Transfer tehnologic<\/strong><\/p>\nPe l\u00e2ng\u0103 serviciile de rutin\u0103 \u0219i activit\u0103\u021bile de cercetare, Laboratorul BIOMOL contribuie activ la transferul tehnologic, facilit\u00e2nd transpunerea rezultatelor cercet\u0103rii \u00een practica clinic\u0103. Acest proces include:<\/p>\n
\n- implementarea tehnologiilor genomice avansate (platforme NGS, PCR \u00een timp real, MLPA) \u00een fluxurile de diagnostic;<\/li>\n<\/ul>\n","publicatii_centru":"
\n- Stoian M, Azamfirei L, Bandila SR, Stoian A, Bab\u0103 DF,\u00a0B\u0103nescu C. Circulating microRNAs and Plasma Gelsolin as Biomarkers of Sepsis: Molecular Insights and Prospects for Precision Medicine. 2025;15(11):1621, doi: 10.3390\/biom15111621. https:\/\/pubmed.ncbi.nlm.nih.gov\/41301539\/<\/a><\/li>\n
- Anciuc-Crauciuc M, Crauciuc GA, Tripon F, Simon M, Cucerea MC,\u00a0B\u0103nescu CV. Exploring\u00a0IL-10<\/em>and\u00a0NOS3<\/em>\u00a0Genetic Variants as a Risk Factor for Neonatal Respiratory Distress Syndrome and Its Outcome. Diagnostics (Basel). 2025 Sep 6;15(17):2259. doi: 10.3390\/diagnostics15172259. https:\/\/pubmed.ncbi.nlm.nih.gov\/40941746\/<\/a><\/li>\n
- Anciuc-Crauciuc M, Cucerea MC, Tripon F, Crauciuc GA, B\u0103nescu CV.Descriptive and Functional Genomics in Neonatal Respiratory Distress Syndrome: From Lung Development to Targeted Therapies. Int J Mol Sci. 2024, 25(1):649. doi: 10.3390\/ijms25010649. https:\/\/pubmed.ncbi.nlm.nih.gov\/38203821\/<\/a><\/li>\n
- Stoian A, Bajko Z, B\u0103la\u0219a R, Andone S, Stoian M, Ormeni\u0219an I, Muntean C, B\u0103nescu C. Characteristics of Developmental and Epileptic Encephalopathy Associated with PACS2 p.Glu209Lys Pathogenic Variant-Our Experience and Systematic Review of the Literature. Biomolecules. 2024 Feb 23;14(3):270. doi: 10.3390\/biom14030270. https:\/\/pubmed.ncbi.nlm.nih.gov\/38540691\/<\/a><\/li>\n
- Ognean ML, Anciuc-Crauciuc M, Gali\u0219 R, Stepan AE, Stepan MD, B\u0103nescu C, Grosu F, Kramer BW, Cucerea M. ABCA3 c.838C>T (p.Arg280Cys, R280C) and c.697C>T (p.Gln233Ter, Q233X, Q233*) as Causative Variants for RDS: A Family Case Study and Literature Review. Biomedicines. 2024 Oct 18;12(10):2390. doi: 10.3390\/biomedicines12102390. https:\/\/pubmed.ncbi.nlm.nih.gov\/39457702\/<\/a><\/li>\n
- Anciuc-Crauciuc M, Cucerea MC, Crauciuc GA, Tripon F, B\u0103nescu CV. Evaluation of the Copy Number Variants and Single-Nucleotide Polymorphisms of ABCA3 in Newborns with Respiratory Distress Syndrome-A Pilot Study. Medicina (Kaunas). 2024 Feb 29;60(3):419. doi: 10.3390\/medicina60030419. https:\/\/pubmed.ncbi.nlm.nih.gov\/38541145\/<\/a><\/li>\n
- Cri\u0219an AS, Tripon F, Bogli\u0219 A, Crauciuc GA, Trifa AP, L\u00e1z\u00e1r E, Macarie I, Gabor MR, B\u0103nescu C. The Role of DNA Repair (XPC, XPD, XPF, and XPG) Gene Polymorphisms in the Development of Myeloproliferative Neoplasms. Medicina (Kaunas). 2024 Mar 19;60(3):506. doi: 10.3390\/medicina60030506. https:\/\/pubmed.ncbi.nlm.nih.gov\/38541232\/<\/a><\/li>\n
