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Life (Basel, Switzerland)|October 31, 2020
Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global BurdenSamuel Mawuli Adadey, Edmond Wonkam-Tingang, Elvis Twumasi Aboagye, et al.
Diabetology & Metabolic Syndrome|June 19, 2026
Diagnostic utility of fasting versus non-fasting blood glucose: contextualising testing strategies-a narrative reviewRichmond Owusu Ateko, Andrew Decker, Eric N Y Nyarko, et al.
Frontiers in Genetics|August 29, 2022
Cell-based analysis of <i>CLIC5A</i> and <i>SLC12A2</i> variants associated with hearing impairment in two African familiesSamuel Mawuli Adadey, Edmond Wonkam-Tingang, Leonardo Alves de Souza Rios, et al.
BMC Medical Genomics|November 11, 2022
A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in GhanaSamuel Mawuli Adadey, Elvis Twumasi Aboagye, Kevin Esoh, et al.
Molecular Genetics & Genomic Medicine|June 14, 2022
A monoallelic variant in EYA1 is associated with Branchio-Otic syndrome in a Malian familyAbdoulaye Yalcouyé, Oumou Traoré, Salimata Diarra, et al.
Genes|November 27, 2019
The Hearing Impairment Ontology: A Tool for Unifying Hearing Impairment Knowledge to Enhance Collaborative ResearchJade Hotchkiss, Noluthando Manyisa, Samuel Mawuli Adadey, et al.
Frontiers in Genetics|March 4, 2022
Genetic Analysis of TB Susceptibility Variants in Ghana Reveals Candidate Protective Loci in <i>SORBS2</i> and <i>SCL11A1</i> GenesAdwoa Asante-Poku, Portia Morgan, Stephen Osei-Wusu, et al.
International Journal of Molecular Sciences|April 17, 2025
Bi-Allelic <i>MARVELD2</i> Variant Identified with Exome Sequencing in a Consanguineous Multiplex Ghanaian Family Segregating Non-Syndromic Hearing LossElvis Twumasi Aboagye, Samuel Mawuli Adadey, Leonardo Alves de Souza Rios, et al.
Biology|May 28, 2022
<i>GJB2</i> Is a Major Cause of Non-Syndromic Hearing Impairment in SenegalYacouba Dia, Samuel Mawuli Adadey, Jean Pascal Demba Diop, et al.
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