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Balogh István

Balogh István

Balogh István
DE
Medical and Health Science Center
Name: Balogh István
Other profiles: Google Scholar, MTMT
Profession: molecular biologist, geneticist
Source: NEPTUN system

Publication list

Uploaded publications:
96
Publications in DEA:
96
OA:
31
Date range:
1997-2020
2020
  1. Mokánszki, A., Molnár, Z., Tóthné Varga, E., Bodnár, B., Jakab, A., Bálint, B., Balogh, I.: Altered microRNAs expression levels of sperm and seminal plasma in patients with infertile ejaculates compared with normozoospermic males.
    Hum. Fertil. (Camb). 23 (4), 246-255, 2020.
    Journal metrics:
    Q2 Medicine (miscellaneous) (2019)
    Q2 Obstetrics and Gynecology (2019)
    Q2 Reproductive Medicine (2019)
  2. Bene, Z., Fejes, Z., Macek, J., Amaral, M., Balogh, I., Nagy, B.: Laboratory biomarkers for lung disease severity and progression in cystic fibrosis.
    Clin. Chim. Acta. 508 277-286, 2020.
    Journal metrics:
    Q2 Biochemistry (2019)
    Q2 Biochemistry (medical) (2019)
    Q2 Clinical Biochemistry (2019)
    Q1 Medicine (miscellaneous) (2019)
2019
  1. 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)
  2. Madar, L., Szakszon, K., Pfliegler, G., P. Szabó, G., Brúgós, B., Ronen, N., Papp, J., Zahuczky, K., Szakos, E., Fekete, G., Oláh, É., Koczok, K., Balogh, I.: FBN1 gene mutations in 26 Hungarian patients with suspected Marfan syndrome or related fibrillinopathies.
    J. Biotechnol. 301 105-111, 2019.
    Journal metrics:
    Q1 Applied Microbiology and Biotechnology
    Q2 Bioengineering
    Q1 Biotechnology
    Q1 Medicine (miscellaneous)
  3. Nagy, B., Bene, Z., Fejes, Z., Heltshe, S., Reid, D., Ronan, N., McCarthy, Y., Smith, D., Nagy, A., Joseloff, E., Balla, G., Kappelmayer, J., Macek, J., Bell, S., Plant, B., Amaral, M., Balogh, I.: Human epididymis protein 4 (HE4) levels inversely correlate with lung function improvement (delta FEV1) in cystic fibrosis patients receiving ivacaftor treatment.
    J. Cyst. Fibros. 18 (2), 271-277, 2019.
    Journal metrics:
    D1 Pediatrics, Perinatology and Child Health
    Q1 Pulmonary and Respiratory Medicine
  4. Koczok, K., Gurumurthy, C., Balogh, I., Korade, Z., Mirnics, K.: Subcellular localization of sterol biosynthesis enzymes.
    J. Mol. Histol. 50 (1), 63-73, 2019.
    Journal metrics:
    Q3 Cell Biology
    Q2 Histology
    Q2 Medicine (miscellaneous)
    Q2 Physiology
  5. 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
  1. Ivády, G., Madar, L., Dzsudzsák, E., Koczok, K., Kappelmayer, J., Krulisova, V., Macek, J., Horváth, A., Balogh, I.: Analytical parameters and validation of homopolymer detection in a pyrosequencing-based next generation sequencing system.
    BMC Genomics. 19 1-8, 2018.
    Journal metrics:
    D1 Biotechnology
    Q1 Genetics
  2. Koczok, K., Merő, G., P. Szabó, G., Madar, L., Gombos, É., Ajzner, É., Mótyán, J., Hortobágyi, T., Balogh, I.: A novel point mutation affecting Asn76 of dystrophin protein leads to dystrophinopathy.
    Neuromusc. Disord. 28 (2), 129-136, 2018.
    Journal metrics:
    Q2 Genetics (clinical)
    Q2 Neurology
    Q1 Neurology (clinical)
    Q1 Pediatrics, Perinatology and Child Health
  3. Szabó, T., Orosz, P., Balogh, E., Jávorszky, E., Máttyus, I., Bereczki, C., Maróti, Z., Kalmár, T., Szabó, A., Reusz, G., Várkonyi, I., Marián, E., Gombos, É., Orosz, O., Madar, L., Balla, G., Kappelmayer, J., Tory, K., Balogh, I.: Comprehensive genetic testing in children with a clinical diagnosis of ARPKD identifies phenocopies.
    Pediatr. Nephrol. 33 (10), 1713-1721, 2018.
    Journal metrics:
    Q1 Nephrology
    Q1 Pediatrics, Perinatology and Child Health