- Pastorello Y, Russo AP, B\u0103nescu C, Caprio V, G\u00e1ll Z, Potempa L, Cordo\u0219 B, Di Napoli M, Slevin M. Brain Vascular Expression of Monomeric C-Reactive Protein Is Blocked by C10M Following Intraperitoneal Injection in an ApoE-\/- Murine Model of Dyslipidemia: An Immunohistochemical Analysis. Cureus. 2024 May 20;16(5):e60682. doi: 10.7759\/cureus.60682. eCollection 2024 May. https:\/\/pubmed.ncbi.nlm.nih.gov\/38899254\/<\/a><\/li>\n
- Onisor D, Brusnic O, Banescu C, Carstea C, Sasaran M, Stoian M, Avram C, Boicean A, Boeriu A, Dobru D. miR-155 and miR-21 as Diagnostic and Therapeutic Biomarkers for Ulcerative Colitis: There Is Still a Long Way to Go. Biomedicines. 2024 Jun 13;12(6):1315. doi: 10.3390\/biomedicines12061315. https:\/\/pubmed.ncbi.nlm.nih.gov\/38927522\/<\/a><\/li>\n
- Pastorello Y, Manu D, Sawkulycz X, Caprio V, Banescu C, Dobreanu M, Potempa L, Di Napoli M, Slevin M. mCRP-Induced Focal Adhesion Kinase-Dependent Monocyte Aggregation and M1 Polarization, Which Was Partially Blocked by the C10M Inhibitor. Int J Mol Sci. 2024 Mar 7;25(6):3097. doi: 10.3390\/ijms25063097. https:\/\/pubmed.ncbi.nlm.nih.gov\/38542070\/<\/a><\/li>\n
- Balla B, Tripon F, Lazar E, B\u0103nescu C. Analysis of Mutational Status of IGHV, and Cytokine Polymorphisms as Prognostic Factors in Chronic Lymphocytic Leukemia: The Romanian Experience. Int J Mol Sci. 2024;25(3):1799. doi: 10.3390\/ijms25031799. https:\/\/pubmed.ncbi.nlm.nih.gov\/38339076\/<\/a><\/li>\n
- M\u0103nescu IB, Gabor MR, Moldovan GV, Hadadi L, Hu\u021banu A, B\u0103nescu C, Dobreanu M. An 8-SNP LDL Cholesterol Polygenic Score: Associations with Cardiovascular Risk Traits, Familial Hypercholesterolemia Phenotype, and Premature Coronary Heart Disease in Central Romania. Int J Mol Sci. 2024 Sep 18;25(18):10038. doi: 10.3390\/ijms251810038. https:\/\/pubmed.ncbi.nlm.nih.gov\/39337524\/<\/a><\/li>\n
- B\u0103nescu C, Tripon F, Muntean C. The Genetic Landscape of Myelodysplastic Neoplasm Progression to Acute Myeloid Leukemia. Int J Mol Sci. 2023 Mar 17;24(6):5734. doi: 10.3390\/ijms24065734. PMID: 36982819. Review. https:\/\/pubmed.ncbi.nlm.nih.gov\/36982819\/<\/a><\/li>\n
- Muntean C, Chirtes C, Baczoni B, Banescu C. PAX2<\/em> Gene Mutation in Pediatric Renal Disorders-A Narrative Review. Int J Mol Sci. 2023 Aug 13;24(16):12737. doi: 10.3390\/ijms241612737. https:\/\/pubmed.ncbi.nlm.nih.gov\/37628926\/<\/a><\/li>\n
- Balla B, Tripon F, Candea M,\u00a0Banescu C. Copy Number Variations and Gene Mutations Identified by Multiplex Ligation-Dependent Probe Amplification in Romanian Chronic Lymphocytic Leukemia Patients. J Pers Med. 2023;13(8):1239. doi: 10.3390\/jpm13081239. https:\/\/pubmed.ncbi.nlm.nih.gov\/37623489\/<\/a><\/li>\n
- F\u0103g\u0103r\u0103\u0219an A, S\u0103s\u0103ran M, Gozar L, Crauciuc A, B\u0103nescu C. The Role of Galectin-3 in Predicting Congenital Heart Disease Outcome: A Review of the Literature. Int J Mol Sci. 2023 22;24(13):10511. doi: 10.3390\/ijms241310511. Review. https:\/\/pubmed.ncbi.nlm.nih.gov\/37445687\/<\/a><\/li>\n
