Wonkam A - Search Results

1

Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden.

Adadey SM, Wonkam-Tingang E, Twumasi Aboagye E, Nayo-Gyan DW, Boatemaa Ansong M, Quaye O, Awandare GA, Wonkam A. Adadey SM, et al. Among authors: wonkam a, wonkam tingang e. Life (Basel). 2020 Oct 28;10(11):258. doi: 10.3390/life10110258. Life (Basel). 2020. PMID: 33126609 Free PMC article. Review.

2

Public Health Burden of Hearing Impairment and the Promise of Genomics and Environmental Research: A Case Study in Ghana, Africa.

Adadey SM, Awandare G, Amedofu GK, Wonkam A. Adadey SM, et al. Among authors: wonkam a. OMICS. 2017 Nov;21(11):638-646. doi: 10.1089/omi.2017.0145. OMICS. 2017. PMID: 29140768 Free PMC article. Review.

3

Genomics and Epigenomics of Congenital Heart Defects: Expert Review and Lessons Learned in Africa.

Thomford NE, Dzobo K, Yao NA, Chimusa E, Evans J, Okai E, Kruszka P, Muenke M, Awandare G, Wonkam A, Dandara C. Thomford NE, et al. Among authors: wonkam a. OMICS. 2018 May;22(5):301-321. doi: 10.1089/omi.2018.0033. OMICS. 2018. PMID: 29762087 Free PMC article. Review.

4

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

Adadey SM, Manyisa N, Mnika K, de Kock C, Nembaware V, Quaye O, Amedofu GK, Awandare GA, Wonkam A. Adadey SM, et al. Among authors: wonkam a. Front Genet. 2019 Sep 18;10:841. doi: 10.3389/fgene.2019.00841. eCollection 2019. Front Genet. 2019. PMID: 31620164 Free PMC article.

5

GJB2 and GJB6 Mutations in Hereditary Recessive Non-Syndromic Hearing Impairment in Cameroon.

Tingang Wonkam E, Chimusa E, Noubiap JJ, Adadey SM, F Fokouo JV, Wonkam A. Tingang Wonkam E, et al. Among authors: wonkam a. Genes (Basel). 2019 Oct 25;10(11):844. doi: 10.3390/genes10110844. Genes (Basel). 2019. PMID: 31731535 Free PMC article.

6

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

Hotchkiss J, Manyisa N, Adadey SM, Oluwole OG, Wonkam E, Mnika K, Yalcouye A, Nembaware V, Haendel M, Vasilevsky N, Mulder NJ, Jupp S, Wonkam A, Mazandu GK. Hotchkiss J, et al. Among authors: wonkam e, wonkam a. Genes (Basel). 2019 Nov 21;10(12):960. doi: 10.3390/genes10120960. Genes (Basel). 2019. PMID: 31766582 Free PMC article.

7

Enhancing Genetic Medicine: Rapid and Cost-Effective Molecular Diagnosis for a GJB2 Founder Mutation for Hearing Impairment in Ghana.

Adadey SM, Tingang Wonkam E, Twumasi Aboagye E, Quansah D, Asante-Poku A, Quaye O, Amedofu GK, Awandare GA, Wonkam A. Adadey SM, et al. Among authors: wonkam a. Genes (Basel). 2020 Jan 27;11(2):132. doi: 10.3390/genes11020132. Genes (Basel). 2020. PMID: 32012697 Free PMC article.

8

Cascade Testing for Fragile X Syndrome in a Rural Setting in Cameroon (Sub-Saharan Africa).

Kengne Kamga K, Nguefack S, Minka K, Wonkam Tingang E, Esterhuizen A, Nchangwi Munung S, De Vries J, Wonkam A. Kengne Kamga K, et al. Among authors: wonkam a, wonkam tingang e. Genes (Basel). 2020 Jan 28;11(2):136. doi: 10.3390/genes11020136. Genes (Basel). 2020. PMID: 32012997 Free PMC article.

9

Hearing Impairment Overview in Africa: the Case of Cameroon.

Wonkam Tingang E, Noubiap JJ, F Fokouo JV, Oluwole OG, Nguefack S, Chimusa ER, Wonkam A. Wonkam Tingang E, et al. Among authors: wonkam a. Genes (Basel). 2020 Feb 22;11(2):233. doi: 10.3390/genes11020233. Genes (Basel). 2020. PMID: 32098311 Free PMC article. Review.

10

GJB4 and GJC3 variants in non-syndromic hearing impairment in Ghana.

Adadey SM, Esoh KK, Quaye O, Amedofu GK, Awandare GA, Wonkam A. Adadey SM, et al. Among authors: wonkam a. Exp Biol Med (Maywood). 2020 Sep;245(15):1355-1367. doi: 10.1177/1535370220931035. Epub 2020 Jun 11. Exp Biol Med (Maywood). 2020. PMID: 32524838 Free PMC article.

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