Follow
Khuthala Mnika
Khuthala Mnika
University of Cape Town
Verified email at nhls.ac.za
Title
Cited by
Cited by
Year
Clinical and genetic factors are associated with pain and hospitalisation rates in sickle cell anaemia in Cameroon
A Wonkam, K Mnika, VJ Ngo Bitoungui, B Chetcha Chemegni, ...
British journal of haematology 180 (1), 134-146, 2018
412018
Genetic modifiers of long‐term survival in sickle cell anemia
A Wonkam, ER Chimusa, K Mnika, GD Pule, VJ Ngo Bitoungui, N Mulder, ...
Clinical and Translational medicine 10 (4), e152, 2020
382020
GJB2 and GJB6 Mutations in Non-Syndromic Childhood Hearing Impairment in Ghana
SM Adadey, N Manyisa, K Mnika, C De Kock, V Nembaware, O Quaye, ...
Frontiers in Genetics 10, 841, 2019
332019
Hydroxyurea-induced miRNA expression in sickle cell disease patients in Africa
K Mnika, GK Mazandu, M Jonas, GD Pule, ER Chimusa, NA Hanchard, ...
Frontiers in genetics 10, 437181, 2019
232019
The Sickle Cell Disease Ontology: enabling universal sickle cell-based knowledge representation
Database 2019, baz118, 2019
222019
An expert review of pharmacogenomics of sickle cell disease therapeutics: not yet ready for global precision medicine
K Mnika, GD Pule, C Dandara, A Wonkam
OMICS: A Journal of Integrative Biology 20 (10), 565-574, 2016
202016
Association of genetic polymorphisms of TGF-β1, HMOX1, and APOL1 with CKD in Nigerian patients with and without HIV
UE Ekrikpo, K Mnika, EE Effa, SO Ajayi, C Okwuonu, B Waziri, A Bello, ...
American Journal of Kidney Diseases 76 (1), 100-108, 2020
162020
Beta-globin gene haplotypes and selected Malaria-associated variants among black Southern African populations
GD Pule, ER Chimusa, K Mnika, K Mhandire, E Kampira, C Dandara, ...
Global health, epidemiology and genomics 2, e17, 2017
162017
The hearing impairment ontology: A tool for unifying hearing impairment knowledge to enhance collaborative research
J Hotchkiss, N Manyisa, S Mawuli Adadey, OG Oluwole, E Wonkam, ...
Genes 10 (12), 960, 2019
102019
Investigations of kidney dysfunction-related gene variants in sickle cell disease patients in Cameroon (Sub-Saharan Africa)
VJ Ngo-Bitoungui, S Belinga, K Mnika, T Masekoameng, V Nembaware, ...
Frontiers in Genetics 12, 595702, 2021
62021
The sickle cell disease ontology: enabling collaborative research and co-designing of new planetary health applications
V Nembaware, GK Mazandu, J Hotchkiss, JM Safari Serufuri, J Kent, ...
OMICS: A Journal of Integrative Biology 24 (10), 559-567, 2020
62020
Genetic analysis of TB susceptibility variants in Ghana reveals candidate protective loci in SORBS2 and SCL11A1 genes
A Asante-Poku, P Morgan, S Osei-Wusu, SY Aboagye, P Asare, ...
Frontiers in Genetics 12, 729737, 2022
52022
Burden, genotype and phenotype profiles of adult patients with sickle cell disease in Cape Town, South Africa
GD Pule, K Mnika, M Joubert, S Mowla, N Novitzky, A Wonkam
South African Medical Journal 107 (2), 149-155, 2017
42017
The implementation of laboratory information management system in multi-site genetics study in Africa: the challenges and up-scaling opportunities
OG Oluwole, C Oosterwyk, D Anderson, SM Adadey, K Mnika, N Manyisa, ...
Journal of Molecular Pathology 3 (4), 262-272, 2022
32022
Biomarkers of sickle cell nephropathy in Senegal
EHM Ndour, K Mnika, FG Tall, M Seck, ID Ly, V Nembaware, GK Mazandu, ...
Plos one 17 (11), e0273745, 2022
22022
An expert review of voxelotor for the treatment of hemolytic anemia in patients with sickle cell disease:‘Bridging the gap between laboratory data and patient related outcomes’
BPD Inusa, K Mnika, S Babiker
Expert Review of Hematology 16 (8), 585-591, 2023
12023
Clinical characteristics and risk factors of relative systemic hypertension and hypertension among sickle cell patients in Cameroon
A Nguweneza, VJ Ngo Bitoungui, K Mnika, G Mazandu, V Nembaware, ...
Frontiers in Medicine 9, 924722, 2022
12022
Effects of Senegal haplotype (Xmn1-rs7412844), alpha-thalassemia (3.7 kb HBA1/HBA2 deletion), NPRL3-rs11248850 and BCL11A-rs4671393 variants on sickle cell nephropathy
K Mnika, FG Tall, M Seck, ID Ly, V Nembaware, HAT Sagna-Bassène, ...
International Journal of Biochemistry and Molecular Biology 13 (2), 5, 2022
12022
The ESHG-Young & the Young Investigator Forum: Partnership, networking and innovation
E Avram, R Barbosa-Matos, M Johari, AR Gouveia Freitas da Silva, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 32, 756-756, 2024
2024
Advancing intercontinental collaboration in human genetics: success story of the African and European Young Investigator Forum
MZ Alimohamed, K Mnika, SM Adadey, R Barbosa-Matos, E Avram, ...
European Journal of Human Genetics 32 (1), 3-5, 2024
2024
The system can't perform the operation now. Try again later.
Articles 1–20