@CONFERENCE{MTMT:34813318,
	title = {Inequity in uptake of maternal health care services in developing countries: a systematic review and meta-analysis},
	url = {https://m2.mtmt.hu/api/publication/34813318},
	author = {Gube, Addisu Alemayehu and Murányi, Edit and Vitrai, József and Lohner, Szimonetta},
	booktitle = {Absztraktkötet: XII. Interdiszciplináris Doktorandusz Konferencia = Book of Abstract: XII. Interdisciplinary Doctoral Conference},
	unique-id = {34813318},
	year = {2024},
	pages = {27-27},
	orcid-numbers = {Gube, Addisu Alemayehu/0000-0002-8389-9554; Vitrai, József/0000-0001-9267-806X}
}

@{MTMT:34794735,
	title = {A baleseti agysérülés epidemiológiája},
	url = {https://m2.mtmt.hu/api/publication/34794735},
	author = {Maróti, Péter and Kiss, István},
	booktitle = {Súlyos baleseti agysérültek ellátása},
	unique-id = {34794735},
	year = {2024},
	pages = {9789632269177},
	orcid-numbers = {Maróti, Péter/0000-0001-7538-0675}
}

@article{MTMT:34788027,
	title = {In Vitro Inhibition of Colorectal Cancer Gene Targets by Withania somnifera L. Methanolic Extracts: A Focus on Specific Genome Regulation},
	url = {https://m2.mtmt.hu/api/publication/34788027},
	author = {Macharia, John Macharia and O. Pande, Daniel and Zand, Afshin and Budán, Ferenc Csaba and Káposztás, Zsolt and Kövesdi, Orsolya Liza and Varjas, Tímea and Raposa, Bence},
	doi = {10.3390/nu16081140},
	journal-iso = {NUTRIENTS},
	journal = {NUTRIENTS},
	volume = {16},
	unique-id = {34788027},
	year = {2024},
	eissn = {2072-6643},
	orcid-numbers = {Macharia, John Macharia/0000-0002-7535-9478; Kövesdi, Orsolya Liza/0009-0006-2992-6503; Varjas, Tímea/0000-0002-4950-0669; Raposa, Bence/0000-0001-9551-8440}
}

@article{MTMT:34786852,
	title = {Consumption Pattern of Tea Is Associated with Serum Ferritin Levels of Women of Childbearing Age in Nandi County, Kenya : A Cross-Sectional Study},
	url = {https://m2.mtmt.hu/api/publication/34786852},
	author = {Patrick Nyamemba, Nyakundi and Kiio, Juliana and Munyaka, Ann Wambui and Galgalo, Dahabo and Lohner, Szimonetta},
	doi = {10.1159/000536196},
	journal-iso = {ANN NUTR METAB},
	journal = {ANNALS OF NUTRITION AND METABOLISM},
	volume = {80},
	unique-id = {34786852},
	issn = {0250-6807},
	abstract = {Tea consumption with meals affects iron absorption, increasing the risk of iron deficiency. Our study investigated the association between tea consumption patterns and serum ferritin levels among women of childbearing age (WCA) in Nandi County, Kenya.We conducted a cross-sectional analytical study among 160 WCA selected using a systematic random sampling technique from Kapsabet Ward. Information on tea consumption practices was gathered using a researcher-administered questionnaire, and serum ferritin and C-reactive protein were measured. We assessed associations between tea consumption and iron status of respondents by multivariable regression analysis, adjusting for potential confounders, including parasitic infections and recent severe blood losses.The prevalence of anaemia and iron deficiency among the study participants were 86.2% and 45%, respectively. Majority (90.6%) of the respondents consumed tea or coffee, with an infusion time of more than 5 min (60.0%) and a moderate tea strength (64.1%), within 1 h before or after meals. Iron deficiency was associated the number of teacups consumed (adjusted odds ratio = 7.282, 95% CI = 3.580-14.812).High tea consumption is positively associated with iron deficiency among WCA. Lower tea infusion strength, shorter tea infusion duration, and a lower number of teacups overall consumed, as well as consuming tea 1 h before or after meals instead of with meals, may be recommended for better outcomes in iron status among WCA.},
	keywords = {polyphenols; Serum ferritin; Women of childbearing age; iron status; Tea consumption patterns},
	year = {2024},
	eissn = {1421-9697},
	pages = {109-116},
	orcid-numbers = {Patrick Nyamemba, Nyakundi/0000-0001-8132-6886; Galgalo, Dahabo/0000-0002-9508-7182}
}

