Poster Presentations

Poster Board Submission No. Presenting Author Title
P01 4 Kimberly Coetzer Advancing Gene Function and Disease Mechanism Insight Through a Containerized Multi-Omics Integration Tool
P02 7 Leticia Camargo Tavares Rare pathogenic variants in G-protein coupled receptor genes involved in gut-to-host communication are associated with cardiovascular disease risk
P03 8 Kamal Kishor Identification of anti-TB therapy induced ADRs genetic markers using In-Silico approaches
P04 9 Sarmistha Adhikari Molecular Heterogeneity of Aplastic Anaemia in Eastern Region of India: Are Telomeres the Explanations?
P05 10 Oluwafemi Oluwole COMPUTATIONAL PHARMACOLOGY AND MOLECULAR DOCKING STUDIES OF SMALL PEPTIDE FOR PLAUSIBLE ANTI-AGING PROPERTIES
P06 11 Sathiya Maran Decoding the Pathogenic Impact of MYH Gene Variants: Insights into Congenital Heart Defects Through Integrative Computational Analysis
P07 12 Paolo Gasparini Drug Repurposing for Rare Diseases: An Effective Clinical Trial for White-Sutton Syndrome
P08 16 Carola Oelofse Characterisation of the complex TB pharmacogenomic landscape in Africa using bioinformatic tools
P09 18 Weiming Li Tissue Regeneration and Functional Recovery of the Tail and Spinal Cord in Amputated Larval Lamprey
P10 19 Lusanda Madula Computational Workflow to Identify Pathogenic Variants for Parkinson’s Disease Using the NeuroBooster Array
P11 20 Dayna Croock Mitochondrial DNA Imputation in Southern Africa: A Study Investigating Accuracy and Reliability.
P12 23 Christopher Kintu Polygenic Prediction of estimated Glomerular Filtration Rate in East Africa
P13 27 Giovanna Giudicelli Identification of Individuals of African Ancestry Affected by G6PD Deficiency in the 1000 Genomes Database
P14 32 Ayoade Desmond Babalola Glucose-6-Phosphate Dehydrogenase (G6PD) Evaluation of Ontologies and Mechanisms: A Systems Biology Approach
P15 33 Ayoade Desmond Babalola Glucose-6-Phosphate Dehydrogenase Possible Modifying Roles in Cancer and Neurodegenerative Diseases: A Bioinformatic Approach
P16 34 Vadim Stepanov Y-chromosomal haplogroup N1a2b: phylogeny and the age of sublineages in the peoples of Siberia based on whole-genome sequencing and median networks of YSTR haplotypes
P17 39 Linda Lillian Fine-Mapping, Replication and Causal Inference of Genetic Loci Associated with Major Depressive Disorder Among Participants in the Uganda Genome Resource.
P18 40 Cristian Rubiano Turner Syndrome Due to Unbalanced Translocation Between X And Chromosome 21: Language Dyspraxia as a Cardinal Criterion
P19 41 Citra Mattar In-vivo Base Editing of Human Haematopoietic Stem Cells carrying IVS1-5G>C mutation in a Patient-derived Humanized Mouse Model of ß-Thalassemia Major
P20 43 Terisha Ghazi Fusaric acid induces hepatic global m6A RNA methylation and differential expression of m6A regulatory genes in vivo – a pilot study
P21 44 Erin Kinghorn Investigating the Ancestral Origin of Amyotrophic Lateral Sclerosis Pathogenic Variants in South Africa
P22 51 Thina Gcobo NPHS2 p.V260E In Steroid Resistant Nephrotic Syndrome in South African Paediatric Patients
P23 56 Sesethu Ntanjana Title: TITLE: Title: Approach to Congenital Disorders: Referral Pathways for Genetic Services in The Eastern Cape
P24 59 Migael Mouton Drug-Drug Interactions: Evaluating Effects on Tamoxifen Efficacy.
P25 60 Faridah Nassolo Time-series Models for HIV-1 Gag Gene Mutation Frequencies from Uganda: A Machine Learning Approach
P26 62 Cassidy Gray How Mitochondrial Dysfunction Affects the Prevalence and Disease Progression of Alzheimer’s Disease, OCD And Schizophrenia in The Cape Admixed Population
P27 64 Allyson Andrea Abram Exploring The Genome for Discoveries on The Role of GPCR Receptors in Autism Spectrum Disorder (ASD)
P28 69 Oumou Maiga Causal relationship between COVID-19 and renal function in Afro-descendant populations: A bidirectional Mendelian randomization study
P29 70 Giuseppe Novelli MDPL Syndrome: human dermal fibroblasts as a reservoir providing insights into pathogenic mechanisms
P30 77 Big Charles Bifu Wa Bifu Is the whole genome sequencing the best way for reducing the diagnostic odessey in Affrica?
P31 82 Yentl Lamprecht Bioinformatics Pipeline for Whole Genome Sequencing Data Generated to Investigate Genetic Variants Associated With COVID-19 Vaccination Status
P32 83 Nomfundo Sikhakhane Three Pathways of Complement Activation: Genetic Variants Associated with Extreme SARS-CoV-2 Infection Outcomes
P33 84 Thilona Arumugam Exploring the Human Leukocyte Antigen (HLA) Landscape in TB and HIV-Affected South African Populations
P34 85 Pavithra Sampath Latent Tuberculosis: Understanding The Prevalence in A High Burden Area and Evaluation of Detection Assays
P35 86 Fekadu Urgessa Fita MiRNA for predicting bad molecular response among CML patients
P36 87 Anmol Gokul The role of African diversity within the OAS-1 gene in HIV infection
P37 88 Ntombikhona Maphumulo Assessing the Prevalence of high-burden STIs among Young South African women
P38 90 Edward Tobias New Globally Accessible Genomics Education-Related Resources from the Univ. of Glasgow (UK), the HUGO and ESHG Education Committees and the Apogee E-Textbook and ECMGG-Examination Committees.
P39 91 Mohammed Farahat Building an African Pangenome Reference Graph
P40 92 Peace Bassey Osim Topic Genetic Analysis of TERT Promoter Mutations and Their Role in Hepatocellular Carcinoma Progression in Cross River State, Nigeria.
P41 93 Rahaba Marima TUG1 and MALAT 1 as active role players in prostate cancer

Poster Presentations

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