Noluthando R. Manyisa

University Of Cape Town
Cape Town, WC, South Africa

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 12 publications

Genetic susceptibility to aminoglycoside cochleotoxicity in South African multidrug-resistant and rifampicin-resistant tuberculosis patients.

Genetic susceptibility to aminoglycoside cochleotoxicity in South African multidrug-resistant and rifampicin-resistant tuberculosis patients.

Journal: The South African journal of communication disorders = Die Suid-Afrikaanse tydskrif vir Kommunikasieafwykings

Published: February 06, 2026

The Diverse Genetic Landscape of Hearing Impairment in South African Families.

The Diverse Genetic Landscape of Hearing Impairment in South African Families.

Journal: Clinical genetics

Published: January 22, 2025

Craniofacial, dental, and molecular features of Pyle disease in a South African child.

Craniofacial, dental, and molecular features of Pyle disease in a South African child.

Journal: BDJ open

Published: May 18, 2022

Cell-based analysis of CLIC5A and SLC12A2 variants associated with hearing impairment in two African families.

Cell-based analysis of CLIC5A and SLC12A2 variants associated with hearing impairment in two African families.

Journal: Frontiers in genetics

Published: April 20, 2022

Hearing Impairment in South Africa and the Lessons Learned for Planetary Health Genomics: A Systematic Review.

Hearing Impairment in South Africa and the Lessons Learned for Planetary Health Genomics: A Systematic Review.

Journal: Omics : a journal of integrative biology

Published: January 18, 2022

Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes.

Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes.

Journal: Communications biology

Published: January 04, 2022

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

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

Journal: Genes

Published: October 05, 2021

Whole exome sequencing identifies rare coding variants in novel human-mouse ortholog genes in African individuals diagnosed with non-syndromic hearing impairment.

Whole exome sequencing identifies rare coding variants in novel human-mouse ortholog genes in African individuals diagnosed with non-syndromic hearing impairment.

Journal: Experimental biology and medicine (Maywood, N.J.)

Published: September 30, 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 Cameroon.

Whole exome sequencing reveals pathogenic variants in MYO3A, MYO15A and COL9A3 and differential frequencies in ancestral alleles in hearing impairment genes among individuals from Cameroon.

Journal: Human molecular genetics

Published: June 03, 2020

The Hearing Impairment Ontology: A Tool for Unifying Hearing Impairment Knowledge to Enhance Collaborative Research.

The Hearing Impairment Ontology: A Tool for Unifying Hearing Impairment Knowledge to Enhance Collaborative Research.

Journal: Genes

Published: September 18, 2019

GJB2 and GJB6 Mutations in Non-Syndromic Childhood Hearing Impairment in Ghana.

GJB2 and GJB6 Mutations in Non-Syndromic Childhood Hearing Impairment in Ghana.

Journal: Frontiers in genetics

Published: February 28, 2019

A Genomic and Protein-Protein Interaction Analyses of Nonsyndromic Hearing Impairment in Cameroon Using Targeted Genomic Enrichment and Massively Parallel Sequencing.

A Genomic and Protein-Protein Interaction Analyses of Nonsyndromic Hearing Impairment in Cameroon Using Targeted Genomic Enrichment and Massively Parallel Sequencing.

Journal: Omics : a journal of integrative biology

Published: January 12, 2017

Showing 1-12 of 12

Last Updated: 09/26/2026