Researchers



Results 81-100 of 101
Issue DateTitleAuthor(s)TypeМp-cat.
2017Genetic modifiers of -thalassemia: a rise of a novel therapy approachesUgrin M.  ; Stojiljković M.; Zukić B.  ; Klaassen K.  ; Jovana Komazec  ; Skakić A.  ; Dokmanović, L.; Janić D.; Patrinos GP.; Pavlović S.Conference Paper
Mp. category will be shown later
2017Precision molecular diagnostic of hepatic GSD revealed unexpectedly high incidence of gsd ib in serbian population and three novel variants in the SLC37A4 geneSkakic, Anita  ; Djordjevic, Maja; Adrijan Sarajlija; Kristel Klaassen  ; Tosic, Natasa  ; Bozica Kecman; Milena Ugrin; Vesna Spasovski  ; Pavlovic, Sonja  ; Stojiljkovic, Maja  Conference Paper
Mp. category will be shown later
2016Functional Analysis of an (A)gamma-Globin Gene Promoter Variant (HBG1: g.-225_-222delAGCA) Underlines Its Role in Increasing Fetal Hemoglobin Levels Under Erythropoietic StressUgrin, Milena  ; Stojiljković, Maja  ; Zukić, Branka  ; Klaassen, Kristel  ; Katsila, Theodora; Komazec, Jovana  ; Dokmanović, Lidija  ; Janić, Dragana  ; Patrinos, George P.; Pavlović, Sonja  Article
23M23
2016Molecular and phenotypic characteristics of seven novel mutations causing branched-chain organic aciduriasStojiljković, Maja  ; Klaassen, Kristel  ; Đorđević, Maja  ; Sarajlija, Adrijan  ; Brasil, S.; Kecman, Božica; Grković, Sanja; Perić, Jelena  ; Rodriguez-Pombo, P.; Desviat, L.R.;
Pavlović, Sonja  ; Perez, B.;
Article
21M21
2016Functional analysis of an Aγ-globin gene promoter variant (HBG1: g.-225_-222delAGCA) underlines its role in increasing fetal hemoglobin levels under erythropoietic stressJovana Komazec  ; Ugrin M  ; Stojiljkovic, M; Zukic, B  ; Klaassen K  ; Katsila T; Dokmanovic, L; Janic, D; Patrinos GP; Pavlovic, SConference Paper
Mp. category will be shown later
2016Molecular genetic testing of inborn metabolic diseases in SerbiaStojiljkovic, Maja  ; Kristel Klaassen  ; Skakic, Anita  ; Kostic, Jelena; Tosic, Natasa  ; Pavlovic, Sonja  Conference Paper
Mp. category will be shown later
2015Tetrahydrobiopterin deficiency among Serbian patients presenting with hyperphenylalaninemiaStojiljković, Maja  ; Klaassen, Kristel  ; Đorđević, Maja; Sarajlija, Adrijan  ; Kecman, Bozica; Ugrin, Milena  ; Zukić, Branka  ; Desviat, Lourdes R.; Pavlović, Sonja  ; Perez, BelenArticle
23M23
2015Functional analysis of the four base pair deletion upstream of the Aγ-globin gene associated with decreased gene expressionJovana Komazec  ; Stojiljkovic, M; Klaassen K  ; Zukic, B  ; Dokmanovic, L; Janic, D; Ugrin M  ; Pavlovic, SConference Paper
Mp. category will be shown later
2015Influence of Promoter Polymorphisms of the Tnf-α (-308g/A) and IL-6 (-174g/C) Genes on Therapeutic Response to Etanercept in Rheumatoid ArthritisJančić, Ivan  ; Sefik-Bukilica, Mirjana; Živojinović, Slađana; Damjanov, Nemanja ; Spasovski, Vesna  ; Kotur, Nikola  ; Klaassen, Kristel  ; Pavlović, Sonja  ; Bufan, Biljana  ; Arsenović-Ranin, Nevena  Article
23M23
2015Molecular genetic study of congenital adrenal hyperplasia in serbia: two novel CYP21A2 gene mutationsSkakic, Anita  ; Milacic, Iva; M Barac; Milenkovic, Tatjana; Milena Ugrin  ; Kristel Klaassen  ; Jesic, Maja; Joksic, I; Mitrovic, K; Todorovic, S;
Vujovic, S; Pavlovic, Sonja  ; Stojiljkovic, Maja  ;
Conference Paper
Mp. category will be shown later
