István Balogh

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 27

Top Topics

Top Venues

International journal of molecular sciences

Pediatric nephrology (Berlin, Germany)

This page only lists publications with an associated author ORCID identifier.

Publications

Éva Márton, Alexandra Varga, András Penyige, Zsuzsanna Birkó, István Balogh, Bálint Nagy, Melinda Szilágyi
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) (2023)
Éva Márton, Alexandra Varga, András Penyige, Zsuzsanna Birkó, István Balogh, Bálint Nagy, Melinda Szilágyi
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) (2023)
László Madar, Viktória Majoros, Zsuzsanna Szűcs, Orsolya Nagy, Tamás Babicz, Henriett Butz, Attila Patocs, István Balogh, Katalin Koczok
Double Heterozygosity for Rare Deleterious Variants in the BRCA1 and BRCA2 Genes in a Hungarian Patient with Breast Cancer. International journal of molecular sciences 24 (20) (2023)
Andrea Xue, István Lénárt, Judit Kincs, Hajnalka Szabó, Andrea Párniczky, István Balogh, Anna Deák, Péter Béla Monostori, Krisztina Hegedűs, Attila J Szabó, Ildikó Szatmári
Neonatal Screening for Cystic Fibrosis in Hungary-First-Year Experiences. International journal of neonatal screening 9 (3) (2023)
Éva Márton, Alexandra Varga, András Penyige, Zsuzsanna Birkó, István Balogh, Bálint Nagy, Melinda Szilágyi
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) (2023)
Gréta Gombos, Nikolett Németh, Ondrej Pös, Jakub Styk, Gergely Buglyó, Tomas Szemes, Ludovit Danihel, Bálint Nagy, István Balogh, Beáta Soltész
New Possible Ways to Use Exosomes in Diagnostics and Therapy via JAK/STAT Pathways. Pharmaceutics 15 (7) (2023)
Ádám Csók, Tamás Micsik, Zsófia Magyar, Tamás Tornóczky, Levente Kuthi, Yumika Nishi, Krisztina Szirák, Monika Csóka, Gábor Ottóffy, Beáta Soltész, István Balogh, Gergely Buglyó
Alterations of miRNA Expression in Diffuse Hyperplastic Perilobar Nephroblastomatosis: Mapping the Way to Understanding Wilms' Tumor Development and Differential Diagnosis. International journal of molecular sciences 24 (10) (2023)
Éva Márton, Alexandra Varga, András Penyige, Zsuzsanna Birkó, István Balogh, Bálint Nagy, Melinda Szilágyi
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) (2023)
Éva Márton, Alexandra Varga, András Penyige, Zsuzsanna Birkó, István Balogh, Bálint Nagy, Melinda Szilágyi
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) (2023)
Tímea Margit Szabó, István Balogh, Anikó Ujfalusi, Zsuzsanna Szűcs, László Madar, Katalin Koczok, Beáta Bessenyei, Ildikó Csürke, Katalin Szakszon
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) (2022)
Tímea Margit Szabó, István Balogh, Anikó Ujfalusi, Zsuzsanna Szűcs, László Madar, Katalin Koczok, Beáta Bessenyei, Ildikó Csürke, Katalin Szakszon
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) (2022)
Tímea Margit Szabó, István Balogh, Anikó Ujfalusi, Zsuzsanna Szűcs, László Madar, Katalin Koczok, Beáta Bessenyei, Ildikó Csürke, Katalin Szakszon
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) (2022)
Tímea Margit Szabó, István Balogh, Anikó Ujfalusi, Zsuzsanna Szűcs, László Madar, Katalin Koczok, Beáta Bessenyei, Ildikó Csürke, Katalin Szakszon
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) (2022)
László Madar, Lilla Juhász, Zsuzsanna Szűcs, Lóránt Kerkovits, Mariann Harangi, István Balogh
Establishing the Mutational Spectrum of Hungarian Patients with Familial Hypercholesterolemia. Genes 13 (1) (2022)
