Tudóstér: Nagy Orsolya publikációi

Nagy, O., Kárteszi, J., Elmont, B., Ujfalusi, A.: Case Report: Expressive Speech Disorder in a Family as Hallmark of 7q31 Deletion Involving the FOXP2 Gene.
Front. Pediatr. 9 1-8, 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.

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.

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.

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.

Nagy, O., Baráth, S., Ujfalusi, A.: The role of microRNAs in congenital heart disease.
EJIFCC. 30 (2), 165-178, 2019.

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.