- S\u0103s\u0103ran MO, B\u0103nescu C. Role of salivary miRNAs in the diagnosis of gastrointestinal disorders: a mini-review of available evidence. Front Genet. 2023;14:1228482. doi: 10.3389\/fgene.2023.1228482. Review. https:\/\/pubmed.ncbi.nlm.nih.gov\/37456668\/<\/a><\/li>\n
- Chirte\u0219 C, Bogli\u0219 A, Toth A, Rac C, B\u0103nescu C. Compound heterozygous FAM20C<\/em> gene variants in a patient with severe Raine syndrome: a case report. Front Genet. 2023 Apr 26;14:1179163. doi: 10.3389\/fgene.2023.1179163. https:\/\/pubmed.ncbi.nlm.nih.gov\/37158450\/<\/a><\/li>\n
- Banescu C, Tripon F, Bojan AS, et al. Association of TLR4 Rs4986791 Polymorphism and TLR9 Haplotypes with Acute Myeloid Leukemia Susceptibility: A Case-Control Study of Adult Patients. J Pers Med. 2022;12(3):409. https:\/\/pubmed.ncbi.nlm.nih.gov\/35330409\/<\/a><\/li>\n
- Muntean C, Starcea IM, Banescu C. Diabetic kidney disease in pediatric patients: A current review. World J Diabetes. 2022;13(8):587-599. doi:10.4239\/wjd.v13.i8.587 https:\/\/pubmed.ncbi.nlm.nih.gov\/36159227\/<\/a><\/li>\n
- Muntean C, Starcea IM, Stoica C, Banescu C. Clinical Characteristics, Renal Involvement, and Therapeutic Options of Pediatric Patients With Fabry Disease [published correction appears in Front Pediatr. 2022;10:1045199]. Front Pediatr.;10:908657. https:\/\/pubmed.ncbi.nlm.nih.gov\/35722479\/<\/a><\/li>\n
- Muntean C, Tripon F, Bogli\u0219 A, B\u0103nescu C. Pathogenic Biallelic Mutations in ECHS1 in a Case with Short-Chain Enoyl-CoA Hydratase (SCEH) Deficiency-Case Report and Literature Review. Int J Environ Res Public Health. 2022;19(4):2088. https:\/\/pubmed.ncbi.nlm.nih.gov\/35206276\/<\/a><\/li>\n
- Muntean C, Sasaran MO, Crisan A, Banescu C. Effects of PPARG and PPARGC1A gene polymorphisms on obesity markers. Front Public Health. 2022;10:962852. https:\/\/pubmed.ncbi.nlm.nih.gov\/36466447\/<\/a><\/li>\n
- Meli\u021b LE, M\u0103rginean CO, S\u0103s\u0103ran MO, Mocanu S, Ghiga DV, Cri\u0219an A, B\u0103nescu C. Innate Immune Responses in Pediatric Patients with Gastritis-A Trademark of Infection or Chronic Inflammation?. Children (Basel). 2022;9(2):121. https:\/\/pubmed.ncbi.nlm.nih.gov\/35204842\/<\/a><\/li>\n
- Tripon F, B\u0103nescu C, Trifa AP, et al. TERT rs2853669 as a predictor for overall survival in patients with acute myeloid leukaemia. Arch Med Sci. 2021;18(1):103-111 https:\/\/pubmed.ncbi.nlm.nih.gov\/35154531\/<\/a><\/li>\n
- B\u0103nescu C, Tripon F, Trifa A et al Presence of copy number aberration and clinical prognostic factors in patients with acute myeloid leukemia: an analysis of effect modification. Pol Arch Intern Med 2019;129(12):898-906. doi:10.20452\/pamw.15093; IF=2.8 https:\/\/pubmed.ncbi.nlm.nih.gov\/31808755\/<\/a><\/u><\/li>\n
- Balla B, Tripon F,\u00a0Banescu C. From Descriptive to Functional Genomics of Leukemias Focusing on Genome Engineering Techniques.Int J Mol Sci. 2021 17;22(18):10065. doi: 10.3390\/ijms221810065, (IF=5.923) https:\/\/pubmed.ncbi.nlm.nih.gov\/34576226\/<\/a><\/li>\n
- Duicu C, Pitea AM, S\u0103s\u0103ran OM, Cozea I, Man L,\u00a0B\u0103nescu C. Nephrogenic diabetes insipidus in children (Review). Exp Ther Med. 2021 Jul;22(1):746. doi: 10.3892\/etm.2021.10178. https:\/\/pubmed.ncbi.nlm.nih.gov\/34055061\/<\/a><\/li>\n
