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Szűcs Zsuzsanna

Szűcs Zsuzsanna

Szűcs Zsuzsanna
Name: Szűcs Zsuzsanna

Publication list

Uploaded publications:
8
Publications in DEA:
8
OA:
8
Date range:
2021-2022
2022
  1. Deák, A., Koczok, K., Bessenyei, B., Szűcs, Z., Madar, L., Csorba, G., Orosz, O., Laki, I., Halász, A., Marsal, G., Balogh, I.: A magyar Cystás Fibrosis Regiszter genetikai revíziója.
    Orv. hetil. 163 (51), 2052-2059, 2022.
    Journal metrics:
    Q4 Medicine (miscellaneous)
  2. Szűcs, Z., Pinti, É., Haltrich, I., Pálné, S., Nagy, T., Barta, E., Méhes, G., Bidiga, L., Török, O., Ujfalusi, A., Koczok, K., Balogh, I.: An Ultra-Rare Manifestation of an X-Linked Recessive Disorder: duchenne Muscular Dystrophy in a Female Patient.
    Int. J. Mol. Sci. 23 (21), 1-15, 2022.
    Journal metrics:
    Q2 Catalysis
    Q1 Computer Science Applications
    D1 Inorganic Chemistry
    Q1 Medicine (miscellaneous)
    Q2 Molecular Biology
    Q1 Organic Chemistry
    Q1 Physical and Theoretical Chemistry
    D1 Spectroscopy
  3. Madar, L., Juhász, L., Szűcs, Z., Kerkovits, L., Harangi, M., Balogh, I.: Establishing the Mutational Spectrum of Hungarian Patients with Familial Hypercholesterolemia.
    Genes. 13 (1), 1-13, 2022.
    Journal metrics:
    Q2 Genetics
    Q2 Genetics (clinical)
2021
  1. Gaál, Z., Szűcs, Z., Kántor, I., Luczay, A., Tóth, -., Benn, O., Felszeghy, E., Karádi, Z., Madar, L., Balogh, I.: A Comprehensive Analysis of Hungarian MODY Patients-Part I: Gene Panel Sequencing Reveals Pathogenic Mutations in HNF1A, HNF1B, HNF4A, ABCC8 and INS Genes.
    Life (Basel). 11 (755), 1-13, 2021.
    Journal metrics:
    Q2 Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Q2 Ecology, Evolution, Behavior and Systematics
    Q2 Paleontology
    Q3 Space and Planetary Science
  2. Gaál, Z., Szűcs, Z., Kántor, I., Luczay, A., Tóth, -., Benn, O., Felszeghy, E., Karádi, Z., Madar, L., Balogh, I.: A Comprehensive Analysis of Hungarian MODY Patients-Part II: glucokinase MODY Is the Most Prevalent Subtype Responsible for about 70% of Confirmed Cases.
    Life (Basel). 11 (8), 1-20, 2021.
    Journal metrics:
    Q2 Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Q2 Ecology, Evolution, Behavior and Systematics
    Q2 Paleontology
    Q3 Space and Planetary Science
  3. Szűcs, Z., Fitala, R., Nyuzó, Á., Fodor, K., Czemmel, É., Vrancsik, N., Bessenyei, M., Szabó, T., Szakszon, K., Balogh, I.: Four New Cases of Hypomyelinating Leukodystrophy Associated with the UFM1 c.-155_-153delTCA Founder Mutation in Pediatric Patients of Roma Descent in Hungary.
    Genes. 12 (9), 1-13, 2021.
    Journal metrics:
    Q2 Genetics
    Q2 Genetics (clinical)
  4. Kozma, K., Bembea, M., Jurca, C., Ioana, M., Streaţă, I., Şoşoi, S., Pirvu, A., Petchesi, C., Szilágyi, A., Sava, C., Jurca, A., Ujfalusi, A., Szűcs, Z., Szakszon, K.: Greig Cephalopolysyndactyly Contiguous Gene Syndrome: case Report and Literature Review.
    Genes. 12 (11), 1-9, 2021.
    Journal metrics:
    Q2 Genetics
    Q2 Genetics (clinical)
updated: 2024-10-13, 01:51

SCImago quartiles of
scientific journal articles

Number of scientific articles: 8
Q1/D1 1 (12.5%)
Q1 1 (12.5%)
Q2 6 (75%)
Q4 1 (12.5%)
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SCImago subject areas and categories

Biochemistry, Genetics and Molecular Biology (7)
Genetics (4)
Biochemistry, Genetics and Molecular Biology (miscellaneous) (2)
Molecular Biology (1)
Medicine (6)
Genetics (clinical) (4)
Medicine (miscellaneous) (2)
Agricultural and Biological Sciences (2)
Ecology, Evolution, Behavior and Systematics (2)
Earth and Planetary Sciences (2)
Paleontology (2)
Space and Planetary Science (2)
Chemical Engineering (1)
Catalysis (1)
Chemistry (1)
Inorganic Chemistry (1)
Organic Chemistry (1)
Physical and Theoretical Chemistry (1)
Spectroscopy (1)
Computer Science (1)
Computer Science Applications (1)

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