2015Molecular characterization of mutations in Serbian patients with glycogen storage diseases.Skakic, Anita  ; Kristel Klaassen  ; Kostić, Jelena; Đorđević, Maja; Sarajlija, Adrijan; Boyica Kecman; Kotur, Nikola  ; Stanković, Biljana; Srzentić, Sanja  ; Pavlović, Sonja  ;
Stojiljković, Maja  ;
Conference Paper
Mp. category will be shown later
2015Molecular characterization of mutations in Serbian patients with glycogen storage diseases - an NGS approachSkakic, Anita  ; Kristel Klaassen  ; Kostić, Jelena; Đorđević, Maja; Adrijan Sarajlija; Kecman, Božica; Spasovski, Vesna  ; Anđelković, Marina  ; Vreca, Misa; Pavlović, Sonja  ;
Stojiljković, Maja  ;
Conference Paper
Mp. category will be shown later
2015Molecular genetic study of congenital adrenal hyperplasia in Serbia: novel p.Leu129Pro and p.Ser165Pro CYP21A2 gene mutationsMilačić, I.; Barać, M.; Milenković, Tatjana; Ugrin, Milena  ; Klaassen, Kristel  ; Skakić, Anita  ; Ješić, Maja  ; Joksić, Ivana  ; Mitrović, Katarina; Todorović, Slađana;
Vujović, Svetlana  ; Pavlović, Sonja  ; Stojiljković, Maja  ;
Article
22M22
2015Molecular genetic testing of inborn metabolic diseases in SerbiaStojiljkovic, Maja  ; Kristel Klaassen  ; Skakic, Anita  ; Milena Ugrin; Pavlovic, Sonja  Conference Paper
Mp. category will be shown later
2014Association of variants in FTO, FABP2, PPARG, ADRB2 and ADRB3 genes with obesity in Serbian population: A prerequisite for nutrigenetic algorithm development.Skakić, Anita  ; Kristel Klaassen  ; Zukic, Branka; Spasovski, Vesna  ; Kotur, Nikola  ; Stanković, Biljana; Vreća, Miša; Nikcević, Gordana; Pavlović, Sonja  ; Stojiljković, Maja  Conference Paper
Mp. category will be shown later
2014Molekularne karakteristike, fenotipska raznolikost i procena odgovora na terapiju zasnovana na genotipu kod srpskih pacijenata sa fenilketonurijomStojiljković, Maja  ; Klaassen, Kristel  ; Pavlović, Sonja  Article
23M23
2014Molecular genetic characteristics of hyperphenylalaninemias in Serbia and implications for personalized medicine.Stojiljković Maja  ; Kristel Klaassen  ; Đorđević, Maja; Adrijan Sarajlija; Bozica Kecman; Skakic, Anita  ; Ugrin, Milena  ; Zukić, Branka  ; Nikčević, Gordana; Pavlović, Sonja  Conference Paper
Mp. category will be shown later
2013Association of mitochondrial DNA variants and cognitive impairment of phenylketonuria patientsKlaassen Kristel  ; Đorđević, Maja; Petrović Stojiljković, Maja  ; Pavlović, Sonja  Article
23M23
2012Molecular genetics and genotype-based estimation of BH4-responsiveness in serbian PKU patients: Spotlight on phenotypic implications of p.L48SĐorđević, M.  ; Klaassen, Kristel  ; Sarajlija, A.  ; Tošić, Nataša  ; Zukić, Branka  ; Kecman, B.; Radmilović Milena  ; Spasovski, Vesna  ; Pavlović, Sonja  ; Stojiljković, Maja  Article
Mp. category will be shown later
20126-mercaptopurine influences TPMT gene transcription in a TPMT gene promoter variable number of tandem repeats-dependent mannerKotur, Nikola  ; Stanković, Biljana  ; Katerina , Kassela; Georgitsi, Marianthi; Vicha, Anna; Leontari, Iliana; Dokmanović, Lidija  ; Janić, Dragana  ; Krstovski, Nada; Klaassen, Kristel  ;
Radmilović Milena  ; Stojiljković, Maja  ; Nikčević, Gordana  ; Simeonidis, Argiris; Sivolapenko, Gregory; Pavlović, Sonja  ; Partinos, George P.; Zukić, Branka  ;
Article
21M21