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Scientific Reports|January 31, 2020
Genome-Wide Association Study of Brain Connectivity Changes for Alzheimer's DiseaseSamar S M Elsheikh, Emile R Chimusa, Nicola J Mulder, et al.Human Molecular Genetics|October 20, 2020
Whole exome sequencing reveals pathogenic variants in MYO3A, MYO15A and COL9A3 and differential frequencies in ancestral alleles in hearing impairment genes among individuals from CameroonAmbroise Wonkam, Noluthando Manyisa, Christian D Bope, et al.Briefings in Bioinformatics|April 28, 2018
Post genome-wide association analysis: dissecting computational pathway/network-based approachesEmile R Chimusa, Shareefa Dalvie, Collet Dandara, et al.Frontiers in Human Neuroscience|January 10, 2022
Relating Global and Local Connectome Changes to Dementia and Targeted Gene Expression in Alzheimer's DiseaseSamar S M Elsheikh, Emile R Chimusa, , et al.African Journal of Laboratory Medicine|June 10, 2026
Burden of rare genetic variants in genes associated with cancer among Malawian cervical cancer patientsSamuel D Gwayi, Tamiwe Tomoka, Emile R Chimusa, et al.Omics : a Journal of Integrative Biology|January 12, 2017
A Genomic and Protein-Protein Interaction Analyses of Nonsyndromic Hearing Impairment in Cameroon Using Targeted Genomic Enrichment and Massively Parallel SequencingKamogelo Lebeko, Noluthando Manyisa, Emile R Chimusa, et al.Journal of Personalized Medicine|April 27, 2026
Genetic Variation in CYP2B6, UGT1A4 and Sulfotransferases Is Associated with Disease-Free Survival in South African Breast Cancer Patients Treated with TamoxifenBianca Kruger, Emile R Chimusa, Aron B Abera, et al.Briefings in Functional Genomics|December 24, 2019
A broad survey of DNA sequence data simulation toolsShatha Alosaimi, Armand Bandiang, Noelle van Biljon, et al.Plos One|October 6, 2022
A whole genome sequencing approach to anterior cruciate ligament rupture-a twin study in two unrelated familiesDaneil Feldmann, Christian D Bope, Jon Patricios, et al.Briefings in Bioinformatics|July 17, 2018
A comprehensive survey of models for dissecting local ancestry deconvolution in human genomeEphifania Geza, Jacquiline Mugo, Nicola J Mulder, et al.Pageof 8