  4. Mokánszki, A., Ujfalusi, A., Gombos, É., Balogh, I.: Examination of Y-Chromosomal Microdeletions and Partial Microdeletions in Idiopathic Infertility in East Hungarian Patients.
    J. Hum. Reprod. Sci. 11 (4), 329-336, 2018.
    Journal metrics:
    Q2 Reproductive Medicine
  5. 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, 2018.
  6. Koczok, K., Gombos, É., Madar, L., Török, O., Balogh, I.: Interfering effect of maternal cell contamination on invasive prenatal molecular genetic testing.
    Prenat. Diagn. 38 (9), 713-719, 2018.
    Journal metrics:
    Q2 Genetics (clinical)
    D1 Obstetrics and Gynecology
  7. Orosz, O., Fodor, M., Balogh, I., Losonczy, G.: Relative anterior microphthalmos in oculodentodigital dysplasia.
    Indian J. Ophthalmol. 66 (2), 334-336, 2018.
    Journal metrics:
    Q3 Ophthalmology
2017
  1. Zádori, D., Szpisjak, L., Madar, L., Varga, V., Csányi, B., Bencsik, K., Balogh, I., Harangi, M., Kereszty, É., Vécsei, L., Klivényi, P.: Different phenotypes in identical twins with cerebrotendinous xanthomatosis: case series.
    Neurol. Sci. 38 (3), 481-483, 2017.
    Journal metrics:
    Q2 Dermatology
    Q2 Medicine (miscellaneous)
    Q2 Neurology (clinical)
    Q2 Psychiatry and Mental Health
  2. Orosz, O., Rajta, I., Vajas, A., Takács, L., Csutak, A., Fodor, M., Kolozsvári, B., Resch, M., Sényi, K., Lesch, B., Szabó, V., Berta, A., Balogh, I., Losonczy, G.: Myopia and Late-Onset Progressive Cone Dystrophy Associate to LVAVA/MVAVA Exon 3 Interchange Haplotypes of Opsin Genes on Chromosome X.
    Invest. Ophthalmol. Vis. Sci. 58 (3), 1834-1842, 2017.
    Journal metrics:
    Q1 Cellular and Molecular Neuroscience
    D1 Ophthalmology
    D1 Sensory Systems
  3. Losonczy, G., Orosz, O., Vajas, A., Takács, L., Csutak, A., Kolozsvári, B., Fodor, M., Resch, M., Sényi, K., Lesch, B., Balogh, I., Szabó, V., Berta, A.: Nem-szindrómás myopia vagy más betegség?.
    Szemészet. 154 50-51, 2017.
  4. Orosz, P., Durányik, M., Biró, E., Körhegyi, I., Balogh, I., Szabó, T.: Question of Prophylactic Anticoagulation in Steroid Sensitive Nephrotic Syndrome: rare Complication in Pediatrics.
    J. Pediatr. & Child Health Care. 2017 (2(1)), 1-3, 2017.
  5. Korade, Z., Genaro-Mattos, T., Tallman, K., Liu, W., Garbett, K., Koczok, K., Balogh, I., Mirnics, K., Porter, N.: Vulnerability of DHCR7+/- mutation carriers to aripiprazole and trazodone exposure.
    J. Lipid Res. 58 (11), 2139-2146, 2017.
    Journal metrics:
    D1 Biochemistry
    Q1 Cell Biology
    D1 Endocrinology
2016
  1. Mizzi, C., Dalabira, E., Kumuthini, J., Dzimiri, N., Balogh, I., Başak, N., Böhm, R., Borg, J., Borgiani, P., Bozina, N., Bruckmueller, H., Burzynska, B., Carracedo, A., Cascorbi, I., Deltas, C., Dolzan, V., Fenech, A., Grech, G., Kasiulevicius, V., Kádaši, L., Kučinskas, V., Khusnutdinova, E., Loukas, Y., Macek, J., Makukh, H., Mathijssen, R., Mitropoulos, K., Mitropoulou, C., Novelli, G., Papantoni, I., Pavlovic, S., Saglio, G., Setric, J., Stojiljkovic, M., Stubbs, A., Squassina, A., Torres, M., Turnovec, M., van Schaik, R., Voskarides, K., Wakil, S., Werk, A., del Zompo, M., Zukic, B., Katsila, T., Lee, M., Motsinger-Rief, A., Mc Leod, H., Van der, S., Patrinos, G.: A European Spectrum of Pharmacogenomic Biomarkers: implications for Clinical Pharmacogenomics.
    PLoS One. 11 (9), e0162866, 2016.
    Journal metrics:
    Q1 Agricultural and Biological Sciences (miscellaneous)
    Q1 Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Q1 Medicine (miscellaneous)
  2. Antal-Szalmás, P., Balogh, I.: Anyagcsere rendellenességek molekuláris genetikai diagnosztikája.
    In: Laboratóriumi Diagnosztikai Gyakorlatok. Szerk.: Kappelmayer János, Muszbek László, Debrecen, Debreceni Egyetem, 11-20, 2016.
Show all
updated: 2021-04-11, 01:07