- Negovan A, Iancu M, Tripon F, Crauciuc A, Mocan S,\u00a0B\u0103nescu C. Cytokine\u00a0TGF-\u03b21, TNF-\u03b1<\/em>,\u00a0IFN-\u03b3<\/em>and\u00a0IL-6<\/em>\u00a0Gene Polymorphisms and Localization of Premalignant Gastric Lesions in Immunohistochemically\u00a0 pylori<\/em>-negative Patients. Int J Med Sci. 2021;18(12):2743-2751. doi: 10.7150\/ijms.60517. https:\/\/pubmed.ncbi.nlm.nih.gov\/34104107\/<\/a><\/li>\n
- Negovan A, Sz\u0151ke AR, Mocan S, B\u0103nescu C. Helicobacter pylori-Positive Gastric Biopsies-Association with Clinical Predictors. Life (Basel). 2022;12(11):1789. doi:10.3390\/life12111789, https:\/\/pubmed.ncbi.nlm.nih.gov\/36362946\/<\/a><\/li>\n
- Tripon F, Iancu M, Trifa A, Crauciuc GA, Boglis A, Dima D, Lazar E, B\u0103nescu C. Modelling the Effects of MCM7 Variants, Somatic Mutations, and Clinical Features on Acute Myeloid Leukemia Susceptibility and Prognosis. J Clin Med. 2020 Jan 8;9(1):158. doi: 10.3390\/jcm9010158. (IF=3,303) https:\/\/www.mdpi.com\/2077-0383\/9\/1\/158<\/a><\/li>\n
- Crauciuc GA, Iancu M, Olah P, Tripon F, \u2026, B\u0103nescu C. Significant Associations between AXIN1 rs1805105, rs12921862, rs370681 Haplotypes and Variant Genotypes of AXIN2 rs2240308 with Risk of Congenital Heart Defects. Int J Environ Res Public Health. 2020, 17(20):7671. doi:10.3390\/ijerph17207671. (IF=2,84) https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC7589771\/<\/a><\/li>\n
- Tripon F, Bogli\u0219 A, Micheu C, Strea\u021b\u0103 I, B\u0103nescu C. Pitt-Hopkins Syndrome: Clinical and Molecular Findings of a 5-Year-Old Patient. Genes (Basel). 2020 May 28;11(6):596. doi: 10.3390\/genes11060596. (IF=3,759) https:\/\/www.mdpi.com\/2073-4425\/11\/6\/596<\/a><\/li>\n
- Georgescu AM, Banescu C, Azamfirei R, Hutanu A, Moldovan V, Badea I, Voidazan S, Dobreanu M, Chirtes IR, Azamfirei L. Evaluation of TNF-\u03b1 genetic polymorphisms as predictors for sepsis susceptibility and progression. BMC Infect Dis. 2020 Mar 14;20(1):221. doi: 10.1186\/s12879-020-4910-6. (IF=2,688) https:\/\/bmcinfectdis.biomedcentral.com\/articles\/10.1186\/s12879-020-4910-6<\/a><\/li>\n
- Lighezan DL, Bojan AS, Iancu M, .., B\u0103nescu C, Trifa AP. TET2 rs1548483 SNP Associating with Susceptibility to Molecularly Annotated Polycythemia Vera and Primary Myelofibrosis. J Pers Med. 2020,10(4):259. doi: 10.3390\/jpm10040259. (IF=4,43) https:\/\/pubmed.ncbi.nlm.nih.gov\/33271790\/<\/a><\/li>\n
- Tripon F, Iancu M, Trifa A, Crauciuc GA, Boglis A, .., Banescu C. Association Analysis of TP53 rs1042522, MDM2 rs2279744, rs3730485, MDM4 rs4245739 Variants and Acute Myeloid Leukemia Susceptibility, Risk Stratification Scores, and Clinical Features: An Exploratory Study. J Clin Med. 2020;9(6):1672. doi: 10.3390\/jcm9061672. (IF=3,303) https:\/\/pubmed.ncbi.nlm.nih.gov\/32492903\/<\/a><\/li>\n
- Bogli\u015f A, Cosma AS, Tripon F, B\u00e3nescu C. Exon 21 deletion in the OPHN1 gene in a family with syndromic X-linked intellectual disability: Case report. Medicine (Baltimore). 2020 ;99(33):e21632. doi: 10.1097\/MD.0000000000021632. (IF=1,552) https:\/\/pubmed.ncbi.nlm.nih.gov\/32872024\/<\/a><\/li>\n
