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R. Petrovič · SciRah

Researcher profile · Semantic Scholar

R. Petrovič

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R. Petrovič — researcher profile on SciRah

h-index: 8
Works: 36
Citations: 186

Most-cited papers

Rapid and simple method for determination of Nε‐(carboxymethyl)lysine and Nε‐(carboxyethyl)lysine in urine using gas chromatography[sol ]mass spectrometry
R. Petrovič, J. Futas, J. Chandoga, V. Jakuš
200525 citations
Semantic Scholar
Smith‐Lemli‐Opitz syndrome — Fetal phenotypes with special reference to the syndrome‐specific internal malformation pattern
K. Schoner, M. Witsch-Baumgartner, J. Behunova, R. Petrovič +10 more
2019Birth Defects Research19 citations Open access
Semantic Scholar
Neuropathology and biochemistry of early onset familial Alzheimer’s disease caused by presenilin-1 missense mutation Thr116Asn
S. Šutovský, T. Smolek, P. Turčáni, R. Petrovič +5 more
2018Journal of neural transmission17 citations Open access
Semantic Scholar
Adult onset cerebral form of X-linked adrenoleukodystrophy with dementia of frontal lobe type with new L160P mutation in ABCD1 gene.
S. Šutovský, R. Petrovič, J. Chandoga, P. Turčáni
2007Journal of Neurological Sciences15 citations
Semantic Scholar
Rapid and simple method for determination of Nepsilon-(carboxymethyl)lysine and Nepsilon-(carboxyethyl)lysine in urine using gas chromatography/mass spectrometry.
R. Petrovič, J. Futas, J. Chandoga, V. Jakuš
2005Biomedical chromotography12 citations
Semantic Scholar
Frequency of selected single nucleotide polymorphisms influencing the warfarin pharmacogenetics in Slovak population
Ľ. Krajčíová, R. Petrovič, L. Déžiová, J. Chandoga +1 more
2014European Journal of Haematology11 citations
Semantic Scholar
Prevalence of Low Serum Alkaline Phosphatase and Hypophosphatasia in Adult Patients with Atypical Femur Fractures
E. Tsiantouli, E. Biver, T. Chevalley, R. Petrovič +2 more
2022Calcified Tissue International10 citations Open access
Semantic Scholar
Congenital Proximal Radioulnar Synostosis in an Elite Athlete–Case Report
Iľja Chandoga, R. Petrovič, I. Varga, Boris Šteňo +1 more
2023Medicina9 citations Open access
Semantic Scholar
Peroxisomal D-bifunctional protein deficiency: First case reports from Slovakia.
Jana Konkoľová, R. Petrovič, J. Chandoga, Marcel Repiský +6 more
2015Gene8 citations
Semantic Scholar
Frequencies of polymorphisms in CYP2C9 and VKORC1 genes influencing warfarin metabolism in Slovak population: implication for clinical practice
Ľ. Krajčíová, L. Déžiová, R. Petrovič, J. Luha +2 more
2014Bratislava Medical Journal8 citations Open access
Semantic Scholar
Genetic and clinical characteristics including occurrence of testicular adrenal rest tumors in Slovak and Slovenian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Robert Šáhó, V. Dolžan, Mojca Žerjav Tanšek, Andrea Pastorakova +10 more
2023Frontiers in Endocrinology7 citations Open access
Semantic Scholar
A novel mutation in the PEX12 gene causing a peroxisomal biogenesis disorder
J. Konkoľová, R. Petrovič, J. Chandoga, E. Halasová +2 more
2015Molecular Biology Reports7 citations
Semantic Scholar
Influence of different spectra of NOTCH3 variants on the clinical phenotype of CADASIL – experience from Slovakia
M. Juhosová, J. Chandoga, F. Cisárik, S. Dallemule +13 more
2022Neurogenetics5 citations
Semantic Scholar
TREM2 coding variants in Slovak Alzheimer's disease patients.
V. Durmanova, J. Javor, Z. Párnická, G. Minárik +6 more
2022Journal of Integrative Neuroscience4 citations Open access
Semantic Scholar
Transthyretin-related familial amyloid polyneuropathy (ATTR-FAP) in Poland - genetic and clinical presentation.
M. Lipowska, H. Drac, D. Rowczenio, J. Gilbertson +13 more
2020Neurologia i Neurochirurgia Polska4 citations Open access
Semantic Scholar
Differing clinical presentations of two unrelated cases of X-linked adrenoleukodystrophy with identical mutation Y296C in the ABCD1 gene.
S. Šutovský, M. Kolniková, R. Petrovič, B. Kollár +4 more
2014Neuro - endocrinology letters4 citations
Semantic Scholar
Adrenoleukodystrophy--a new mutation identified.
I. Vachalová, J. Chandoga, R. Petrovič, D. Čopíková-Cudráková +2 more
