Ambroise Wonkam

54PUBLICATIONS
142CO-AUTHORS
Infant and child healthEpigenetics (incl. genome methylation and epigenomics)MultimorbidityEarly English languagesGeneral practice
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Publications (54)

|Mar 25, 2026
Exome sequencing identifies known and candidate genes in hearing impairment in Cameroon.

Ambroise Wonkam, Edmond Wonkam-Tingang, Abdoulaye Yalcouyé

|Feb 20, 2026
The Sickle Africa Data Coordinating Centre (SADaCC): a data science hub for interdisciplinary sickle cell disease research and training.

Ambroise Wonkam, Nchangwi Syntia Munung, Mario Jonas

|May 15, 2025
The Diverse Genetic Landscape of Hearing Impairment in South African Families.

Thashi Bharadwaj, Anushree Acharya, Noluthando Rearabetswe Manyisa

|May 07, 2025
Sickle Cell Disease in Africa: SickleInAfrica Registry in Ghana, Nigeria and Tanzania.

Jack Morrice, Wilson Mupfururirwa, Reuben I Chianumba

|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

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