SCImago quartiles of
scientific journal articles

Number of scientific articles: 82
Q1/D1 21 (25.6%)
Q1 43 (52.4%)
Q2 10 (12.2%)
Q3 7 (8.5%)
Q4 5 (6.1%)
N/A 17 (20.7%)

SCImago subject areas and categories

Medicine (60)
Medicine (miscellaneous) (25)
Hematology (11)
Obstetrics and Gynecology (7)
Pediatrics, Perinatology and Child Health (7)
Ophthalmology (6)
Neurology (clinical) (5)
Reproductive Medicine (5)
Genetics (clinical) (4)
Biochemistry (medical) (3)
Histology (3)
Pathology and Forensic Medicine (3)
Pulmonary and Respiratory Medicine (3)
Cardiology and Cardiovascular Medicine (2)
Nephrology (2)
Critical Care and Intensive Care Medicine (1)
Dermatology (1)
Immunology and Allergy (1)
Pharmacology (medical) (1)
Physiology (medical) (1)
Psychiatry and Mental Health (1)
Rheumatology (1)
Biochemistry, Genetics and Molecular Biology (20)
Cell Biology (6)
Genetics (6)
Biochemistry (4)
Biotechnology (3)
Clinical Biochemistry (3)
Molecular Biology (3)
Biochemistry, Genetics and Molecular Biology (miscellaneous) (2)
Cancer Research (1)
Endocrinology (1)
Molecular Medicine (1)
Physiology (1)
Immunology and Microbiology (7)
Immunology (5)
Applied Microbiology and Biotechnology (2)
Neuroscience (4)
Neurology (3)
Cellular and Molecular Neuroscience (1)
Sensory Systems (1)
Pharmacology, Toxicology and Pharmaceutics (3)
Drug Discovery (1)
Pharmaceutical Science (1)
Pharmacology (1)
Agricultural and Biological Sciences (2)
Agricultural and Biological Sciences (miscellaneous) (2)
Chemical Engineering (2)
Bioengineering (2)

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Journals

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iDEa co-authors

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Other co-authors

Amaral, Margarida D.
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Amaral, Margarida D.
Molnár Mária Judit
Tóthné Varga Emese
Andrikovics Hajnalka
Austerlitz, Frederic
Biró Brigitta Orsolya
Bruckmueller, Henrike
Czajkowski, Krzysztof
de Frutos, Pablo Garcia
Deltas, Constantinos
Garbett, Krassimira A.
Genaro-Mattos, Thiago C.
Gurumurthy, Channabasavaiah B.
Hammarström, Lennart
Kalaydjieva, Luba V.
Kasiulevicius, Vytautas
Kučinskas, Vaidutis
Lee, Ming Ta Michael
Mitropoulos, Konstantinos
Mitropoulou, Christina
Motsinger-Rief, Alison
Van der Spek, Peter J.
Voskarides, Konstantinos