Nagy Orsolya

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Name: Nagy Orsolya

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Date range:

2018-2023

2023

Madar, L., Majoros, V., Szűcs, Z., Nagy, O., Babicz, T., Butz, H., Patócs, A., Balogh, I., Koczok, K.: Double Heterozygosity for Rare Deleterious Variants in the BRCA1 and BRCA2 Genes in a Hungarian Patient with Breast Cancer.
Int. J. Mol. Sci. 24 (20), 1-7, 2023.

Journal metrics:

Q2 Catalysis (2022)
Q1 Computer Science Applications (2022)
D1 Inorganic Chemistry (2022)
Q1 Medicine (miscellaneous) (2022)
Q2 Molecular Biology (2022)
Q1 Organic Chemistry (2022)
Q1 Physical and Theoretical Chemistry (2022)
D1 Spectroscopy (2022)

2021

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.

Journal metrics:

Q1 Pediatrics, Perinatology and Child Health
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)
Bessenyei, B., Mokánszki, A., Nagy, O., Szakszon, K., Zimmermann, A., Zombor, M., Horváth, E., Ujfalusi, A., Balogh, I., Sztriha, L.: Genetic investigation of the LIS1, DCX and TUBA1A genes in patients with lissencephaly.
Eur. J. Hum. Genet. 27 286, 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.

Journal metrics:

Q4 Genetics
Q2 Medicine (miscellaneous)
Q4 Molecular Biology
Nagy, O., Baráth, S., Ujfalusi, A.: The role of microRNAs in congenital heart disease.
EJIFCC. 30 (2), 165-178, 2019.

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: 2024-04-21, 01:06

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Nagy Orsolya

Nagy Orsolya

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Nagy Orsolya

Nagy Orsolya

Publication list

SCImago quartiles ofscientific journal articles

SCImago subject areas and categories

Genre chart

Year chart

Language chart

Journals

iDEa co-authors

Other co-authors

SCImago quartiles of
scientific journal articles