Suchergebnisse - "Dandara, Collet"

PubPharm (240)

31

The clinical utility of polygenic risk scores in genomic medicine practices: a systematic review

enthalten in: Human genetics | 2022

von Kumuthini, J. | Zick, B. | Balasopoulou, A. | +16

32

The clinical utility of polygenic risk scores in genomic medicine practices: a systematic review

enthalten in: Human genetics | 2022

von Kumuthini, J. | Zick, B. | Balasopoulou, A. | +16

33

The clinical utility of polygenic risk scores in genomic medicine practices: a systematic review

enthalten in: Human genetics | 2022

von Kumuthini, J. | Zick, B. | Balasopoulou, A. | +16

34

Editorial : Metabolism of anti-cancer drugs: Interplay involving pharmacology and pharmacokinetics

enthalten in: Frontiers in oncology | 2022

von Bapiro, T. | Hayeshi, R. | Dandara, C.

35

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

enthalten in: Omics : a journal of integrative biology | 2022

von Muyambo, S. | Ndadza, A. | Soko, N. | +7

36

Competency-based Training Needs Assessment for Research Managers and Administrators in Africa and the United Kingdom to Strengthen Equitable Partnerships

enthalten in: AAS open research | 2022

von Nembaware, V. | Glasser, S. | Priest, A. | +10

37

The importance of including African populations in pharmacogenetics studies of warfarin response

enthalten in: Pharmacogenomics | 2022

von Dandara, C. | Ndadza, A. | Soko, N.

38

Clinical and demographic characteristics of cervical cancer patients presenting at Parirenyatwa Hospital, Zimbabwe

enthalten in: African journal of reproductive health | 2021

von Kuguyo, O. | Tsikai, N. | Muradzikwa, S. | +6

39

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

enthalten in: Journal of thrombosis and haemostasis : JTH | 2021

von Ndadza, A. | Muyambo, S. | Mntla, P. | +5

40

A Monoallelic Variant in REST Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family

enthalten in: Genes | 2021

von Manyisa, N. | Schrauwen, I. | de Souza Rios, L. | +13