Influence of XPC, XPD, XPF, and XPG gene polymorphisms on the risk and the outcome of acute myeloid leukemia in a Romanian population C Bănescu, M Iancu, AP Trifa, M Dobreanu, VG Moldovan, C Duicu, ... Tumor Biology 37, 9357-9366, 2016 | 41* | 2016 |
Cytokine rs361525, rs1800750, rs1800629, rs1800896, rs1800872, rs1800795, rs1800470, and rs2430561 SNPs in relation with prognostic factors in acute myeloid leukemia C Bănescu, F Tripon, AP Trifa, AG Crauciuc, VG Moldovan, A Bogliş, ... Cancer medicine 8 (12), 5492-5506, 2019 | 27 | 2019 |
Simultaneous FLT3, NPM1 and DNMT3A mutations in adult patients with acute myeloid leukemia–case study F Tripon, GA Crauciuc, VG Moldovan, A Bogliș, I Benedek, E Lázár, ... Revista Romana de Medicina de Laborator 27 (3), 245-254, 2019 | 17 | 2019 |
The relationship between TLR4 rs4986790 and rs4986791 gene polymorphisms and Helicobacter pylori infection in children with gastritis LE Meliţ, CO Mărginean, C Bănescu, A Bogliş, S Mocan, M Iancu Pathology-Research and Practice 215 (12), 152692, 2019 | 13 | 2019 |
Innate immunity–the hallmark of Helicobacter pylori infection in pediatric chronic gastritis LE Meliț, CO Mărginean, MO Săsăran, S Mocan, DV Ghiga, A Bogliş, ... World Journal of Clinical Cases 9 (23), 6686, 2021 | 11 | 2021 |
Presence of copy number aberration and clinical prognostic factors in patients with acute myeloid leukemia: An analysis of effect modification C Bănescu, F Tripon, AP Trifa, AG Crauciuc, A Bogliș, E Lazar, D Dima, ... Pol. Arch. Intern. Med 129, 898-906, 2019 | 11 | 2019 |
Multiplex ligation dependent probe amplification-A useful, fast and cost-effective method for identification of small supernumerary marker chromosome in children with … GA Crauciuc, F Tripon, A Bogliş, A Făgărăşan, C Bănescu Revista Romana de Medicina de Laborator 26 (4), 461-470, 2018 | 11 | 2018 |
The utility of molecular genetic techniques in craniosynostosis cases associated with intellectual disability A Boglis, F Tripon, C Banescu REVISTA ROMANA DE MEDICINA DE LABORATOR 26 (4), 471-477, 2018 | 10 | 2018 |
Exon 21 deletion in the OPHN1 gene in a family with syndromic X-linked intellectual disability: Case report A Boglis, AS Cosma, F Tripon, C Bãnescu Medicine 99 (33), e21632, 2020 | 9 | 2020 |
Modelling the effects of MCM7 variants, somatic mutations, and clinical features on acute myeloid leukemia susceptibility and prognosis F Tripon, M Iancu, A Trifa, GA Crauciuc, A Boglis, D Dima, E Lazar, ... Journal of Clinical Medicine 9 (1), 158, 2020 | 9 | 2020 |
Association analysis of TP53 rs1042522, MDM2 rs2279744, rs3730485, MDM4 rs4245739 variants and acute myeloid leukemia susceptibility, risk stratification scores, and clinical … F Tripon, M Iancu, A Trifa, GA Crauciuc, A Boglis, B Balla, A Cosma, ... Journal of Clinical Medicine 9 (6), 1672, 2020 | 8 | 2020 |
Pathogenic biallelic mutations in ECHS1 in a case with short-chain enoyl-CoA hydratase (SCEH) deficiency-case report and literature review C Muntean, F Tripon, A Bogliș, C Bănescu International Journal of Environmental Research and Public Health 19 (4), 2088, 2022 | 7 | 2022 |
Co-occurrence of PML-RARA gene fusion, chromosome 8 trisomy, and FLT3 ITD mutation in a young female patient with de novo acute myeloid leukemia and early death: A CARE case report F Tripon, GA Crauciuc, A Bogliş, V Moldovan, J Sándor-Kéri, AP Trifa, ... Medicine 99 (14), e19730, 2020 | 7 | 2020 |
Pitt-hopkins syndrome: Clinical and molecular findings of a 5-year-old patient F Tripon, A Bogliș, C Micheu, I Streață, C Bănescu Genes 11 (6), 596, 2020 | 6 | 2020 |
The influence of GPX1 Pro198Leu, CAT C262T and MnSOD Ala16Val gene polymorphisms on susceptibility for non-hodgkin lymphoma and overall survival rate at five years from diagnosis AS Cosma, C Radu, A Moldovan, A Bogliș, GA Crauciuc, E Horváth, ... Acta Marisiensis-Seria Medica 65 (1), 25-30, 2019 | 5 | 2019 |
Association of TLR4 Rs4986791 polymorphism and TLR9 haplotypes with acute myeloid leukemia susceptibility: a case-control study of adult patients C Banescu, F Tripon, AS Bojan, AP Trifa, C Muntean, GA Crauciuc, ... Journal of Personalized Medicine 12 (3), 409, 2022 | 4 | 2022 |
No association between GSTT1, GSTM1 and GSTP1 gene polymorphism and risk of non-Hodgkin lymphoma in a population from Romania A Bogliș, AG Crauciuc, F Tripon, CG Radu, S Demian, C Duicu, ... International Journal of Innovation and Applied Studies 19 (1), 1-8, 2017 | 2 | 2017 |
TERT rs2853669 as a predictor for overall survival in patients with acute myeloid leukaemia F Tripon, C Bănescu, AP Trifa, AG Crauciuc, VG Moldovan, A Boglis, ... Archives of Medical Science: AMS 18 (1), 103, 2022 | 1 | 2022 |
The Role of DNA Repair (XPC, XPD, XPF, and XPG) Gene Polymorphisms in the Development of Myeloproliferative Neoplasms AS Crișan, F Tripon, A Bogliș, GA Crauciuc, AP Trifa, E Lázár, I Macarie, ... Medicina 60 (3), 506, 2024 | | 2024 |
Compound heterozygous FAM20C gene variants in a patient with severe Raine syndrome: a case report C Chirteș, A Bogliș, A Toth, C Rac, C Bănescu Frontiers in Genetics 14, 1179163, 2023 | | 2023 |