日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Pharmacogenomic Pathways Underlying Variable Vedolizumab Response in Crohn's Disease Patients: A Rare-Variant Analysis

克罗恩病患者对维多珠单抗反应差异的药物基因组学通路:一项罕见变异分析

Stankovic, Biljana; Stasuk, Mihajlo; Gasic, Vladimir; Ristivojevic, Bojan; Grubisa, Ivana; Zukic, Branka; Toplicanin, Aleksandar; Latinovic Bosnjak, Olgica; Smolovic, Brigita; Markovic, Srdjan; Sokic Milutinovic, Aleksandra; Pavlovic, Sonja

Role of Next-Generation Sequencing in Diagnosis of Familial Hypercholesterolemia in Serbia

下一代测序技术在塞尔维亚家族性高胆固醇血症诊断中的作用

Lukac, Sandra Singh; Gasic, Vladimir; Komazec, Jovana; Grubisa, Ivana; Popovic, Ljiljana; Rasulic, Iva; Pavlovic, Sonja; Lalic, Katarina

Genetic risk of alcohol-related liver cirrhosis: Associations of PNPLA3, TM6SF2, and a two-variant polygenic risk score

酒精相关性肝硬化的遗传风险:PNPLA3、TM6SF2 和双变异多基因风险评分的关联

Nesic, Branka; Jelovac, Marina; Karan-Djurasevic, Teodora; Vrinic Kalem, Dusica; Svorcan, Petar; Zukic, Branka; Grubisa, Ivana

Combined GSTM1 and GSTT1 null genotypes are strong risk factors for atherogenesis in a Serbian population

在塞尔维亚人群中,GSTM1 和 GSTT1 双重缺失基因型是动脉粥样硬化发生的强风险因素。

Grubisa, Ivana; Otasevic, Petar; Vucinic, Nada; Milicic, Biljana; Jozic, Tanja; Krstic, Slobodan; Milasin, Jelena

Enlarged follicles and temporomandibular joint abnormalities in mucolipidosis Type III

III型黏脂沉积症的毛囊增大和颞下颌关节异常

Khalifa, H; Grubisa, H S; Lee, L; Lam, E W N

Individual phenotypic variances in a family with Avellino corneal dystrophy

阿韦利诺角膜营养不良症家族中的个体表型变异

Abazi, Zihret; Magarasevic, Lidija; Grubisa, Ivana; Risovic, Dusica