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

Whole-Exome Sequencing for Molecular Diagnosis of Paediatric Nephrotic Syndrome in Africa: A Call for Implementation

在非洲开展全外显子组测序以进行儿童肾病综合征的分子诊断:呼吁实施

Gcobo, Thina; Katsukunya, Jonathan N; Lamola, Lindie; Awany, Denis; Ndadza, Arinao; Dandara, Collet; Mnika, Khuthala

Very low prevalence of validated kelch13 mutations and absence of hrp2/3 double gene deletions in South African malaria-eliminating districts (2022-2024)

南非疟疾消除地区(2022-2024 年)已验证的 kelch13 突变患病率极低,且未发现 hrp2/3 双基因缺失。

Raman, Jaishree; Mabona, Maxwell; Nyawo, Qedusizi; Mangena, Brighton; Kok, Gerdalize; Mathaba, Lihle; Malatje, Gillian; Lauterbach, Sonja B; Makhanthisa, Takalani I; Gwarinda, Hazel; Letinić, Blaženka D; Ndadza, Arinao; Raswiswi, Eric; Shandukani, Mbavhalelo; Baloyi, Ednah; Fekema, Ziyanda; Ismail, Arshad; Featherston, Jonathan; Greenhouse, Bryan; Smith, Jennifer L; Aranda-Diaz, Andres

Meta-analysis of genome-wide association studies of stable warfarin dose in patients of African ancestry

对非洲裔患者稳定华法林剂量的全基因组关联研究进行荟萃分析

Asiimwe, Innocent G; Blockman, Marc; Cavallari, Larisa H; Cohen, Karen; Cupido, Clint; Dandara, Collet; Davis, Brittney H; Jacobson, Barry; Johnson, Julie A; Lamorde, Mohammed; Limdi, Nita A; Morgan, Jennie; Mouton, Johannes P; Muyambo, Sarudzai; Nakagaayi, Doreen; Ndadza, Arinao; Okello, Emmy; Perera, Minoli A; Schapkaitz, Elise; Sekaggya-Wiltshire, Christine; Semakula, Jerome R; Tatz, Gayle; Waitt, Catriona; Yang, Guang; Zhang, Eunice J; Jorgensen, Andrea L; Pirmohamed, Munir

Warfarin Pharmacogenomics for Precision Medicine in Real-Life Clinical Practice in Southern Africa: Harnessing 73 Variants in 29 Pharmacogenes

华法林药物基因组学在南部非洲真实临床实践中的精准医疗应用:利用29个药物基因中的73个变异

Muyambo, Sarudzai; Ndadza, Arinao; Soko, Nyarai D; Kruger, Bianca; Kadzirange, Gerard; Chimusa, Emile; Masimirembwa, Collen M; Ntsekhe, Mpiko; Nhachi, Charles F B; Dandara, Collet

Profiling of warfarin pharmacokinetics-associated genetic variants: Black Africans portray unique genetic markers important for an African specific warfarin pharmacogenetics-dosing algorithm

华法林药代动力学相关遗传变异分析:黑人非洲人具有独特的遗传标记,这些标记对于制定非洲特有的华法林药代动力学剂量算法至关重要。

Ndadza, Arinao; Muyambo, Sarudzai; Mntla, Pindile; Wonkam, Ambroise; Chimusa, Emile; Kengne, Andre P; Ntsekhe, Mpiko; Dandara, Collet