Publication list
2021
Zodanu, G.,
Oszlánczi, M.,
Havasi, K.,
Kalapos, A.,
Rácz, G.,
Katona, M.,
Ujfalusi, A.,
Nagy, O.,
Széll, M.,
Nagy, D.:
Systemic Screening for 22q11.2 Copy Number Variations in Hungarian Pediatric and Adult Patients With Congenital Heart Diseases Identified Rare Pathogenic Patterns in the Region.
Front. Genet. 12 1-11, 2021.
Journal metrics:
Q2 Genetics
Q2 Genetics (clinical)
Q2 Molecular Medicine
2020
Ujfalusi, A.,
Nagy, O.,
Bessenyei, B.,
Lente, G.,
Kántor, I.,
Borbély, Á.,
Szakszon, K.:
22q13 microduplication syndrome in siblings with mild clinical phenotype: broadening the clinical and behavioral spectrum.
Mol Syndromol. 11 (3), 146-152, 2020.
Journal metrics:
Q3 Genetics
Q3 Genetics (clinical)
2019
Nagy, O.,
Szakszon, K.,
Biró, B.,
Mogyorósy, G.,
Nagy, D.,
Nagy, B.,
Balogh, I.,
Ujfalusi, A.:
Copy number variants detection by microarray and multiplex ligation-dependent probe amplification in congenital heart diseases.
J. Biotechnol. 299 86-95, 2019.
Journal metrics:
Q1 Applied Microbiology and Biotechnology
Q2 Bioengineering
Q1 Biotechnology
Q1 Medicine (miscellaneous)
Nagy, O.,
Kárteszi, J.,
Hartwig, M.,
Bertalan, R.,
Jávorszky, E.,
Erhardt, É.,
Patócs, A.,
Tornóczky, T.,
Balogh, I.,
Ujfalusi, A.:
The importance of the multiplex ligation-dependent probe amplification in the identification of a novel two-exon deletion of the NR5A1 gene in a patient with 46,XY differences of sex development.
Mol. Biol. Rep. 46 (5), 5595-5601, 2019.
Journal metrics:
Q4 Genetics
Q2 Medicine (miscellaneous)
Q4 Molecular Biology
2018
Tóth, N.,
Székely, E.,
Czuriga-Kovács, K.,
Sarkady, F.,
Nagy, O.,
Lánczi, L.,
Berényi, E.,
Fekete, K.,
Fekete, I.,
Csiba, L.,
Bagoly, Z.:
Elevated factor VIII and von Willebrand factor levels predict unfavorable outcome in stroke patients treated with intravenous thrombolysis.
Front. Neurol. 8 1-10, 2018.
Journal metrics:
Q2 Neurology
Q2 Neurology (clinical)
updated: 2023-03-26, 01:07