- Tripon F, Iancu M, Trifa A, Crauciuc GA, Boglis A, Dima D, Lazar E, B\u0103nescu C. Modelling the Effects of MCM7 Variants, Somatic Mutations, and Clinical Features on Acute Myeloid Leukemia Susceptibility and Prognosis. J Clin Med. 2020 Jan 8;9(1). pii: E158. doi: 10.3390\/jcm9010158. IF=5.688 https:\/\/www.mdpi.com\/2077-0383\/9\/1\/158<\/a><\/li>\n
- Tripon F, Crauciuc GA, Bogli\u015f A, Moldovan V, S\u00e1ndor-K\u00e9ri J, Benedek IJ, Trifa AP, B\u0103nescu C. 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. Medicine (Baltimore). 2020 Apr;99(14):e19730. doi: 10.1097\/MD.0000000000019730. (IF=1,552) https:\/\/pubmed.ncbi.nlm.nih.gov\/32243411\/<\/a><\/li>\n
- Nechifor-Boil\u0103 A, Banescu C, Zahan AE, Moldovan V, Szasz E, Borda A. DNA isolation from achieved formalin-fixed paraffin-embedded tissues in a series of 212 thyroid carcinoma cases: the influence of preanalytical factors on DNA quantity and purity. J Investig Med. 2020 Mar;68(3):792-798. doi: 10.1136\/jim-2019-001134. (IF=2,304) https:\/\/pubmed.ncbi.nlm.nih.gov\/31801793\/<\/a><\/li>\n
- Trifa AP, Lighezan DL, Jucan C, Tripon F, Arbore DR, Bojan A, Gligor-PopaS, Pop M R, Dima D, Banescu C. SH2B3 (LNK) rs3184504 polymorphism is correlated with JAK2 V617F-positive myeloproliferative neoplasms. Rev Romana Med Lab. 2020;28(3):267-77. DOI:10.2478\/rrlm-2020-0025 (IF=0,945), https:\/\/www.rrml.ro\/articole\/2020\/2020_3_3.pdf<\/a><\/li>\n
- Vasilache SL, M\u0103rginean CO, Boaghi A, Pop RM, Banescu C, et al. Implications of visfatin genetic variants in the metabolic profile of the Romanian pediatric population. Rev Romana Med Lab. 2020;28(2):163-74. DOI:10.2478\/rrlm-2020-0015, https:\/\/www.rrml.ro\/articole\/2020\/2020_2_5.pdf<\/a><\/li>\n
- B\u0103nescu C, Tripon F, Trifa AP, Crauciuc AG, et al. Cytokine rs361525, rs1800750, rs1800629, rs1800896, rs1800872, rs1800795, rs1800470, and rs2430561 SNPs in relation with prognostic factors in acute myeloid leukemia.\u00a0Cancer Med<\/em>. 2019;8(12):5492-5506.IF=3.35 https:\/\/pubmed.ncbi.nlm.nih.gov\/31373163\/<\/a><\/u><\/li>\n
- M\u00e1rtha K, Kerekes M\u00e1th\u00e9 B, Moldovan VG, B\u0103nescu C. Study of rs12532, rs8670 Polymorphism of Msh Homeobox 1 (MSX1), rs61754301, rs4904155 Polymorphism of Paired Box Gene 9 (PAX9), and rs2240308 Polymorphism of Axis Inhibitor Protein 2 (AXIN2) Genes in Nonsyndromic Hypodontia. Biomed Res Int. 2019 Nov 5;2019:2183720. doi: 10.1155\/2019\/2183720. eCollection 2019. IF=2.197 https:\/\/pubmed.ncbi.nlm.nih.gov\/31781599\/<\/a><\/li>\n
- Meli\u0163 LE, M\u0103rginean CO, B\u0103nescu et al. The relationship between TLR4 rs4986790 and rs4986791 gene polymorphisms and Helicobacter pylori infection in children with gastritis.Pathol Res Pract. 2019;215(12):152692,doi:10.1016\/j.prp.2019.152692; https:\/\/pubmed.ncbi.nlm.nih.gov\/31690518\/<\/a><\/li>\n
