Elvis Twumasi Aboagye

5PUBLICATIONS
39CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)NeurogeneticsTe hauora me te oranga ā-whaea, ā-pēpi o te Māori (Māori mothers and babies health and wellbeing)Gene mapping
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Publications (5)

|Jan 10, 2026
Genetics of Waardenburg Syndrome in Africa: A Systematic Review.

Elvis Twumasi Aboagye, Ramses Peigou Wonkam, Carmen de Kock

|Apr 17, 2025
Bi-Allelic MARVELD2 Variant Identified with Exome Sequencing in a Consanguineous Multiplex Ghanaian Family Segregating Non-Syndromic Hearing Loss.

Elvis Twumasi Aboagye, Samuel Mawuli Adadey, Leonardo Alves de Souza Rios

|Mar 28, 2025
Etiologies of Early-Onset Hearing Impairment in Rwanda.

Esther Uwibambe, Leon Mutesa, Charles Muhizi

|Feb 22, 2023
Variants of LRP2, encoding a multifunctional cell-surface endocytic receptor, associated with hearing loss and retinal dystrophy.

Rabia Faridi, Rizwan Yousaf, Shoujun Gu

|Oct 31, 2020
Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden.

Samuel Mawuli Adadey, Edmond Wonkam-Tingang, Elvis Twumasi Aboagye

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Frequent Collaborators

4 joint publications

Samuel Mawuli Adadey

4 joint publications

Ambroise Wonkam

3 joint publications

Carmen DeKock

2 joint publications

Isabelle Schrauwen