@article{MTMT:34763929,
	title = {Same Old Challenges in Subgroup Analysis-Should We Do More About Methods Implementation?},
	url = {https://m2.mtmt.hu/api/publication/34763929},
	author = {Schandelmaier, Stefan and Guyatt, Gordon},
	doi = {10.1001/jamanetworkopen.2024.3339},
	journal-iso = {JAMA NETW OPEN},
	journal = {JAMA NETWORK OPEN},
	volume = {7},
	unique-id = {34763929},
	year = {2024},
	eissn = {2574-3805}
}

@article{MTMT:34760472,
	title = {Aromatase Inhibitors and Plasma Lipid Changes in Postmenopausal Women with Breast Cancer: A Systematic Review and Meta-Analysis},
	url = {https://m2.mtmt.hu/api/publication/34760472},
	author = {Bérczi, Bálint and Borbásné Farkas, Kornélia and Hegyi, Péter and Tóth, Barbara and Csupor, Dezső and Németh, Balázs and Lukács, Anita and Czumbel, László Márk and Kerémi, Beáta and Kiss, István and Szabó, Andrea and Varga, Gábor and Gerber, Gábor and Gyöngyi, Zoltán},
	doi = {10.3390/jcm13061818},
	journal-iso = {J CLIN MED},
	journal = {JOURNAL OF CLINICAL MEDICINE},
	volume = {13},
	unique-id = {34760472},
	abstract = {Background: Women are typically diagnosed with estrogen receptor-positive breast cancer around the postmenopausal period when declining estrogen levels initiate changes in lipid profiles. Aromatase inhibitors (AI) are used to prevent the progression of cancer; however, a further reduction in estrogen levels may have detrimental effects on lipid levels, which was our working hypothesis. Methods: Our meta-analysis was conducted on the lipid profiles of postmenopausal breast cancer patients at baseline and at different treatment time points. Results: We identified 15 studies, including 1708 patients. Studies using anastrozole (ANA), exemestane (EXE), letrozole (LET), and tamoxifen (TMX) were involved. Subgroup analyses revealed that 3- and 12-month administrations of LET and EXE lead to negative changes in lipid profiles that tend to alter the lipid profile undesirably, unlike ANA and TMX. Conclusions: Our results suggest that, despite statistically significant results, EXE and LET may not be sufficient to cause severe dyslipidemia in patients without cardiovascular comorbidities according to the AHA/ACC Guideline on the Management of Blood Cholesterol. However, the results may raise the question of monitoring the effects of AIs in patients, especially those with pre-existing cardiovascular risk factors such as dyslipidemia.},
	keywords = {[Meta-analysis]},
	year = {2024},
	eissn = {2077-0383},
	orcid-numbers = {Borbásné Farkas, Kornélia/0000-0002-5349-6527; Hegyi, Péter/0000-0003-0399-7259; Tóth, Barbara/0000-0002-6086-8819; Csupor, Dezső/0000-0002-4088-3333; Németh, Balázs/0000-0002-4914-9872; Lukács, Anita/0000-0002-0746-8920; Czumbel, László Márk/0000-0002-5915-0383; Kerémi, Beáta/0000-0003-4000-9440; Szabó, Andrea/0000-0003-4949-9431; Varga, Gábor/0000-0002-5506-8198; Gerber, Gábor/0000-0003-0256-2608; Gyöngyi, Zoltán/0000-0001-9330-9119}
}

@article{MTMT:34743842,
	title = {Searching a methods topic: practical challenges and implications for search design},
	url = {https://m2.mtmt.hu/api/publication/34743842},
	author = {Hirt, Julian and Ewald, Hannah and Briel, Matthias and Schandelmaier, Stefan},
	doi = {10.1016/j.jclinepi.2023.10.017},
	journal-iso = {J CLIN EPIDEMIOL},
	journal = {JOURNAL OF CLINICAL EPIDEMIOLOGY},
	volume = {166},
	unique-id = {34743842},
	issn = {0895-4356},
	keywords = {Health Care Sciences & Services},
	year = {2024},
	eissn = {1878-5921},
	orcid-numbers = {Ewald, Hannah/0000-0002-5081-1093; Briel, Matthias/0000-0002-2070-5230}
}