- B\u0103nescu C. Do we really need genetic tests in current practice?. Rev Romana Med Lab<\/em>. 2019;27(1):9-14. DOI:10.2478\/rrlm-2019-0010, https:\/\/www.rrml.ro\/articole\/2019\/2019_1_1.pdf<\/a><\/li>\n
- B\u0103nescu C, Skrypnyk C. The Value of FLT3, NPM1 and DNMT3A Gene Mutation Analysis in Acute Myeloid Leukemia Diagnosis. Rev Romana Med Lab<\/em>. 2019;27(3):239-43. DOI:10.2478\/rrlm-2019-0024 , IF=0.8<\/li>\n
- Negovan A, Iancu M, F\u00fcl\u00f6p E, B\u0103nescu C. Helicobacter pylori and cytokine gene variants as predictors of premalignant gastric lesions. World J Gastroenterol. 2019 Aug 14;25(30):4105-4124. doi: 10.3748\/wjg.v25.i30.4105. (IF=3.411), https:\/\/www.rrml.ro\/articole\/2019\/2019_3_1.pdf<\/a><\/li>\n
- Negovan A, Pantea M, Banescu C, Mocan S. Response to: Comment on \"Factors Associated with Recurrent Ulcers in Patients with Gastric Surgery after More Than 15 Years: A Cross-Sectional Single-Center Study\". Gastroenterol Res Pract. 2019 Feb 24;2019:9214597. doi: 10.1155\/2019\/9214597. eCollection 2019. (IF=1.825), https:\/\/pubmed.ncbi.nlm.nih.gov\/30918517\/<\/a><\/li>\n
- M\u0103rginean CO, M\u0103rginean C, Iancu M, Moldovan VG, Melit LE, B\u0103nescu C. The impact of TNF-\u03b1 308G>A gene polymorphism on children's overweight risk and an assessment of biochemical variables: A cross-sectional single-center experience. Pediatr Neonatol. 2019 Feb;60(1):19-27. doi: 10.1016\/j.pedneo.2018.03.003. (IF=1.497), https:\/\/pubmed.ncbi.nlm.nih.gov\/29605384\/<\/a><\/li>\n
- M\u0103rginean C, M\u0103rginean CO, B\u0103nescu C, Meli\u0163 LE, Tripon F, Iancu M. The relationship among GNB3 rs5443, PNPLA3 rs738409, GCKR rs780094 gene polymorphisms, type of maternal gestational weight gain and neonatal outcomes (STROBE-compliant article). Medicine (Baltimore). 2019 Jul;98(28):e16414. doi: 10.1097\/MD.0000000000016414.(IF=1.870), https:\/\/pubmed.ncbi.nlm.nih.gov\/31305457\/<\/a><\/li>\n
- Crauciuc GA, Tripon F, Bogli\u015f A, F\u0103g\u0103r\u0103\u015fan A, B\u0103nescu C. Multiplex ligation dependent probe amplification - A useful, fast and cost-effective method for identification of small supernumerary marker chromosome in children with developmental delay and congenital heart defect.\u00a0Rev Romana Med Lab<\/em>. 2018;26(4):461-70. DOI:10.2478\/rrlm-2018-0032, IF=0.8, https:\/\/rrml.ro\/articole\/articol.php?year=2018&vol=4&poz=7<\/a><\/li>\n
- Bogli\u015f A, Tripon F, B\u0103nescu C. The utility of molecular genetic techniques in craniosynostosis cases associated with intellectual disability.\u00a0Rev Romana Med Lab<\/em>. 2018;26(4):471-7. DOI:10.2478\/rrlm-2018-0033, ISSN 2284-5623, IF=0.8, https:\/\/reference-global.com\/download\/article\/10.2478\/rrlm-2018-0033.pdf<\/a><\/li>\n
- Negovan A, Iancu M, Tripon F, Crauciuc A, Mocan S, B\u0103nescu C. The CAT-262 C>T, MnSOD Ala16Val, GPX1 Pro198Leu Polymorphisms Related to Oxidative Stress and the Presence of Gastric Lesions. J Gastrointestin Liver Dis; 2018:27(4):371-78. IF=2.063, https:\/\/pubmed.ncbi.nlm.nih.gov\/30574618\/<\/a><\/li>\n
