Carmen DeKock

4PUBLICATIONS
16CO-AUTHORS
People with disabilityGene 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)
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Publications (4)

|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

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