Division of Clinical Genetics

1.

Torner, B., Géczi, D., Klekner, Á., Balogh, I., Penyige, A., Hádáné Birkó, Z.: Construction of a miRNA Panel for Differentiating Lung Adenocarcinoma Brain Metastases and Glioblastoma.
Cancers. 17 (4), 1-23, (article identifier: 581), 2025.

doi DEA WoS Scopus

Journal metrics:

Q2 Cancer Research (2024)

Q1 Oncology (2024)

2.

Géczi, D., Klekner, Á., Balogh, I., Penyige, A., Szilágyi, M., Virga, J., Bakó, A., Nagy, B., Torner, B., Hádáné Birkó, Z.: Identification of Deregulated miRNAs and mRNAs Involved in Tumorigenesis and Detection of Glioblastoma Patients Applying Next-Generation RNA Sequencing.
Pharmaceuticals. 18 (3), 1-29, (article identifier: 431), 2025.

doi DEA WoS Scopus

Journal metrics:

Q1 Drug Discovery (2024)

Q2 Molecular Medicine (2024)

Q1 Pharmaceutical Science (2024)

3.

Márton, É., Beke-Varga, A. E., Domoszlai, D., Buglyó, G., Balázs, A., Penyige, A., Balogh, I., Nagy, B., Szilágyi, M.: Non-Coding RNAs in Cancer: structure, Function, and Clinical Application.
Cancers (Basel). 17 (4), 1-41, (article identifier: 579), 2025.

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Journal metrics:

Q2 Cancer Research (2024)

Q1 Oncology (2024)

4.

Csók, Á., Micsik, T., Magyar, Z., Tornóczky, T., Kuthi, L., Nishi, Y., Soltész, B., Szirák, K., Balogh, I., Buglyó, G.: Assessing the potential of miRNA biomarkers for the differential diagnosis of Wilms' tumor and diffuse hyperplastic perilobar nephroblastomatosis.
Eur. J. Hum. Genet. 32 (S1), 553, 2024.

DEA WoS

5.

Ujfalusi, A.: Citogenetikai vizsgálatok helye a malignus hematológiai betegségek diagnosztikájában.
Magyar Onkol. 68, 341-349, 2024.

DEA

6.

Feró, O., Szabóné, V. D., Nagy, É., Karányi, Z., Sipos, É., Engelhardt, J., Török, N., Balogh, I., Vető, B., Liko, I., Fóthi, Á., Szabó, Z., Halmos, G., Vécsei, L., Arányi, T., Székvölgyi, L.: DNA methylome, R-loop and clinical exome profiling of patients with sporadic amyotrophic lateral sclerosis.
Sci Data. 11 (1), 1-12, (article identifier: 123), 2024.

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Journal metrics:

D1 Computer Science Applications

D1 Education

D1 Information Systems

D1 Library and Information Sciences

D1 Statistics, Probability and Uncertainty

D1 Statistics and Probability

7.

Hudák, R., Szegedi, I., Petrás, M., Gaál, Z., Macsi, L., Szakszon, K., Merő, G., Nagy, O., Balogh, I., Bedekovics, J., Méhes, G., Baráth, S., Kiss, C.: Generalizált lymphadenopathia hátterében álló ritka ok: esetismertetés.
Gyermekgyógyászat. 75 (5), 365, 2024.

DEA

8.

Mianesaz, H., Ghalamkari, S., Abbasi, F., Razzaghy-Azar, M., Sayarifard, F., Vakili, R., Sedghi, M., Noroozi Asl, S., Hosseini, S., Amoli, M. M., Yaghootkar, H.: Genetic variant profiling of neonatal diabetes mellitus in Iranian patients: unveiling 58 distinct variants in 14 genes.
J of Diabetes Invest. 15 (10), 1390-1402, 2024.

doi DEA WoS Scopus

9.

Csók, Á., Micsik, T., Magyar, Z., Tornóczky, T., Kuthi, L., Nishi, Y., Szirák, K., Csóka, M., Ottóffy, G., Soltész, B., Balogh, I., Buglyó, G.: Alterations of miRNA Expression in Diffuse Hyperplastic Perilobar Nephroblastomatosis: Mapping the Way to Understanding Wilms' Tumor Development and Differential Diagnosis.
Int. J. Mol. Sci. 24 (10), 1-16, (article identifier: 8793), 2023.

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Journal metrics:

Q2 Catalysis

Q1 Computer Science Applications

D1 Inorganic Chemistry

Q1 Medicine (miscellaneous)

Q2 Molecular Biology

D1 Organic Chemistry

Q1 Physical and Theoretical Chemistry

D1 Spectroscopy

10.

Sira, L., Zsíros, N., Bidiga, L., Barna, S., Kanyári, Z., Nagy, E. B., Guillaume, N., Wild, D., Molnárné Rázsó, K., Andó, S., Balogh, I., Nagy, E. V., Balogh, Z.: Case report: Metastatic pancreatic neuroendocrine tumour associated with portal vein thrombosis; successful management with subsequent pregnancies.
Front Endocrinol (Lausanne). 14, 1-7, (article identifier: 1095815), 2023.

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Journal metrics:

Q1 Endocrinology, Diabetes and Metabolism

11.

Mianesaz, H., Ghalamkari, S., Salehi, M., Behnam, M., Hosseinzadeh, M., Basiri, K., Ghasemi, M., Sedghi, M., Ansari, B.: Causative variants linked with limb girdle muscular dystrophy in an Iranian population: 6 novel variants.
Molec Gen & Gen Med. 11 (2), 1-14, (article identifier: 2101), 2023.

doi DEA WoS Scopus

Journal metrics:

Q3 Genetics (clinical)

Q3 Genetics

Q3 Molecular Biology

12.

