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Journal of Medical Biochemistry|January 2, 2019
Variants in TPMT, ITPA, ABCC4 and ABCB1 Genes As Predictors of 6-mercaptopurine Induced Toxicity in Children with Acute Lymphoblastic LeukemiaGoran Milosevic, Nikola Kotur, Nada Krstovski, et al.
Pharmacogenomics|March 31, 2010
Functional analysis of the role of the TPMT gene promoter VNTR polymorphism in TPMT gene transcriptionBranka Zukic, Milena Radmilovic, Maja Stojiljkovic, et al.
Medical Oncology (Northwood, London, England)|January 8, 2013
Expression of Bcl2L12 in chronic lymphocytic leukemia patients: association with clinical and molecular prognostic markersTeodora Karan-Djurasevic, Vuk Palibrk, Branka Zukic, et al.
Frontiers in Genetics|August 1, 2022
Genome-Wide Association Study of COVID-19 Outcomes Reveals Novel Host Genetic Risk Loci in the Serbian PopulationMarko Zecevic, Nikola Kotur, Bojan Ristivojevic, et al.
International Journal of Laboratory Hematology|September 19, 2022
Expression of BCL11A in chronic lymphocytic leukaemiaNatasa Tosic, Milena Ugrin, Irena Marjanovic, et al.
Frontiers in Immunology|March 19, 2024
Case report: Rapidly progressive neurocognitive disorder with a fatal outcome in a patient with PU.1 mutated agammaglobulinemiaRada Miskovic, Jelena Ljubicic, Branka Bonaci-Nikolic, et al.
Radiology and Oncology|December 2, 2016
Somatic mutations of isocitrate dehydrogenases 1 and 2 are prognostic and follow-up markers in patients with acute myeloid leukaemia with normal karyotypeMarijana Virijevic, Teodora Karan-Djurasevic, Irena Marjanovic, et al.
Clinical Immunology (Orlando, Fla.)|September 9, 2018
Importance of TLR9-IL23-IL17 axis in inflammatory bowel disease development: Gene expression profiling studySanja Dragasevic, Biljana Stankovic, Aleksandra Sokic-Milutinovic, et al.
Metabolic Syndrome and Related Disorders|November 22, 2019
Metabolic Syndrome in Inflammatory Bowel Disease: Association with Genetic Markers of Obesity and InflammationSanja Dragasevic, Biljana Stankovic, Nikola Kotur, et al.
Plos One|October 10, 2018
Genomic profiling supports the diagnosis of primary ciliary dyskinesia and reveals novel candidate genes and genetic variantsMarina Andjelkovic, Predrag Minic, Misa Vreca, et al.
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