Уноси

• Пројекат-Повезаност полиморфизама гена значајних за метаболизам масти и угљених хидрата са липидним параметрима код пацијената са акутним инфарктом миокарда (2024-01)

  S. Vidović, R. Škrbić, V. Vidovic, I. Milovac, N. Maksimović, Ž. Radić Savić, N. Malešević, J. Bećarević, Пројекат-Повезаност полиморфизама гена значајних за метаболизам масти и угљених хидрата са липидним параметрима код пацијената са акутним инфарктом миокарда, МИНИСТАРСТВО ЗА НАУЧНОТЕХНОЛОШКИ РАЗВОЈ И ВИСОКО ОБРАЗОВАЊЕ РЕПУБЛИКЕ СРПСКЕ, Jan, 2024

• Galectin 3 rs4644 gene polymorphism is associated with metabolic traits in Serbian adolescent population (2023-05)

  V. Vidović, I. Novaković, T. Damjanović, Ž. Radić, S. Vidović, R. Škrbić, Galectin 3 rs4644 gene polymorphism is associated with metabolic traits in Serbian adolescent population, JOURNAL OF MEDICAL BIOCHEMISTRY, May, 2023

• Prevalence of five pharmacologically most important CYP2C9 and CYP2C19 allelic variants in the population from the Republic of Srpska in Bosnia and Herzegovina (2021-06)

  S. Vidović, R. Škrbić, М. Stojiljković, V. Vidović, J. Bećarević, S. Stoisavljević-Šatara, N. Maksimović, Prevalence of five pharmacologically most important CYP2C9 and CYP2C19 allelic variants in the population from the Republic of Srpska in Bosnia and Herzegovina, ARHIV ZA HIGIJENU RADA I TOKSIKOLOGIJU, Vol. 72, No. 2, pp. 129 - 134, Jun, 2021

• Association of MDR1 rs1045642 Polymorphism with Susceptibility to Balkan Endemic Nephropathy (2023-10)

  Z. Radic Savic, V. Vidovic, S. Vidović, I. Milovac, J. Bećarević, A. Marić, V. Coric, M. Matic, T. Simić, Association of MDR1 rs1045642 Polymorphism with Susceptibility to Balkan Endemic Nephropathy, Book of Abstracts Genetics&Applications CONGUB&H 2023 –Special Edition, 69, Oct, 2023

• Significance of TPMT genotyping in clinical practice (2024-05)

  V. Vidovic, S. Vidović, J. Bećarević, R. Skrbic, Significance of TPMT genotyping in clinical practice, Book of Abstracts Genetics&Applications, Special Edition, May, 2024

• Significance of CYP2C9 in Prescribing Siponimod Therapy in Patients with Multiple Sclerosis (2024-06)

  J. Bećarević, I. Milovac, V. Vidovic, R. Skrbic, S. Vidović, Significance of CYP2C9 in Prescribing Siponimod Therapy in Patients with Multiple Sclerosis, Book of Abstracts, Jun, 2024

• Association of PRDM16 rs12409277 and CtBP2 rs1561589 gene polymorphisms with lipid profile of adolescents (2023-01)

  N. Maksimović, V. Vidovic, T. Damjanović, B. Jekić, N. Majkic-Singh, S. Simeunovic, D. Savic Bozovic, S. Vidović, I. Novaković, Association of PRDM16 rs12409277 and CtBP2 rs1561589 gene polymorphisms with lipid profile of adolescents, ARCHIVES OF MEDICAL SCIENCE, Vol. 19, No. 3, pp. 593 - 599, Jan, 2023

• GPX3 rs8177412 Polymorphism Modifies Risk of Upper Urothelial Tumors in Patients with Balkan Endemic Nephropathy (2023-08)

  Ž. Radić Savić, V. Ćorić, S. Vidović, V. Vidovic, J. Bećarević, I. Milovac, Z. Reljić, B. Mirjanić-Azarić, R. Škrbić, R. Gajanin, M. Matić, T. Simić, GPX3 rs8177412 Polymorphism Modifies Risk of Upper Urothelial Tumors in Patients with Balkan Endemic Nephropathy, MEDICINE, Vol. 59, No. 8, Aug, 2023

• Galectin 3 rs4644 Gene Polymorphism is Associated with Metabolic Traits in Serbian Adolescent Population (2024-01)

  V. Vidovic, I. Novaković, T. Damjanović, Ž. Radić Savić, S. Vidović, R. Škrbić, N. Maksimović, Galectin 3 rs4644 Gene Polymorphism is Associated with Metabolic Traits in Serbian Adolescent Population, JOURNAL OF MEDICAL BIOCHEMISTRY, Vol. 43, pp. 1 - 6, Jan, 2024

• Farmakogenetika - uloga genetičkog polimorfizma CYP enzima u terapiji (2023-03)