@article{MTMT:34741555,
	title = {Betanin Attenuates Epigenetic Mechanisms and UV-Induced DNA Fragmentation in HaCaT Cells: Implications for Skin Cancer Chemoprevention},
	url = {https://m2.mtmt.hu/api/publication/34741555},
	author = {Zand, Afshin and Sodbuyan, Enkhbilguun and Macharia, John Macharia and Varajti, Krisztina and Szabó, István and Gerencsér, Gellért and Tisza, Boglárka Bernadett and Raposa, Bence and Gyöngyi, Zoltán and Varjas, Tímea},
	doi = {10.3390/nu16060860},
	journal-iso = {NUTRIENTS},
	journal = {NUTRIENTS},
	volume = {16},
	unique-id = {34741555},
	year = {2024},
	eissn = {2072-6643},
	orcid-numbers = {Sodbuyan, Enkhbilguun/0000-0002-9889-7877; Macharia, John Macharia/0000-0002-7535-9478; Raposa, Bence/0000-0001-9551-8440; Gyöngyi, Zoltán/0000-0001-9330-9119; Varjas, Tímea/0000-0002-4950-0669}
}

@article{MTMT:34725861,
	title = {Editorial : Women in science: public health education and promotion 2023},
	url = {https://m2.mtmt.hu/api/publication/34725861},
	author = {Kang, Sunjoo and Rákosy, Zsuzsa and Park, Se Eun and Nguyen, Thi Anh Phuong},
	doi = {10.3389/fpubh.2024.1368704},
	journal-iso = {FRONT PUBLIC HEALTH},
	journal = {FRONTIERS IN PUBLIC HEALTH},
	volume = {12},
	unique-id = {34725861},
	keywords = {education; public health; health promotion; health literacy; health disparity; Women in science},
	year = {2024},
	eissn = {2296-2565}
}

@article{MTMT:34725857,
	title = {Association Between AIRE Polymorphisms rs870881(C>T), rs1003854(T>C) and Rheumatoid Arthritis Risk : A Hungarian Case-control Study},
	url = {https://m2.mtmt.hu/api/publication/34725857},
	author = {Bérczi, Bálint and Nusser, Nóra and Péter, Iván and Németh, Balázs and Gyöngyi, Zoltán},
	doi = {10.21873/invivo.13501},
	journal-iso = {IN VIVO},
	journal = {IN VIVO},
	volume = {38},
	unique-id = {34725857},
	issn = {0258-851X},
	abstract = {Autoimmune regulator (AIRE) is a transcription factor that plays pivotal role in controlling autoimmunity. In the thymus, it supports the presentation of peripheral tissue antigens to developing T cells, where recognition of these self-antigens negatively selects the autoimmune naïve T-cells by central tolerance. Studies demonstrated that single-nucleotide polymorphisms (SNPs) in AIRE alter transcription and propagate clonal survival of autoimmune T cells, therefore increase susceptibility to autoimmune diseases. This study intended to identify SNPs in exon and intron sequences that determine AIRE transcription, where their genotypes are associated with rheumatoid arthritis (RA) risk and clinical parameters.After a thorough in silico research, we enrolled 100 patients with RA and 100 healthy controls to analyze the association of SNP rs870881(C>T) and rs1003854(T>C) in AIRE coding sequence with RA risk by using five different genetic models and selected clinical parameters. Multiplex quantitative polymerase chain reaction was used to determine allelic discrimination of SNPs. RA risk was assessed by odds ratios (ORs) and confidence intervals (CIs).In a recessive model of rs878081, minor allele TT homozygotes were associated with RA (p=0.032, OR=5.44, 95%CI=1.16-25.52); in a recessive model of rs1003854, minor allele CC homozygotes were associated with RA (p=0.047, OR=4.84, 95%CI=1.02-23.02). Higher C-reactive protein (CRP) levels in patients with RA were significantly associated with minor allele homozygotes in recessive and codominant genetic models (p=0.029 and p=0.043, respectively) of rs1003854.Genotypes for minor alleles of rs878081 and rs1003854 might be involved in RA pathogenesis and risk prediction.},
	keywords = {C-REACTIVE PROTEIN; rheumatoid arthritis; SINGLE-NUCLEOTIDE POLYMORPHISM; autoimmune regulator; Allelic discrimination},
	year = {2024},
	eissn = {1791-7549},
	pages = {774-784},
	orcid-numbers = {Németh, Balázs/0000-0002-4914-9872; Gyöngyi, Zoltán/0000-0001-9330-9119}
}