich-Jordà, (unknown), (unknown)	2
3	Simultaneous reduction of all ORMDL proteins decreases the threshold of mast cell activation 2023 ·Scientific Reports ·(unknown), Viktor Bugajev, (unknown), Ladislav Kuchař, Björn Schuster, Petr Dráber, Ivana Hálová	5
4	Skin inflammation and impaired adipogenesis in a mouse model of acid ceramidase deficiency 2022 ·Journal of Inherited Metabolic Disease ·(unknown), Ladislav Kuchař, Jakub Sikora, William M. McKillop, Jeffrey A. Medin	6
5	Crosstalk between ORMDL3, serine palmitoyltransferase, and 5-lipoxygenase in the sphingolipid and eicosanoid metabolic pathways 2021 ·Journal of Lipid Research ·Viktor Bugajev, (unknown), (unknown), (unknown), Ivana Hálová, Ladislav Kuchař, Ondřej Kuda, (unknown), Björn Schuster, (unknown), (unknown), Daniel Smrž, (unknown), Lubica Dráberová, Monika Bambousková, Petr Dráber	7
6	ORMDL2 Deficiency Potentiates the ORMDL3-Dependent Changes in Mast Cell Signaling 2021 ·Frontiers in Immunology ·Viktor Bugajev, Ivana Hálová, (unknown), (unknown), (unknown), (unknown), (unknown), Lubica Dráberová, Ladislav Kuchař, Björn Schuster, Petr Dráber	10
7	Lipidomic characterization of exosomes isolated from human plasma using various mass spectrometry techniques 2020 ·Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids ·Ondřej Peterka, Robert Jirásko, Michaela Chocholoušková, Ladislav Kuchař, Denise Wolrab, Roman Hájek, David Vrána, (unknown), Bohuslav Melichar, Michal Holčapek	47
8	Transcript, protein, metabolite and cellular studies in skin fibroblasts demonstrate variable pathogenic impacts of NPC1 mutations 2020 ·Orphanet Journal of Rare Diseases ·(unknown), (unknown), Ladislav Kuchař, Ondřej Lukšan, Befekadu Asfaw, Hana Vlášková, (unknown), (unknown), Helena Poupětová, Helena Jahnová, Helena Hůlková, J. Ledvinová, Lenka Dvořáková, Jakub Sikora, M Jirsa, Marie T. Vanier, Martin Hřebı́ček	4
9	A new role for dolichol isoform profile in the diagnostics of CDG disorders 2020 ·Clinica Chimica Acta ·(unknown), Ladislav Kuchař, Nina Ondrušková, Tomáš Honzík, Hana Hansíková	4
10	Chronic visceral acid sphingomyelinase deficiency (Niemann-Pick disease type B) in 16 Polish patients: long-term follow-up 2019 ·Orphanet Journal of Rare Diseases ·Patryk Lipiński, Ladislav Kuchař, Ekaterina Zakharova, Galina Baydakova, Agnieszka Ługowska, Anna Tylki‐Szymańska	17
11	Neural cells generated from human induced pluripotent stem cells as a model of CNS involvement in mucopolysaccharidosis type II 2017 ·Journal of Inherited Metabolic Disease ·(unknown), J. Ledvinová, Jakub Sikora, Ladislav Kuchař, Robert Dobrovolný	17
12	N-butyldeoxynojirimycin delays motor deficits, cerebellar microgliosis, and Purkinje cell loss in a mouse model of mucolipidosis type IV 2017 ·Neurobiology of Disease ·(unknown), Jakub Sikora, Ladislav Kuchař, J. Ledvinová, Yulia Grishchuk, (unknown), Kostantin Dobrenis, Steven U. Walkley	14
13	Quantitation of plasmatic lysosphingomyelin and lysosphingomyelin-509 for differential screening of Niemann-Pick A/B and C diseases 2017 ·Analytical Biochemistry ·Ladislav Kuchař, Jakub Sikora, Maria Gulinello, Helena Poupětová, Agnieszka Ługowska, Vĕra Malinová, Helena Jahnová, Befekadu Asfaw, J. Ledvinová	52
14	Tandem Mass Spectrometry of Sphingolipids 2016 ·Advances in clinical chemistry ·Ladislav Kuchař, Befekadu Asfaw, (unknown), J. Ledvinová	7
15	Fabry disease: renal sphingolipid distribution in the α-Gal A knockout mouse model by mass spectrometric and immunohistochemical imaging 2014 ·Analytical and Bioanalytical Chemistry ·Ladislav Kuchař, (unknown), Lukáš Krásný, Robert Dobrovolný, Helena Hůlková, J. Ledvinová, Michael Volný, Martin Strohalm, Karel Lemr, (unknown), Befekadu Asfaw, (unknown), Robert J. Desnick, Vladimı́r Havlı́ček	17
16	Rapid Isolation of Lysosomal Membranes from Cultured Cells 2013 ·Folia Biologica ·(unknown), J. Lukáš, (unknown), (unknown), Eva Svobodová, Ladislav Kuchař, (unknown), Helena Hůlková, J. Ledvinová, Martin Hřebı́ček	2
17	Direct tandem mass spectrometric profiling of sulfatides in dry urinary samples for screening of metachromatic leukodystrophy 2013 ·Clinica Chimica Acta ·Ladislav Kuchař, Befekadu Asfaw, Helena Poupětová, (unknown), František Tureček, J. Ledvinová	15
18	Glycosphingolipid profile of the apical pole of human placental capillaries: The relevancy of the observed data to Fabry disease 2012 ·Glycobiology ·Helena Hůlková, J. Ledvinová, Ladislav Kuchař, F. Šmíd, (unknown), M. Elleder	7
19	Semisynthesis of C17:0 isoforms of sulphatide and glucosylceramide using immobilised sphingolipid ceramide N‐deacylase for application in analytical mass spectrometry 2010 ·Rapid Communications in Mass Spectrometry ·Ladislav Kuchař, (unknown), Befekadu Asfaw, J Lenfeld, Daniel Horák, Lucie Korecká, Zuzana Bı́lková, J. Ledvinová	10
20	Prosaposin deficiency and saposin B deficiency (activator‐deficient metachromatic leukodystrophy): Report on two patients detected by analysis of urinary sphingolipids and carrying novel PSAP gene mutations 2009 ·American Journal of Medical Genetics Part A ·Ladislav Kuchař, J. Ledvinová, Martin Hřebı́ček, (unknown), Lenka Dvořáková, Linda Berná, Petr Chrastina, Befekadu Asfaw, M. Elleder, (unknown), (unknown), Martin Staudt, Ingeborg Krägeloh‐Mann, Barbara C. Paton, K. Harzer	60

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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