  V. Vidovic, S. Vidović, Farmakogenetika - uloga genetičkog polimorfizma CYP enzima u terapiji, Mar, 2023

• Findings from ACGH in patient with psychomotor delay-case report (2019-12)

  V. Vidovic, N. Maksimović, T. Damjanović, B. Jekić, I. Milovac, M. Grk, S. Vidović, Findings from ACGH in patient with psychomotor delay-case report, Genetics&Applications, Vol. 3, No. 3, pp. 38 - 41, Dec, 2019

• Findings from ACGH in patient with psychomotor delay-case report (2019-12)

  Vanja Vidović, Nela Maksimović, Tatjana Damnjanović, Biljana Jekić, Irina Milovac, Milka Grk, Stojko Vidović, Findings from ACGH in patient with psychomotor delay-case report, Genetics&Applications, Vol. 3, No. 3, pp. 38 - 41, Dec, 2019

• Association of the Brain-Derived Neurotrophic Factor Val66met Polymorphism with Body Mass Index, Fasting Glucose Levels and Lipid Status in Adolescents (2020)

  V. Vidovic, N. Maksimović, I. Novakovic, T. Damjanović, B. Jekić, S. Vidović, N. Majkic-Singh, M. Stamenkovic-Radak, D. Nikolic, D. Marisavljevic, Association of the Brain-Derived Neurotrophic Factor Val66met Polymorphism with Body Mass Index, Fasting Glucose Levels and Lipid Status in Adolescents, BALKAN JOURNAL OF MEDICAL GENETICS, Vol. 23, No. 1, pp. 77 - 82, 2020

• Prevalence of five pharmacologically most important CYP2C9 and CYP2C19 allelic variants in the population from the Republic of Srpska in Bosnia and Herzegovina (2021)

  S. Vidović, Р. Шкрбић, M. Stojiljković, V. Vidovic, J. Bećarević, S. Stoisavljević Šatara, N. Maksimović, Prevalence of five pharmacologically most important CYP2C9 and CYP2C19 allelic variants in the population from the Republic of Srpska in Bosnia and Herzegovina, ARHIV ZA HIGIJENU RADA I TOKSIKOLOGIJU, No. 72, pp. 129 - 134, 2021

• Association of PRDM16 rs12409277 and CtBP2 rs1561589 gene polymorphisms with lipid profile of adolescents (2021-01)

  N. Maksimović, V. Vidovic, T. Damnjanovic, B. Jekić, N. Majkic-Singh, S. Simeunovic, D. Savic Bozovic, S. Vidović, I. Novakovic, Association of PRDM16 rs12409277 and CtBP2 rs1561589 gene polymorphisms with lipid profile of adolescents, ARCHIVES OF MEDICAL SCIENCE, pp. 1 - 7, Jan, 2021

• Association of PPARG rs3856806 C>T polymorphism with BMI, fasting glucose levels and lipid profile in Serbian adolescents (2021-03)

  V. Vidovic, N. Maksimović, S. Vidović, T. Damnjanovic, I. Novakovic, Association of PPARG rs3856806 C>T polymorphism with BMI, fasting glucose levels and lipid profile in Serbian adolescents, SCRIPTA MEDICA, Vol. 1, No. 52, pp. 15 - 21, Mar, 2021

• PPARGC1A gene polymorphism and its association with obesityrelated metabolic traits in Serbian adolescent population (2022-11)

  V. Vidovic, N. Maksimović, S. Vidović, T. Damnjanović, I. Milovac, I. Novaković, PPARGC1A gene polymorphism and its association with obesityrelated metabolic traits in Serbian adolescent population, Genetika, Vol. 54, No. 3, pp. 1375 - 1384, Nov, 2022

• Identification of Gene Candidates Associated with Irritable Bowel Syndrome (2022-12)

  I. Milovac, V. Vidovic, J. Ramic, N. Lojo-Kadrić, M. Hadžić, Z. Mavija, S. Vidović, L. Pojskic, Identification of Gene Candidates Associated with Irritable Bowel Syndrome, SCRIPTA MEDICA, Vol. 53, No. 4, pp. 327 - 331, Dec, 2022

• Genetic diagnosis by ACGH in patient with development delay and congenital anomalies – case report (2019)

  S. Vidović, N. Maksimović, V. Vidovic, T. Damjanović, B. Jekić, I. Milovac, M. Grk, Genetic diagnosis by ACGH in patient with development delay and congenital anomalies – case report, Book of Apstracts 6th Congress Of The Serbian Genetic Society, 2019

• DAT polymorphism and its association with irittable bowl syndrome (2019)

  Irina Milovac, Vanja Vidović, Stojko Vidović, Naida Lojo-Kadrić, Jasmin Ramić, Maida Hadžić, Zoran Mavija, Lejla Pojskić, DAT polymorphism and its association with irittable bowl syndrome, Genetics&Applications, Vol.3, No.2, 2019