Wonkam A - Search Results

1

GJB2 Is a Major Cause of Non-Syndromic Hearing Impairment in Senegal.

Dia Y, Adadey SM, Diop JPD, Aboagye ET, Ba SA, De Kock C, Ly CAT, Oluwale OG, Sène ARG, Sarr PD, Diallo BK, Diallo RN, Wonkam A. Dia Y, et al. Among authors: wonkam a. Biology (Basel). 2022 May 23;11(5):795. doi: 10.3390/biology11050795. Biology (Basel). 2022. PMID: 35625523 Free PMC article.

2

In search of genetic markers for nonsyndromic deafness in Africa: a study in Cameroonians and Black South Africans with the GJB6 and GJA1 candidate genes.

Bosch J, Lebeko K, Nziale JJ, Dandara C, Makubalo N, Wonkam A. Bosch J, et al. Among authors: wonkam a. OMICS. 2014 Jul;18(7):481-5. doi: 10.1089/omi.2013.0166. Epub 2014 May 2. OMICS. 2014. PMID: 24785695 Free PMC article.

3

Sequencing of GJB2 in Cameroonians and Black South Africans and comparison to 1000 Genomes Project Data Support Need to Revise Strategy for Discovery of Nonsyndromic Deafness Genes in Africans.

Bosch J, Noubiap JJ, Dandara C, Makubalo N, Wright G, Entfellner JB, Tiffin N, Wonkam A. Bosch J, et al. Among authors: wonkam a. OMICS. 2014 Nov;18(11):705-10. doi: 10.1089/omi.2014.0063. Epub 2014 Aug 27. OMICS. 2014. PMID: 25162826 Free PMC article.

4

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.

5

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.

6

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.

7

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.

8

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.

9

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.

10

Whole exome sequencing identifies rare coding variants in novel human-mouse ortholog genes in African individuals diagnosed with non-syndromic hearing impairment.

Oluwole OG, Esoh KK, Wonkam-Tingang E, Manyisa N, Noubiap JJ, Chimusa ER, Wonkam A. Oluwole OG, et al. Among authors: wonkam a, wonkam tingang e. Exp Biol Med (Maywood). 2021 Jan;246(2):197-206. doi: 10.1177/1535370220960388. Epub 2020 Sep 30. Exp Biol Med (Maywood). 2021. PMID: 32996353 Free PMC article.

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