2007Bratislava Medical Journal4 citations Open access
Semantic Scholar
GAI – distinct genotype and phenotype characteristics in reported Slovak patients
J. Lisyová, R. Petrovič, Katarína Juríčková, K. Brennerová +4 more
2016Bratislava Medical Journal3 citations Open access
Semantic Scholar
[The role of cholesterol in embryogenesis and the Smith-Lemli-Opitzov syndrom].
Katarína Kolejáková, R. Petrovič, Peter Turčáni, D. Böhmer +1 more
2010Ceskoslovenska fysiologie3 citations
Semantic Scholar
Atypical Huntington’s disease with the clinical presentation of behavioural variant of frontotemporal dementia
S. Šutovský, T. Smolek, I. Alafuzoff, Andrej Blaho +6 more
2016Journal of neural transmission2 citations
Semantic Scholar
Spectrum of DHCR7 mutations in Slovak patients with Smith-Lemli-Opitz syndrome and detection of common mutations by PCR-based assays.
K. Kolejáková, R. Petrovič, J. Futas, P. Turčáni +2 more
2009General Physiology and Biophysics2 citations Open access
Semantic Scholar
[Peroxisomal hereditary metabolic disorders].
J. Chandoga, R. Petrovič
2001Casopis lekaru ceskych2 citations
Semantic Scholar
Dysfibrinogenemia and hypofibrinogenemia - Spectrum of pathogenic variants in Slovak patients.
D. Jarásková, J. Chandoga, A. Bátorová, Tatiana Prigancová +8 more
2024Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia1 citations Open access
Semantic Scholar
Partial hydatidiform moles with unclear histopathological profile - importance of genetic diagnostics.
L. Gergely, R. Petrovič, Zuzana Feketová, D. Klimova +6 more
2021Ceska gynekologie1 citations
Semantic Scholar
Kennedy’s Disease in the Neuromuscular Centre in Bratislava
F. Cibulčík, I. Martinka, A. Hergottová, I. Urminska +3 more
20151 citations
Semantic Scholar
Tumour suppressor gene and protein TP53/P53 in normal endometrium and endometrial carcinoma
Vladimir Sisovsky, Z. Lasabová, Ľ. Straka, M. Telkova +8 more
20141 citations
Semantic Scholar
[Peroxisomes--characteristics, biogenesis and regulation of peroxisomal genes].
J. Chandoga, R. Petrovič
2001Casopis lekaru ceskych1 citations
Semantic Scholar
Artificial Intelligence‐Driven Multidimensional Phenotyping of Gut Metabolic States for Personalized Prebiotic, Probiotic, and Postbiotic Strategies
Andrej Tóth, S. Furka, Jerguš Vengríni, P. Neogrády +6 more
2026Molecular Nutrition & Food Research0 citations Open access
Semantic Scholar
SOD1 Variants in Patients With Amyotrophic Lateral Sclerosis in Central Eastern Europe: From Genetic Testing to SOD1 Targeted Therapy
Magui Khazaal, Paula Stretavská, M. Kuźma-Kozakiewicz, Krzysztof Nieporęcki +17 more
2026European Journal of Neurology0 citations Open access
Semantic Scholar
Prevalence of clinical manifestations among patients with hypophosphatasia in Central and Eastern European countries
M. Kužma, J. Payer, R. Petrovič, A. Bandura +6 more
2026Frontiers in Endocrinology0 citations Open access
Semantic Scholar
Derivation of a new induced pluripotent stem cell line ORIONi004-A for modelling Duchenne muscular dystrophy.
Dominika Hajduchova, Stanislava Suroviaková, S. Mersakova, V. Nosáľ +33 more
2026Stem Cell Research0 citations Open access
Semantic Scholar
Fabry Disease in Slovakia: How the Situation Has Changed over 20 Years of Treatment
Katarína Juríčková, P. Jungová, R. Petrovič, S. Mattošová +3 more
2022Journal of Personalized Medicine0 citations Open access
Semantic Scholar
Kennedyho choroba v materiáli Centra pre neuromuskulárne ochorenia Bratislava
F. Cibulčík, Ivan Martinka, Andrea Hergottová, I. Urminska +3 more
20150 citations
Semantic Scholar
Pilotná štúdia prevalencie familiárnej amyloidnej polyneuropatie medzi pacientmi s diagnózou idiopatickej polyneuropatie
Ivan Martinka, R. Petrovič, J. Chandoga, Peter Turčáni +1 more
20150 citations
Semantic Scholar
[Hypophosphatasia--biochemical and clinical manifestations, molecular genetic principles].
Iľja Chandoga, J. Futas, R. Petrovič, J. Chandoga
2011Casopis lekaru ceskych0 citations
Semantic Scholar
X-viazaná adrenoleukodystrofia – najčastejšia dedičná metabolická porucha peroxizómov
J. Chandoga, R. Petrovič
20060 citations
Semantic Scholar

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