Association of the TYMS 3G/3G genotype with poor response and GGH 354GG genotype with the bone marrow toxicity of the methotrexate in RA patients

Biljana Jekić, Ljiljana Luković, Vera Bunjevački, +10

European Journal of Clinical Pharmacology

Hematological MalignancyBone Marrow FailureAutoimmune DiseaseImmunologyHematology +8

Bcl‐2 Expression in Oral Squamous Cell Carcinoma

Branka Popović, Biljana Jekić, Ivana Novaković, +5

Annals of the New York Academy of Sciences

Cancer genes alterations and HPV infection in oral squamous cell carcinoma

Branka Popović, Biljana Jekić, Ivana Novaković, +4

International Journal of Oral and Maxillofacial Surgery

Cancer Genes AlterationsHuman Papillomavirus VaccinesOral CavityPathogenesisImmunology +8

Clinical Pharmacogenetic Models of Treatment Response to Methotrexate Monotherapy in Slovenian and Serbian Rheumatoid Arthritis Patients: Differences in Patient's Management May Preclude Generalization of the Models

Barbara Jenko, Matija Tomšič, Biljana Jekić, +3

Frontiers in Pharmacology

Association of dihydrofolate reductase (DHFR) -317AA genotype with poor response to methotrexate in patients with rheumatoid arthritis.

Vera Milic, Biljana Jekić, Ljiljana Luković, +10

PubMed

Association Between the Methylenetetrahydrofolate Reductase Polymorphisms and Risk of Acute Lymphoblastic Leukemia in Serbian Children

Tatjana Damnjanović, Radomir Milicevic, Tanja Novkovic, +7

Journal of Pediatric Hematology/Oncology

Mthfr PolymorphismsMixed-phenotype Acute LeukemiaGeneticsPolygenic RiskGenetic Epidemiology +16

Degree of genetic homozygosity and distribution of AB0 blood types among patients with spina bifida occulta and spina bifida aperta

Dejan Nikolić, Suzana Cvjeticanin, Ivana Petronić, +5

Archives of Medical Science

Chromosomal microarray in postnatal diagnosis of congenital anomalies and neurodevelopmental disorders in Serbian patients

Dijana Perović, Tatjana Damnjanović, Biljana Jekić, +6

Journal of Clinical Laboratory Analysis

Association between Tumor Necrosis Factor-<i>α</i> Promoter -308 G/A Polymorphism and Early Onset Sepsis in Preterm Infants

Tatjana Varljen, Olgica Rakic, Gordana Sekulovic, +5

The Tohoku Journal of Experimental Medicine

ImmunohematologyImmunodeficienciesImmunologyGenetic EpidemiologyPathology +25

Genetic variant rs16944 in IL1B gene is a risk factor for early-onset sepsis susceptibility and outcome in preterm infants

Tatjana Varljen, Gordana Sekulovic, Olgica Rakic, +4

Inflammation Research

Genetic Variant Rs16944Immune Cell DevelopmentPathogenesisImmunologyGenetic Epidemiology +8