Márton, É., Beke-Varga, A. E., Penyige, A., Hádáné Birkó, Z., Balogh, I., Nagy, B., Szilágyi, M.: Comparative Analysis of Transcriptomic Changes including mRNA and microRNA Expression Induced by the Xenoestrogens Zearalenone and Bisphenol A in Human Ovarian Cells.
Toxins. 15 (2), 1-22, (article identifier: 140), 2023.

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Journal metrics:

Q1 Health, Toxicology and Mutagenesis

Q1 Toxicology

13.

Kárteszi, J., Ziegler, A., Tihanyi, M., Elmont, B., Zhang, Y., Patócs, B., Molnár, M. J., Méhes, G., Wells, K., Jakus, R., Bessenyei, B., Ranatunga, W., Morava, É.: Compound heterozygous variants in MAPK8IP3 were detected in severe congenital hypotonia mimicking lethal spinal muscular atrophy.
Am. J. Med. Genet. A. 191 (9), 2428-2432, 2023.

doi DEA WoS Scopus

Journal metrics:

Q2 Genetics

Q3 Genetics (clinical)

14.

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, (article identifier: 15334), 2023.

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Journal metrics:

Q2 Catalysis

Q1 Computer Science Applications

D1 Inorganic Chemistry

Q1 Medicine (miscellaneous)

Q2 Molecular Biology

D1 Organic Chemistry

Q1 Physical and Theoretical Chemistry

D1 Spectroscopy

15.

Pócsi, M., Fejes, Z., Bene, Z., Nagy, A. C., Balogh, I., Amaral, M. D., Macek, J. M., Nagy, B. J.: Human epididymis protein 4 (HE4) plasma concentration inversely correlates with the improvement of cystic fibrosis lung disease in p.Phe508del-CFTR homozygous cases treated with the CFTR modulator lumacaftor/ivacaftor combination.
J. Cyst. Fibros. 22 (6), 1085-1092, 2023.

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Journal metrics:

D1 Pediatrics, Perinatology and Child Health

D1 Pulmonary and Respiratory Medicine

16.

Xue, A., Lénárt, I., Kincs, J., Szabó, H., Párniczky, A., Balogh, I., Deák, A., Monostori, P. B., Hegedűs, K., Szabó, A., Szatmári, I.: Neonatal Screening for Cystic Fibrosis in Hungary-First-Year Experiences.
Int. J. Neonatal Screen. 9 (3), 1-10, (article identifier: 47), 2023.

doi DEA WoS Scopus

Journal metrics:

Q1 Immunology and Microbiology (miscellaneous)

D1 Obstetrics and Gynecology

D1 Pediatrics, Perinatology and Child Health

17.

Gombos, G., Németh, N., Pös, O., Styk, J., Buglyó, G., Szemes, T., Danihel, L., Nagy, B., Balogh, I., Soltész, B.: New Possible Ways to Use Exosomes in Diagnostics and Therapy via JAK/STAT Pathways.
Pharmaceutics. 15 (7), 1-17, (article identifier: 1904), 2023.

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Journal metrics:

Q1 Pharmaceutical Science

18.

Deák, A., Koczok, K., Bessenyei, B., Szűcs, Z., Madar, L., Csorba, G. É., Orosz, O., Laki, I., Halász, A., Marsal, G., Balogh, I.: A magyar Cystás Fibrosis Regiszter genetikai revíziója.
Orv. hetil. 163 (51), 2052-2059, 2022.

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Q4 Medicine (miscellaneous)

19.

Zsíros, N., Paragh, G., Balogh, I., Harangi, M.: A MODY jelentősége a diabéteszes betegek ellátásában: irodalmi áttekintés egy eset kapcsán.
Metabolizmus. 20 (2), 51-58, 2022.

DEA

20.

Szűcs, Z., Pinti, É., Haltrich, I., Pálné, S. O., 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, (article identifier: 13076), 2022.

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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

21.

Berta, E., Zsíros, N., Bodor, M., Balogh, I., Lőrincz, H., Paragh, G., Harangi, M.: Clinical Aspects of Genetic and Non-Genetic Cardiovascular Risk Factors in Familial Hypercholesterolemia.
Genes. 13 (7), 1-19, (article identifier: 1158), 2022.

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Journal metrics:

Q2 Genetics

Q2 Genetics (clinical)

22.

Horváth, O., Reusz, G., Goda, V., Kelen, K., Balogh, I., Kardos, M., Kállay, K., Cseh, Á., Szabó, A., Kriván, G.: Correction to: Non-lupus full-house nephropathy - immune dysregulation as a rare cause of pediatric nephrotic syndrome: answers.
Pediatr. Nephrol. 37 (6), 1429, 2022.

doi DEA WoS Scopus

23.

Andó, S., Koczok, K., Bessenyei, B., Balogh, I., Ujfalusi, A.: Cytogenetic Investigation of Infertile Patients in Hungary: a 10-Year Retrospective Study.
Genes. 13 (11), 1-13, (article identifier: 2086), 2022.

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Journal metrics:

Q2 Genetics

Q2 Genetics (clinical)

24.

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, (article identifier: 153), 2022.

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Journal metrics:

Q2 Genetics

Q2 Genetics (clinical)

25.

Szabó, T. M., Balogh, I., Ujfalusi, A., Szűcs, Z., Madar, L., Koczok, K., Bessenyei, B., Csürke, I., Szakszon, K.: Helsmoortel-Van der Aa Syndrome: Cardiothoracic and Ectodermal Manifestations in Two Patients as Further Support of a Previous Observation on Phenotypic Overlap with RASopathies.
Genes. 13 (12), 1-13, (article identifier: 2367), 2022.

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Journal metrics:

Q2 Genetics

Q2 Genetics (clinical)

Division of Clinical Genetics

Publication list