- Adler G, Valjevac A, Skonieczna-Żydecka K, Mačkić-Đurović M,Parczewski M, Urbańska A,  Salkic N. Frequency of CCR5Δ32 allele in healthyBosniak population. Bosn J Basic Med Sci. 2014;14(3):150-154.

- Rakanović-Todić M, Burnazović-Ristić L, Ibrulj S,  Mulabegović N.Effect of met-enkephalin on chromosomal aberrations in the lymphocytes of the peripheral blood of patients with multiple sclerosis.Bosn J Basic Med Sci 2014;14(2): 75 – 80.

- Mačkić-Đurović M, Projić P, Ibrulj S, Čakar J, Marjanović D. “A comparative analysis of the effectiveness of cytogenetic and molecular genetic methods in the detection of Down syndrome.Bosn J Basic Med Sci. 2014 Maj;14(2):94-8.

- Kiseljaković E, Wiesner JR. Last cycle “hot” polymerase chain reaction - restriction fragment length polymorphism PCR – RFLP analysis for quantification of  mitochondrial DNA mutation.  Folia Medica  2014; 49. (Suppl. 1): 39.

- Mačkić-Đurović M,Projić P,Ibrulj S, Čakar J,Marjanović D. Effectivenessof molecular - geneticdetection of down syndrome using 6 STR markers. Folia Medica  2014; 49. (Suppl. 1): 45.

- Hajdarpašić-Saračević A, Mušanović J, Mačkić-Đurović M, Alić L. Cystic fibrosis genetic testing. Folia Medica  2014; 49. (Suppl. 1): 52.

- Hajdarpašić-Saračević A, Mušanović J, Mačkić-Đurović M, Mehić B. Epidermal growth factor receptor (EGFR) mutation detection. Folia Medica  2014; 49. (Suppl. 1): 53.

- Valjevac A, Adler A,Skonieczna-Żydecka K, Mačkić-Đurović M, Parczewski M, Urbańska A,  Salkić N. Frequency of the CCR5δ32allele inhealthy Bosnian population. Folia Medica  2014; 49. (Suppl. 1): 58.

- Kiseljaković E, Mačkić-Đurović M, Hasić S, Jadrić R, Valjevac A, Ibrulj S. Mannose-binding lectin 2 polymorphism in postmenopausal women.
Folia Medica  2014; 49. (Suppl. 1): 62.

- Adler G,Kiseljaković E, Valjevac A, Pawińska-Matecka A, Salkić N. Polymorphism3435C>TMDR1inpatientswith crohn'sdisease in the populationof Bosniaand  Herzegovina. Folia Medica  2014; 49. (Suppl. 1): 64.

- Aganović-Musinović I, Mačkić-Đurović M, Lepara O, Ibrulj S. Frequency of chromosomal aberrations among the healthy population of B&H. Folia Medica  2014; 49. (Suppl. 1): 66.

- Mušanović J,Godinjak Z, Mačkić-Đurović M, Hajdarpašić-Saračević A,Kiseljaković E, Ibrulj S. Y chromosome microdeletions detection by molecular genetics methods. Folia Medica  2014; 49. (Suppl. 1): 67.

- Kiseljaković E, Hasić S, Valjevac A, Mačkić-Đurović M, Jadrić R, Mehić B, Kučukalić-Selimović E, Ibrulj S. Association of mannose-binding lectin-2 (MBL2) gene heterogeneity and its serum concentration with osteoporosis in postmenopausal women. Bosn J Basic Med Sci. 2014 Feb;14(1):25-9

 - Hasić S, Hadžović-Džuvo A, Jadrić R, Kiseljaković E. B-type natriuretic peptide and adiponectin releases in rat model of myocardial damage induced by isoproterenol administration. Bosnian Journal of Basic Medical Sciences 2013;13(4):225-229.

 - Valjevac A, Mehić B, Kiseljaković E, Ibrulj S, Garstka A, Adler G. Prevalence of 1691G>A FV mutation in females from Bosnia and Herzegovina - a preliminary report. Bosn J Basic Med Sci. 2013 Feb; 13(1): 31-3.

- Mušanović J, Mačkić-Đurović M, Stomornjak M, Ibrulj S. Molecular and cytogenetic diagnosis of disorders of sex development in persons: a case report. Folia Medica 2012; 47. (Suppl. 2): 64.

- Mačkić-Đurović M, Mušinović-Aganović I, Ibrulj S. Chromosomal aberrations among a population with reproductive problems. Folia Medica 2012; 47. (Suppl. 2): 65.

- Mušinović-Aganović I, Mačkić-Đurović M, Ibrulj S. Frequency of chromosomal aberrations among general human population. Eur. J. of Hum. Genet. 2012; 20.(Supp 1): 119.

- Mačkić-Đurović M, Mušinović- Aganović I, Beganović S, Kučukalić E, Ibrulj S. Chromosomal aberrations and Micronuclei frequency in patents treated with J-131 for therapeutic causes. Eur. J. of Hum. Genet. 2012; 20.(Supp 1): 110.

- Ibrulj S, Mačkić-Đurović M, Mušinović- Aganović I, Čelik D. Cytogenetic biomonitoring of general population of FB&H using micronucleus assay test. Eur. J. of Hum. Genet. 2012; 20.(Supp 1): 374.

- Mačkić-Đurović M, Mušinović- Aganović I, Čelik D, Ibrulj S. Cytogenetic causes of infertility and recurrent spontaneus abortions. Journal of Life Sciences 2012; 6(4): 374-377.

- Mačkić-Đurović M, Mušinović- Aganović I, Ibrulj S. Cytogenetic study for couples with reproductive problems. Eur. J. of Hum. Genet. 2010; 18.(Supp 1): 136.

- Sokolović Š, Kasumagić Š, Mačkić-Đurović M, Mušinović-Aganović I. The impact of rituximab therapy on the chromosomes of patients with rheumatoid arthritis. Bosnian J 2010;10(2): 121-124.

- Mušinović- Aganović I, Mačkić-Đurović M, Ibrulj S. Chromosomal aberrations in blood cancers. Eur. J. of Hum. Genet. 2010; 18.(Supp 1): 200.

Mušinović- Aganović I, Mačkić-Đurović M, Ibrulj S. Chromosomal changes in a boy with disharmonic development and allaly. Chromosome Research 2009; 17 (Suppl 1): 70.

- Mačkić-Đurović M, Mušinović-Aganović I, Ibrulj S. Incidence of syndrome Down during 1998-2008 period. Chromosome Research 2009; 17 (Suppl 1): 72.

- Mačkić-Đurović M, Ibrulj S, Aganović I. Results of 3248 cytogenetic analyses: a retrospective study in karyotype abnormalities. Eur. J. of Hum. Genet. 2009; 17.(Supp 2): 127.

- Mušinović- Aganović I, Mačkić-Đurović M, Ibrulj S. Clinical caracteristics of syndrome 47, XY + 18 and 47, XX + 18/ 46, XX. Eur. J. of Hum. Genet. 2009; 17 (Suppl.2): 131.

- Mušinović- Aganović I, Mačkić-Đurović M, Šeremet Z. Trisomija 18. HealthMed 2008; 2(4); 293-296.

- Heljić S, Ćatibušić F, Mačkić-Đurović M. Wolf-Hirschhorn syndrome: report of two cases in Bosnia and Herzegovina. BJMG 2007; 10(2): 77-82.

- Heljić S, Mačkić-Đurović M, Džinović A. Frys-ov syndrom. Med Arh 2006; 60(5): 317- 319.