Zsuzsanna Szűcs, Eva Pinti, Irén Haltrich, Orsolya Pálné Szén, Tibor Nagy, Endre Barta, Gábor Méhes, László Bidiga, Olga Török, Anikó Ujfalusi, Katalin Koczok, István Balogh
An Ultra-Rare Manifestation of an X-Linked Recessive Disorder: Duchenne Muscular Dystrophy in a Female Patient. International journal of molecular sciences 23 (21) (2022)
Alexandra Varga, Éva Márton, Arnold Markovics, András Penyige, István Balogh, Bálint Nagy, Melinda Szilágyi
Suppressing the PI3K/AKT Pathway by miR-30d-5p Mimic Sensitizes Ovarian Cancer Cells to Cell Death Induced by High-Dose Estrogen. Biomedicines 10 (9) (2022)
Szilvia Andó, Katalin Koczok, Beáta Bessenyei, István Balogh, Anikó Ujfalusi
Cytogenetic Investigation of Infertile Patients in Hungary: A 10-Year Retrospective Study. Genes 13 (11) (2022)
Eszter Berta, Noémi Zsíros, Miklós Bodor, István Balogh, Hajnalka Lőrincz, György Paragh, Mariann Harangi
Clinical Aspects of Genetic and Non-Genetic Cardiovascular Risk Factors in Familial Hypercholesterolemia. Genes 13 (7) (2022)
Orsolya Horváth, George S Reusz, Veronika Goda, Kata Kelen, István Balogh, Magdolna Kardos, Krisztián M Kállay, Áron Cseh, Attila J Szabo, Gergely Krivan
Non-lupus full-house nephropathy-immune dysregulation as a rare cause of pediatric nephrotic syndrome: Questions. Pediatric nephrology (Berlin, Germany) 37 (5) (2021)
Katalin Koczok, László Horváth, Zeljka Korade, Zoltán András Mezei, Gabriella P Szabó, Ned A Porter, Eszter Kovács, Karoly Mirnics, István Balogh
Biochemical and Clinical Effects of Vitamin E Supplementation in Hungarian Smith-Lemli-Opitz Syndrome Patients. Biomolecules 11 (8) (2021)
Zsolt Gaál, Zsuzsanna Szűcs, Irén Kántor, Andrea Luczay, Péter Tóth-Heyn, Orsolya Benn, Enikő Felszeghy, Zsuzsanna Karádi, László Madar, István Balogh
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, Switzerland) 11 (8) (2021)
Orsolya Horváth, George S Reusz, Veronika Goda, Kata Kelen, István Balogh, Magdolna Kardos, Krisztián M Kállay, Áron Cseh, Attila J Szabo, Gergely Krivan
Non-lupus full-house nephropathy-immune dysregulation as a rare cause of pediatric nephrotic syndrome: Answers. Pediatric nephrology (Berlin, Germany) 37 (5) (2021)
Beáta Soltész, Gergely Buglyó, Nikolett Németh, Melinda Szilágyi, Ondrej Pös, Tomas Szemes, István Balogh, Bálint Nagy
The Role of Exosomes in Cancer Progression. International journal of molecular sciences 23 (1) (2021)
Zsuzsanna Szűcs, Réka Fitala, Ágnes Renáta Nyuzó, Krisztina Fodor, Éva Czemmel, Nóra Vrancsik, Mónika Bessenyei, Tamás Szabó, Katalin Szakszon, István Balogh
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) (2021)
Zsolt Gaál, Zsuzsanna Szűcs, Irén Kántor, Andrea Luczay, Péter Tóth-Heyn, Orsolya Benn, Enikő Felszeghy, Zsuzsanna Karádi, László Madar, István Balogh
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, Switzerland) 11 (8) (2021)
Katalin Koczok, Éva Gombos, László Madar, Olga Török, István Balogh
Interfering effect of maternal cell contamination on invasive prenatal molecular genetic testing. Prenatal diagnosis 38 (9) (2018)
Tamás Szabó, Petronella Orosz, Eszter Balogh, Eszter Jávorszky, István Máttyus, Csaba Bereczki, Zoltán Maróti, Tibor Kalmár, Attila J Szabó, George Reusz, Ildikó Várkonyi, Erzsébet Marián, Éva Gombos, Orsolya Orosz, László Madar, György Balla, János Kappelmayer, Kálmán Tory, István Balogh
Comprehensive genetic testing in children with a clinical diagnosis of ARPKD identifies phenocopies. Pediatric nephrology (Berlin, Germany) 33 (10) (2018)