- Trifa AP, B\u0103nescu C, et al. Modest contribution of JAK2 V617F allele burden to the occurrence of major thrombosis in polycthemia vera and essential thrombocythemia. Blood Cells Mol Dis. 2018; 73:45-6. doi:10.1016\/j.bcmd.2018.09.003.(IF=2.3) https:\/\/pubmed.ncbi.nlm.nih.gov\/30249383\/<\/a><\/li>\n
- M\u0103rgineanCO, M\u0103rginean C, B\u0103nescu C, et al. The relationship between MMP9 and ADRA2A gene polymorphisms and mothers\u2013newborns\u2019 nutritional status: an exploratory path model (STROBE compliant article). Pediatric Research. 2019;85(6):822-829. doi: 10.1038\/s41390-019-0347-2 , https:\/\/pubmed.ncbi.nlm.nih.gov\/30791043\/<\/a><\/li>\n
- Tripon F, Crauciuc GA, Moldovan VG, Bogli\u0219 A, Benedek IJ, L\u00e1z\u00e1r E, B\u0103nescu C. Simultaneous FLT3, NPM1 and DNMT3A mutations in adult patients with acute myeloid leukemia \u2013 case study.\u00a0Rev Romana Med Lab<\/em>. 2019;27(3):245-54, <\/u>https:\/\/rrml.ro\/articole\/articol.php?year=2019&vol=3&poz=2<\/a><\/li>\n
- Marginean C, M\u0103rginean CO, B\u0103nescu C, Melit LE, Tripon F, Iancu M. The relationship among GNB3 rs5443, PNPLA3 rs738409, GCKR rs780094 gene polymorphisms, type of maternal gestational weight gain and neonatal outcomes (STROBE-compliant article). Medicine. 2019; 98:28(e16414) DOI: 10.1097\/MD.0000000000016414. https:\/\/pubmed.ncbi.nlm.nih.gov\/31305457\/<\/a><\/li>\n
- C M\u0103rginean, CO M\u0103rginean, M Iancu, LE Meli\u021b, F Tripon, C B\u0103nescu. MC4R and ENPP1 gene polymorphisms and their implication in maternal and neonatal risk for obesity. Scientific reports 2019; 9: https:\/\/www.nature.com\/articles\/s41598-019-47402-2<\/a><\/li>\n
- Negovan A, Iancu M, Mocan S, Banescu C. Immunohistochemistry as confirmatory test for current Helicobacter pylori infection in patients treated with proton pump inhibitors. Eur J Intern Med. 2018; 50:e31-e32. doi: 10.1016\/j.ejim.2017.11.013. https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/29203056<\/a><\/li>\n
- M\u0103rginean CO, M\u0103rginean C, Iancu M, \u2026 B\u0103nescu C. The impact of TNF-\u03b1 308G>A gene polymorphism on children's overweight risk and an assessment of biochemical variables: A cross-sectional single-center experience. Pediatr Neonatol. 2018. pii: S1875-9572(17)30211-5. doi: 10.1016\/j.pedneo.2018.03.003. https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/29605384<\/a><\/li>\n
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- Negovan A, Iancu M, Moldovan V, et al. Influence of MDR1 <\/em>C3435T, CYP2C19*2 <\/em>and CYP2C19*3 <\/em>gene polymorphisms and clinical characteristics on the severity of gastric lesions: a case-control study. J Gastrointestin Liver Dis, 2016, 25(2):2-4. (IF=1.891), http:\/\/www.jgld.ro\/wp\/archive\/y2016\/n2\/a23\/<\/a><\/li>\n
- Loghin A, B\u0103nescu C, Nechifor-Boila A, et al. XRCC3 Thr241Met and XPD Lys751Gln gene polymorphisms and risk of clear cell renal cell carcinoma. Cancer Biomark. 2016 Feb 23;16(2):211-7. doi: 10.3233\/CBM-150558. (IF=1.736) http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/26682510<\/a><\/li>\n<\/ul>\n","patente_brevete_de_inventie":"
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